The DOI matches its Crossref record.
Regulation of Pituitary ACTH Secretion during Chronic Stress
Abstract
Maintenance of adequate levels of response of the hypothalamic-pituitary-adrenal axis during chronic stress is important for survival. Three basic patterns of response can be identified depending on the type of stress: (a) desensitization of ACTH responses to the sustained stimulus, but hyperresponsiveness to a novel stress despite elevated plasma glucocorticoid levels, as occurs in physical-psychological paradigms; (b) no desensitization of ACTH response to the repeated stimulus and hyperresponsiveness to a novel stress, as occurs during repeated painful stress and insulin hypoglycemia; and (c) small and transient increases in ACTH, but sustained elevations of plasma corticosterone and diminished ACTH responses. The level of response of the pituitary corticotroph is determined by differential regulation of the hypothalamic regulators, corticotropin-releasing hormone (CRH) and vasopressin (VP), and the sensitivity of the negative glucocorticoid feedback. While osmotic stimulation increases VP expression in magnocellular neurons of the paraventricular (PVN) and supraoptic nuclei of the hypothalamus, chronic stress paradigms with high pituitary responsiveness are associated with activation of CRH and CRH/VP parvicellular neurons of the PVN, predominantly of the VP-containing population. While moderate increase of CRH output is important for stimulation of POMC transcription, the increase of the VP:CRH secretion ratio appears to be important in maintaining the secretory capacity of the pituitary corticotroph during chronic stimulation. Decreased sensitivity of the glucocorticoid feedback, probably due to interaction of glucocorticoid receptors with transcription factors induced by CRH and VP, is critical for the maintenance of ACTH responses in the presence of elevated plasma glucocorticoid levels during chronic stress. Although both CRH and VP receptors are activated and undergo regulatory variations during chronic stress, only the changes in VP receptor levels are parallel to the changes in pituitary ACTH responsiveness. The inhibitory effect of chronic osmotic stimulation on ACTH secretion in spite of high circulating levels of VP is probably the result of diminished activity of parvicellular PVN neurons and downregulation of pituitary VP receptors. Although the exact interaction between regulatory factors and the molecular mechanisms controlling the sensitivity of the corticotroph during adaptation to chronic stress remain to be determined, it is clear that regulation of the proportional secretion of CRH and VP in the PVN, modulation of pituitary VP receptors, and the sensitivity to feedback inhibition play a critical role.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“In essence, CRH and AVP are both required as stimulatory inputs to corticotrope cells for a complete ACTH response in physiologically normal as well as in various stressful conditions (32, 38, 48–51).”
From Influence of arginine vasopressin on the ultradian dynamics of Hypothalamic-Pituitary-Adrenal axis (2022) · cites this paper as [49]
Citations
Cited by
Sorted by citations
Items 401–500 of 553
Kouhnavardi, S., Cabatic, M., Mañas‐Padilla, M. C., Malabanan, M.-A., Smani, T., Cicvaric, A., Aranzalez, E. M., Koenig, X., Urban, E., Lübec, G., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119565 · Cited by 8
Sharma, D. K., Cornett, L. E., & Chaturvedi, C. M. (2009) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2008.12.019 · Cited by 7
Noguchi, T., Makino, S., Maruyama, H., & Hashimoto, K. (2006) · Neuroendocrinology · doi:10.1159/000096824 · Cited by 7
de Souza, L. M., & Franci, C. R. (2010) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2010.05.009 · Cited by 9
Kocaman, A., Gül, M., Yurt, K., et al. (2017) · Journal of Microscopy and Ultrastructure · doi:10.1016/j.jmau.2017.08.003 · Cited by 7
Saroj, N., Shanker, S., Fernández-Parilla, M. A., López‐Sánchez, P., & Terrón, J. A. (2019) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/cjpp-2019-0080 · Cited by 7
“…17 of 30 https://mc06.manuscriptcentral.com/cjpp-pubs Canadian Journal of Physiology and Pharmacology Draft 18 desensitization of the ACTH output to the persistent stimulus has taken place, as reported in studies with other physical/psychological stress paradigms (see Aguilera 1994 for review).”
BackgroundGlucocorticoids and the HPA axis
Cowell, A.-M., & Buckingham, J. C. (2001) · Birkhäuser Basel eBooks · doi:10.1007/978-3-0348-8348-1_8 · Cited by 7
Immunocytochemical Analysis of Pituitary Cells in Pre-spawning Chum Salmon
Salam, M., Ando, H., Ban, M., et al. (2000) · ZOOLOGICAL SCIENCE · doi:10.2108/zsj.17.805 · Cited by 7
The pulsatility of ACTH secretion in the rat anterior pituitary cell perifusion system
Deng, Q., Zhang, Z., & Wu, Y. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000455984 · Cited by 6
Przygodda, F., Manfredi, L. H., Machado, J., Gonçalves, D. A. P., Zanon, N. M., Bonagamba, L. G. H., Machado, B. H., Kettelhut, Í. D. C., & Navegantes, L. C. C. (2016) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00977.2015 · Cited by 6
“During stress conditions, several behavior, visceral, and endocrine changes are activated as part of homeostatic control (1).”
BackgroundWalker, C. D., Tilders, F. J. H., & Burlet, A. J. (2001) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2001.00589.x · Cited by 6
Liu, H., Yi, R., Wang, C., Zhao, P. Y., Zhang, M., Xu, S., & Bao, J. (2018) · PLoS ONE · doi:10.1371/journal.pone.0197152 · Cited by 7
Endothelium-Dependent, Vasopressin-Induced Contractions in Rabbit Renal Arteries
Streefkerk, J. O., Pfaffendorf, M., & van Zwieten, P. A. (2003) · Journal of Cardiovascular Pharmacology · doi:10.1097/00005344-200312000-00002 · Cited by 6
Hurwitz, B. E., Brownley, K. A., FLETCHER, M. A., et al. (2000) · Journal of Chronic Fatigue Syndrome · doi:10.1300/j092v06n02_06 · Cited by 6
Responses of hypothalamo–pituitary–adrenal axis to a cholinesterase inhibitor
Umegaki, H., Yamamoto, A., Suzuki, Y., et al. (2009) · Neuroreport · doi:10.1097/wnr.0b013e3283313eb7 · Cited by 6
Virtual reality environmental enrichment effects on heart rate variability in healthy volunteers
Benvegnù, G., Graffer, R., Lorusso, F. M., Ceccato, S., Tedesco, E., & Chiamulera, C. (2025) · Psychopharmacology · doi:10.1007/s00213-025-06870-3 · Cited by 7
“Cortisol response may therefore be a biomarker of both acute and sustained physiological response to stress (Aguilera 1994).”
Goudochnikov, V. I. (2023) · Journal of Endocrinological Science · doi:10.29245/2767-5157/2023/1.1125 · Cited by 5
A Preliminary Assessment of Equine Affect in Equine-Assisted Services
Rudd, C. C., Pasiuk, E. L., Anderson, N., Hall, N. J., Foster, R., & Schroeder, K. (2024) · Anthrozoös · doi:10.1080/08927936.2024.2333163 · Cited by 5
“Research exploring the general equine experience often focusses on identifying markers of negative stress, such as cortisol (Hovey et al., 2021; Mazzola et al., 2021; Rizzo et al., 2017) and adrenocorticotrophin hormone (Aguilera, 1994; Johnson et al., 2017; Marc et al., 2000).”
BackgroundBorraccia, V., Sblano, S., Carabellese, F., et al. (2012) · Journal of Forensic Sciences · doi:10.1111/j.1556-4029.2012.02161.x · Cited by 5
“It is characterized by an increased production of fluid in the internal ear, secondary to hypersecretion of ADH in response to either exogenous stimuli, largely of an environmental nature (weather, temperature, and atmospheric pressure changes), or endogenous stimuli (stress) (11,12), and by an anomalous response by t…”
BackgroundSugimoto, K., Ohmomo, H., Shutoh, F., Nogami, H., & Hisano, S. (2014) · Neuroscience Research · doi:10.1016/j.neures.2014.11.010 · Cited by 6
Zhang, M., Li, X., Li, J., Sun, H., Zhang, X., & Bao, J. (2017) · Asian-Australasian Journal of Animal Sciences · doi:10.5713/ajas.17.0013 · Cited by 5
“cause stress closer to delivery and then weaken the human PLR response [25], significantly lowering the pupillary contraction amplitude [26].”
BackgroundAnother Side of the Antidiuretic Hormone, Vasopressin: Its Role in Stress Regulation
Zelena, D. R., & Jain, S. K. (2011) · Journal of Experimental Sciences · Cited by 5
Dynamics of the HPA Axis: A Systems Modeling Approach
Terry, J. R., Walker, J. J., Spiga, F., & Lightman, S. L. (2016) · Computational Neuroendocrinology · doi:10.1002/9781119159438.ch8 · Cited by 5
Distinct adrenal gland macrophages regulate corticosteroid productionPreprint
O’Brien, C. J. O., Sidarta-Oliveira, D., Stawiarski, A., Ratti, G., Loyher, P.-L., Makhlouf, M., AbouMoussa, E. H., Haberman, E. R., Sweeney, C. A. P., Mizuno, Y., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.05.556330 · Cited by 5
Mornagui, B., Rezg, R., Grissa, A., Duvareille, M., Gharib, C., Kamoun, A., El‐Fazâa, S., & Gharbi, N. (2010) · Journal of Physiology and Biochemistry · doi:10.1007/s13105-010-0026-6 · Cited by 5
“Thus, stress paradigms in which ACTH responses are reduced show vasopressin receptor downregulation in the pituitary, whereas stress paradigms with enhanced ACTH responses to a novel stress are associated with vasopressin receptor upregulation [4].”
An Introduction: Overview of Nervous System and Brain Disorders
Ayub, M., & Mallamaci, A. (2023) · Food bioactive ingredients · doi:10.1007/978-3-031-41188-5_1 · Cited by 8
Sarahian, N., Sahraei, H., Zardooz, H., Alibeik, H., Sadeghi, B., Javadifar, T.-S., Herfehdoost, G., Ehteram, B. Z., Ghanbari, Z., & Hoseini-Namvar, F. (2015) · Cited by 4
The surgical patient taking glucocorticoids
Welsh, G. A., Manzullo, E. F., & Nieman, L. K. (2007) · Cited by 4
UNDERSTANDING THE ROLE OF VASOPRESSIN IN THE HYPOTHALAMO-PITUITARY ADRENOCORTICAL AXIS
Buckingham, J. C. (2009) · IMPERIAL COLLEGE PRESS eBooks · doi:10.1142/9781848162952_0009 · Cited by 4
Schmidt, B. L., Santos, M. J., Cariaga-Martínez, A. E., Hill, L., Barloese, M. C. J., & Hall, Z. J. (2017) · Cited by 4
Repaske, D. R. (2009) · Wiley eBooks · doi:10.1002/9781444316728.ch15 · Cited by 4
Green, R. P., Majzoub, J. A., & Muglia, L. J. (2005) · Clinical Pediatric Endocrinology · doi:10.1002/9780470987117.ch17 · Cited by 4
Adrenocorticotropic Hormone (ACTH)
Rhodes, M. E. (2007) · Elsevier eBooks · doi:10.1016/b978-012373947-6.00012-x · Cited by 4
Williams, A. F., Boles, J. A., Herrygers, M. R., et al. (2016) · Journal of Animal Science · doi:10.2527/jam2016-1094 · Cited by 4
“Stimuli identification initiates a complex cascade of neuroendocrine signals allowing animals to change metabolic and physiological processes to maintain homeostasis (Aguilera, 1994).”
BackgroundNovel molecular insights into the role of CRH type 1 receptor in the pathophysiology of depression
Rakeshkumar, P. P., Bommaraju, S., Datusalia, A. K., & Nayak, P. K. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117430 · Cited by 4
Siddiqui, S. H., Komnenov, D., Olayonwa, A., & Rossi, N. F. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70105 · Cited by 3
“18 Nota-bly, CMS increases expression of V 1b R within the PVN. 19,20 When compared with unstressed counterparts, male rats that have undergone a 4-week CMS paradigm display elevated resting blood pressure and renal sympathetic nerve activity (RSNA) and display a profoundly augmented RSNA response…”
Intermittent Hypoxia and Weight Loss: Insights into the Etiology of the Sleep Apnea Phenotype
Gagnon, M., Fournier, S., Marcouiller, F., Guay, L. M., Joseph, V., Michael, N. J., & Kinkead, R. (2023) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-32371-3_7 · Cited by 3
CRHBP, a novel multiple cancer biomarker connected with better prognosis and anti-tumorigenicity
Yoo, W., Choi, H., Lee, J., Lee, Y., Park, K. C., & Noh, K. (2024) · Cancer Cell International · doi:10.1186/s12935-024-03562-4 · Cited by 4
Sinen, O., Akçalı, İ., Akkan, S. S., & Bülbül, M. (2023) · Neurogastroenterology & Motility · doi:10.1111/nmo.14719 · Cited by 4
“46 In rats, it was shown that icv administration of OXA stimulated the increases in plasma concentrations of CORT and ACTH within 40 min and 90 min postinjection phases, respectively.”
BackgroundAcceleration of irregular estrous cycle in forced running by midbrain raphe lesions in female rats
Shimizu, H., & Yamanouchi, K. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.03.063 · Cited by 3
Different Types of Stress as Highly Complex Endocrine and Biochemical Phenomena: A Reappraisal
Goudochnikov, V. I. (2022) · Open Access Journal of Endocrinology · doi:10.23880/oaje-16000171 · Cited by 3
Primary and secondary thrombocytosis induced by exercise and environmental luminosity
Beck, W. R., Menezes, P. P., & Gobatto, C. A. (2014) · Bratislavské lekárske listy/Bratislava medical journal · doi:10.4149/bll_2014_117 · Cited by 3
“Probably the adverse conditions increased adrenocorticotropic hormone (24) and consequently adrenaline and corticosterone (25).”
Morphofunctional Characteristics of Pituitary Adrenocorticotropes in An Animal Model of Heat Stress
Perčinić-Popovska, F., Ajdžanović, V. Z., Dinevska-Kofkarovska, S., et al. (2011) · Journal of Medical Biochemistry · doi:10.2478/v10011-011-0030-6 · Cited by 3
“ACTH, re leased into the peripheral circulation in response to stress, stimulates the synthesis and secretion of adre nal glucocorticoids (3, 5, 6).”
BackgroundNikoo, G. B., Khosravi, M., Sahraei, H., Ranjbaran, M., Sarahian, N., Zardooz, H., Bourbour, Z., Alemaref, M., Jahromi, G. P., & Herfehdoost, G. (2014) · Cited by 3
The genomic profiling and MAMLD1 expression in human and canines with Cushing’s disease
Wang, A., Neill, S. G., Newman, S., et al. (2021) · BMC Endocrine Disorders · doi:10.1186/s12902-021-00845-z · Cited by 3
Bethin, K. E., & Muglia, L. J. (2013) · Humana Press eBooks · doi:10.1007/978-1-60761-395-4_12 · Cited by 3
Regulation and Actions of Corticotropin‐Releasing Hormone
Weninger, S. C., & Majzoub, J. A. (2001) · Comprehensive physiology · doi:10.1002/cphy.cp070406 · Cited by 5
Oliveira, P., Soares, M. C., & Trigo, S. (2024) · Hormones and Behavior · doi:10.1016/j.yhbeh.2024.105646 · Cited by 4
“AVT is involved in the vertebrate stress response by triggering the production of adrenocorticotropin (ACTH) in the hypothalamic – pituitary – adrenal (HPA) axis, both in mammals and birds (Aguilera, 1994; Harding and Rowe, 2003; Rotondo et al., 2016; Stewart et al., 2008).”
BackgroundRaghavendhira, H., Srinivasan, D., Paul, J., Rajan, R., & Bhaskaran, R. S. (2025) · Gene Expression Patterns · doi:10.1016/j.gep.2025.119391 · Cited by 2
Brain peptides in Alzheimer’s disease - pathophysiology and therapeutic advances
Pahal, S., Gupta, A., Kumar, V., Singh, P. B. R. P., Kaushik, M., Pahal, V., Atluri, G., & Chaudhary, A. (2026) · Cell and Tissue Research · doi:10.1007/s00441-026-04055-8 · Cited by 3
The gut as a central hub for multi-organ crosstalk in aging
Zhang, X., Li, R., Gao, Y., Zhang, W., Ni, T., & Liu, Y. (2026) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-026-06129-w · Cited by 7
Toleкova, A., Hadzhibozheva, P., Georgiev, T., Mihailova, S., Ilieva, G., Gulubova, M. V., Leventieva-Necheva, E., Milenov, K., & Kalfi, R. (2012) · InTech eBooks · doi:10.5772/48417 · Cited by 1
“Aguilera supposed that in chronic stress there is preferential activation of vasopressin rather than corticoliberin and as a consequence a feedback mechanism is disintegrated (Aguilera, 1994).”
BackgroundHypothalamo-pituitary-adrenocortical and sympatho-adrenomedullar systems in stress response
Cvijić, G., & Djordjevic, J. D. (2003) · Jugoslovenska medicinska biohemija · doi:10.2298/jmh0301003c · Cited by 2
Single‐cell genomics meets systems neuroscience: Insights from mapping the brain circuitry of stress
Hanchate, N. K. (2025) · Journal of Neuroendocrinology · doi:10.1111/jne.70005 · Cited by 2
“69,70 The co-expression of other neuropeptides (e.g., neurotensin, galanin) in PVN CRHNs and their precise physiological roles are yet to be determined.”
Disorders of the Adrenal Gland
Fechner, P. Y. (2018) · Elsevier eBooks · doi:10.1016/b978-0-323-40139-5.00096-6 · Cited by 2
Arginine Vasopressin Gene Variation and Behavioural Inhibition in Children: an Exploratory Study
Bisceglia, R., Jenkins, J. M., Barr, C. L., Wigg, K. G., & Schmidt, L. A. (2014) · Infant and Child Development · doi:10.1002/icd.1866 · Cited by 2
Aguilera, G. (2015) · Interdisciplinary Information Sciences · doi:10.4036/iis.2015.b.13 · Cited by 2
Self-citationDisorders of the Adrenal Gland
Nimkarn, S., & New, M. I. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4377-0134-0.10091-5 · Cited by 2
Hypothalamic–Pituitary–Adrenal Cortical Axis
Rhodes, M. E., McKlveen, J. M., Ripepi, D. R., & Gentile, N. E. (2009) · Elsevier eBooks · doi:10.1016/b978-008088783-8.00073-5 · Cited by 5
Bethin, K. E., Majumdar, I., & Muglia, L. J. (2024) · Springer eBooks · doi:10.1007/978-3-031-66296-6_10 · Cited by 2
Nonpeptide vasopressin V1b receptor antagonists
Griebel, G., & Gal, C. S. (2005) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(05)80066-5 · Cited by 3
Gatehouse, M. (2008) · UC Research Repository (University of Canterbury) · doi:10.26021/5671 · Cited by 2
Parker, C. R. (1997) · Humana Press eBooks · doi:10.1007/978-1-4757-2584-1_2 · Cited by 2
Novel Targets for Drug Treatment in Psychiatry
Kurita, M., García‐Bea, A., & González‐Maeso, J. (2016) · Springer eBooks · doi:10.1007/978-1-4939-2528-5_30 · Cited by 1
Disorders of the Adrenal Gland
Fechner, P. Y. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-82823-9.00084-2 · Cited by 1
Nociceptive sensitivity and body weight in rats under chronic unpredictable stress
Skripkina, D. V., Abramova, A. Y., Nikenina, E. V., et al. (2024) · Russian Journal of Pain · doi:10.17116/pain2024220215 · Cited by 1
Shiozaki, H., Fujioka, S., Takano, Y., Shimazaki, T., Suka, M., Sakamoto, T., Gocho, T., Nakamoto, K., Toya, N., & Ikegami, T. (2025) · Surgery Today · doi:10.1007/s00595-025-03128-5 · Cited by 1
“Acute physical stress activates the hypothalamic–pituitary–adrenal (HPA) axis, increasing plasma adrenocorticotropic hormone (ACTH) and serum cortisol levels [7].”
Cicha, E., Blatkiewicz, M., Jopek, K., Szyszka, M., Malendowicz, P. W., Olechnowicz, A., Malendowicz, L. K., & Ruciński, M. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48020135 · Cited by 2
“Hypothalamic corticotropin-releasing hormone (CRH) has been shown to stimulate the release of adrenocorticotropic hormone (ACTH) from the anterior pituitary, which in turn acts on the adrenal cortex to promote glucocorticoid synthesis and secretion [1,2].”
Marques, D. A., Guay, L. M., Koogler, A. A., Ostrowski, T. D., de Souza, A. M. A., Sandberg, K. L., & Kinkead, R. (2026) · Experimental Physiology · doi:10.1113/ep093539 · Cited by 1
“However, a dissociation between ACTH and corticosterone can occur (Aguilera, 1994) and the results observed in ageing females are in line with previous evidence from male studies showing that early-life stress reduces adrenal sensitivity to ACTH stimulation, resulting in lower corticosterone output…”
Identification of Cushing's syndrome (CS) and its history from Harvey Cushing to today
Poirier, J., Martel‐Duguech, L., Bourdeau, I., & Lacroix, A. (2026) · Elsevier eBooks · doi:10.1016/b978-0-323-96100-4.00012-0 · Cited by 1
Vasoactive Hormones and Regulation of the Hypothalamic-Pituitary-Adrenal Axis
Aguilera, G., Rabadan‐Diehl, C., Kiss, A., & Ochędalski, T. (2002) · Advances in behavioral biology · doi:10.1007/978-1-4757-3538-3_66 · Cited by 1
Self-citationRole of the ACTH/MC2R System in the Hair Cycle in Mice
Hiramoto, K., Orita, K., Yamate, Y., & Kasahara, E. (2016) · Journal of Biosciences and Medicines · doi:10.4236/jbm.2016.47001 · Cited by 1
Disorders of the Adrenal Gland
Bethin, K. E., & Muglia, L. J. (2005) · Elsevier eBooks · doi:10.1016/b978-072169347-7.50092-5 · Cited by 1
Sivukhina, E. V., & Jirikowski, G. F. (2018) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2018.12.008 · Cited by 1
Zimmer, P., & Rüffer, J. U. (2012) · Springer eBooks · doi:10.1007/978-3-642-25066-8_7 · Cited by 1
KOBAY ADRENAL KORTEKSİNDE GESTASYONEL DEĞİŞİKLİKLER: MORFOMETRİK VE HİSTOLOJİK BİR ÇALIŞMA
Özbek, E. (1999) · Turkiye Klinikleri Journal of Case Reports · Cited by 1
Beck, W. R., Forte, L. D. M., & Gobatto, C. A. (2015) · journal of physical education · doi:10.4025/reveducfis.v26i1.23186 · Cited by 1
“Essas condições podem causar aumento nas concentrações de hormônio adrenocorticotrópico (AGUILERA, 1994), conduzindo à liberação de adrenalina e corticosterona (AXELROD; REISINE, 1984).”
BackgroundCruickshank, N. C. (2017) · ScholarWorks -A service of University of Vermont Libraries (University of Vermont) · Cited by 1
Amri, N., Habbachi, S., Ibtissem, S., et al. (2020) · Journal of Animal Behaviour and Biometeorology · doi:10.31893/jabb.21005 · Cited by 1
“An extended maternal separation (SM) is enough to increase the ACTH and corticosterone levels, especially when the studied rat is aged 07 days (Aguilera 1994).”
BackgroundThe Endocrine Response to Stress
Henley, D., Upton, T. J., & Lightman, S. L. (2022) · doi:10.1093/med/9780198870197.003.0203 · Cited by 1
Bethin, K. E., Majumdar, I., & Muglia, L. J. (2018) · Springer eBooks · doi:10.1007/978-3-319-73782-9_13 · Cited by 1
Neuroendocrinology of Bipolar Illness
Dinan, T. G., & Bauer, M. (2010) · doi:10.1002/9780470661277.ch19 · Cited by 1
Consequences of chronic psychosocial stress in male wistar rats
Nyuyki, K. D. (2013) · University of Regensburg Publication Server (University of Regensburg) · doi:10.5283/epub.27726 · Cited by 1
Ježová, D., Kiss, A., & Aguilera, G. (1996) · Stress · doi:10.3109/10253899609001097 · Cited by 1
Self-citationVasopressin: The neglected target for stress modulation?
Dinan, T. G. (2005) · Stress and Health · doi:10.1002/smi.1054 · Cited by 1
Naugle, A. L. (2003) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 1
Cummings, S. A. (2011) · UC Research Repository (University of Canterbury) · doi:10.26021/8934 · Cited by 1
Høyland, M. (2018) · NORA - Norwegian Open Research Archives · Cited by 1
Stress-induced neuronal hypertrophy decreases the intrinsic excitability in stress habituationPreprint
Matovic, S., Ichiyama, A., Igarashi, H., Salter, E. W., Wang, X.-F., Henry, M. S., Vernoux, N., Tremblay, M., & Inoue, W. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/593665
Dorin, R. I., & Crapo, L. M. (1997) · Humana Press eBooks · doi:10.1007/978-1-4612-3954-3_8 · Cited by 1
Manière, M. (2015) · theses.fr (ABES) · doi:10.70675/0be8e854za3f5z48bcz81c6zbe779562a135 · Cited by 1
Papel da corticosterona na vigência do estresse sobre a função pineal em ratos.
Moraes, R. C. (2010) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.42.2010.tde-18102010-153227
Aguilera, G. (2004) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-18497-0_6
“The regulation of ACTH synthesis and secretion is multifactorial, involving the stimulatory effect of the neuropeptides, corticotropin-releasing hormone (CRH) and vasopressin (VP), produced by parvocellular neurons of the hypothalamic paraventricular nucleus (PVN) and negative feedback by glucocorticoids ( Aguilera 19…”
BackgroundSelf-citationPolli, S. (2008) · doi:10.11606/d.42.2008.tde-07102008-131916
“…de corticosteróides naturais ou dexametasona, um corticosteróide sintético presente na corrente sanguínea, de maneira que, por efeito de uma retroalimentação negativa, este corticosteróide chega ao hipotálamo e a adeno-hipófise e inibe a produção, respectivamente, do CRF e do ACTH (AGUILERA, 1994).”
BackgroundFreiwilliger Alkoholkonsum bei Nagern: Einfluss von Emotionalität und Stress
Henniger, M. S. H. (2002) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.248
Lakic, I. V., Vujovic, P. Z., Jasnic, N. I., Djurasevic, S. F., & Cvijić, G. (2011) · Archives of Biological Sciences · doi:10.2298/abs1103579l
“an important role in corticotrophe cell responsiveness to stressors, as judged by the good correlation between receptor concentration and ACTH responses in the pituitary (Aguilera, 1994; Aguilera et al., 1994).”
BackgroundResultInfluentialGasperi, D. D., da Silveira, E. A., da Silva, D. R. P., Pereira, R. C. D. F., Portela, L. O. C., Brass, K. E., & Côrte, F. D. D. L. (2011) · Ciência Rural · doi:10.1590/s0103-84782011000300016
Fan, S. (2006) · UC Research Repository (University of Canterbury) · doi:10.26021/7257
Metadata
- Authors
- Aguilera, G.
- Affiliations
- National Institutes of Health (US)
- Corresponding author
- Aguilera, Greti
- Venue
- Frontiers in Neuroendocrinology
- Publisher
- Elsevier BV
- Published
- 1994-12
- Volume
- 15
- Issue
- 4
- Pages
- 321-350
- ISSN
- 0091-3022 (ISSN-L)
- OpenAlex
- W2031934304
- Cited by
- 557
- References
- 0
- Citations by year
- 2026: 10 · 2025: 11 · 2024: 14 · 2023: 16 · 2022: 11 · 2021: 12 · 2020: 11 · 2019: 14 · 2018: 11 · 2017: 17 · 2016: 21 · 2015: 19 · 2014: 14 · 2013: 18 · 2012: 18
- FWCI
- 5.50
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Frontiers in Neuroendocrinology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Keywords
- ACTH secretion, chronic stress, hypothalamic-pituitary-adrenal axis, corticotropin-releasing factor, vasopressin, corticotrophs, glucocorticoid negative feedback, paraventricular nucleus, supraoptic nucleus, osmotic stimulation, glucocorticoid receptor, stress adaptation, corticosterone, insulin-induced hypoglycemia
- MeSH terms
- Adrenocorticotropic Hormone, Animals, Corticosterone, Corticotropin-Releasing Hormone, Glucocorticoids, Homeostasis, Humans, Hypothalamus, Pituitary Gland, Stress, Physiological, Vasopressins
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.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review