Corticosterone effects on corticotropin-releasing hormone mRNA in the central nucleus of the amygdala and the parvocellular region of the paraventricular nucleus of the hypothalamus

The rat brain in stereotaxic coordinates

Palkovits, M. (1983) · Neuropeptides · doi:10.1016/0143-4179(83)90049-5 · Cited by 28,959

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585

Physiological functions of glucocorticoids in stress and their relation to pharmacological actions

MUNCK, A., GUYRE, P. M., & HOLBROOK, N. J. (1984) · Endocrine Reviews · doi:10.1210/edrv-5-1-25 · Cited by 3,083

The Concepts of Stress and Stress System Disorders: Overview of Physical and Behavioral Homeostasis

Chrousos, G. P. (1992) · JAMA · doi:10.1001/jama.1992.03480090092034 · Cited by 2,689

The role of the amygdala in fear and anxiety

Davis, M. (1992) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.15.030192.002033 · Cited by 2,357

Organization of ovine corticotropin-releasing factor immunoreactive cells and fibers in the rat brain: an immunohistochemical study

Swanson, L. W., Sawchenko, P. E., Rivier, J., & Vale, W. W. (2008) · Neuroendocrinology · doi:10.1159/000123454 · Cited by 1,953

The amygdala: Neurobiological aspects of emotion, memory, and mental dysfunction.

Aggleton, J. P. (1992) · Wiley-Liss eBooks · Cited by 1,536

Elevated Concentrations of CSF Corticotropin-Releasing Factor-Like Immunoreactivity in Depressed Patients

Nemeroff, C. B., Widerlöv, E., Bissette, G., Walléus, H., Karlsson, I., Eklund, K., Kilts, C. D., Loosen, P. T., & Vale, W. (1984) · Science · doi:10.1126/science.6334362 · Cited by 1,485

Physiological and behavioral responses to corticotropin-releasing factor administration: is CRF a mediator of anxiety or stress responses?

Dunn, A. J., & Berridge, C. W. (1990) · Brain Research Reviews · doi:10.1016/0165-0173(90)90012-d · Cited by 1,352

Clinical and Biochemical Manifestations of Depression

Gold, P. W., Goodwin, F. K., & Chrousos, G. P. (1988) · New England Journal of Medicine · doi:10.1056/nejm198808183190706 · Cited by 1,057

Corticosterone Acts Directly at the Amygdala to Alter Spinal Neuronal Activity in Response to Colorectal Distension

Qin, C., Meerveld, B. G., Myers, D. A., & Foreman, R. D. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00834.2002 · Cited by 41

Levels of maternal serum corticotropin-releasing hormone (CRH) at midpregnancy in relation to maternal characteristics

Chen, Y., Holzman, C., Chung, H., Senagore, P. K., Talge, N. M., & Siler-Khodr, T. M. (2009) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2009.11.007 · Cited by 41

Prophylactic and therapeutic effects of acute systemic injections of EMD 281014, a selective serotonin 2A receptor antagonist on anxiety induced by predator stress in rats

Adamec, R. E., Creamer, K., Bartoszyk, G. D., & Burton, P. (2004) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2004.09.017 · Cited by 41

Knockdown of steroid receptors in the central nucleus of the amygdala induces heightened pain behaviors in the rat

Johnson, A. C., & Meerveld, B. G. (2015) · Neuropharmacology · doi:10.1016/j.neuropharm.2015.01.018 · Cited by 40

Isoform switching of steroid receptor co-activator-1 attenuates glucocorticoid-induced anxiogenic amygdala CRH expression

Zalachoras, I., Verhoeve, S. L., Toonen, L. J. A., van Weert, L. T. C. M., van Vlodrop, A. M., Mol, I., Meelis, W., de Kloet, E. R., & Meijer, O. C. (2016) · Molecular Psychiatry · doi:10.1038/mp.2016.16 · Cited by 40

Regulation of Corticotropin-Releasing Factor (CRF) Messenger Ribonucleic Acid and CRF Peptide in the Amygdala: Studies in Primary Amygdalar Cultures

Kasckow, J. W., Regmi, A., Gill, P. S., Parkes, D. G., & Geracioti, T. D. (1997) · Endocrinology · doi:10.1210/endo.138.11.5543 · Cited by 40

Exposure to repeated low-level formaldehyde in rats increases basal corticosterone levels and enhances the corticosterone response to subsequent formaldehyde

Sorg, B. A., Bailie, T. M., Tschirgi, M. L., Li, N., & Wu, W.-R. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02208-9 · Cited by 39

Mechanisms of Stress‐Induced Visceral Pain: Implications in Irritable Bowel Syndrome

Meerveld, B. G., Moloney, R. D., Johnson, A. C., & Vicario, M. (2016) · Journal of Neuroendocrinology · doi:10.1111/jne.12361 · Cited by 39

Increased mRNA for corticotrophin releasing hormone in the amygdala of Fawn‐hooded rats: A potential animal model of anxiety

Altemus, M. M., Smith, M. A., Diep, V., Aulakh, C. S., & Murphy, D. L. (1994) · Anxiety · doi:10.1002/anxi.3070010602 · Cited by 39

The Interplay between the Hippocampus and Amygdala in Regulating Aberrant Hippocampal Neurogenesis during Protracted Abstinence from Alcohol Dependence

Mandyam, C. D. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00061 · Cited by 41

Corticotropin-releasing hormone signals adversity in both the placenta and the brain: regulation by glucocorticoids and allostatic overload

Schulkin, J. A. (1999) · Journal of Endocrinology · doi:10.1677/joe.0.1610349 · Cited by 38

The debate over neurotransmitter interaction in aspartame usage

Choudhary, A. K., & Lee, Y. Y. (2018) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2018.06.043 · Cited by 39

Different Views of Anxiety Disorders

Selek, S. (2011) · InTech eBooks · doi:10.5772/1022 · Cited by 39

Can the Behaviour Abnormalities Induced by Gestational Stress in Rats be Prevented or Reversed?

Weinstock, M. (2002) · Stress · doi:10.1080/1025389021000010503 · Cited by 37

Rapid Induction of Corticotropin-Releasing Hormone Gene Transcription in the Paraventricular Nucleus of the Developing Rat

Dent, G. W. (2000) · Endocrinology · doi:10.1210/en.141.5.1593 · Cited by 37

Amygdala microglia modify neuronal plasticity via complement C1q/C3-CR3 signaling and contribute to visceral pain in a rat model

Yuan, T., Orock, A. M., & Meerveld, B. G. (2021) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00123.2021 · Cited by 36

Effects of Sodium Valproate on Corticotropin-Releasing Factor Systems in Rat Brain

Stout, S. (2001) · Neuropsychopharmacology · doi:10.1016/s0893-133x(00)00243-8 · Cited by 36

Distinct populations of corticotropin-releasing factor (CRF) neurons mediate divergent yet complementary defensive behaviors in response to a threat

Chudoba, R., & Dabrowska, J. (2023) · Neuropharmacology · doi:10.1016/j.neuropharm.2023.109461 · Cited by 38

Hormonal and molecular effects of restraint stress on formalin-induced pain-like behavior in male and female mice

Long, C. C., Sadler, K. E., & Kolber, B. J. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.08.009 · Cited by 37

Treatment with CRH‐1 antagonist antalarmin reduces behavioral and endocrine responses to social stressors in marmosets (Callithrix kuhlii)

French, J. A., Fite, J. E., Jensen, H., Oparowski, K., Rukstalis, M. R., Fix, H., Jones, B., Maxwell, H., Pacer, M., Power, M. L., et al. (2007) · American Journal of Primatology · doi:10.1002/ajp.20385 · Cited by 31

Nutraceuticals to promote neuronal plasticity in response to corticosterone-induced stress in human neuroblastoma cells

Gite, S., Ross, R. P., Kirke, D. A., Guihéneuf, F., Aussant, J., Stengel, D. B., Dinan, T. G., Cryan, J. F., & Stanton, C. (2018) · Nutritional Neuroscience · doi:10.1080/1028415x.2017.1418728 · Cited by 35

Glucocorticoids Regulation of FosB/ΔFosB Expression Induced by Chronic Opiate Exposure in the Brain Stress System

García‐Pérez, D., Laorden, M. L., Milanés, M. V., & Núñez, C. (2012) · PLoS ONE · doi:10.1371/journal.pone.0050264 · Cited by 34

Differential disinhibition of the neonatal hypothalamic– pituitary–adrenal axis in brain‐specific CRH receptor 1‐knockout mice

Schmidt, M. V., Deussing, J. M., Oitzl, M. S., Ohl, F., Levine, S., Wurst, W., Holsboer, F., Müller, M. B., & de Kloet, E. R. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05121.x · Cited by 34

Neuropeptides and Anxiety-Related Behavior.

Landgraf, R. (2001) · Endocrine Journal · doi:10.1507/endocrj.48.517 · Cited by 34

Repeated low level formaldehyde exposure produces enhanced fear conditioning to odor in male, but not female, rats

Sorg, B. A., Swindell, S., & Tschirgi, M. L. (2004) · Brain Research · doi:10.1016/j.brainres.2004.02.015 · Cited by 33

Adrenal Activity during Repeated Long-Access Cocaine Self-Administration is Required for Later CRF-Induced and CRF-Dependent Stressor-Induced Reinstatement in Rats

Graf, E. N., Hoks, M. A., Baumgardner, J., Sierra, J. F. R., Vranjkovic, O., Bohr, C., Baker, D. L., & Mantsch, J. R. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.28 · Cited by 32

Gene–environment interactions resulting in risk alcohol drinking behaviour are mediated by CRF and CRF1

Clarke, T., & Schumann, G. (2009) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2009.04.014 · Cited by 32

Coordinate and Divergent Regulation of Corticotropin-Releasing Factor (CRF) and CRF-Binding Protein Expression in an Immortalized Amygdalar Neuronal Cell Line**Portions of this report were presented in abstract form at the 1997 and 1998 annual meetings of The Endocrine Society.

Mulchahey, J. J., Regmi, A., Sheriff, S., Balasubramaniam, A., & Kasckow, J. W. (1999) · Endocrinology · doi:10.1210/endo.140.1.6406 · Cited by 32

Pathways to relapse: factors controlling the reinitiation of drug seeking after abstinence.

Stewart, J. (2004) · PubMed · Cited by 32

Central Role of the Brain in Stress and Adaptation

McEwen, B. S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-800951-2.00005-4 · Cited by 39

The effects of repeated corticosterone exposure on the interoceptive effects of alcohol in rats

Besheer, J., Fisher, K. R., Grondin, J. J. M., Cannady, R., & Hodge, C. W. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2533-8 · Cited by 32

The dissociation of catecholamine and hypothalamic-pituitary-adrenal responses to daily stressors using dexamethasone

Malarkey, W. B., Lipkus, I. M., & Cacioppo, J. T. (1995) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.80.8.7629242 · Cited by 31

Effect of glucocorticoids on the adrenocortical axis responses to electrical stimulation of the amygdala and the ventral noradrenergic bundle

Weidenfeld, J., Itzik, A., & Feldman, S. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00078-4 · Cited by 31

Corticotropin‐releasing hormone‐synthesizing neurons of the human hypothalamus receive neuropeptide Y‐immunoreactive innervation from neurons residing primarily outside the infundibular nucleus

Mihály, E., Fekete, C., Lechan, R. M., & Liposits, Z. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10193 · Cited by 31

The nature of personality disorder

Adshead, G. M. J., & Sarkar, J. (2012) · Advances in Psychiatric Treatment · doi:10.1192/apt.bp.109.006981 · Cited by 31

Organic cation transporter 3 and the dopamine transporter differentially regulate catecholamine uptake in the basolateral amygdala and nucleus accumbens

Holleran, K. M., Rose, J. H., Fordahl, S., Benton, K. C., Rohr, K. E., Gasser, P., & Jones, S. R. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14927 · Cited by 25

Molecular Biology of Glucocorticoid Signaling

Arango-Lievano, M., Lambert, W. M., & Jeanneteau, F. D. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-1-4939-2895-8_2 · Cited by 28

Stress and eating: a dual role for bombesin-like peptides

Merali, Z., Graitson, S., MacKay, J. C., & Kent, P. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00193 · Cited by 30

Crossroads of corticotropin releasing hormone, corticosteroids and monoamines

van Praag, H. M. (2002) · Neurotoxicity Research · doi:10.1080/1029842021000022115 · Cited by 29

Differential Influence of Early Life and Adult Stress on Urogenital Sensitivity and Function in Male Mice

Fuentes, I. M., Pierce, A. N., Silvestro, E. R. D., Maloney, M. O., & Christianson, J. A. (2018) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2017.00097 · Cited by 28

Rodent anxiety and kindling of the central amygdala and nucleus basalis

Adamec, R., & Shallow, T. (2000) · Physiology & Behavior · doi:10.1016/s0031-9384(00)00250-x · Cited by 27

Neurobiological aspects of pain in the context of alcohol use disorder

Cucinello‐Ragland, J. A., & Edwards, S. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2020.09.001 · Cited by 27

The importance of corticosterone in mediating restraint-induced weight loss in rats

Scherer, I. J., Holmes, P. V., & Harris, R. B. S. (2010) · Physiology & Behavior · doi:10.1016/j.physbeh.2010.11.014 · Cited by 27

Glucocorticoid Receptor Signaling Contributes to Constitutive Activation of the Noncanonical NF-κB Pathway in Term Human Placenta

Wang, B., Palomares, K. T. S., Parobchak, N., Cece, J. A., Rosen, M., Nguyen, A., & Rosen, T. (2012) · Molecular Endocrinology · doi:10.1210/me.2012-1309 · Cited by 27

Transient forebrain over-expression of CRF induces plasma corticosterone and mild behavioural changes in adult conditional CRF transgenic mice

Vicentini, E., Arban, R., Angelici, O., Maraia, G., Perico, M. E., Mugnaini, M., Ugolini, A., Large, C. H., Domenici, E., Gerrard, P. A., et al. (2009) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2009.03.015 · Cited by 27

Adaptation and well-being : social allostasis

Schulkin, J. A. (2011) · Cited by 26

Molecular reactivity of mesocorticolimbic brain areas of high and low grooming rats after elevated plus maze exposure

Koya, E., Spijker, S., Homberg, J. R., Voorn, P., Schoffelmeer, A. N. M., Vries, T. J. D., & Smit, A. B. (2005) · Molecular Brain Research · doi:10.1016/j.molbrainres.2005.03.005 · Cited by 27

Amygdala Kindling and Rodent Anxiety

Adamec, R. E. (1998) · Advances in behavioral biology · doi:10.1007/978-1-4615-5375-5_24 · Cited by 27

Desipramine prevents the sustained increase in corticotropin‐releasing hormone‐like immunoreactivity induced by repeated immobilization stress in the rat central extended amygdala

Santibañez, M., Gysling, K., & Forray, M. I. (2006) · Journal of Neuroscience Research · doi:10.1002/jnr.21023 · Cited by 26

Role of testosterone in mediating prenatal ethanol effects on hypothalamic–pituitary–adrenal activity in male rats

Lan, N., Hellemans, K. G. C., Ellis, L. A., Viau, V., & Weinberg, J. (2009) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2009.04.001 · Cited by 27

Hepatic vagotomy alters limbic and hypothalamic neuropeptide responses to insulin‐dependent diabetes and voluntary lard ingestion

la Fleur, S. E., Manalo, S. L., Roy, M., Houshyar, H., & Dallman, M. F. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04125.x · Cited by 26

Environmental stressors and alcoholism development: Focus on molecular targets and their epigenetic regulation

Pucci, M., Bonaventura, M. V. M. D., Wille‐Bille, A., Fernández, M. S., Maccarrone, M., Pautassi, R. M., Cifani, C., & D’Addario, C. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.07.004 · Cited by 27

Reduced brain CRH and GR mRNA expression precedes obesity in juvenile rats bred for diet-induced obesity

Michel, C., Dunn-Meynell, A. A., & Levin, B. E. (2004) · Behavioural Brain Research · doi:10.1016/j.bbr.2004.03.019 · Cited by 25

Neuroanatomical distribution and colocalisation of nuclear receptor corepressor (N-CoR) and silencing mediator of retinoid and thyroid receptors (SMRT) in rat brain.

van der Laan, S., Lachize, S. B., Schouten, T. G., Vreugdenhil, E., de Kloet, E. R., & Meijer, O. C. (2005) · Brain Research · doi:10.1016/j.brainres.2005.08.011 · Cited by 27

Up-regulation of galanin and corticotropin-releasing hormone mRNAs in the key hypothalamic and amygdaloid nuclei in a mouse model of visceral pain

Nishii, H., Nomura, M. J., Aono, H., Fujimoto, N., & Matsumoto, T. (2007) · Regulatory Peptides · doi:10.1016/j.regpep.2006.12.022 · Cited by 24

Anxiogenesis induced by social defeat in male mice: Role of nitric oxide, NMDA, and CRF1 receptors in the medial prefrontal cortex and BNST

Faria, M. P., Laverde, C. F., & Nunes‐de‐Souza, R. L. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.107973 · Cited by 24

Sleep Endocrine Effects of the 11-β-Hydroxysteroiddehydrogenase Inhibitor Metyrapone

Jahn, H., Kiefer, F., Schick, M., Yassouridis, A., Steiger, A., Kellner, M. B., & Wiedemann, K. (2003) · SLEEP · doi:10.1093/sleep/26.7.823 · Cited by 24

Adrenalectomy decreases corticotropin-releasing hormone gene expression and increases noradrenaline and dopamine extracellular levels in the rat lateral bed nucleus of the stria terminalis

Santibáñez, M., Gysling, K., & Forray, M. I. (2005) · Journal of Neuroscience Research · doi:10.1002/jnr.20538 · Cited by 24

Coping with Danger: The Neural Basis of Defensive Behavior and Fearful Feelings

LaBar, K. S., & LeDoux, J. E. (2000) · Comprehensive physiology · doi:10.1002/cphy.cp070408 · Cited by 24

Intact Catecholamine Inputs to the Forebrain are Required for Appropriate Regulation of Corticotrophin‐Releasing Hormone and Vasopressin Gene Expression by Corticosterone in the Rat Paraventricular Nucleus

Kaminski, K. L., & Watts, A. G. (2012) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2012.02363.x · Cited by 23

Corticotropin releasing factor type-1 receptor antagonism in the dorsolateral bed nucleus of the stria terminalis disrupts contextually conditioned fear, but not unconditioned fear to a predator odor

Asok, A., Schulkin, J. A., & Rosen, J. B. (2016) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2016.04.021 · Cited by 22

Lack of Decrease in Hypothalamic and Hippocampal Glucocorticoid Receptor mRNA during Starvation

Makino, S., Kaneda, T., Nishiyama, M., Asaba, K., & Hashimoto, K. (2001) · Neuroendocrinology · doi:10.1159/000054677 · Cited by 23

Identifying Early Behavioral and Molecular Markers of Future Stress Sensitivity

Goel, N., & Bale, T. L. (2007) · Endocrinology · doi:10.1210/en.2007-0479 · Cited by 23

Contrasting Effects of Pretraining, Posttraining, and Pretesting Infusions of Corticotropin-Releasing Factor into the Lateral Amygdala: Attenuation of Fear Memory Formation but Facilitation of its Expression

Isogawa, K., Bush, D. E. A., & LeDoux, J. E. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.08.021 · Cited by 22

Amygdaloid Corticotropin-releasing Factor is Involved in the Anxiolytic Effect of Acupuncture during Ethanol Withdrawal in Rats

Zhao, Z., Jin, X., Wu, Y., Yang, X., Xu, Y., Jiang, J. Z., Kim, S. C., Lee, B. H., Yang, C. H., & Zhao, R. (2013) · Journal of Acupuncture and Meridian Studies · doi:10.1016/j.jams.2013.01.017 · Cited by 22

Prenatal stress and enhanced developmental plasticity

Hartman, S., & Belsky, J. (2018) · Journal of Neural Transmission · doi:10.1007/s00702-018-1926-9 · Cited by 26

What Is Stress?

McEwen, B. S., & Karatsoreos, I. N. (2019) · Springer eBooks · doi:10.1007/978-3-030-16996-1_4 · Cited by 25

Associations among parenting experiences during childhood and adolescence, hypothalamus‐pituitary‐adrenal axis hypoactivity, and hippocampal gray matter volume reduction in young adults

Narita, K., Fujihara, K., Takei, Y., Suda, M., Aoyama, Y., Uehara, T., Majima, T., Kosaka, H., Amanuma, M., Fukuda, M., et al. (2011) · Human Brain Mapping · doi:10.1002/hbm.21354 · Cited by 22

Sleep-Disturbance-Induced Microglial Activation Involves CRH-Mediated Galectin 3 and Autophagy Dysregulation

Guo, L., Reed, K. M., Carter, A. M., Cheng, Y., Roodsari, S. K., Pineda, D. M., Wellman, L. L., Sanford, L. D., & Guo, M. (2022) · Cells · doi:10.3390/cells12010160 · Cited by 21

Binge Eating in Female Rats Induced by Yo-Yo Dieting and Stress

Cifani, C., Bonaventura, M. V. M. D., Ciccocioppo, R., & Massi, M. (2012) · Neuromethods · doi:10.1007/978-1-62703-104-2_3 · Cited by 21

Evidence that preimmunization with a heat-killed preparation of Mycobacterium vaccae reduces corticotropin-releasing hormone mRNA expression in the extended amygdala in a fear-potentiated startle paradigm

Loupy, K. M., Arnold, M. R., Hassell, J. E., Lieb, M. W., Milton, L. N., Cler, K. E., Fox, J. H., Siebler, P. H., Schmidt, D., Noronha, S. I. S. R., et al. (2018) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2018.12.015 · Cited by 20

Gene Regulation System of Vasopressin and Corticotoropin-Releasing Hormone

Yoshida, M. (2008) · Gene Regulation and Systems Biology · doi:10.4137/grsb.s424 · Cited by 20

Presence of Corticotrophin‐Releasing Factor and /or Tyrosine Hydroxylase in Cells of a Neural Brain‐Testicular Pathway That are Labelled by a Transganglionic Tracer

James, P., RIVIER, C. L., & Lee, S. (2007) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2007.01630.x · Cited by 20

The neurobiology of stress and its relevance to psychotherapy

Gold, P. W. (2005) · Clinical Neuroscience Research · doi:10.1016/j.cnr.2005.03.006 · Cited by 24

Steroid hormone mediated regulation of corticotropin-releasing hormone gene expression

Ni, X. (2006) · Frontiers in bioscience · doi:10.2741/2019 · Cited by 19

Effects of generalized convulsive seizures on corticotropin-releasing factor neuronal systems

Piekut, D. T., Phipps, B. S., Pretel, S., & Applegate, C. D. (1996) · Brain Research · doi:10.1016/s0006-8993(96)00970-5 · Cited by 19

Regulation of Corticotropin‐Releasing Factor‐Binding Protein Expression in Amygdalar Neuronal Cultures

Kasckow, Regmi, Seasholtz, & Mulchahey (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00413.x · Cited by 18

The role of corticotropin-releasing hormone in the regulation of energy balance

Richard, D. (1999) · Current Opinion in Endocrinology & Diabetes · doi:10.1097/00060793-199902000-00003 · Cited by 18

Corticosterone effects on rat calretinin mRNA in discrete brain nuclei and the testes

Strauss, K. I., Schulkin, J. A., & Jacobowitz, D. M. (1995) · Molecular Brain Research · doi:10.1016/0169-328x(94)00186-i · Cited by 18

Regulation of Corticotropin‐Releasing Factor Secretion and Synthesis in the Human Neuroblastoma Clones‐ BE(2)‐M17 and BE(2)‐C

Kasckow, J., Han, J., Parkes, D. G., MULCHAHEY, J. J., Owens, M. J., Risby, E. D., Fisher, J. M., & Nemeroff, C. B. (1995) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1995.tb00782.x · Cited by 17

Anti-stress and nootropic activity of drugs affecting the renin-angiotensin system in rats based on indirect biochemical evidence

Kumar, K. A., Nagwar, S., Thyloor, R., & Satyanarayana, S. (2014) · Journal of the Renin-Angiotensin-Aldosterone System · doi:10.1177/1470320313516173 · Cited by 16

Reinterpretation of Basal Glucocorticoid Feedback: Implications to Behavioral and Metabolic Disease

Laugero, K. D. (2004) · Vitamins and hormones · doi:10.1016/s0083-6729(04)69001-7 · Cited by 16

Coordinate and Divergent Regulation of Corticotropin-Releasing Factor (CRF) and CRF-Binding Protein Expression in an Immortalized Amygdalar Neuronal Cell Line

Mulchahey, J. J. (1999) · Endocrinology · doi:10.1210/en.140.1.251 · Cited by 16

Immunological stress in rats induces bodily alterations in saline-treated conspecifics

Fernandes, G. A. (2000) · Physiology & Behavior · doi:10.1016/s0031-9384(99)00226-7 · Cited by 16

Differential CRH expression level determines efficiency of Cre- and Flp-dependent recombination

Zhao, C., Ries, C., Du, Y., Zhang, J., Sakimura, K., Itoi, K., & Deussing, J. M. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1163462 · Cited by 15

Chronic corticosterone administration does not potentiate unconditioned freezing to the predator odor, trimethylthiazoline

Rosen, J. B., Donley, M. P., Gray, D., West, E. A., Morgan, M. A., & Schulkin, J. A. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.06.019 · Cited by 15

Prednisolone Blocks Extreme Intermale Social Aggression in Seizure-Induced, Brain-Damaged Rats: Implications for the Amygdaloid Central Nucleus, Corticotrophin-Releasing Factor, and Electrical Seizures

Bedard, A. W., & Persinger, M. A. (1995) · Psychological Reports · doi:10.2466/pr0.1995.77.1.3 · Cited by 15

A cell-specific role for the adrenal gland in regulating CRH mRNA levels in rat hypothalamic neurosecretory neurons after cellular dehydration

Watts, A. G., & Sanchez‐Watts, G. (1995) · Brain Research · doi:10.1016/0006-8993(95)00451-u · Cited by 15

Gene expression changes in the brain of a Cushing's syndrome mouse model

Amaya, J. M., Viho, E. M. G., Sips, H. C. M., Lalai, R. A., Sahut‐Barnola, I., Dumontet, T., Montanier, N., Pereira, A. M., Martinez, A., & Meijer, O. C. (2022) · Journal of Neuroendocrinology · doi:10.1111/jne.13125 · Cited by 14

Functional interactions between stress neuromediators and the locus coeruleus–norepinephrine system

Valentino, R. J., & Bockstaele, E. J. V. (2005) · Techniques in the behavioral and neural sciences · doi:10.1016/s0921-0709(05)80026-4 · Cited by 14

The visible burrow system: A view from across the hall

Herman, J. P., & Tamashiro, K. L. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.01.021 · Cited by 17

Functional Hypothalamic Amenorrhea Due to Increased CRH Tone in Melanocortin Receptor 2-Deficient Mice

Matsuwaki, T., Nishihara, M., Sato, T., Yoda, T., Iwakura, Y., & Chida, D. (2010) · Endocrinology · doi:10.1210/en.2010-0687 · Cited by 14

Mind over matter:

Gaab, J., Jucker, P., Staub‐Bartelt, F., & Ehlert, U. (2005) · Zeitschrift für Klinische Psychologie und Psychotherapie · doi:10.1026/1616-3443.34.2.121 · Cited by 14

Adolescent Brain Development

Galván, A., & Tottenham, N. (2016) · Wiley eBooks · doi:10.1002/9781119125556.devpsy218 · Cited by 14

The Impact of Stressor Exposure and Glucocorticoids on Anxiety and Fear

Hassell, J. E., Nguyen, K., Gates, C. A., & Lowry, C. A. (2018) · Current topics in behavioral neurosciences · doi:10.1007/7854_2018_63 · Cited by 13

Impaired hypothalamic feedback dysregulates brain glucocorticoid signaling in genetically‐selected Marchigian Sardinian alcohol‐preferring rats

Natividad, L. A., Steinman, M. Q., McGinn, M. A., Sureshchandra, S., Kerr, T. M., Ciccocioppo, R., Messaoudi, I., Edwards, S., & Roberto, M. (2020) · Addiction Biology · doi:10.1111/adb.12978 · Cited by 13

Involvement of regulatory elements on corticotropin-releasing factor gene promoter in nypothalamic 4B cells

Kageyama, K., Hanada, K., Takayasu, S., Iwasaki, Y., Sakihara, S., Nigawara, T., & Suda, T. (2008) · Journal of Endocrinological Investigation · doi:10.1007/bf03345656 · Cited by 13

Neuropeptide and cytokine regulation of pain in the context of substance use disorders

Delery, E., & Edwards, S. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.108153 · Cited by 12

Glucocorticoid receptors regulate central amygdala GABAergic synapses in Marchigian-Sardinian alcohol-preferring rats

Khom, S., Borgonetti, V., Vozella, V., Kirson, D., Rodriguez, L., Gandhi, P. J., Bianchi, P., Snyder, A. E., Vlkolinský, R., Bajo, M., et al. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100547 · Cited by 12

Effects of corticosterone on CRH mRNA and content in the bed nucleus of the stria terminalis; comparison with the effects in the central nucleus of the amygdala and the paraventricular nucleus of the hypothalamus

Makino, S., Gold, P. W., & Schulkin, J. A. (1994) · Brain Research · doi:10.1016/0006-8993(94)90961-x · Cited by 249

Differential regulation of corticotropin-releasing hormone mRNA in rat brain

Frim, D. M., Robinson, B. G., Pasieka, K. B., & Majzoub, J. A. (1990) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1990.258.4.e686 · Cited by 55

Regulation of corticotropin-releasing hormone receptor messenger ribonucleic acid in the rat brain and pituitary by glucocorticoids and stress

Makino, S., Schulkin, J. A., Smith, M. A., Pacák, K., Palkovits, M., & Gold, P. W. (1995) · Endocrinology · doi:10.1210/endo.136.10.7664672 · Cited by 193

Rapid stress-induced elevations in corticotropin-releasing hormone mRNA in rat central amygdala nucleus and hypothalamic paraventricular nucleus: An in situ hybridization analysis

Hsu, D. T., Chen, F.-L., Takahashi, L. K., & Kalin, N. H. (1998) · Brain Research · doi:10.1016/s0006-8993(98)00032-8 · Cited by 154

Expression of α1bAdrenoceptor mRNA in Corticotropin-Releasing Hormone-Containing Cells of the Rat Hypothalamus and Its Regulation by Corticosterone

Day, H. E. W., Campeau, S., Watson, S. J., & Akil, H. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-22-10098.1999 · Cited by 98