Cited by 199Stress Responses and CortisolRegulation of Appetite and ObesityNeuropeptides and Animal Physiology

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Glucocorticoids, chronic stress, and obesity

Dallman, Mary F., Pecoraro, Norman C., La Fleur, Susanne E., Warne, James P., Ginsberg, Abigail B., Akana, Susan F., Laugero, Kevin C., Houshyar, Hani, Strack, Alison M., Bhatnagar, Seema, Bell, Mary E.·2006·Progress in Brain Research

DOI 10.1016/s0079-6123(06)53004-3

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Abstract

Glucocorticoids either inhibit or sensitize stress-induced activity in the hypothalamo-pituitary-adrenal (HPA) axis, depending on time after their administration, the concentration of the steroids, and whether there is a concurrent stressor input. When there are high glucocorticoids together with a chronic stressor, the steroids act in brain in a feed-forward fashion to recruit a stress-response network that biases ongoing autonomic, neuroendocrine, and behavioral outflow as well as responses to novel stressors. We review evidence for the role of glucocorticoids in activating the central stress-response network, and for mediation of this network by corticotropin-releasing factor (CRF). We briefly review the effects of CRF and its receptor antagonists on motor outflows in rodents, and examine the effects of glucocorticoids and CRF on monoaminergic neurons in brain. Corticosteroids stimulate behaviors that are mediated by dopaminergic mesolimbic "reward" pathways, and increase palatable feeding in rats. Moreover, in the absence of corticosteroids, the typical deficits in adrenalectomized rats are normalized by providing sucrose solutions to drink, suggesting that there is, in addition to the feed-forward action of glucocorticoids on brain, also a feedback action that is based on metabolic well being. Finally, we briefly discuss the problems with this network that normally serves to aid in responses to chronic stress, in our current overindulged, and underexercised society.

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Items 201–371 of 371

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Stansfeld, S. A., & Marmot, M. G. (2002) · Cited by 139
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Feldman, S., & Weidenfeld, J. (1998) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00384-5 · Cited by 137
Corticosterone circadian secretion differentially facilitates dopamine- mediated psychomotor effect of cocaine and morphine
Marinelli, M., Piazza, P., Deroche, V., Maccari, S., Moal, M. L., & Simon, H. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-05-02724.1994 · Cited by 135
Long‐Lasting Deficient Dexamethasone Suppression of Hypothalamic‐Pituitary‐Adrenocortical Activation Following Peripheral CRF Challenge in Socially Defeated Rats
Buwalda, de Boer, S. F., Schmidt, Felszeghy, Nyakas, Sgoifo, A., der Vegt, V., Tilders, Bohus, & Koolhaas (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00350.x · Cited by 135
Effects of repeated stress on pituitary cyclic AMP, and plasma prolactin, corticosterone and growth hormone in male rats12
Kant, G. J., Bunnell, B. A., Mougey, E. H., Pennington, L. L., & Meyerhoff, J. L. (1983) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(83)80022-7 · Cited by 133
Decreased Sensitivity to Glucocorticoid Fast Feedback in Chronically Stressed Rats
Young, E. A., Akana, S. F., & Dallman, M. F. (2008) · Neuroendocrinology · doi:10.1159/000125388 · Cited by 130
Self-citation
Region‐specific regulation of neuropeptide mRNAs in rat limbic forebrain neurones by aldosterone and corticosterone.
Watts, A. G., & Sanchez‐Watts, G. (1995) · The Journal of Physiology · doi:10.1113/jphysiol.1995.sp020698 · Cited by 130
Projections from the paraventricular nucleus of the thalamus to the rat prefrontal cortex and nucleus accumbens shell: Ultrastructural characteristics and spatial relationships with dopamine afferents
Pinto, A., Jankowski, M. P., & Sesack, S. R. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10596 · Cited by 130
Nibbling at CRF receptor control of feeding and gastrocolonic motility
Zorrilla, E. P., Taché, Y., & Koob, G. F. (2003) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(03)00177-9 · Cited by 130
Short-Term Plasticity of a Thalamocortical Pathway Dynamically Modulated by Behavioral State
Castro‐Alamancos, M. A., & Connors, B. W. (1996) · Science · doi:10.1126/science.272.5259.274 · Cited by 129
A spoonful of sugar: feedback signals of energy stores and corticosterone regulate responses to chronic stress
Dallman, M. F., Akana, S. F., Laugero, K. D., Gómez-Oliver, F., Manalo, S. L., Bell, M. E., & Bhatnagar, S. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00100-8 · Cited by 129
Self-citation
Suppression of glucocorticoid secretion and antipsychotic drugs have similar effects on the mesolimbic dopaminergic transmission
Piazza, P. V., Barrot, M., Rougé‐Pont, F., Marinelli, M., Maccari, S., Abrous, D. N., Simon, H., & Moal, M. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15445 · Cited by 129
Basolateral amygdala-nucleus accumbens interactions in mediating glucocorticoid enhancement of memory consolidation
Roozendaal, B., de Quervain, D. J.-F., Ferry, B., Setlow, B., & McGaugh, J. L. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-07-02518.2001 · Cited by 128
Sucrose Ingestion Normalizes Central Expression of Corticotropin-Releasing-Factor Messenger Ribonucleic Acid and Energy Balance in Adrenalectomized Rats: A Glucocorticoid-Metabolic-Brain Axis?
Laugero, K. D., Bell, M. E., Bhatnagar, S., Soriano, L., & Dallman, M. F. (2001) · Endocrinology · doi:10.1210/endo.142.7.8250 · Cited by 123
Self-citation
Stress induces CRF release in the paraventricular nucleus, and both CRF and GABA release in the amygdala
Cook, C. J. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.06.013 · Cited by 123
Evidence for regional heterogeneity in corticotropin‐releasing factor interactions in the dorsal raphe nucleus
Valentino, R. J., Liouterman, L., & Bockstaele, E. J. V. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1043 · Cited by 122
The paraventricular nucleus of the thalamus alters rhythms in core temperature and energy balance in a state-dependent manner
Bhatnagar, S., & Dallman, M. F. (1999) · Brain Research · doi:10.1016/s0006-8993(99)02108-3 · Cited by 122
Self-citation
Chronic Stress and Energy Balance: Role of the Hypothalamo‐Pituitary‐Adrenal Axis
Dallman, M. F., & Bhatnagar, S. (2000) · Comprehensive physiology · doi:10.1002/cphy.cp070410 · Cited by 121
Self-citation
Behavioral sensitization to amphetamine is dependent on corticosteroid receptor activation
Rivet, J., Stinus, L., Moal, M. L., & Mormède, P. (1989) · Brain Research · doi:10.1016/0006-8993(89)90411-3 · Cited by 121
Direct Evidence for Chronic Stress-Induced Facilitation of the Adrenocorticotropin Response to a Novel Acute Stressor
Martı́, O., Gavaldà, A., Gómez-Oliver, F., & Armario, A. (2008) · Neuroendocrinology · doi:10.1159/000126713 · Cited by 121
In vitro analysis of a mammalian retinal progenitor that gives rise to neurons and glia
Ahmad, I., Dooley, C. M., Thoreson, W. B., Rogers, J. A., & Afiat, S. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01376-1 · Cited by 121
Afferent connections of the thalamic paraventricular and parataenial nuclei in the rat — a retrograde tracing study with iontophoretic application of Fluoro-Gold
Chen, S., & Su, H. (1990) · Brain Research · doi:10.1016/0006-8993(90)91570-7 · Cited by 118
The behavioural effects of corticotropin-releasing factor-related peptides in rats
Jones, D. N. C., Kortekaas, R., Slade, P. D., Middlemiss, D. N., & Hagan, J. J. (1998) · Psychopharmacology · doi:10.1007/s002130050654 · Cited by 115
Evidence for corticotropin-releasing factor regulation of serotonin in the lateral septum during acute swim stress: adaptation produced by repeated swimming
Price, M. L., Kirby, L. G., Valentino, R. J., & Lucki, I. (2002) · Psychopharmacology · doi:10.1007/s00213-002-1114-2 · Cited by 115
Evidence for arginine vasopressin as the primary activator of the HPA axis during adjuvant‐induced arthritis
Chowdrey, H. S., Larsen, P. J., Harbuz, M. S., Jessop, D. S., Aguilera, G., Eckland, D. J. A., & Lightman, S. L. (1995) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1995.tb15089.x · Cited by 114
Voluntary Sucrose Ingestion, Like Corticosterone Replacement, Prevents the Metabolic Deficits of Adrenalectomy
Bell, S., Bhatnagar, Liang, L., Soriano, Nagy, T. R., & Dallman (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00488.x · Cited by 112
Chronic activation of the hypothalamo-pituitary-adrenal axis and loss of circadian rhythm during adjuvant-induced arthritis in the rat
Sarlis, N. J., Chowdrey, H. S., Stephanou, A., & Lightman, S. L. (1992) · Endocrinology · doi:10.1210/endo.130.4.1312424 · Cited by 112
Reset of Feedback in the Adrenocortical System: An Apparent Shift in Sensitivity of Adrenocorticotropin to Inhibition by Corticosterone between Morning and Evening*
AKANA, S. F., CASCIO, C. S., DU, J.-Z., LEVIN, N., & DALLMAN, M. F. (1986) · Endocrinology · doi:10.1210/endo-119-5-2325 · Cited by 112
Self-citation
Corticotropin-Releasing Factor and Acute Stress Prolongs Serotonergic Regulation of GABA Transmission in Prefrontal Cortical Pyramidal Neurons
Tan, H., Zhong, P., & Yan, Z. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0143-04.2004 · Cited by 112
Life-Course Exposure to Job Strain and Ambulatory Blood Pressure in Men
Landsbergis, P. A. (2003) · American Journal of Epidemiology · doi:10.1093/aje/kwg095 · Cited by 112
Corticotropin‐releasing factor 1 receptor‐mediated mechanisms inhibit colonic hypersensitivity in rats
Meerveld, B. G., Johnson, A. C., Cochrane, S. W., Schulkin, J. A., & Myers, D. A. (2005) · Neurogastroenterology & Motility · doi:10.1111/j.1365-2982.2005.00648.x · Cited by 111
Peptides that fine-tune the serotonin system
Valentino, R. J., & Commons, K. G. (2004) · Neuropeptides · doi:10.1016/j.npep.2004.09.005 · Cited by 111
A chronic stress state in rats: Effects of repeated stress on basal corticosterone and behavior
Ottenweller, J. E., Servatius, R. J., Tapp, W. N., Drastal, S. D., Bergen, M. T., & Natelson, B. H. (1992) · Physiology & Behavior · doi:10.1016/0031-9384(92)90104-a · Cited by 111
Effect of a chronic stress on CRF neuronal activity and expression of its type 1 receptor in the rat brain
Bonaz, B. L., & Rivest, S. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.275.5.r1438 · Cited by 111
Prevention of stress-induced weight loss by third ventricle CRF receptor antagonist
Smagin, G. N., Howell, L. A., Redmann, S. M., Ryan, D. H., & Harris, R. B. S. (1999) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1999.276.5.r1461 · Cited by 111
Corticotropin‐Releasing Factor Neurones of the Central Nucleus of the Amygdala Mediate Locus Coeruleus Activation by Cardiovascular Stress
Curtis, A., Bello, N. T., Connolly, K., & Valentino, R. (2002) · Journal of neuroendocrinology · doi:10.1046/j.1365-2826.2002.00821.x · Cited by 110
Glucocorticoid feedback increases the sensitivity of the limbic system to stress
Cook, C. J. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00650-9 · Cited by 110
Stereotaxic localization of corticosterone to the amygdala enhances hypothalamo-pituitary–adrenal responses to behavioral stress
Shepard, J. D., Barron, K. W., & Myers, D. A. (2003) · Brain Research · doi:10.1016/s0006-8993(02)03978-1 · Cited by 110
Corticotropin-releasing factor administered into the locus coeruleus, but not the parabrachial nucleus, stimulates norepinephrine release in the prefrontal cortex.
Smagin, G., Świergiel, A., & Dunn, A. (1995) · Brain Research Bulletin · doi:10.1016/0361-9230(94)00166-x · Cited by 110
Central administration of a CRF antagonist blocks the development of stress-induced behavioral sensitization
Cole, B. J., Cador, M., Stinus, L., Rivier, J., Vale, W., Koob, G. F., & Moal, M. L. (1990) · Brain Research · doi:10.1016/0006-8993(90)90646-s · Cited by 109
The Effects of Corticotropin-Releasing Factor on Adrenocorticotropin Secretion from Perifused Pituitariesin vitro: Rapid Inhibition by Glucocorticoids*
Widmaier, E. P., & Dallman, M. F. (1984) · Endocrinology · doi:10.1210/endo-115-6-2368 · Cited by 108
Self-citation
Effects of immobilization on in vivo release of norepinephrine in the bed nucleus of the stria terminalis in conscious rats
Pacák, K., McCarty, R. C., Palkovits, M., Kopin, I. J., & Goldstein, D. S. (1995) · Brain Research · doi:10.1016/0006-8993(95)00566-9 · Cited by 106
Corticosteroid Feedback Control of ACTH Secretion: Rapid Effects of Bilateral Adrenalectomy on Plasma ACTH in the Rat1
Dallman, M. F., Jones, M. T., Vernikos, J., & Ganong, W. F. (1972) · Endocrinology · doi:10.1210/endo-91-4-961 · Cited by 106
Self-citation
Differential stress responsivity in diet-induced obese and resistant rats
Levin, B. E., Richard, D., Michel, C., & Servatius, R. J. (2000) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.2000.279.4.r1357 · Cited by 106
Differential behavioral actions of corticotropin-releasing factor (CRF)
Veldhuis, H. D., & de Wied, D. (1984) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(84)80007-6 · Cited by 105
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Bhatnagar, Bell, S., Liang, L., Soriano, Nagy, T. R., & Dallman (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00487.x · Cited by 104
The role of afferents to the locus coeruleus in the handling stress-induced increase in the release of noradrenaline in the medial prefrontal cortex: a dual-probe microdialysis study in the rat brain.
Kawahara, H., Kawahara, Y., & Westerink, B. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(99)00793-1 · Cited by 104
Corticosterone facilitates retention of contextually conditioned fear and increases CRH mRNA expression in the amygdala
Thompson, B. L., Erickson, K., Schulkin, J. A., & Rosen, J. B. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00216-x · Cited by 103
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Arborelius, L., Skelton, K. H., Thrivikraman, K. V., Plotsky, P. M., Schulz, D. W., & Owens, M. J. (2000) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)39110-4 · Cited by 101
Modulation of memory consolidation by the basolateral amygdala or nucleus accumbens shell requires concurrent dopamine receptor activation in both brain regionsPreprint
LaLumiere, R. T., Nawar, E. M., & McGaugh, J. L. (2005) · Learning & Memory · doi:10.1101/lm.93205 · Cited by 99
Thalamic paraventricular nucleus lesions facilitate central amygdala neuronal responses to acute psychological stress
Spencer, S. J., Fox, J. C., & Day, T. A. (2004) · Brain Research · doi:10.1016/j.brainres.2003.10.054 · Cited by 99
Corticotrope Response to Removal of Releasing Factors and Corticosteroids in Vivo*
Dallman, M. F., Makara, G. B., Roberts, J. L., LEVIN, N., & Blum, M. (1985) · Endocrinology · doi:10.1210/endo-117-5-2190 · Cited by 98
Self-citation
Viewing the ventromedial hypothalamus from the adrenal gland
Dallman, M. F. (1984) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1984.246.1.r1 · Cited by 98
Self-citation
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Viau, V., Soriano, L., & Dallman, M. F. (2001) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2001.00653.x · Cited by 97
Self-citation
The Corticotropin-Releasing Factor (CRF)-system and monoaminergic afferents in the central amygdala: Investigations in different mouse strains and comparison with the rat
Asan, E., Yilmazer‐Hanke, D., Eliava, M., Hantsch, M., Lesch, K., & Schmitt, A. G. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.11.040 · Cited by 95
Diminishing Corticotrope Capacity to Release ACTH During Sustained Stimulation: The Twenty-four Hours After Bilateral Adrenalectomy in the Rat1
Dallman, M. F., DEMANINCOR, D., & Shinsako, J. (1974) · Endocrinology · doi:10.1210/endo-95-1-65 · Cited by 95
Self-citation
Effects of the CRH Receptor Antagonist CP-154,526 on Intravenous Cocaine Self-administration in Rats
Goeders, N. (2000) · Neuropsychopharmacology · doi:10.1016/s0893-133x(00)00148-2 · Cited by 94
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Matsuzaki, I., Takamatsu, Y., & Moroji, T. (1989) · Neuropeptides · doi:10.1016/0143-4179(89)90085-1 · Cited by 92
Intermittent Morphine Administration Induces Dependence and is a Chronic Stressor in Rats
Houshyar, H., Gómez-Oliver, F., Manalo, S. L., Bhargava, A., & Dallman, M. F. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300271 · Cited by 90
Self-citation
Thalamic paraventricular nucleus neurons collateralize to innervate the prefrontal cortex and nucleus accumbens
Bubser, M., & Deutch, A. Y. (1998) · Brain Research · doi:10.1016/s0006-8993(97)01373-5 · Cited by 90
Physiological and behavioral effects of chronic intracerebroventricular infusion of corticotropin-releasing factor in the rat
Buwalda, B., de Boer, S. F., van Kalkeren, A. A., & Koolhaas, J. M. (1997) · Psychoneuroendocrinology · doi:10.1016/s0306-4530(97)00032-2 · Cited by 89
Vagal afferent signaling of a gastric mucosal acid insult to medullary, pontine, thalamic, hypothalamic and limbic, but not cortical, nuclei of the rat brain
Michl, T., Jocič, M., Heinemann, Á., Schuligoi, R., & Holzer, P. D. (2001) · Pain · doi:10.1016/s0304-3959(00)00467-x · Cited by 88
Corticosterone acts on the brain to inhibit adrenalectomy-induced adrenocorticotropin secretion
LEVIN, N., SHINSAKO, J., & DALLMAN, M. F. (1988) · Endocrinology · doi:10.1210/endo-122-2-694 · Cited by 87
Self-citation
Corticotropin-releasing factor is preferentially colocalized with excitatory rather than inhibitory amino acids in axon terminals in the peri-locus coeruleus region
Valentino, R. J., Rudoy, C., Saunders, A., Liu, X.-B., & Bockstaele, E. J. V. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00279-2 · Cited by 86
Association of glucocorticoid receptor immunoreactivity with cell membrane and transport vesicles in hippocampal and hypothalamic neurons of the rat
Liposits, Z., & Bohn, M. C. (1993) · Journal of Neuroscience Research · doi:10.1002/jnr.490350103 · Cited by 86
The Role of Limbic and Hypothalamic Corticotropin‐Releasing Factor in Behavioral Responses to Stress
Menzaghi, F., Heinrichs, S. C., Pich, E. M., Weiss, F., & Koob, G. F. (1993) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1993.tb49929.x · Cited by 86
Stress-induced expression of co-localized neuropeptides in hypothalamic and amygdaloid neurons
Palkovits, M. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00549-5 · Cited by 84
Role of corticotropin-releasing factor, vasopressin and the autonomic nervous system in learning and memory
Croiset, G., Nijsen, M., & Kamphuis, P. J. G. H. (2000) · European Journal of Pharmacology · doi:10.1016/s0014-2999(00)00556-2 · Cited by 84
Does amygdaloid corticotropin‐releasing hormone (CRH) mediate anxiety‐like behaviors? Dissociation of anxiogenic effects and CRH release
Merali, Z., Khan, S. A., Michaud, D. S., Shippy, S. A., & Anisman, H. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03468.x · Cited by 82
Negative feedback functions in chronically stressed rats: role of the posterior paraventricular thalamus
Jaferi, A., Nowak, N., & Bhatnagar, S. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00014-3 · Cited by 81
Self-citation
Inhibition of central actions of cytokines on fever and thermogenesis by lipocortin-1 involves CRF
Strijbos, P. J. L. M., Hardwick, A. J., Relton, J. K., Carey, F., & Rothwell, N. J. (1992) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1992.263.4.e632 · Cited by 80
Corticosterone-Induced Changes in Hypothalamic Corticotropin-Releasing Factor (CRF) Content After Stress1
Sato, T., Sato, M., Shinsako, J., & Dallman, M. F. (1975) · Endocrinology · doi:10.1210/endo-97-2-265 · Cited by 80
Self-citation
Chronic Cold in Adrenalectomized, Corticosterone (B)-Treated Rats: Facilitated Corticotropin Responses to Acute Restraint Emerge as B Increases1
Akana, S. F., & Dallman, M. F. (1997) · Endocrinology · doi:10.1210/endo.138.8.5291 · Cited by 79
Self-citation
The Effects of Thalamic Paraventricular Nucleus Lesions on Cocaine-Induced Locomotor Activity and Sensitization
Young, C. (1998) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(98)00051-3 · Cited by 78
Activation of the central nervous system in obese Zucker rats during food deprivation
Timofeeva, E., & Richard, D. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1398 · Cited by 78
Chronic cold exposure potentiates CRH-evoked increases in electrophysiologic activity of locus coeruleus neurons.
Jedema, H., Finlay, J. M., Sved, A., & Grace, A. A. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(00)01057-x · Cited by 77
Non-Peptide Corticotropin-Releasing Hormone Antagonists: Syntheses and Structure−Activity Relationships of 2-Anilinopyrimidines and -triazines
Arvanitis, A. G., Gilligan, P. J., Chorvat, R. J., Cheeseman, R. S., Christos, T. E., Bakthavatchalam, R., Beck, J. P., Cocuzza, A. J., Hobbs, F. W., Wilde, R. G., et al. (1999) · Journal of Medicinal Chemistry · doi:10.1021/jm980222w · Cited by 76
Psychostimulant-Induced Fos Protein Expression in the Thalamic Paraventricular Nucleus
Deutch, A. Y., Bubser, M., & Young, C. D. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10680.1998 · Cited by 76
The adrenals and the regulatory nature of running wheel activity
Leshner, A. I. (1971) · Physiology & Behavior · doi:10.1016/0031-9384(71)90204-6 · Cited by 75
The metabolic syndrome: an emerging health epidemic in women
Steinbaum, S. (2004) · Progress in Cardiovascular Diseases · doi:10.1016/j.pcad.2003.08.005 · Cited by 75
Chronic stress enhances vasopressin but not corticotropin-releasing factor secretion during hypoglycemia
de Goeij, D. C. E., Binnekade, R., & Tilders, F. J. H. (1992) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1992.263.2.e394 · Cited by 73
Corticosterone Infused Intracerebroventricularly Inhibits Energy Storage and Stimulates the Hypothalamo-Pituitary Axis in Adrenalectomized Rats Drinking Sucrose
Laugero, K. D., Gómez-Oliver, F., Manalo, S. L., & Dallman, M. F. (2002) · Endocrinology · doi:10.1210/en.2002-220613 · Cited by 72
Self-citation
Effect of experimental and pathological weight loss upon the hypothalamo-pituitary-adrenal axis
Fichter, M. M., & Pirke, K. M. (1986) · Psychoneuroendocrinology · doi:10.1016/0306-4530(86)90015-6 · Cited by 71
Persistent stress-induced sensitization of adrenocortical and startle responses
Servatius, R. J., Ottenweller, J. E., Bergen, M. T., Soldan, S. A., & Natelson, B. H. (1994) · Physiology & Behavior · doi:10.1016/0031-9384(94)90328-x · Cited by 70
Corticosterone implants to the amygdala and type 1 CRH receptor regulation: Effects on behavior and colonic sensitivity
Myers, D. A., Gibson, M. S., Schulkin, J. A., & van-Meerveld, B. G. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.03.001 · Cited by 69
Amygdala kindling, anxiety, and corticotrophin releasing factor (CRF)
Adamec, R. E., & McKay, D. W. (1993) · Physiology & Behavior · doi:10.1016/0031-9384(93)90230-d · Cited by 68
Regulation of a Putative Neurotransmitter Effect of Corticotropin-Releasing Factor: Effects of Adrenalectomy
Pavcovich, L. A., & Valentino, R. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-01-00401.1997 · Cited by 68
Altered Serotonergic Neurotransmission but Normal Hypothalamic–Pituitary–Adrenocortical Axis Activity in Mice Chronically Treated with the Corticotropin-Releasing Hormone Receptor Type 1 Antagonist NBI 30775
Oshima, A., Flachskamm, C., Reul, J. M. H. M., Holsboer, F., & Linthorst, A. C. E. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300267 · Cited by 67
Corticosterone Can Facilitate as Well as Inhibit Corticotropin-Releasing Hormone Gene Expression in the Rat Hypothalamic Paraventricular Nucleus*
Tanimura, S. M., & Watts, A. G. (1998) · Endocrinology · doi:10.1210/endo.139.9.6192 · Cited by 67
Sucrose Intake and Corticosterone Interact with Cold to Modulate Ingestive Behaviour, Energy Balance, Autonomic Outflow and Neuroendocrine Responses During Chronic Stress
Bell, M. E., Bhargava, A., Soriano, L., Laugero, K. D., Akana, S. F., & Dallman, M. F. (2002) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2002.00784.x · Cited by 65
Self-citation
Ultrastructural evidence for a role of γ‐aminobutyric acid in mediating the effects of corticotropin‐releasing factor on the rat dorsal raphe serotonin system
Waselus, M., Valentino, R. J., & Bockstaele, E. J. V. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20360 · Cited by 65
Habituation and Cross‐Sensitization of Stress‐Induced Hypothalamic‐Pituitary‐Adrenal Activity: Effect of Lesions in the Paraventricular Nucleus of the Thalamus or Bed Nuclei of the Stria Terminalis
Fernandes, G. A., Perks, P., Cox, N. K., Lightman, S. L., Ingram, C. D., & Shanks, N. M. (2002) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2002.00819.x · Cited by 64
Colocalization of peptide- and tyrosine hydroxylase-like immunoreactivities with Fos-immunoreactive neurons in rat central amygdaloid nucleus after immobilization stress
Honkaniemi, J. (1992) · Brain Research · doi:10.1016/0006-8993(92)90173-7 · Cited by 64
Constrained Corticotropin Releasing Factor Antagonists (Astressin Analogues) with Long Duration of Action in the Rat
Rivier, J., Kirby, D. A., Lahrichi, S. L., CORRIGAN, A. Z., Vale, W., & RIVIER, C. L. (1999) · Journal of Medicinal Chemistry · doi:10.1021/jm9902133 · Cited by 64
HPA axis responses to acute stress and adrenalectomy during adjuvant-induced arthritis in the rat
Harbuz, M. S., Rees, R. G., & Lightman, S. L. (1993) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1993.264.1.r179 · Cited by 63
Glucocorticoids and insulin: complex interaction on brown adipose tissue
Strack, A. M., Horsley, C. J., Sebastian, R. J., Akana, S. F., & Dallman, M. F. (1995) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1995.268.5.r1209 · Cited by 63
Self-citation
Anatomical and Functional Mapping of Central Neural Input and Feedback Pathways of the Adrenocortical System
Dallman, M. F., & Yates, F. E. (1967) · Proceedings of the Royal Society of Medicine · doi:10.1177/003591576706000942 · Cited by 63
Self-citation
Chronic stress increases the opioid-mediated inhibition of the pituitary-adrenocortical response to acute stress in pigs
Janssens, C. J., Helmond, F. A., Loyens, L. W. S., Schouten, W. G. P., & Wiegant, V. M. (1995) · Endocrinology · doi:10.1210/endo.136.4.7895656 · Cited by 61
Effect of corticotropin-releasing factor antagonist on behavioral and neuroendocrine responses during exposure to defensive burying paradigm in rats
Korte, S. M., Korte-Bouws, G. A. H., Bohus, B., & Koob, G. F. (1994) · Physiology & Behavior · doi:10.1016/0031-9384(94)90268-2 · Cited by 61
Central mechanism of neural activation with cold acclimation of rats using Fos immunohistochemistry
Miyata, S., Ishiyama, M., Shido, O., Nakashima, T., Shibata, M., & Kiyohara, T. (1995) · Neuroscience Research · doi:10.1016/0168-0102(95)00900-x · Cited by 60
Low doses of corticotropin-releasing hormone injected into the dorsal raphe nucleus block the behavioral consequences of uncontrollable stress
Hammack, S. E., Pepin, J. L., DesMarteau, J. S., Watkins, L. R., & Maier, S. F. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00133-5 · Cited by 60
Role of glucocorticoids in the regulation of dopaminergic neurotransmission.
Czyrak, A., Maćkowiak, M., Chocyk, A., Fijał, K., & Wedzony, K. (2003) · PubMed · Cited by 59
Negative Feedback Regulation following Administration of Chronic Exogenous Corticosterone
Young, E. A., Kwak, S., & Kottak, J. (1995) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1995.tb00665.x · Cited by 58
Effects of chronic stress on anterior pituitary and brain corticotropin-releasing factor receptors
Anderson, S. M., Kant, G. J., & Souza, E. B. D. (1993) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(93)90002-b · Cited by 57
Central Actions of Corticotropin‐Releasing Factor on Autonomic Nervous Activity and Cardiovascular Functioning
Fisher, L. A. (2007) · Novartis Foundation symposium · doi:10.1002/9780470514368.ch12 · Cited by 56
Temporal and spatial dynamics of corticosteroid receptor down-regulation in rat brain following social defeat
Buwalda, B., Felszeghy, K., Horváth, K. M., Nyakas, C. J., de Boer, S. F., Bohus, B., & Koolhaas, J. M. (2001) · Physiology & Behavior · doi:10.1016/s0031-9384(00)00414-5 · Cited by 56
CRF receptor antagonist attenuates immobilization stress-induced norepinephrine release in the prefrontal cortex in rats.
Smagin, G., Zhou, J., Harris, R., & Ryan, D. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(96)00368-1 · Cited by 55
Influence of glucocorticoids on dopaminergic transmission in the rat dorsolateral striatum
Barrot, M., Abrous, D. N., Marinelli, M., Rougé‐Pont, F., Moal, M. L., & Piazza, P. V. (2001) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2001.01434.x · Cited by 55
Behavioral Effects of Corticotropin-Releasing Factor
Baldwin, H. A., Britton, K. T., & Koob, G. F. (1990) · Current topics in neuroendocrinology · doi:10.1007/978-3-642-75837-9_1 · Cited by 54
Stress-induced sensitization of CRH-ir but not P-CREB-ir responsivity in the rat central nervous system
Bruijnzeel, A. W., Stam, R., Compaan, J. C., & Wiegant, V. M. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02646-4 · Cited by 53
Effects of chronic modification of dietary fat and carbohydrate on the insulin, corticosterone and metabolic responses of rats fed acutely with glucose, fructose or ethanol
Brindley, D. N., COOLING, J., Glenny, H. P., Burditt, S. L., & McKechnie, I. S. (1981) · Biochemical Journal · doi:10.1042/bj2000275 · Cited by 53
Glucocorticoid receptor-immunoreactivity in corticotrophin-releasing factor afferents to the locus coeruleus
Lechner, S. M., & Valentino, R. J. (1999) · Brain Research · doi:10.1016/s0006-8993(98)00900-7 · Cited by 51
Regulation of dopamine function in the nucleus accumbens of the rat by the thalamic paraventricular nucleus and adjacent midline nuclei
Jones, M. W., Kilpatrick, I. C., & Phillipson, O. T. (1989) · Experimental Brain Research · doi:10.1007/bf00248914 · Cited by 50
Stress responsiveness of hypothalamic corticotrophin-releasing factor and pituitary pro-opiomelanocortin mRNAs following high-dose glucocorticoid treatment and withdrawal in the rat
Harbuz, M. S., Nicholson, S. A., Gillham, B., & Lightman, S. L. (1990) · Journal of Endocrinology · doi:10.1677/joe.0.1270407 · Cited by 50
Streptozotocin-diabetic rats exhibit facilitated adrenocorticotropin responses to acute stress, but normal sensitivity to feedback by corticosteroids
Scribner, K. A., Akana, S. F., Walker, C. D., & Dallman, M. F. (1993) · Endocrinology · doi:10.1210/endo.133.6.8243290 · Cited by 50
Self-citation
Differential release of corticotropin-releasing hormone (CRH) in the amygdala during different types of stressors
Hand, G. A., Hewitt, C. B., Fulk, L. J., Stock, H. S., Carson, J. A., Davis, J. M., & Wilson, M. A. (2002) · Brain Research · doi:10.1016/s0006-8993(02)02972-4 · Cited by 50
Corticotropin-releasing factor as well as opioid and dopamine are involved in tail-pinch-induced food intake of rats
Samarghandian, S., Ohata, H., Yamauchi, N., & Shibasaki, T. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00712-1 · Cited by 48
Activation of Noradrenergic Neurons in the Locus coeruleus by Corticotropin-Releasing Factor
Schulz, C., & Lehnert, H. (2008) · Neuroendocrinology · doi:10.1159/000127071 · Cited by 48
Lesions of the Hippocampal Efferent Pathway (Fimbria-Fornix) Do Not Alter Sensitivity of Adrenocorticotropin to Feedback Inhibition by Corticosterone in Rats
BRADBURY, M. J., Strack, A. M., & Dallman, M. F. (2008) · Neuroendocrinology · doi:10.1159/000126569 · Cited by 47
Self-citation
Clamped Corticosterone (B) Reveals the Effect of Endogenous B on Both Facilitated Responsivity to Acute Restraint and Metabolic Responses to Chronic Stress
Akana, S. F., Hanson, E. S., Horsley, C. J., Strack, A. M., Bhatnagar, S., BRADBURY, M. J., Milligan, E. D., & Dallman, M. F. (1996) · Stress · doi:10.3109/10253899609001094 · Cited by 47
Self-citation
Dissecting the components of the central response to stress
Mayer, E. A., & Fanselow, M. S. (2003) · Nature Neuroscience · doi:10.1038/nn1003-1011 · Cited by 45
c-Fos After Incentive Shifts: Expectancy, Incredulity, and Recovery.
Pecoraro, N. C., & Dallman, M. F. (2005) · Behavioral Neuroscience · doi:10.1037/0735-7044.119.2.366 · Cited by 45
Self-citation
Corticotropin-releasing factor in the dorsal raphe nucleus regulates activity of lateral septal neurons
Thomas, E., Pernar, L. I. M., Lucki, I., & Valentino, R. J. (2003) · Brain Research · doi:10.1016/s0006-8993(02)03882-9 · Cited by 43
Viscerosensory activation of noradrenergic inputs to the amygdala in rats
MYERS, E., & Rinaman, L. (2002) · Physiology & Behavior · doi:10.1016/s0031-9384(02)00925-3 · Cited by 42
Glucocorticoids dose-dependently remodel energy stores and amplify incentive relativity effects
Pecoraro, N. C., Gómez-Oliver, F., & Dallman, M. F. (2005) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2005.03.010 · Cited by 42
Self-citation
Alterations in corticotropin-releasing hormone gene expression of central amygdaloid neurons following long-term paraventricular lesions and adrenalectomy
Palkovits, M., Young, W. S., Kovács, K., Tóth, Z., & Makara, G. B. (1998) · Neuroscience · doi:10.1016/s0306-4522(97)00621-0 · Cited by 42
Effects of Adrenal Steroids on Basal Ganglia Neuropeptide mRNA and Tyrosine Hydroxylase Radioimmunoreactive Levels in the Adrenalectomized Rat
Lucas, L., Pompei, P., Ono, J. G., & McEwen, B. S. (1998) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1998.71020833.x · Cited by 41
Hypophysiotropic CRF Neurons Display a Sustained Immediate‐Early Gene Response to Chronic Stress but not to Adrenalectomy
Brown, E. R., & Sawchenko, P. E. (1997) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1997.00586.x · Cited by 41
Long double-stranded RNA-mediated RNA interference as a tool to achieve site-specific silencing of hypothalamic neuropeptides
Bhargava, A., Dallman, M. F., Pearce, D., & Choi, S. (2004) · Brain Research Protocols · doi:10.1016/j.brainresprot.2004.03.003 · Cited by 40
Self-citation
Measuring of extracellular cortisol and corticotropin-releasing hormone in the amygdala using immunosensor coupled microdialysis
Cook, C. J. (2001) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(01)00421-6 · Cited by 39
Peptide Gene Activation, Secretion, and Steroid Feedback during Stimulation of Rat Neuroendocrine Corticotropin-Releasing Hormone Neurons1
Tanimura, S. M., Sanchez‐Watts, G., & Watts, A. G. (1998) · Endocrinology · doi:10.1210/endo.139.9.6191 · Cited by 39
Poststress glucose mitigates behavioral impairment in rats in the “learned helplessness” model of psychopathology
Minor, T. R., & Saade, S. (1997) · Biological Psychiatry · doi:10.1016/s0006-3223(96)00467-2 · Cited by 39
CRHR1 Receptor binding and lipophilicity of pyrrolopyrimidines, potential nonpeptide corticotropin-releasing hormone type 1 receptor antagonists
Hsin, L., Tian, X., WEBSTER, E. L., Coop, A., Caldwell, T. M., Jacobson, A. E., Chrousos, G. P., Gold, P. W., Habib, K. E., Ayala, A. R., et al. (2002) · Bioorganic & Medicinal Chemistry · doi:10.1016/s0968-0896(01)00261-9 · Cited by 38
Activation of the hypothalamic-pituitary axis in adrenalectomised rats: potentiation by chronic stress
Martı́, O., Harbuz, M. S., Andrés, R. M., Lightman, S. L., & Armario, A. (1999) · Brain Research · doi:10.1016/s0006-8993(98)01212-8 · Cited by 38
Changes at multiple levels of the hypothalamo-pituitary adrenal axis following repeated electrically induced seizures
Young, E. A., Spencer, R. L., & McEwen, B. S. (1990) · Psychoneuroendocrinology · doi:10.1016/0306-4530(90)90027-7 · Cited by 38
Impact of stress on diet: processes and implications
Wardle, J., & Gibson, E. L. (2002) · UCL Discovery (University College London) · Cited by 37
The effect of corticotropin-releasing factor (CRF) on autonomic and behavioral responses during shock-prod burying test in rats
Diamant, M., Croiset, G., & de Wied, D. (1992) · Peptides · doi:10.1016/0196-9781(92)90022-u · Cited by 37
Involvement of hypothalamic corticotropin-releasing factor neurons in behavioral responses to novelty in rats
Menzaghi, F., Heinrichs, S. C., Merlo‐Pich, E., Tilders, F. J. H., & Koob, G. F. (1994) · Neuroscience Letters · doi:10.1016/0304-3940(94)90435-9 · Cited by 37
Glucocorticoid regulation of preproenkephalin gene expression in the rat forebrain
Ahima, R. S., Garcia, M. M., & Harlan, R. E. (1992) · Molecular Brain Research · doi:10.1016/0169-328x(92)90201-l · Cited by 37
Limbic Thalamic Lesions, Appetitively Motivated Discrimination Learning, and Training-Induced Neuronal Activity in Rabbits
Smith, D. M., Freeman, J. H., Nicholson, D. A., & Gabriel, M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-18-08212.2002 · Cited by 37
Behavioural activation produced by crh but not α-helical CRH (CRH-receptor antagonist) when microinfused into the central nucleus of the amygdala under stress-free conditions
Wiersma, A. T., Baauw, A., Bohus, B., & Koolhaas, J. M. (1995) · Psychoneuroendocrinology · doi:10.1016/0306-4530(94)00074-3 · Cited by 37
Positive Rate-Sensitive Corticosteroid Feedback Mechanism of ACTH Secretion in Cushing's Disease
Fehm, H. L., Voigt, K. H., Kummer, G., & Pfeiffer, E. F. (1979) · Journal of Clinical Investigation · doi:10.1172/jci109428 · Cited by 36
Glucocorticoid Receptor Agonist Enhances Pavlovian Appetitive Conditioning but Disrupts Outcome-Specific Associations.
Zorawski, M., & Killcross, S. (2003) · Behavioral Neuroscience · doi:10.1037/0735-7044.117.6.1453 · Cited by 33
The Effects of Repeated Intra-Amygdala CRF Injections on Rat Behavior and HPA Axis Function After Stress
Daniels, W. M. U., Richter, L., & Stein, D. J. (2004) · Metabolic Brain Disease · doi:10.1023/b:mebr.0000027413.42946.61 · Cited by 32
Corticotropin-Releasing Factor Induces Differential Behavioral and Cardiovascular Effects after Intracerebroventricular and Lateral Hypothalamic/Perifornical Injections in Rats
Diamant, M., Kashtanov, S. I., Fodor, M., & de Wied, D. (2008) · Neuroendocrinology · doi:10.1159/000126303 · Cited by 30
LHRH and mating behavior: Sexual receptivity versus sexual preference
Dudley, C. A., & Moss, R. L. (1985) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(85)90304-1 · Cited by 29
Prevention of Inhibitory Effect of Free Fatty Acids on Insulin Binding and Action in Isolated Rat Hepatocytes by Etomoxir
Svedberg, J., Björntorp, P. A., Lönnroth, P., & Smith, U. (1991) · Diabetes · doi:10.2337/diab.40.6.783 · Cited by 28
Receptor-Independent Activation of GABAergic Neurotransmission and Receptor-Dependent Nontranscriptional Activation of Phosphatidylinositol 3-kinase/Protein Kinase Akt Pathway in Short-Term Cardiovascular Actions of Dexamethasone at the Nucleus Tractus Solitarii of the Rat
Ling-lin, W., Ou, C.-C., & Chan, J. Y. H. (2004) · Molecular Pharmacology · doi:10.1124/mol.104.005595 · Cited by 27
Nonsteroidal adrenal feedback demarcates two types of pathways to CRF-ACTH release
Wilkinson, C. W., Engeland, W. C., Shinsako, J., & Dallman, M. F. (1981) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1981.240.2.e136 · Cited by 25
Self-citation
Intraventricular corticosterone injection facilitates memory of an appetitive discriminative task in mice
Micheau, J., Destrade, C., & Soumireu-Mourat, B. (1981) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(81)91162-6 · Cited by 24
Neuroendocrinology of insulin resistance: metabolic and endocrine aspects of adiposity
van Dijk, G., de Vries, K., Benthem, L., Nyakas, C. J., Buwalda, B., & Scheurink, A. J. W. (2003) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2003.08.090 · Cited by 24
Midline thalamic lesions enhance conditioned bradycardia and the cardiac orienting reflex in rabbits
Buchanan, S. L., Thompson, R. H., & Powell, D. A. (1989) · Psychobiology · doi:10.1007/bf03337784 · Cited by 24
Specific and Time‐Dependent Effects of Glucocorticoid Receptor Agonist RU28362 on Stress‐Induced Pro‐Opiomelanocortin hnRNA, c‐fos mRNA and zif268 mRNA in the Pituitary
Ginsberg, A. B., Frank, M. G., Francis, A. B., Rubin, B. A., O’Connor, K., & Spencer, R. L. (2005) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.2005.01396.x · Cited by 24
Self-citation
Differential influence of corticosterone and dexamethasone on schedule-induced polydipsia in adrenalectomized rats
Cirulli, F., van Oers, H. J. J., de Kloet, E. R., & Levine, S. D. (1994) · Behavioural Brain Research · doi:10.1016/0166-4328(94)90070-1 · Cited by 21
Chronic cortisol exposure promotes the development of a GABAergic phenotype in the primate hippocampus
McMillan, P. J., Wilkinson, C. W., Greenup, L., Raskind, M. A., Peskind, E. R., & Leverenz, J. B. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02760.x · Cited by 20
Overfeeding-induced obesity in rats: Insulin sensitivity and autonomic regulation of metabolism
Balkan, B., STRUBBE, J. H., Bruggink, J. E., & Steffens, A. B. (1993) · Metabolism · doi:10.1016/0026-0495(93)90144-d · Cited by 18
Recovery of the Hypothalamo-Pituitary-Adrenocortical Axis in the Rat after Long-Term Dexamethasone Treatment
Nicholson, S., Campbell, E., Torrellas, A., Beckford, U., Altaher, R., Sandford, R. N., Scraggs, R., Gillham, B., & Jones, M. T. (2008) · Neuroendocrinology · doi:10.1159/000124002 · Cited by 18
Effect of adrenalectomy and dexamethasone treatment on circadian running in the rat
Moberg, G. P., & Clark, C. R. (1976) · Pharmacology Biochemistry and Behavior · doi:10.1016/0091-3057(76)90207-0 · Cited by 18
Recovery of the components of the hypothalamo-pituitary-adrenocortical axis in the rat after chronic treatment with prednisolone
Nicholson, S. A., Campbell, E. A., Gillham, B., & Jones, M. T. (1987) · Journal of Endocrinology · doi:10.1677/joe.0.1130239 · Cited by 17
Corticosterone modulation of ACTH secretogogue gene expression in the paraventricular nucleus
Tanimura, S. M., & Watts, A. G. (2001) · Peptides · doi:10.1016/s0196-9781(01)00391-6 · Cited by 17
Increased expression of corticotropin-releasing factor receptor mRNA in the locus coeruleus of stress-induced rat model of depression
Zeng, J., Kitayama, I. T., Yoshizato, H., Zhang, K., & Okazaki, Y. (2003) · Life Sciences · doi:10.1016/s0024-3205(03)00417-x · Cited by 15
Effects of High-Fat Diet Intake on Glucose Uptake in Central and Peripheral Tissues of Non-Obese Rats.
Matsuo, T., Iwashita, S., Komuro, M., & Suzuki, M. (1999) · Journal of Nutritional Science and Vitaminology · doi:10.3177/jnsv.45.667 · Cited by 12
The medial thalamus and the opposite effect of corticosteroids and adrenocorticotrophic hormone on avoidance extinction in the rat.
Bohus, B. (1970) · PubMed · Cited by 11
Alteration of pituitary-adrenal responses to adrenalectomy by the immunological targeting of CRF neurons
Menzaghi, F., Burlet, A. J., Chapleur-Chateau, M., Nicolas, J., & Burlet, C. R. (1992) · Neuroscience Letters · doi:10.1016/0304-3940(92)90133-r · Cited by 8
Single, but not multiple pairings of sucrose and corticosterone enhance memory for sucrose drinking and amplify remote reward relativity effects
Pecoraro, N. C., Gómez-Oliver, F., la Fleur, S. E., Roy, M., & Dallman, M. F. (2005) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2004.11.005 · Cited by 8
Self-citation
Influence of prolonged glucocorticoid treatment on intracellular mechanisms involved in ACTH secretion in the rat
Nicholson, S. A., Gillham, B., & Jones, M. T. (1988) · Journal of Molecular Endocrinology · doi:10.1677/jme.0.0010203 · Cited by 8
Short Stature Due to Growth Hormone Deficiency Associated with Cushing's Disease and Ulcerative Colitis
Kotake, M., Nakai, A., Mokuno, T., Oda, N., Sawai, Y., Itoh, Y., Shimazaki, K., Kato, R., HAYAKAWA, N., Uchikawa, A., et al. (1996) · Hormone and Metabolic Research · doi:10.1055/s-2007-979854 · Cited by 5
Brain Catecholamine Systems in Stress
Palkovits, M., Baffi, J., Tóth, Z., & Pacák, K. (1997) · Advances in pharmacology · doi:10.1016/s1054-3589(08)60815-7 · Cited by 3
Distribution of mRNAs encoding CRF receptors in brain and pituitary of rat and mouse
Van Pett, K., Viau, V., Bittencourt, J. C., Chan, R. K. W., Li, H.-Y., Arias, C., Prins, G. S., Perrin, M., Vale, W., & Sawchenko, P. E. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001211)428:2
Distinct neurochemical populations in the rat central nucleus of the amygdala and bed nucleus of the stria terminalis: Evidence for their selective activation by interleukin-1?
Day, H. E. W., Curran, E. J., Watson, S. J., & Akil, H. (1999) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19991011)413:1
Stress induces Fos expression in neurons of the thalamic paraventricular nucleus that innervate limbic forebrain sites
Bubser, M., & Deutch, A. Y. (1999) · Synapse · doi:10.1002/(sici)1098-2396(199904)32:1

Research works printed but not linked: 10

Aguilera, 1994, Regulation of piutuitary ACTH secretion during chronic stress, Front. Neuroendocrinol., 15, 321, 10.1006/frne.1994.1013 · DOI · Paper page
Bhatnagar, 1998, Neuroanatomical basis for facilitation of hypothalamic-pituitary-adrenal responses to a novel stressor after chronic stress, Neuroscience, 84, 1025, 10.1016/S0306-4522(97)00577-0 · DOI · Paper page
Bhatnagar, 1998, Neuroanatomical basis for facilitation of the hypothalamo-pituitary-adrenal responses to a novel stress after chronic stress, Neuroscience, 84, 1025, 10.1016/S0306-4522(97)00577-0 · DOI · Paper page
Britton, 1986, Corticotropin-releasing factor (CRF) receptor antagonist blocks activating and ‘anxiogenic’ actions of CRF in the rat, Brain Res., 369, 303, 10.1016/0006-8993(86)90539-1 · DOI
Dallman, 1989, Pharmacological evidence that the inhibition of diurnal adrenocorticotropin secretion by corticosteroids is mediated via type I corticosterone-preferring receptors, Endocrinology, 124, 2844, 10.1210/endo-124-6-2844 · DOI · Paper page
Gray, 1993, Amydgaloid CRF pathways. Role in autonomic, neuroendocrine, and behavioral responses to stress, Vol. 697, 53
Krahn, 1986, CRF antagonist partially reverses CRF- and stress-induced effects on feeding, Brain Res. Bull., 17, 285, 10.1016/0361-9230(86)90233-9 · DOI
Laugero, 2001, Sucrose ingestion normalizes central expression of corticotropin-releasing-factor messenger ribonucleic acid and energy balance in adrenalectomized rats: a glucocorticoid-metabolic-brain axis?, Endocrinology, 142, 2796, 10.1210/endo.142.7.8250 · DOI
Merlo Pich, 1994, Release of corticotropin releasing factor (CRF) from the amygdala of ethanol-dependent rats measured with microdialysis, Alcohol Clin. Exp. Res., 18, 522
Valentino, 2001, Evidence for regional heterogeneity in corticotropin-releasing factor interactions in the dorsal raphe nuclei, J. Comp. Neurol., 435, 450, 10.1002/cne.1043 · DOI

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Authors: Dallman, M. F., Pecoraro, N. C., La Fleur, S. E., Warne, J. P., Ginsberg, A. B., Akana, S. F., Laugero, K. C., Houshyar, H., Strack, A. M., Bhatnagar, S., & Bell, M. E.
Affiliations: University of California, San Francisco (US)
Corresponding author: Dallman, Mary F.
ORCID: Bhatnagar, Seema
Venue: Progress in Brain Research
Publisher: Elsevier
Published: 2006
Volume: 153
Pages: 75-105
ISSN: 0079-6123 (ISSN-L)
DOI: 10.1016/s0079-6123(06)53004-3
OpenAlex: W1553637564
Cited by: 198
References: 374
Citations by year: 2026: 2 · 2025: 2 · 2024: 6 · 2023: 11 · 2022: 4 · 2021: 9 · 2020: 4 · 2019: 9 · 2018: 8 · 2017: 5 · 2016: 12 · 2015: 12 · 2014: 16 · 2013: 14 · 2012: 12
FWCI: 33.08
Type: book chapter
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Progress in brain research (publishedVersion)
PubMed (publishedVersion)
Data Archiving and Networked Services (DANS) (submittedVersion)
Pure Amsterdam UMC (submittedVersion)
Funders: National Institute on Drug Abuse (DA-16944, R01DA016944)
National Institute of Diabetes and Digestive and Kidney Diseases (DK28172)
Topics: Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
Keywords: glucocorticoids, chronic stress, obesity, hypothalamic-pituitary-adrenal axis, corticotropin-releasing factor, CRF receptor antagonists, stress response networks, monoaminergic neurons, dopaminergic reward pathways, sucrose intake, adrenalectomy, metabolic feedback
MeSH terms: Animals, Chronic Disease, Glucocorticoids, Humans, Hypothalamo-Hypophyseal System, Obesity, Pituitary-Adrenal System, Stress, Physiological

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