The DOI matches its Crossref record; 112 of the 113 references it cites were found in a registry or an index; 126 of the 224 sources its claims cite were checked for support.
Emerging insights into hypothalamic‐pituitary‐gonadal axis regulation and interaction with stress signalling
Open accessAbstract
Reproduction and fertility are regulated via hormones of the hypothalamic-pituitary-gonadal (HPG) axis. Control of this reproductive axis occurs at all levels, including the brain and pituitary, and allows for the promotion or inhibition of gonadal sex steroid secretion and function. In addition to guiding proper gonadal development and function, gonadal sex steroids also act in negative- and positive-feedback loops to regulate reproductive circuitry in the brain, including kisspeptin neurones, thereby modulating overall HPG axis status. Additional regulation is also provided by sex steroids made within the brain, including neuroprogestins. Furthermore, because reproduction and survival need to be coordinated and balanced, the HPG axis is able to modulate (and be modulated by) stress hormone signalling, including cortiscosterone, from the hypothalamic-pituitary-adrenal (HPA) axis. This review covers recent data related to the neural, hormonal and stress regulation of the HPG axis and emerging interactions between the HPG and HPA axes, focusing on actions at the level of the brain and pituitary.
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Claims the paper makes
126 of 224 cited sources checked · 52 supported · 3 flagged · accuracy not yet measured
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“Additionally in the last decade, a new pathway of ALLO action through membrane P4 receptors (mPR α and β) was discovered allowing for rapid responses65.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 5. Neuroprogesterone Control of the Reproductive Axis
What the sources say
- Disputedcites [65] sourceExperimental — accuracy not yet measured
In “Is the LH Surge Stimulated by Progesterone or a Metabolite?” (page not specified), the paper says progesterone acted through mPRα and mPRβ, while allopregnanolone did not affect GnRH release in that study. It describes allopregnanolone as acting primarily at GABAA receptors, not as having a discovered pathway through those membrane progesterone receptors. (LLM, conf=0.88)
Checked by a reasoning model — may be wrong.
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Disputed
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Subsequent studies from numerous species have now provided a wealth of information supporting the model that hypothalamic-derived kisspeptin directly activates GnRH neurons via kisspeptin receptor (Kiss1R) to stimulate the reproductive axis (reviewed in 1,2).”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Not checked — no full text of the sourcecites [1] source
- Supportedcites [2] source
Section 2.2 states that hypothalamic kisspeptin directly activates GnRH neurons to stimulate the reproductive axis. The same section reports that GnRH neurons express Kiss1R and that kisspeptin’s effects on the GnRH axis are mediated by Kiss1R. (LLM, conf=0.95)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesThe cited sources support only part of this claim — read each source’s verdict below.
In the paper
“RFRP-3 neurons are found exclusively in the dorsal-medial nucleus of the hypothalamus (DMN) of rodents7,8”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Not checked — no full text of the sourcecites [7] source
- Partly supportedcites [8] sourceExperimental — accuracy not yet measured
The Introduction says that, in rodents, RFRP-3-producing neurons are localized exclusively within and immediately adjacent to the hypothalamic DMN. The claim omits the neurons immediately adjacent to the DMN, so its 'exclusively in' wording is too narrow. (LLM, conf=0.88)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesThe sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“In contrast to kisspeptin, another neuropeptide, RFamide-related peptide-3 (RFRP-3), has potent inhibitory actions on LH secretion in many mammalian species6–8.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Not checked — no full text of the sourcecites [6] source
- Not checked — no full text of the sourcecites [7] source
- Supportedcites [8] source
The Introduction says exogenous RFRP-3 potently inhibits the reproductive axis and that RFRP-3 treatment suppresses LH secretion. The Conclusion likewise states that exogenous RFRP-3 suppresses LH secretion. The reported stimulatory effects in two hamster species do not conflict with the claim's qualification of 'many' rather than all mammals. (LLM, conf=0.91)
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesThe cited sources support only part of this claim — read each source’s verdict below.
In the paper
“The proximal 140bp consist of tandem copies of DNA binding motifs for the early growth response protein 1 (Egr-1) and steroidogenic factor 1 (SF-1) transcription factors22,23.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
- Partly supportedcites [22] sourceExperimental — accuracy not yet measured
The Results (page unavailable) describe a proximal 142-bp LHβ promoter fragment with an SF-1 element at −120 and an Egr-1 motif at −45, supporting the approximate length and presence of both motifs. The paper does not describe these motifs as tandem copies; it also identifies a Ptx1 site in the fragment. (LLM, conf=0.86)
- Partly supportedcites [23] sourceExperimental — accuracy not yet measured
The section “A Consensus SF-1 Binding Site Resides within the 5′ Flanking Regions” reports an SF-1 binding sequence in LHβ promoters, and its EMSA results establish SF-1 binding in the bovine promoter (page not provided). Our copy does not report Egr-1 motifs, tandem copies, or a proximal 140-bp region, so those parts of the attributed claim are unsupported. (LLM, conf=0.86)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“It is well established that GnRH induces the release of stored LH secretory granules into the systemic circulation14,15.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
- Partly supportedcites [14] sourceExperimental — accuracy not yet measured
The section “Hormonal Signals During the Menstrual Cycle” (p. 17) reports that injections of LHRH (GnRH) can induce LH pulses measured in plasma. The cited paper does not establish that the released LH comes from stored secretory granules; that mechanism is the unsupported part of the claim. (LLM, conf=0.86)
- Not checked — no full text of the sourcecites [15] source
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
The sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Early experiments determined that exogenous kisspeptin treatment of rodents and other species, including humans, robustly increases circulating LH and FSH levels (reviewed in 1,2).”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Not checked — no full text of the sourcecites [1] source
- Supportedcites [2] source
Section 2.2 states that kisspeptin treatment potently stimulates LH and FSH secretion in mice, rats, hamsters, sheep, primates (including humans), and other mammals. This directly supports the citing sentence’s claim about rodents, humans, and other species. (LLM, conf=0.94)
Strength:boosted· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesThe sources with a verdict support this claim; the rest weren’t checked yet, have no full text we could read, or their verdicts aren’t rated yet.
In the paper
“Data from transgenic mice suggest that the GSE and the Pitx1 elements are required for GnRH induced LHβ gene promoter activity23,25.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
- Supportedcites [23] source
In “The GSE Is Essential for LHβ Promoter Activity in Transgenic Mice” (page unavailable), mutation of the GSE markedly reduced promoter activity, and the authors report that a physiological rise in GnRH could not compensate for its loss. This supports the GSE portion of the sentence, which carries two citations. (LLM, conf=0.91)
- Not checked — no full text of the sourcecites [25] source
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“In contrast, kisspeptin neurons in the AVPV/PeN are thought to be involved in mediating E2-positive feedback which triggers the preovulatory LH surge in females5.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Supportedcites [5] source
In “Putting the Pieces Together: Current Model of the Circadian-Regulated Preovulatory LH Surge in Rodents,” the paper says AVPV/PeN Kiss1 neurons are thought to be key players in positive feedback and integrate E2 signals essential for the LH surge. The Introduction explains that E2 positive feedback leads to the preovulatory LH surge in females. The claim preserves the paper’s tentative wording. (LLM, conf=0.94)
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Both POMC and NPY neurons express ERα protein, although at strikingly different levels54,61.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [54] sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) explicitly says NPY/AgRP neurons express ERα transcript and protein. It also discusses ERα deletion in POMC neurons, but does not compare ERα protein levels between the two populations or establish that the difference is striking. (LLM, conf=0.85)
- Not checked — no full text of the sourcecites [61] source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passes- Partly supported
- It may state two separate claims as one. 60
- Probably not a substantial claim. 5
At least one cited source doesn’t support this claim or points to a different paper, and none confirmed it — see the verdicts below.
In the paper
“Furthermore, NPY can excite and inhibit GnRH neurons through the Y1 and Y4 receptors, respectively, and AgRP, an endogenous agonist to MC4 receptors, can also excite and inhibit GnRH neurons33,60.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Not checked — no full text of the sourcecites [33] source
- Disputedcites [60] sourceExperimental — accuracy not yet measured
The Results and Discussion (page unavailable) report that NPY inhibits GnRH-1 neuronal activity through Y1 receptors—the opposite of the claim that Y1 mediates excitation. The paper discusses context-dependent stimulation of GnRH-1 secretion, but the passages do not link it to Y1; they also do not substantiate the Y4 or AgRP/MC4 assertions. (LLM, conf=0.88)
Checked by a reasoning model — may be wrong.
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
Some cited sources support this claim and some don’t — read each source’s verdict below.
In the paper
“Reduction of the seminiferous tubules diameter as well as reduced T production were also observed by Borges et al107,108.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6c. Betamethasone Effects on the HPG Axis in Development and Adulthood
What the sources say
- Disputedcites [107] sourceExperimental — accuracy not yet measured
In §3.1 (page unavailable), the paper reports no difference in testicular morphometric measures between control and betamethasone-treated rats, contrary to the claimed reduction in seminiferous tubule diameter. In §4 (page unavailable), it says testosterone levels were unaltered, although Leydig-cell volume and a measure of Leydig-cell function decreased; it does not report reduced testosterone production as an observed result. (LLM, conf=0.88)
Checked by a reasoning model — may be wrong.
- Partly supportedcites [108] sourceExperimental — accuracy not yet measured
The Results report reduced seminiferous tubule diameter at both ages and lower serum testosterone at PND45 after prenatal betamethasone exposure. They report no testosterone difference at PND110. The paper measured circulating testosterone, not testosterone production directly, so the claim omits an important age qualifier and overstates what was measured. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Disputed
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Importantly, GnRH neurons do not express estrogen receptor α (ERα) or the androgen receptor (AR), the receptors that mediate sex steroid feedback, indicating that other sex steroid-sensitive circuits “upstream” of GnRH neurons receive and relay sex steroid feedback signals to GnRH cells3.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Partly supportedcites [3] sourceExperimental — accuracy not yet measured
The ‘Mechanism of estrogen positive feedback to GnRH neurons’ section states that GnRH neurons lack ERα and that ERα-expressing neurons mediate indirect estrogen feedback. It does not address whether GnRH neurons lack androgen receptors or whether upstream circuits relay androgen feedback. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Lim et al. showed that the gene encoding LHβ, Lhb, is occupied by histone deacetylases (HDACs) in αT3-1 cells resulting in transcriptional silencing27.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
- Supportedcites [27] source
The Results report that ChIP detected multiple HDACs at the LHβ gene promoter in αT3-1 cells. They also report that untreated cells did not express LHβ, whereas HDAC inhibition or knockdown allowed its expression, supporting HDAC-mediated transcriptional repression. (LLM, conf=0.94)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Supporting this hypothesis, AVPV/PeN Kiss1 gene expression is greater in females than males (males do not show an LH surge), Kiss1 neurons in the AVPV/PeN express ERα and show increased neuronal activation exclusively during the LH surge, and Kiss1 knockout (KO) mice and Kiss1R KO mice do not exhibit an LH surge even with exogenous E2 treatment3,5.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Partly supportedcites [3] sourceExperimental — accuracy not yet measured
The “Neurochemical phenotypes of RP3V neurons” section describes a female-dominant distribution of AVPV/PVpo kisspeptin neurons, ERα expression, and c-Fos activation at the time of estrogen positive feedback. It also reports evidence that kisspeptin is required for the GnRH surge, but does not report that Kiss1 or Kiss1R knockout mice lack an LH surge despite exogenous E2 treatment. (LLM, conf=0.88)
- Partly supportedcites [5] sourceExperimental — accuracy not yet measured
In “The kisspeptin system: function and neuroanatomy” (page unavailable), the paper reports higher AVPV/PeN Kiss1 expression in females, ERα expression and surge-time activation in these neurons, and absent LH surges in Kiss1- and Kiss1R-null mice after E2 treatment. But it also reports a conflicting study in which E2-treated Kiss1R-null mice displayed small LH surges, so the categorical knockout claim omits an important qualification. (LLM, conf=0.90)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“may be involved in influencing the onset of puberty, the onset of cyclicity in seasonally reproductive mammals, and the suppression of GnRH-induced release of gonadotropins9,10.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Partly supportedcites [9] sourceExperimental — accuracy not yet measured
The Discussion (pp. 8–9) proposes that RFRP helps control seasonal breeding in ewes, and p. 2 reports that RFRP-3 inhibits gonadotropin secretion. The passages do not address puberty onset or establish suppression specifically of GnRH-induced gonadotropin release; searches for those terms found no such result. (LLM, conf=0.87)
- Not checked — no full text of the sourcecites [10] source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“RFRP-3 has been functionally shown to inhibit the electrical firing of some GnRH and ARC kisspeptin neurons11–13 suggesting that RFRP-3 may inhibit the reproductive axis, in part, by signaling to kisspeptin and/or GnRH populations.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Partly supportedcites [11] sourceExperimental — accuracy not yet measured
The Introduction reports that GnIH hyperpolarizes GnRH neurons, and the Results identify RFRP-3 as its mammalian analog. The Results show RFRP-3 reducing firing in arcuate POMC neurons, not ARC kisspeptin neurons; the paper does not report RFRP-3 inhibiting kisspeptin-neuron firing or signaling to that population. Page numbers were not available in our copy. (LLM, conf=0.84)
- Not checked — no full text of the sourcecites [12] source
- Not checked — no full text of the sourcecites [13] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Kisspeptin neurons in the ARC are likely involved in promoting pulsatile GnRH and LH secretion and responding to sex steroid hormone negative feedback1,2.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
What the sources say
- Not checked — no full text of the sourcecites [1] source
- Partly supportedcites [2] sourceExperimental — accuracy not yet measured
Section 2.3 says ARC Kiss1 neurons likely mediate sex-steroid negative feedback and links their activity to GnRH and LH secretion. But Section 4.3 says that although kisspeptin pulses coincide with GnRH pulses, their anatomical source was not determined; the paper does not establish that ARC neurons promote pulsatile GnRH and LH release. Page numbers are unavailable in our copy. (LLM, conf=0.86)
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
Every source the paper cites for this claim was checked and supports it.
In the paper
“Both 5α-reductase and 3α-HSD are expressed in the cortex, hippocampus, and amygdala62, supporting ALLO’s potential ability to modulate behavior.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 5. Neuroprogesterone Control of the Reproductive Axis
What the sources say
- Supportedcites [62] source
The Introduction (page not specified) states that 5α-reductase and 3α-HSD are co-localized in the cortex, hippocampus, and basolateral amygdala. It also describes Allo’s action at GABA_A receptors and its potential role in regulating emotional behaviour. (LLM, conf=0.94)
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“The low expression of ERα and ERβ in RFRP-3 neurons suggests that membrane-initiated estrogen signaling may be key to the regulation of these neurons, as has recently been characterized in ARC NPY neurons54.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Supportedcites [54] source
The Abstract reports rapid membrane-initiated estradiol signaling through Gq-mER and ERα in NPY/AgRP neurons, and the Discussion identifies these neurons as part of the arcuate nucleus (ARC). The suggestion that the same mechanism may regulate RFRP-3 neurons is the citing authors’ inference, not a finding attributed to this source. (LLM, conf=0.93)
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“E2 reduces RFRP-3 expression in the DMN of mice, although only ~20% of RFRP-3 neurons express detectable levels of ERα protein and no detectable ERβ53.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [53] sourceExperimental — accuracy not yet measured
Figure 1 (p. 4) shows that E2 reduced prepro-RFRP mRNA in the mouse dorsomedial nucleus. The receptor results (pp. 4–5) found detectable ERα in 18.7 ± 3.8% of RFRP neurons and no detectable ERβ. The paper measured precursor mRNA and identified neurons using RFRP-1 immunoreactivity; it did not specifically measure RFRP-3 expression or establish those receptor percentages for RFRP-3-identified neurons. (LLM, conf=0.86)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“E2 also modulates GABAergic tone of GABA neurons in the POA, and specific deletion of ERα in hypothalamic GABA neurons produces infertile female mice due to a failure to generate an LH surge and ovulation39.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [39] sourceExperimental — accuracy not yet measured
The Abstract and the results on Esr1 deletion report infertility and an absent estrogen-induced LH surge in female mice lacking ESR1 in GABAergic neurons. The Introduction links the preovulatory surge to ovulation, and the GABAergic-function discussion describes estradiol-modulated GABA transmission near GnRH neurons. However, the deletion targeted GABAergic neurons broadly, not specifically hypothalamic GABA neurons, and ovulation failure was not directly measured. (LLM, conf=0.86)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“α-MSH activation of the melanocortin 4 (MC4) receptor increases GnRH action potential firing while β-endorphin signaling through μ-opioid receptors inhibit GnRH excitability33,59.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Not checked — no full text of the sourcecites [33] source
- Partly supportedcites [59] sourceExperimental — accuracy not yet measured
In “Activation of melanocortin receptors increases GnRH neuron activity” (page not specified), the paper reports increased GnRH firing after treatment with MTII, an MC3/4 receptor agonist; it also reports MC4R expression in GnRH neurons. It does not establish that α-MSH acting specifically through MC4R caused the firing increase, and the passages found do not address β-endorphin inhibition through μ-opioid receptors (searched: endorphin, opioid). (LLM, conf=0.87)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“In females, ARC kisspeptin expression is suppressed through ERα-mediated, ERE-independent mechanisms or de-repressed through a hormone response element44,46.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [44] sourceExperimental — accuracy not yet measured
The Results and Discussion (page not provided) show that estradiol suppresses ARC Kiss1 expression in female mice through an ERα-mediated, ERE-independent mechanism. The Discussion notes that the mouse model may permit signaling through other hormone response elements, but it does not show that ARC kisspeptin expression is de-repressed through one. (LLM, conf=0.86)
- Not matchedcites [46]
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Elevated E2 levels preceding the surge of GnRH and LH activate SCN neurons to accelerate the downstream release of kisspeptin and simultaneously decrease the inhibition of GnRH secretion provided by RFRP-332,52.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [32] sourceExperimental — accuracy not yet measured
The Discussion (page not supplied) proposes that the SCN stimulates the kisspeptin system while suppressing RFRP-3-mediated negative feedback at the LH surge. It does not say that rising estradiol activates SCN neurons or that kisspeptin release accelerates; it describes estrogen-responsive cells as integrating estrogenic and SCN-derived cues. (LLM, conf=0.87)
- Partly supportedcites [52] sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) proposes that E2 permits SCN signals to activate Kiss1 neurons, which may then signal to GnRH neurons. It does not establish that rising E2 activates SCN neurons or accelerates kisspeptin release, and the passages do not address reduced RFRP-3 inhibition. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Both populations of kisspeptin neurons express ERα (with low ERβ expression) but respond differentially to E2 through ERE-dependent and ERE-independent mechanisms44,45.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [44] sourceExperimental — accuracy not yet measured
The Discussion identifies kisspeptin populations in the AVPV and ARC, and reports E2 regulation of ARC Kiss1 through an ERE-independent mechanism. It also says ERα is more highly expressed than ERβ in the ARC. The paper does not establish ERα and low ERβ expression in both kisspeptin populations or compare their E2 responses through these mechanisms; its study focuses on the ARC. Page numbers are unavailable in our copy. (LLM, conf=0.86)
- Partly supportedcites [45] sourceExperimental — accuracy not yet measured
The Abstract and Discussion report that E2 induces Kiss1 in the AVPV through an ERE-dependent ERα pathway but inhibits Kiss1 in the arcuate nucleus through an ERE-independent pathway. The Introduction says regulation in both regions requires ERα. The passages do not establish the claim that both populations have low ERβ expression (page numbers are unavailable in our copy). (LLM, conf=0.85)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Furthermore, activation of GPER by its selective ligand STX in mouse GnRH neurons controlled the expression and activity of cation channels involved in burst firing and membrane hyperpolarization42,43, indicating the E2 has multiple pathways and receptors to control GnRH neuronal excitability, gene expression, and peptide release.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [42] sourceExperimental — accuracy not yet measured
The Results section reports that STX increased Cav3.3 mRNA expression in mouse GnRH neurons, and the Discussion identifies STX as an agonist of a membrane estrogen receptor. The paper does not identify that receptor as GPER or show that STX changed channel activity or channels involved in membrane hyperpolarization. It links E2—not STX—to increased T-type current and excitability, and proposes a possible role in GnRH release. (LLM, conf=0.88)
- Partly supportedcites [43] sourceExperimental — accuracy not yet measured
The Abstract and ‘Estrogen upregulates K ATP channel function in GnRH neurons’ report that E2 enhances K ATP channel activity and hyperpolarization, affecting GnRH neuronal excitability and peptide release. But the paper does not establish activation by STX or GPER; it says the receptor mechanism is uncertain. It also reports that E2 did not increase Kir6.2 or SUR1 transcript expression. (LLM, conf=0.86)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Indeed, membrane-initiated signaling via ERβ activates a PLC-mediated signaling cascade leading to retrograde endocannabinoid signaling to reduce the frequency of presynaptic GABA release and spontaneous postsynaptic currents40.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [40] sourceExperimental — accuracy not yet measured
The Results and Figure 9 caption report that estradiol acting through ERβ engages retrograde 2-AG signaling, suppressing presynaptic GABA release and reducing postsynaptic-current frequency in GnRH neurons of metestrous mice. The Discussion describes membrane-associated signaling as a suggestion, while Figure 9 labels part of its proposed pathway putative; the paper does not establish that ERβ activates PLC. No page numbers are available in our copy. (LLM, conf=0.86)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Furthermore, both neurons express the Gq-mER, which disinhibits GABA and μ-opioid tone in POMC neurons and augments GABAergic tone in NPY neurons54.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Supportedcites [54] source
The Abstract describes Gq-mER signaling in POMC neurons as attenuating GABAB and μ-opioid receptor coupling to GIRK channels, thereby reducing their inhibitory effects. The Discussion reports that the Gq-mER-selective ligand STX enhances GABAB signaling in NPY/AgRP neurons and describes the receptor’s reciprocal effects in the two cell types. The paper calls Gq-mER in NPY/AgRP neurons putative, so the claim is best read as describing functional signaling rather than direct identification of the receptor. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“After ligand-dependent receptor activation, ER disassociates from molecular chaperones, dimerizes, and binds to coactivators or corepressors to initiate or suppress transcription34.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [34] sourceExperimental — accuracy not yet measured
The Introduction says that estradiol-bound intracellular ERs dimerize and recruit transcriptional machinery and cofactors to regulate gene expression. It does not say that ERs dissociate from molecular chaperones or specifically bind coactivators or corepressors to initiate or suppress transcription. No page number is available in our copy. (LLM, conf=0.86)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“These hypothalamic circuits collectively express the range of ER and employ both nuclear-initiated estrogen signaling (through estrogen response element (ERE)-dependent and ERE-independent pathways) and membrane-initiated estrogen signaling (through palmitoylated nuclear ER (α/β) and E2-responsive GPCR)34.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Partly supportedcites [34] sourceExperimental — accuracy not yet measured
The Introduction describes ERE-dependent and ERE-independent nuclear signaling, while Extranuclear ERα and ERβ Expression and Physiology of Membrane ERs describe membrane signaling in hypothalamic-related circuits. The Summary supports palmitoylated ERα/ERβ at membranes, but Novel ERs treats the E2-responsive GPCR candidates as uncertain rather than establishing that these circuits employ them. Page numbers are unavailable in our copy. (LLM, conf=0.84)
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Brain analyses revealed that CORT robustly suppressed the percentage of AVPV/PeN Kiss1 cells co-expressing cfos, as well as reduced the number of AVPV/PeN Kiss1-expressing cells, compared to expression in control brains84.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6a. Influence of Stress on Reproductive Status and Brain Circuitry
What the sources say
- Supportedcites [84] source
The Results report that Cort reduced the percentage of AVPV/PeN Kiss1 neurons coexpressing cfos from 65% in vehicle controls to 14%. The same section reports fewer detectable Kiss1 cells in Cort-treated females than in controls. (LLM, conf=0.95)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“All cholesterol-treated females showed a clear LH surge, whereas LH levels were undetectable in CORT-treated females84.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6a. Influence of Stress on Reproductive Status and Brain Circuitry
What the sources say
- Supportedcites [84] source
The Materials and Methods (LH surge induction) describe ovariectomized mice given an estradiol implant and either a corticosterone or cholesterol pellet. The Results report robust evening LH surges in all vehicle controls, but no surge and undetectable evening LH values in the corticosterone-treated females. (LLM, conf=0.95)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Anxiety and mood disorders are associated with HPA axis dysregulation and show large gender disparities, with women being more likely to experience these disorders86.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Partly supportedcites [86] sourceExperimental — accuracy not yet measured
The Introduction reports that many neuropsychiatric disorders involve HPA-axis dysregulation and sex differences in risk. It specifically says major depressive disorder is at least twice as common in women and is associated with altered HPA activity. The cited passages do not establish that women are also more likely to experience anxiety disorders. (LLM, conf=0.84)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“T treatment reduced CORT release in response to stressors when administered into brain areas that synapse onto the PVN86 as well as when DHT was administered just above the PVN88.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Supportedcites [86] source
Section 5.4 reports that testosterone implanted in the medial preoptic area or bed nucleus of the stria terminalis reduces the corticosterone (CORT) response to acute stress; it identifies these regions as providing input to the PVN or peri-PVN. The same section reports that DHT applied just above the PVN inhibits HPA-axis function. The supplied passages do not give page numbers. (LLM, conf=0.88)
- Supportedcites [88] source
The citation to this paper is attached to the DHT portion of the sentence. In the Results section, the paper reports that DHT pellets implanted directly above the PVN significantly reduced plasma corticosterone after restraint stress compared with vehicle controls. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Oxytocin has been shown to reduce HPA axis reactivity, and E2, via ERβ signaling, increases oxytocin mRNA levels (for review see 93).”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Supportedcites [93] source
The “Oxytocin Regulation of Hypothalamic–Pituitary–Adrenal Axis” section (page unavailable) reports that central oxytocin administration inhibits stress-related HPA axis reactivity in rodents. The “Estrogen Receptor β and Oxytocin Interactions” section (page unavailable) reports that estradiol increases oxytocin mRNA in wild-type mice but not ERβ-knockout mice, supporting the ERβ-mediated part of the claim. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Signaling through these 2 receptors yield opposing effects on HPA axis reactivity, with ERα increasing and ERβ inhibiting HPA axis reactivity (vide infra).”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Supportedcites [86] source
Section 5.3 reports that ERα agonist treatment increases the ACTH and corticosterone responses to stress, whereas ERβ agonist treatment decreases them. The review concludes that ERβ activation reduces the gain of the HPA-axis response to an acute stressor. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“While E2 increases HPA axis reactivity, T has been found to reduce HPA axis reactivity86.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Supportedcites [86] sourceExperimental — accuracy not yet measured
Section 5.4 reports that testosterone replacement reverses heightened stress-induced HPA responses after gonadectomy in male rats and describes an inhibitory effect of androgen treatment on HPA reactivity. Section 5.2 also links higher estradiol levels with stronger stress responses in female rats. These passages support the contrast in the citing sentence, particularly the testosterone claim to which the citation is attached. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Stress increases brain and plasma P4 and ALLO concentrations”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Partly supportedcites [63] sourceExperimental — accuracy not yet measured
The “Neuroactive Steroids and Stress: Background and Research in Laboratory Animals” section (page not provided) states that brain and plasma progesterone (P4) and allopregnanolone (ALLO) rise during stress in rodents. The claim omits that species qualification. In the human-stress section (page not provided), the review describes mixed responses and does not establish increases in both brain and plasma concentrations during stress in humans. (LLM, conf=0.87)
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“T binds to AR, which is expressed in hypothalamic reproductive areas, such as the ARC, VMN and POA nuclei86.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Supportedcites [86] source
Section 4.2, “Androgen receptor distribution in brain” (page not supplied), describes binding sites identified using radiolabeled testosterone and states that AR expression is highest in reproductive hypothalamic areas, including the arcuate nucleus, ventromedial nucleus and medial preoptic area. (LLM, conf=0.93)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“Progesterone and ALLO have also been implicated in HPA axis modulation and in human psychopathology (for review see 63).”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Supportedcites [63] source
The section “A Hypothesis for a Broad Role for Progesterone and Allopregnanolone in Stress Coping and Recovery” (page not provided) links P/ALLO stress responses to HPA-axis activity and depression. The “Stress-Responsive?” section also reports evidence suggesting ALLO down-regulates the HPA axis in humans. Together, these support the review-level claim that the hormones have been implicated in both areas. (LLM, conf=0.92)
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Within the PVN, ERβ is expressed in a large population of oxytocin neurons, in approximately half of CRH neurons, and a small population of AVP neurons92.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Partly supportedcites [92] sourceExperimental — accuracy not yet measured
Results §§3.2–3.3 report ERβ in a large proportion of oxytocin neurons and relatively sparse ERβ–AVP colocalization in the mouse PVN. Results §3.6 finds ERβ in approximately half of CRH neurons in the middle PVN, but substantially fewer in the caudal and rostral PVN; the claim presents that regional figure as applying to the PVN generally. (LLM, conf=0.86)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“When rats were treated with EB or an ERα agonist near the PVN, glucocorticoid receptor (GR)-mediated suppression of CORT release following acute restraint stress was inhibited, and this inhibition was not seen when animals were treated with an ERβ agonist.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Supportedcites [90] source
The Results section on restraint-induced CORT and ACTH reports that EB reduced dexamethasone (DEX) suppression after stress. The peri-PVN Results section reports that local estradiol and the ERα agonist PPT impaired DEX suppression of CORT, whereas suppression remained significant with the ERβ agonist DPN. EB was administered systemically; the near-PVN treatment was estradiol or PPT. (LLM, conf=0.91)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
Every source the paper cites for this claim was checked and supports it.
In the paper
“suggesting that ERα may reduce inhibitory input into the PVN, thereby reducing negative feedback from the glucocorticoids90.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6b. Influence of Reproductive Hormones on the HPA axis
What the sources say
- Supportedcites [90] source
The Discussion explicitly proposes that ERα might impair glucocorticoid negative feedback by reducing inhibitory GABAergic input into the PVN. The citing sentence preserves that proposed, rather than established, mechanism. (LLM, conf=0.95)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Indeed, in utero betamethasone exposure confirmed its effects acting mainly on the HPG axis, since the same pattern of hormonal alteration was observed in both, male and female pups, as well as in the following two generations106–109.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6c. Betamethasone Effects on the HPG Axis in Development and Adulthood
What the sources say
- Partly supportedcites [106] sourceExperimental — accuracy not yet measured
The Results (p. 3) report increased LH and decreased FSH in male rats exposed prenatally to betamethasone. The paper does not establish that betamethasone acts mainly on the HPG axis, nor does it report the same hormonal pattern in female offspring or the following two generations. (LLM, conf=0.88)
- Partly supportedcites [107] sourceExperimental — accuracy not yet measured
The Results (section 3.1; page unavailable) report lower FSH and higher LH in second-generation male rats. The Discussion (section 4; page unavailable) says this resembles the pattern previously observed in prenatally exposed males, but only suggests an effect on the hypophyseal-pituitary-testicular axis. This paper does not report the same hormonal pattern in female pups or establish that betamethasone acts mainly on the HPG axis. (LLM, conf=0.88)
- Partly supportedcites [108] sourceExperimental — accuracy not yet measured
The Discussion (page unavailable) reports altered testosterone and LH levels in male offspring after in utero betamethasone exposure. It does not establish that the drug acts mainly on the HPG axis; it also discusses possible testicular alterations. The paper does not report the same hormonal pattern in female pups or across the following two generations. (LLM, conf=0.88)
- Not checked — no full text of the sourcecites [109] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Piffer et al. observed changes in serum T concentrations, sperm production and sexual preference of adult males following intrauterine betamethasone exposure100.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6c. Betamethasone Effects on the HPG Axis in Development and Adulthood
What the sources say
- Partly supportedcites [100] sourceExperimental — accuracy not yet measured
The Abstract reports lower adult testosterone levels and reduced female-partner preference in male rats exposed prenatally to betamethasone; Section 3.3 confirms the testosterone reduction in plasma. The paper reports changes in ejaculation and other sexual behaviors, but does not report a measure of sperm production, so that part of the claim is unsupported. (LLM, conf=0.88)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“Borges et al. reinforced these findings and also demonstrated that the impact of fetal programming promoted by betamethasone exposure was seen at birth, as low pup weight, at puberty, as reduced serum T levels and delayed puberty onset, and at adulthood, as direct effects on gonadal morphology and function, sperm quality and fertility106–108.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6c. Betamethasone Effects on the HPG Axis in Development and Adulthood
What the sources say
- Partly supportedcites [106] sourceExperimental — accuracy not yet measured
The Results (p. 3) report lower offspring weight at postnatal day 1 and adult changes in reproductive-organ weights and fertility. The Introduction (p. 1) also summarizes adult sperm-quality impairment. The passages do not establish reduced serum testosterone or delayed puberty onset at puberty; the reported hormonal results concern adult animals. (LLM, conf=0.87)
- Partly supportedcites [107] sourceExperimental — accuracy not yet measured
The Results (§3.1; page not provided) report lower birth weight, delayed puberty, reduced Leydig-cell volume and function, poorer sperm measures, and reduced fertility in F2 male rats whose fathers were exposed prenatally to betamethasone. But the same section explicitly says serum testosterone levels were unaltered, contrary to the claimed reduction. (LLM, conf=0.90)
- Partly supportedcites [108] sourceExperimental — accuracy not yet measured
The Results report lower offspring weight at PND1, delayed preputial separation and lower testosterone at PND45, as well as adult testicular abnormalities and reduced fertility. The Discussion links these findings to altered sperm quality, but describes reduced sperm quality as a possible explanation for the fertility result and refers to a previous study; this paper did not directly demonstrate a change in sperm quality. (LLM, conf=0.87)
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
- Partly supported
The cited sources support only part of this claim — read each source’s verdict below.
In the paper
“During this period of intrauterine growth, important changes in fetal development are occurring, such as the gonadogenesis, the establishment of the HPG axis and the morphogenesis of reproductive ducts and glands (epididymis, vas deferens, seminal vesicle and prostate)98–100.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6c. Betamethasone Effects on the HPG Axis in Development and Adulthood
What the sources say
- Not checked — no full text of the sourcecites [98] source
- Not checked — no full text of the sourcecites [99] source
- Partly supportedcites [100] sourceExperimental — accuracy not yet measured
The Introduction (page not specified) identifies gestational days 18–19 as a fetal testosterone-surge period important to sexual differentiation, and Methods §2.2 says treatment on days 18–19 coincided with brain sexual differentiation. Our copy does not say that gonadogenesis, establishment of the HPG axis, or morphogenesis of the listed reproductive ducts and glands occurs during GD 12–19. (LLM, conf=0.84)
Load-bearingStrength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Increased GnRH pulse frequency and amplitude favor LH secretion, while a slower frequency favors FSH secretion16,17.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Hormone binding the GnRHR activates Gαq/11 which initiates multiple phospholipase activities leading to formation of inositol 1,4,5-trisphosphate (IP3) and diacylglycerol19,20.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“In this cell line, GnRH stimulated the export of class IIa HDACs resulting in increased acetylation of gonadotropin genes, while in LβT2 cells, another gonadotrope derived cell line, GnRH treatment enhanced the association of the histone acetyltransferase p300 with the Lhb gene28.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
- Not checked — no full text of the sourcecites [28] source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Chromatin organizing the β-subunit gene promoters also contains low levels of trimethylated histone H3 lysine 4 (H3K4me3). GnRH stimulation increases this modification resulting in chromatin decondensation by menin and the menin-mixed-lineage leukemia (MLL) 1/2 methyl transferase complex29.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
- Not checked — no full text of the sourcecites [29] source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“Additionally, GnRH stimulation results in an increase in Egr-1 mRNA and protein, which is tightly linked to an increase in LHβ synthesis26.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
- Not checked — no full text of the sourcecites [26] source
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“The GnRHR is a member of the rhodopsin like family of seven transmembrane domain G protein coupled receptors (GPCR)18.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
- Not checked — no full text of the sourcecites [18] source
Strength:plain· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
In the paper
“Receptor activation also increases intracellular calcium concentrations through release of intracellular stores and opening of voltage gated L-type calcium channels, which underlie activation of protein kinase C (PKC) isoforms21.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 3. GnRH Regulation of Pituitary Gonadotropin Production
What the sources say
- Not checked — no full text of the sourcecites [21] source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Interestingly, both RFRP-3 and kisspeptin neurons are influenced by stress hormone regulation, as will be discussed further below.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
Strength:plain· not yet calibratedCausal:correlational· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Within the past decade, the neuropeptides kisspeptin and RFRP-3 have been shown to have potent stimulatory or inhibitory actions on GnRH secretion in mammals, thereby modulating reproductive status.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 2. The Neuroendocrine Reproductive Axis and its Upstream Control by Kisspeptin and RFRP-3
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“ERα KO mice are infertile and do not have a normal estrous cycle or the proestrus surge of LH, while ERβ KO mice are subfertile with regular estrous cycles38.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Not checked — no full text of the sourcecites [38] source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“CRH intracerebroventricular (ICV) administration suppresses both LH pulsatility and the LH surge, and this suppression is enhanced by E255, potentially through CRH innervation of the locus coeruleus56.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“CRH neurons are also activated by membrane-initiated E2 signaling through the Gq-mER to suppress the M-current and augment excitatory postsynaptic current amplitude58.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Not checked — no full text of the sourcecites [58] source
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
In the paper
“These SCN neurons synthesize either AVP and project to AVPV/PeN kisspeptin and RFRP-3 neurons or synthesize VIP and project to GnRH and RFRP-3 neurons, thereby controlling the timing of the LH surge47.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Not checked — no full text of the sourcecites [47] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“In the hamster, E2 reduces RFRP-3 neuronal activation, perhaps to promote downstream GnRH surge secretion, with ~40% of RFRP-3 neurons in the female hamster expressing ERα7.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 4. Estrogen Modulation of Reproductive Hypothalamic Circuits
What the sources say
- Not checked — no full text of the sourcecites [7] source
Strength:hedged· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes? Load-bearing: unclear✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“Isolation-restraint stress can block the LH surge in rats, and in sheep and monkeys, the LH surge can be delayed or blocked by stress82,83.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6a. Influence of Stress on Reproductive Status and Brain Circuitry
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Rfrp neuronal activation in female mice was significantly increased after 45 min of restraint stress but not following longer stress durations”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6a. Influence of Stress on Reproductive Status and Brain Circuitry
What the sources say
- Not checked — no full text of the sourcecites [85] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“perhaps as a compensatory response to replenish RFRP-3 stores that were reduced when these neurons were more active during initial stress exposure85.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6a. Influence of Stress on Reproductive Status and Brain Circuitry
What the sources say
- Not checked — no full text of the sourcecites [85] source
Strength:hedged· not yet calibratedCausal:conditional· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
None of the sources cited for this claim have been checked yet.
In the paper
“One ICV administered dose of ALLO on the morning of proestrus has an inhibitory effect on both ovulation rate and sexual receptivity71,72.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 5. Neuroprogesterone Control of the Reproductive Axis
What the sources say
- Not checked — no full text of the sourcecites [71] source
- Not matchedcites [72]
Couldn’t be matched to a paper in Crossref, so it can’t be checked.
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“In females, stress can disrupt ovarian cyclicity as well as upstream gonadotropin synthesis and secretion75,76.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6a. Influence of Stress on Reproductive Status and Brain Circuitry
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“LH pulse frequency and interpulse intervals were significantly and rapidly decreased in stressed female mice compared to controls, with no effects on LH pulse amplitude85.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6a. Influence of Stress on Reproductive Status and Brain Circuitry
What the sources say
- Not checked — no full text of the sourcecites [85] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
In the paper
“Giuliani et al. observed increased GnRH release from hypothalamic slices following treatment with ALLO which was absent when slices were also treated with an NMDA receptor antagonist.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 5. Neuroprogesterone Control of the Reproductive Axis
What the sources say
- Not checked — no full text of the sourcecites [73] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Serotonin signalling disruption is associated with mood disorders thereby suggesting an association between ALLO and serotonergic signalling.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 5. Neuroprogesterone Control of the Reproductive Axis
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“As reproduction and survival are necessary for life, it follows that the two systems promoting these aspects, the HPG and HPA axes respectively, would be interlinked.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 7. Conclusions
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Many components, including neural and hormonal factors, contribute to the proper regulation of the HPG axis and provide many interesting avenues for future research.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 7. Conclusions
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesProbably not a substantial claim.
In the paper
“Pereira & Piffer observed an incomplete masculinization of the hypothalamus followed by damage of seminal vesicle contractility in adult rats exposed in utero to hydrocortisone99.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6c. Betamethasone Effects on the HPG Axis in Development and Adulthood
What the sources say
- Not checked — no full text of the sourcecites [99] source
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A claim is checked only against the cited paper’s full text, never its abstract, and none is available for its sources.
In the paper
“The increase in glucocorticoid concentration with antenatal therapy directly interferes in the control of the HPG axis, leading to a decrease in GnRH release and, consequently, a decrease in FSH and LH102,103.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 6. Stress and Reproduction: Bidirectional Interactions > 6c. Betamethasone Effects on the HPG Axis in Development and Adulthood
What the sources say
Tests✓ Asserted: passes✓ Checkable: passes✓ Load-bearing: passes✓ Based: passesIt may state two separate claims as one.
A conclusion the paper draws from its own results — it cites no other source for it, so there is none to check. The quote shows it is in the paper.
In the paper
“Altogether, we can see that the HPG axis is an elegantly-regulated endocrine system that allows for successful reproduction and species propagation.”
§ Emerging insights into Hypothalamic-pituitary-gonadal (HPG) axis regulation and interaction with stress signaling > 7. Conclusions
Strength:plain· not yet calibratedCausal:direct· not yet calibratedTests✓ Asserted: passes✓ Checkable: passes✗ Load-bearing: fails✓ Based: passesProbably not a substantial claim. The paper’s conclusions may not depend on it.
The paper relies on this without support.
Many key mechanisms and factors controlling GnRH release, including its pulsatile and surge modes, remain poorly defined.
“however, many of the key mechanisms and factors involved in the regulation of GnRH release, including modulation of GnRH pulsatile and surge modes of secretion, remain poorly-defined.”
The authors state this as an assumption.
Inhibition of pulsatile LH release by psychosocial stress or exogenous CORT reflects inhibition of upstream GnRH pulsatile secretion.
“which is assumed to reflect inhibition of upstream GnRH pulsatile secretion.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“Most of the evidence on the dynamic interactions between the HPA and HPG axes comes from animal studies (Acevedo-Rodriguez et al., 2018; McCosh et al., 2019).”
From Dynamic Hormone Control of Stress and Fertility (2020) · cites this paper as Acevedo-Rodriguez et al., 2018
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Each contradiction between two passages listed here was confirmed by an independent check.
Pulse frequency and interpulse interval both reported to decrease
MinorOver the same sampling period, fewer LH pulses would mean longer intervals between pulses, not shorter ones. The reported decreases in both measures conflict.
“LH pulse frequency and interpulse intervals were significantly and rapidly decreased in stressed female mice compared to controls”
“interpulse intervals were significantly and rapidly decreased in stressed female mice compared to controls”
Citations
Cites
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“(1) Gonadal 17β- oestradiol (E2) controls the HPG axis through negative (red circles−) and positive (green circles+) feedback onto hypothalamic neurones and pituitary gonadotrophs.”
BackgroundSeckl, J. R., & Holmes, M. C. (2007) · Nature Clinical Practice Endocrinology & Metabolism · doi:10.1038/ncpendmet0515 · Cited by 754
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Flagged first, then by citations
1 of the 113 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Pelegrina LT, 2015, Pharmacological effect of one icv dose of allogregnanolone in the female rat: behavioral profile, Braz J Biol Sci, 2, 39
Cited by
Sorted by citations
Items 101–200 of 295
Regulation of FSH Synthesis by Differentially Expressed miR-488 in Anterior Adenohypophyseal Cells
Wang, H., Wang, W., Chen, C., et al. (2021) · Animals · doi:10.3390/ani11113262 · Cited by 10
“Feedback regulation also makes the crosstalk among various reproductive hormones in the HPG axis more complicated [41].”
BackgroundRaoof, M., Amanpour, S., Roghani, A., Abbasnejad, M., Kooshki, R., Askari-Zahabi, K., Mohamadi-Jorjafki, E., Majdzadeh, B., Aarab, G., & Lobbezoo, F. (2022) · Neuroscience Letters · doi:10.1016/j.neulet.2022.136444 · Cited by 11
“Various studies have shown that perturbations in the HPA axis activity exacerbate the HPG axis coordination [2,16].”
BackgroundIsaksson, C., & Bonier, F. (2020) · Oxford University Press eBooks · doi:10.1093/oso/9780198836841.003.0013 · Cited by 12
Effects of social environments on male primate HPG and HPA axis developmental programming
Brown, E. R., Gettler, L. T., & Rosenbaum, S. (2024) · Developmental Psychobiology · doi:10.1002/dev.22491 · Cited by 10
Fang, L., Ma, Y., Peng, Y., Ni, J., Ma, C., Wang, G., Zhao, H., Chen, Y., Zhang, T., Cai, G., et al. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.116915 · Cited by 9
de Medeiros, P. D. C., da Silva, A. G. G., Angelo, A. B. S., de Moura, M. J. N., Kannan, U., Gregory, M., Dufresne, J., Borges, C. D. S., & Cyr, D. G. (2025) · Reproductive Toxicology · doi:10.1016/j.reprotox.2025.109002 · Cited by 9
Self-citationSocial status influences relationships between hormones and oxidative stress in a cichlid fish
Culbert, B. M., Border, S. E., Fialkowski, R. J., Bolitho, I., & Dijkstra, P. D. (2023) · Hormones and Behavior · doi:10.1016/j.yhbeh.2023.105365 · Cited by 11
Crewther, B. T., Kasprzycka, W., Cook, C. J., & Rola, R. (2021) · Neurological Sciences · doi:10.1007/s10072-021-05335-7 · Cited by 9
“Additional changes in HPG activity might be expected, as both axes are linked via negative- and positive-feedback loops involving multiple chemical, neuropeptide, and receptor signals [21].”
BackgroundXin, M., He, J., Zhang, Y., Wu, Y., Yang, W., Liang, X., & Yin, X. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.27483 · Cited by 9
“In some papers, mTOR and PI3K signaling had been reported to be associated with secretion of hormones, including sexual hormones, stress hormones as well as kisspeptin and GnRH, which is a potent LH secretion stimulator.(1,4,8,10,11) PI3K regulates the expression of kisspeptin and GnRH might via the PI3K/Akt pathway.”
BackgroundLee, S. (2026) · Toxicology Mechanisms and Methods · doi:10.1080/15376516.2025.2584495 · Cited by 8
Irisin as an emerging target in the regulation of reproductive functions in health and disease
Nalla, S. V., Jayapradha, P., Lalruatmawii, Nandheeswari, K., Naxine, P., Vigneshwaran, G., Rohilla, G., Dubey, I., & Kushwaha, S. (2024) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2024.114529 · Cited by 8
Ruiz‐Pozo, V. A., Cadena-Ullauri, S., Tamayo‐Trujillo, R., Guevara‐Ramírez, P., Paz‐Cruz, E., Cataña, M. A. C., & Zambrano, A. K. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1568828 · Cited by 9
Pathophysiological insights into asprosin: an emerging adipokine in reproductive health
Khan, S., Syeda, S., Raghuvanshi, Y., & Shrivastava, A. (2025) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-025-09975-4 · Cited by 10
Unpacking PCOS Inflammation: From Misconceptions to Immune Networks
Robles, G. D., Wiggins, K. D., Mundo, Z. D. D., Ujagar, N. S., Nguyen, C. M., Seldin, M. M., Pacheco-Sanchez, G., & Nicholas, D. (2025) · Endocrinology · doi:10.1210/endocr/bqaf166 · Cited by 12
“Patients with PCOS typically present with excess androgens, a high LH to FSH ratio driven by abnormally elevated LH, and more recently described, reduced prolactin levels (23, 28-31).”
He, Y., Hou, J., Qiu, Y., et al. (2023) · Toxicology · doi:10.1016/j.tox.2023.153569 · Cited by 8
Lurin, I. A., Seliukova, N. Y., Korenieva, Y. M., Бойко, М., Misiura, K. V., & Nehoduiko, V. V. (2023) · PROBLEMS OF ENDOCRINE PATHOLOGY · doi:10.21856/j-pep.2023.4.08 · Cited by 8
Garcia, C., Vélez, L. M., Ujagar, N. S., Mundo, Z. D. D., Nguyen, T., Fox, C. W., Mark, A., Fisch, K. M., Lawson, M. A., Dulęba, A. J., et al. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1279878 · Cited by 10
Food access modifies GnIH, but not CRH, cell number in the hypothalamus in a female songbird
Wilsterman, K., Alonge, M. M., Bao, X., et al. (2020) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2020.113438 · Cited by 8
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A single GnRH challenge promotes paternal care, changing nestling growth for one day
George, E., Navarro, D., & Rosvall, K. A. (2021) · Hormones and Behavior · doi:10.1016/j.yhbeh.2021.104964 · Cited by 8
Anxiety and ultrastructural consequences of chronic mild stress in rats
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Adedara, I. A., Awogbindin, I. O., Mohammed, K. A., Da‐Silva, O. F., & Farombi, E. O. (2021) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.22741 · Cited by 8
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“160,161 Accordingly, one can hypothesize that aging ‐ related changes in hormonal levels, such as alterations in glucocorticoids (e.g., cortisol) and sex hormones, can in fl uence BDNF and OT expression and function.”
Dai, C., Hao, Z., Liu, D., et al. (2025) · Environment International · doi:10.1016/j.envint.2025.109478 · Cited by 7
A New Bihormonal Model for the Brain Regulation of Gonadotropins in Teleosts
Uju, C. N., Mustapha, U. F., & Unniappan, S. (2025) · Neuroendocrinology · doi:10.1159/000546403 · Cited by 7
“GnRH is indeed the key regulator of the HPG axis in mammals and is indispensable for down-stream reproductive events [22, 23].”
The testobolome in microbial testosterone metabolism and human health
Veerus, L., Subrahmanian, A., & Blaser, M. J. (2026) · npj Biofilms and Microbiomes · doi:10.1038/s41522-025-00861-0 · Cited by 9
Khanna, A., Thomas, J. V., John, F., Maliakel, B. P., & Krishnakumar, I. M. (2021) · Clinical Phytoscience · doi:10.1186/s40816-021-00296-y · Cited by 7
“The reproductive cycle is regulated by the hormones of the hypothalamic-pituitary-gonadal (HPG) axis; mainly the estradiol, progesterone, testosterone, follicle stimulating hormone (FSH), and luteinizing hormone (LH) [1].”
BackgroundChu, L., Liu, S., Wu, Y., Yang, J., Qiao, S., Zhou, Y., Deng, H., Li, X., & Shen, Z. (2022) · Clinica Chimica Acta · doi:10.1016/j.cca.2022.08.023 · Cited by 7
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Neuroendocrine regulation of reproduction, stress, inflammation and energy homeostasis
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Graumann, L., Kulakova, E., Cho, A. B., Deuter, C. E., Wolf, O. T., Schell, J., Hellmann‐Regen, J., Roepke, S., Otte, C., & Wingenfeld, K. (2024) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2024.107232 · Cited by 6
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“Given that the neurobiological mechanisms underlying reproduction and stress response are interlinked [13], sex hormones may modulate the effects of stress in general, and on visuospatial capabilities in particular.”
BackgroundDyson, T., Thomas, S. J., Townsend, M. L., Finch, A. W., South, A., Barkus, E., Walter, E. E., Mendonca, C. J., Grenyer, B. F. S., & Pickard, J. A. (2023) · Frontiers in Psychology · doi:10.3389/fpsyg.2023.1195187 · Cited by 6
“The HPA axis is known to share close bidirectional influences with the hypothalamic-pituitary-gonadal (HPG) axis to support the balance of reproduction and survival (Acevedo-Rodriguez et al., 2018).”
BackgroundMcIlwraith, E. K., Loganathan, N., Mak, K. W. Y., et al. (2024) · Journal of Neuroendocrinology · doi:10.1111/jne.13398 · Cited by 6
Maxon, J. R., & Mahoney, M. M. (2024) · Reproduction · doi:10.1530/rep-24-0145 · Cited by 8
Cáceres, A. R. R., Orozco, A. S. V., Cabrera, R., & Laconi, M. R. (2020) · Journal of Neuroendocrinology · doi:10.1111/jne.12836 · Cited by 6
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Cáceres, A. R. R., Arboccó, F. C. V., Cardone, D. A., Sanhueza, M. D. L. Á., Casais, M., Orozco, A. S. V., & Laconi, M. R. (2021) · Journal of Neuroendocrinology · doi:10.1111/jne.13056 · Cited by 6
Self-citationEditorial: Recent Progress and Perspectives in Neurosteroid Research
Vaudry, H., Ubuka, T., Soma, K. K., & Tsutsui, K. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.951990 · Cited by 6
“The recent years have seen substantial progress in the understanding of the bidirectional interactions between the hypothalamo-pituitary-adrenal (HPA) and the hypothalamopituitary-gonadal (HPG) axes (8).”
BackgroundZhu, Z., Shahab, M., Shahab Uddin, M. S., Imdadullah, & Ishfaq, M. (2025) · Toxicon · doi:10.1016/j.toxicon.2025.108554 · Cited by 5
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Sex steroid hormones and asthma in males: a state-of-the-art review
Ermiş, S. S. Ö., Ercan, S., Malmhäll, C., Adesoba, H., Salisu, M., Bossios, A., Rådinger, M., Kankaanranta, H., & Nwaru, B. I. (2025) · Expert Review of Respiratory Medicine · doi:10.1080/17476348.2025.2501276 · Cited by 5
“…as the hypothalamic–pituitary–gonadal (HPG) axis is activated, pulsatile gonadotropin-releasing hormone (GnRH) secretion promotes luteinizing hormone (LH) and follicle-stimulating hormone (FSH) production [28,36], and LH induces testosterone secretion from Leydig cells in testicles [28,29,37].”
Du, X., He, X., Liu, Q., Liu, Q., Di, R., & Chu, M. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.888207 · Cited by 5
“ACTH in turn stimulates the adrenal gland to secrete cortisol, which then provides negative feedback to the brain in the classic steady-state feedback loop to regulate hypothalamus-pituitary-adrenal gland axis (HPA) signals (10).”
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Li, Y., Tan, Z., Zuo, P., Li, M., Hou, L., & Wang, X. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.168693 · Cited by 7
Stress-mediated convergence of splicing landscapes in male and female rock doves
Lang, A. S., Austin, S. H., Harris, R. M., Calisi, R. M., & MacManes, M. D. (2020) · BMC Genomics · doi:10.1186/s12864-020-6600-6 · Cited by 5
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“LH targets Leydig cells to drive testosterone synthesis and secretion, while FSH acts synergistically with testosterone on Sertoli cells to initiate and maintain spermatogenesis, thereby governing male reproductive function [39].”
Qiu, W., Liu, S., Kang, X., Liu, Y., Xu, B., Pan, C., Magnuson, J. T., Yang, X., Zheng, J., Zheng, C., et al. (2025) · Environmental Science & Technology · doi:10.1021/acs.est.5c07904 · Cited by 6
Too stressed for sex? Associations between stress and sex in daily life
Mües, H. M., Markert, C., Feneberg, A. C., & Nater, U. M. (2025) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2025.107583 · Cited by 4
Mei, Y., Liu, J., Dong, Z., Shi, K., Su, W., Luo, Z., Zhao, J., Li, Y., Yang, M., Wu, J., et al. (2025) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2025.118962 · Cited by 6
Nishan, M. N. H., Ferdous, A., Ahmed, M., & Akter, K. (2025) · PLOS Global Public Health · doi:10.1371/journal.pgph.0005133 · Cited by 4
“While higher humidity supports hydration and metabolic stability, extreme heat exposure—as noted in Maharashtra—can activate stress responses that suppress the hypothalamic–pituitary–gonadal (HPG) axis, delaying hormonal signaling involved in puberty onset [36,37].”
Ovarian status modulates endocrine and neuroinflammatory responses to a murine mammary tumor
Strehle, L. D., Russart, K. L. G., Burch, V. A., Grant, C. V., & Pyter, L. M. (2022) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00124.2022 · Cited by 4
Relationship between semen parameters, serum InhB, and INSL-3 levels, and the degree of varicocele
Liu, L., Huang, W. J., Luo, K., et al. (2024) · Clinics · doi:10.1016/j.clinsp.2024.100339 · Cited by 4
“23 Adult testes secrete testosterone, INSL-3, and InhB into the blood circulation, and these hormone levels are dynamically regulated.”
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Progesterone and suicidality in male combat veterans
Sher, L., Bierer, L. M., Makotkine, I., & Yehuda, R. (2025) · QJM · doi:10.1093/qjmed/hcaf082 · Cited by 4
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PITX2 regulates steroidogenesis in granulosa cells of dairy goat by the WNT/β-catenin pathway
Bu, Q., Liu, S., Wang, Z., Zou, J., Wang, P., Cao, H., Li, D., Cao, B., An, X., Song, Y., et al. (2022) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2022.114027 · Cited by 4
Bar-Sadeh, B., Pnueli, L., Keestra, S., Bentley, G. R., & Melamed, P. (2023) · Journal of the Endocrine Society · doi:10.1210/jendso/bvad108 · Cited by 4
Balancing Act: An Interdisciplinary Exploration of Trade-offs in Reproducing Females
Josefson, C. C., Fitzwater, B. M., Beltran, R. S., da Costa, D. P., Fornara, J. H., Garland, T., Harris, B. N., Hinde, K., Hood, W. R., Hunt, E. S. E., et al. (2024) · Integrative and Comparative Biology · doi:10.1093/icb/icae092 · Cited by 5
Combined Molecular Toxicity Mechanism of Phthalate Mixtures
Liu, Y., & Pei, D. (2025) · Wiley eBooks · doi:10.1002/9781394158355.ch13 · Cited by 4
Yadav, A., & Mishra, R. K. (2025) · Journal of Reproductive Healthcare and Medicine · doi:10.25259/jrhm_27_2024 · Cited by 3
Safari, M., Farahbakht, E., Sharifabadi, A., Sepehri, H., & Jahromi, M. K. (2025) · BMC Research Notes · doi:10.1186/s13104-025-07365-2 · Cited by 4
“Because reproduction and survival need to be coordinated and balanced, the hypothalamic–pituitary–Gonadal (HPG) axis can modulate as well as be modulated by the HPA axis, or there are interactions between the HPG and HPA axes [4].”
Biological Mechanisms Balancing Torpor and Reproduction in Mammals
Vander, P. B., & Correa, S. M. (2025) · Endocrinology · doi:10.1210/endocr/bqaf141 · Cited by 3
Molecular Mechanisms of Dysregulated LH and FSH Secretion in Human Reproductive Failure
Zikopoulos, A., Moustakli, E., Potiris, A., Paraschos, V. S., Katopodis, P., Machairoudias, P., Antsaklis, P. G., Kathopoulis, N., Anagnostaki, I., & Stavros, S. (2026) · Biomedicines · doi:10.3390/biomedicines14040789 · Cited by 5
Feng, H., Zhong, Q., Zhou, H., et al. (2021) · Annals of Palliative Medicine · doi:10.21037/apm-21-3111 · Cited by 3
“For HPRL with non-neurological diseases and tumor compression, when serum PRL decreases, HPO function is gradually restored, enabling hypothalamic kisspeptin expression to normalize the hypothalamic-pituitary-gonadal (HPG) axis (18,19) Serum KP is a peptide hormone widely distributed in the brain and multiple tissues…”
BackgroundAhmed, S. M., Hummadi, Y. M. K. A. M., & Waheed, H. J. (2024) · Pharmacia · doi:10.3897/pharmacia.71.e132062 · Cited by 2
Yang, C., Yang, Y., Zhao, B., Gao, E., Chen, H., Li, Y., Ma, J., Wang, J., Hu, S., Song, X., et al. (2024) · Animal Biotechnology · doi:10.1080/10495398.2024.2427757 · Cited by 3
“Excessive secretion of FSH and threshold secretion of progesterone by the HPG axis triggers negative feedback regulation, inhibiting the secretion of GnRH and FSH, thereby interfering with follicular development and preventing estrus in yaks (56).”
Atopic dermatitis in childhood and pubertal development: A nationwide cohort study
Kjersgaard, C. L., Ernst, A., Clemmensen, P. J., Lunddorf, L. L. H., Arendt, L. H., Brix, N., Arah, O. A., Deleuran, M. S., & Ramlau‐Hansen, C. H. (2024) · JAAD International · doi:10.1016/j.jdin.2024.09.018 · Cited by 3
“28,29 Other potential mechanisms include sleep disturbances, resulting in disturbances of the hormone balance, 30,31 a restricted diet because of food allergies, 32,33 treatment for example topical glucocorticoids, 17,34,35 or the overactive immune system itself may be involved.”
Exploring the Association Between Sleep Quality and Menstrual Abnormalities in Adolescents
Zhang, J., Sarris, G. K., Fernandez-Bergnes, D. G., Salloum, T., Hofmann, K. M., Duncan, E., & Simms-Cendan, J. S. (2025) · Journal of Pediatric and Adolescent Gynecology · doi:10.1016/j.jpag.2025.08.001 · Cited by 3
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Neuroendocrinology of Reproduction
McCartney, C. R., & Marshall, J. C. (2022) · doi:10.1093/med/9780198870197.003.0150 · Cited by 3
The Origins of Gender, not Sex: Evolution and the Reproductive AxisPreprint
Woodhill, B. M., Samuels, C. A., & Jamieson, G. A. (2024) · doi:10.33774/coe-2020-k7gt1-v10 · Cited by 2
Kulakova, E., Graumann, L., Cho, A. B., Deuter, C. E., Wolf, O. T., Hellmann‐Regen, J., Roepke, S., Otte, C., & Wingenfeld, K. (2024) · European Journal of Psychotraumatology · doi:10.1080/20008066.2024.2431368 · Cited by 2
Bick, A. J., Avenant, C., Capitaine, C.-K., Eck, S., Lee, M., Moliki, J. M., Dlamini, S., Erikson, D. W., Smit, J. A., Beksinska, M. E., et al. (2025) · Biology of Reproduction · doi:10.1093/biolre/ioaf292 · Cited by 2
“…gonadotropin-releasing hormone (GnRH) in a pulsatile manner, which stimulates the pituitary gonadotrophs to secrete luteinising hormone (LH) and follicle-stimulating hormone (FSH) to regulate synthesis and release of progesterone (P4), testosterone (T) and estradiol (E2) in the ovaries [4, 5].”
Khan, S., Attaullah, M., Zubair, M., Khan, M. S., Ali, R., & Jahan, S. (2026) · Regulatory Toxicology and Pharmacology · doi:10.1016/j.yrtph.2026.106069 · Cited by 2
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Moss, R. A., Murphy, K., Gardner, S. T., Watkins, M. M., Finger, J. W., Kelley, M. D., Elsey, R. M., Warner, D. A., & Mendonça, M. T. (2023) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cbpc.2023.109767 · Cited by 3
Neuroendocrine Control of the Vascular System
Dalmasso, C., & Loria, A. S. (2023) · Masterclass in neuroendocrinology · doi:10.1007/978-3-031-39995-4_3 · Cited by 2
Different of Hypothalamic-Pituitary-Gonadal Axis in Male and Female
Tammasse, I. F. U., & Fachrul, T. (2023) · Reproductive Medicine International · doi:10.23937/2643-4555/1710023 · Cited by 2
The role of neonatal kisspeptin in long-term social behavior in mammals
Neves, J. R., Castelo-Branco, M. S., & Gonçalves, J. (2025) · Communications Biology · doi:10.1038/s42003-025-08478-x · Cited by 2
Jugulytė, N., & Bartkevičienė, D. (2025) · Endocrines · doi:10.3390/endocrines6040054 · Cited by 3
Sex vs Gender: A Biological Location for Gender, not Sex.Preprint
Woodhill, B. M., & Samuels, C. A. (2021) · doi:10.33774/coe-2020-k7gt1-v4 · Cited by 3
Harnessing BDNF Signaling to Promote Resilience in AgingPreprint
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Toll-like Receptor 4 Contributes to PCOS-like Metabolic and Reproductive PathogenesisPreprint
Wiggins, K. D., Mundo, Z. D. D., Angulo, J. A. A., Naidu, N., Saba, A., Garcia, C., Nguyen, C. M., Ujagar, N. S., Torre, J.-J. D. L., Robles, G. D., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.16.682907 · Cited by 2
Self-citationSynergy under the Sun? Nanoplastics Enhance Estrogenicity of Common UV-Blocker
Schmidt, C. W. (2024) · Environmental Health Perspectives · doi:10.1289/ehp14939 · Cited by 1
Poli, V., & Motireddy, S. R. (2024) · American Journal of Pharmacology and Toxicology · doi:10.3844/ajptsp.2024.1.26 · Cited by 1
Exploring sexual and romantic functioning as early risk factors of schizophrenia: a narrative review
Dospělová, P., Šustová, P., Zakreski, E., & Androvičová, R. (2025) · Sexual Medicine · doi:10.1093/sexmed/qfaf002 · Cited by 2
Senotherapeutic approach to age-related endocrine diseases
Turgut, Ş., & Andican, G. (2025) · Advances in pharmacology · doi:10.1016/bs.apha.2025.02.009 · Cited by 1
Khan, S., Attaullah, M., Jahan, S., Ali, R., & Ahmad, S. (2025) · Toxicological Research · doi:10.1007/s43188-025-00286-z · Cited by 1
Effects of Sulpiride on the Reproductive System of Male Rats after Puberty
Abd, A. A., Al-Juhaishi, O. A., & Jumma, Q. S. (2025) · World s Veterinary Journal · doi:10.54203/scil.2025.wvj5 · Cited by 5
Metadata
- Authors
- Acevedo‐Rodriguez, A., Kauffman, A. S., Cherrington, B. D., Borges, C. S., Roepke, T. A., & Laconi, M.
- Affiliations
- Department of Neuroscience Baylor College of Medicine Houston TX USA
- University of California San Diego (US)
- University of Wyoming (US)
- Department of Morphology Institute of Biosciences São Paulo State University (Unesp) Botucatu Brazil
- Rutgers, The State University of New Jersey (US)
- University of Mendoza (AR)
- Venue
- Journal of neuroendocrinology
- Publisher
- Wiley
- Published
- 2018-08-07
- Volume
- 30
- Issue
- 10
- Pages
- e12590-e12590
- ISSN
- 0953-8194 (ISSN-L)
- 1365-2826
- PMC
- PMC6129417
- OpenAlex
- W2792526589
- Semantic Scholar
- ddaae3f6099839f5eb7b172e24dc865e4fd445d3
- Cited by
- 298
- References
- 113
- Citations by year
- 2026: 63 · 2025: 60 · 2024: 48 · 2023: 32 · 2022: 28 · 2021: 29 · 2020: 25 · 2019: 8 · 2018: 5
- FWCI
- 2.52
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Journal of Neuroendocrinology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Rutgers University Community Repository (Rutgers University) (submittedVersion)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, cc-by-nc-sa)
- eScholarship (California Digital Library) (submittedVersion)
- UNESP Institutional Repository (São Paulo State University) (submittedVersion)
- Funders
- National Institutes of Health (R21 ES027119, R01 HD090161, P50 HD012303)
- National Science Foundation (IOS‐1457226)
- Fundação de Amparo à Pesquisa do Estado de São Paulo (2012/25350‐1, 2014/13660‐1)
- Conselho Nacional de Desenvolvimento Científico e Tecnológico (308842/2013‐8)
- Topics
- Health Sciences › Medicine › Reproductive Medicine › Hypothalamic control of reproductive hormones
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Health Sciences › Medicine › Reproductive Medicine › Reproductive Biology and Fertility
- Keywords
- hypothalamic-pituitary-gonadal axis, stress signaling, hypothalamic-pituitary-adrenal axis, kisspeptin neurons, sex steroid feedback, corticosterone, reproduction, fertility control, pituitary gland
- MeSH terms
- Animals, Estrogens, Female, Humans, Hypothalamic Hormones, Hypothalamo-Hypophyseal System, Luteinizing Hormone, Gonadotropin-Releasing Hormone, Neuropeptides, Pituitary-Adrenal System, Reproduction, Stress, Psychological, Kisspeptins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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