Studies of the secretion of corticotropin-releasing factor and arginine vasopressin into the hypophysial-portal circulation of the conscious sheep: II. The central noradrenergic and neuropeptide Y pathways cause immediate and prolonged hypothalamic-pituitary-adrenal activation. Potential involvement in the pseudo-Cushing’s syndrome of endogenous depression and anorexia nervosa

Molecular Mechanisms of Depression: Perspectives on New Treatment Strategies

Lang, U. E., & Borgwardt, S. (2013) · Cellular Physiology and Biochemistry · doi:10.1159/000350094 · Cited by 8,501 · see citing works

The regulation and function of c-fos and other immediate early genes in the nervous system

Sheng, M., & Greenberg, M. E. (1990) · Neuron · doi:10.1016/0896-6273(90)90106-p · Cited by 2,432 · see citing works

Neuropeptide Y—a novel brain peptide with structural similarities to peptide YY and pancreatic polypeptide

Tatemoto, K., Carlquist, M., & Mutt, V. (1982) · Nature · doi:10.1038/296659a0 · Cited by 2,254 · see citing works

A Specific Laboratory Test for the Diagnosis of Melancholia: Standardization, Validation, and Clinical Utility

Carroll, B. J. (1981) · Archives of General Psychiatry · doi:10.1001/archpsyc.1981.01780260017001 · Cited by 2,243 · see citing works

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 · see citing works

Corticosteroid inhibition of acth secretion

KELLER-WOOD, M. E., & DALLMAN, M. F. (1984) · Endocrine Reviews · doi:10.1210/edrv-5-1-1 · Cited by 1,219 · see citing works

Functional antagonism between oncoprotein c-Jun and the glucocorticoid receptor

Schüle, R., Rangarajan, P. N., Kliewer, S. A., Ransone, L. J., Bolado, J., Yang, N., Verma, I. M., & Evans, R. M. (1990) · Cell · doi:10.1016/0092-8674(90)90397-w · Cited by 1,204 · see citing works

The organization of noradrenergic pathways from the brainstem to the paraventricular and supraoptic nuclei in the rat

Sawchenko, P. E., & Swanson, L. W. (1982) · Brain Research Reviews · doi:10.1016/0165-0173(82)90010-8 · Cited by 1,141 · see citing works

Neuropeptide Y Distribution in the Rat Brain

Allen, Y. S., Adrian, T. E., Allen, J. M., Tatemoto, K., Crow, T. J., Bloom, S. R., & Polak, J. M. (1983) · Science · doi:10.1126/science.6136091 · Cited by 1,097 · see citing works

The anatomy of neuropeptide-y-containing neurons in rat brain

Chronwall, B. M., DiMaggio, D. A., Massari, V. J., Pickel, V. M., Ruggiero, D. A., & O’Donohue, T. L. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90260-x · Cited by 1,088 · see citing works

Corticotropin releasing activity of the new CRF is potentiated several times by vasopressin

Gillies, G. E., Linton, E. A., & Lowry, P. J. (1982) · Nature · doi:10.1038/299355a0 · Cited by 965 · see citing works

THE TEMPORAL RELATIONSHIP BETWEEN GONADOTROPIN RELEASING HORMONE (GnRH) AND LUTEINIZING HORMONE (LH) SECRETION IN OVARIECTOMIZED EWES1

Clarke, I. J., & Cummins, J. T. (1982) · Endocrinology · doi:10.1210/endo-111-5-1737 · Cited by 921 · see citing works

Hypothalamic Control of Adrenocorticotropin Secretion: Advances since the Discovery of 41-Residue Corticotropin-Releasing Factor

Antoni, F. A. (1986) · Endocrine Reviews · doi:10.1210/edrv-7-4-351 · Cited by 888 · see citing works

Differential co-existence of neuropeptide Y (NPY)-like immunoreactivity with catecholamines in the central nervous system of the rat

Everitt, B. J., Hökfelt, T. G. M., Terenius, L. Y., Tatemoto, K., Mutt, V., & Goldstein, M. (1984) · Neuroscience · doi:10.1016/0306-4522(84)90036-8 · Cited by 871 · see citing works

Overflow of catecholamine neurotransmitters to the circulation: source, fate, and functions

Esler, M., Jennings, G., Lambert, G., Meredith, I., Horne, M., & Eisenhofer, G. (1990) · Physiological Reviews · doi:10.1152/physrev.1990.70.4.963 · Cited by 794 · see citing works

Responses to Corticotropin-Releasing Hormone in the Hypercortisolism of Depression and Cushing's Disease

Gold, P. W., Loriaux, D. L., Roy, A., Kling, M. A., Calabrese, J. R., Kellner, C. H., Nieman, L. K., Post, R. M., Pickar, D., Gallucci, W. T., et al. (1986) · New England Journal of Medicine · doi:10.1056/nejm198605223142101 · Cited by 766 · see citing works

Neuropeptide Y distribution in human brain

Adrian, T. E., Allen, J. M., Bloom, S. R., Ghatei, M. A., Rossor, M. N., Roberts, G. W., Crow, T. J., Tatemoto, K., & Polak, J. M. (1983) · Nature · doi:10.1038/306584a0 · Cited by 701 · see citing works

Neuroreptide Y: Stimulation of feeding and drinking by injection into the paraventricular nucleus

Stanley, B. G., & LEIBOWITZ, S. F. (1984) · Life Sciences · doi:10.1016/0024-3205(84)90032-8 · Cited by 665 · see citing works

Neuropeptide Y secretion increases in the paraventricular nucleus in association with increased appetite for food.

Kalra, S. P., Dubé, M., Sahu, A., Phelps, C. P., & Kalra, P. S. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.23.10931 · Cited by 665 · see citing works

Colocalization of neuropeptide Y immunoreactivity in brainstem catecholaminergic neurons that project to the paraventricular nucleus of the hypothalamus

Sawchenko, P. E., Swanson, L. W., Grzanna, R., Howe, P. R. C., Bloom, S. R., & Polak, J. M. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902410203 · Cited by 663 · see citing works

Corticotropin-releasing factor activates noradrenergic neurons of the locus coeruleus

Valentino, R. J., Foote, S. L., & Aston‐Jones, G. (1983) · Brain Research · doi:10.1016/0006-8993(83)90615-7 · Cited by 603 · see citing works

Effects of synthetic ovine corticotropin-releasing factor, glucocorticoids, catecholamines, neurohypophysial peptides, and other substances on cultured corticotropic cells

VALE, W., VAUGHAN, J., SMITH, M., & YAMAMOTO, G. (1983) · Endocrinology · doi:10.1210/endo-113-3-1121 · Cited by 563 · cited 1× · see citing works

An arcuato-paraventricular and -dorsomedial hypothalamic neuropeptide Y-containing system which lacks noradrenaline in the rat

Bai, F.-L., Yamano, M., Shiotani, Y., Emson, P. C., Smith, A. D., Powell, J. F., & Tohyama, M. (1985) · Brain Research · doi:10.1016/0006-8993(85)90730-9 · Cited by 524 · see citing works

Corticotropin-releasing factor produces fear-enhancing and behavioral activating effects following infusion into the locus coeruleus

Butler, P., Weiss, J., Stout, J., & Nemeroff, C. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-01-00176.1990 · Cited by 402 · see citing works

Glucose Inhibition of the Glucose-sensitive Neurone in the Rat Lateral Hypothalamus

Oomura, Y., Ooyama, H., Sugimori, M., Nakamura, T., & YAMADA, Y. (1974) · Nature · doi:10.1038/247284a0 · Cited by 358 · see citing works

Facilitation of Immunoreactive Corticotropin-Releasing Factor Secretion into the Hypophysial-Portal Circulation after Activation of Catecholaminergic Pathways or Central Norepinephrine Injection*

Plotsky, P. M. (1987) · Endocrinology · doi:10.1210/endo-121-3-924 · Cited by 325 · see citing works

Effect of neuropeptide Y on ingestive behaviors in the rat

Morley, J. E., Levine, A. S., Gosnell, B. A., Kneip, J. M., & Grace, M. K. (1987) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1987.252.3.r599 · Cited by 292 · see citing works

Neuropeptide Y (NPY) in the area of the hypothalamic paraventricular nucleus activates the pituitary-adrenocortical axis in the rat

Wahlestedt, C., Skagerberg, G., Ekman, R., Heilig, M. A., Sundler, F., & Håkanson, R. (1987) · Brain Research · doi:10.1016/0006-8993(87)90176-4 · Cited by 285 · see citing works

The origin of the vasopressinergic and oxytocinergic fibres of the external region of the median eminence of the rat hypophysis

Vandesande, F., Dierickx, K., & Mey, J. D. (1977) · Cell and Tissue Research · doi:10.1007/bf00220167 · Cited by 270 · see citing works

Pathways to the Secretion of Adrenocorticotropin: A View from the Portal*

Plotsky, P. M. (1991) · Journal of Neuroendocrinology · doi:10.1111/j.1365-2826.1991.tb00231.x · Cited by 258 · see citing works

Glucose responding neurons in the nucleus tractus solitarius of the rat: In vitro study

Mizuno, Y., & Oomura, Y. (1984) · Brain Research · doi:10.1016/0006-8993(84)90466-9 · Cited by 245 · see citing works

The Responses of Plasma Adrenocorticotropin and Cortisol to Corticotropin-Releasing Hormone (CRH) and Cerebrospinal Fluid Immunoreactive CRH in Anorexia Nervosa Patients*

Hotta, M., Shibasaki, T., Masuda, A., Imaki, T., Demura, H., LING, N. C., & SHIZUME, K. (1986) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-62-2-319 · Cited by 239 · see citing works

Studies of the Secretion of Corticotropin-Releasing Factor and Arginine Vasopressin into the Hypophysial-Portal Circulation of the Conscious Sheep

Engler, D., Pham, T., Fullerton, M. J., Ooi, G., Funder, J. W., & Clarke, I. J. (2008) · Neuroendocrinology · doi:10.1159/000125141 · Cited by 235 · see citing works

Norepinephrine and Its Metabolites in Cerebrospinal Fluid, Plasma, and Urine

Roy, A. (1988) · Archives of General Psychiatry · doi:10.1001/archpsyc.1988.01800330081010 · Cited by 208 · see citing works

Hypophysiotropic Regulation of Adrenocorticotropin Secretion in Response to Insulin-Induced Hypoglycemia*

Plotsky, P. M., BRUHN, T. O., & Vale, W. (1985) · Endocrinology · doi:10.1210/endo-117-1-323 · Cited by 196 · see citing works

Catecholamine effects upon rat hypothalamic corticotropin-releasing hormone secretion in vitro.

Calogero, A. E., Gallucci, W. T., Chrousos, G. P., & Gold, P. W. (1988) · Journal of Clinical Investigation · doi:10.1172/jci113687 · Cited by 188 · see citing works

A generalized computer program for the treatment of data from competitive protein-binding assays including radioimmunoassays.

Burger, H., Vw, L., & Gc, R. (1972) · PubMed · Cited by 185 · see citing works

Neuropeptide-Y and ACTH-immunoreactive innervation of corticotropin releasing factor (CRF)-synthesizing neurons in the hypothalamus of the rat

Liposits, Z., Sievers, L., & Paull, W. K. (1988) · Histochemistry · doi:10.1007/bf00570278 · Cited by 182 · see citing works

Altered Cerebrospinal Fluid Neuropeptide Y and Peptide YY Immunoreactivity in Anorexia and Bulimia Nervosa

Kaye, W. H. (1990) · Archives of General Psychiatry · doi:10.1001/archpsyc.1990.01810180048008 · Cited by 174 · see citing works

Feedback and facilitation in the adrenocortical system: unmasking facilitation by partial inhibition of the glucocorticoid response to prior stress

Akana, S. F., Dallman, M. F., BRADBURY, M. J., Scribner, K. A., Strack, A. M., & Walker, C. D. (1992) · Endocrinology · doi:10.1210/endo.131.1.1319329 · Cited by 168 · see citing works

Hypercortisolism and its possible neural bases

Sapolsky, R. M., & Plotsky, P. M. (1990) · Biological Psychiatry · doi:10.1016/0006-3223(90)90032-w · Cited by 161 · see citing works

PRESENCE OP CORTICOTROPIN RELEASING FACTOR-LIKE IMMUNOREACTIVITY IN HYPOPHYSIAL PORTAL BLOOD

Gibbs, D. M., & Vale, W. (1982) · Endocrinology · doi:10.1210/endo-111-4-1418 · Cited by 159 · see citing works

Relationships between brain noradrenergic activity and blood glucose

Smythe, G. A., Grunstein, H. S., Bradshaw, J. E., Nicholson, M. V., & Compton, P. (1984) · Nature · doi:10.1038/308065a0 · Cited by 155 · see citing works

Adrenergic innervation of corticotropin releasing factor (CRF) ? synthesizing neurons in the hypothalamic paraventricular nucleus of the rat

Liposits, Z., Phelix, C. F., & Paull, W. K. (1986) · Histochemistry and Cell Biology · doi:10.1007/bf00495783 · Cited by 149 · see citing works

The hypothalamic-pituitary-adrenal axis in critical illness: response to dexamethasone and corticotropin-releasing hormone

Reincke, M., Allolio, B., Würth, G., & Winkelmann, W. (1993) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.77.1.8392081 · Cited by 147 · see citing works

Corticotropin-Releasing Factor Regulates Proopiomelanocortin Messenger Ribonucleic Acid Levels in vivo

BRUHN, T. O., Sutton, R. E., RIVIER, C. L., & Vale, W. (2008) · Neuroendocrinology · doi:10.1159/000123974 · Cited by 141 · see citing works

Insulin-induced hypoglycemia stimulates corticotropin-releasing factor and arginine vasopressin secretion into hypophysial portal blood of conscious, unrestrained rams

Caraty, A., Grino, M., Locatelli, A., Guillaume, V, Boudouresque, F., Conte-Devolx, B., & Oliver, C. (1990) · Journal of Clinical Investigation · doi:10.1172/jci114626 · Cited by 128 · see citing works

Morphometrical analysis of the distribution of corticotrophin releasing factor, glucocorticoid receptor and phenylethanolamine-N-methyltransferase immunoreactive structures in the paraventricular hypothalamic nucleus of the rat

Agnati, L. F., Fuxé, K., Yu, Z.-Y., Härfstrand, A., Okret, S., Wikström, A. C., Goldstein, M., Zoli, M., Vale, W., & Gustafsson, J.-Α. (1985) · Neuroscience Letters · doi:10.1016/s0304-3940(85)80070-7 · Cited by 121 · see citing works

Arginine Vasopressin Is a Much More Potent Stimulus to ACTH Release from Ovine Anterior Pituitary Cells than Ovine Corticotropin-Releasing Factor

Familari, M., Smith, I., Smith, R., & Funder, J. W. (2008) · Neuroendocrinology · doi:10.1159/000125214 · Cited by 116 · cited 2× · see citing works

Localization of neuropeptide Y messenger ribonucleic acid in rat and mouse brian by in situ hybridization

Gehlert, D. R., Chronwall, B. M., Schafer, M. P., & O’Donohue, T. L. (1987) · Synapse · doi:10.1002/syn.890010106 · Cited by 114 · see citing works

Acetylcholine and Norepinephrine Stimulate the Release of Corticotropin-Releasing Factor-41 from the Rat Hypothalamusin Vitro*

Tsagarakis, S., Holly, J. M. P., REES, L. H., BESSER, G. M., & Grossman, A. B. (1988) · Endocrinology · doi:10.1210/endo-123-4-1962 · Cited by 107 · see citing works

Pulsatile Rhythms of Adrenocorticotropin (ACTH) and Cortisol in Women with Endogenous Depression: Evidence for Increased ACTH Pulse Frequency*

Mortola, J. F., LIU, J. H., GILLIN, J. C., Rasmussen, D. D., & Yen, S. S. C. (1987) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-65-5-962 · Cited by 105 · see citing works

The biosynthesis and secretion of adrenocorticotropin by the ovine anterior pituitary is predominantly regulated by arginine vasopressin (AVP). Evidence that protein kinase C mediates the action of AVP.

Liu, J., Robinson, P. J., Funder, J. W., & Engler, D. (1990) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)77278-5 · Cited by 91 · see citing works

The Production Rate of Cortisol Declines during Recovery from Anorexia Nervosa*

Walsh, B. T., Katz, J. L., Levin, J., Kream, J., Fukushima, D. K., Weiner, H., & Zumoff, B. (1981) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem-53-1-203 · Cited by 89 · see citing works

Glucoresponsive neurons in rat ventromedial hypothalamic tissue slices in vitro

Ono, T., Nishino, H., Fukuda, M., Sasaki, K., Muramoto, K., & Oomura, Y. (1982) · Brain Research · doi:10.1016/0006-8993(82)90295-5 · Cited by 85 · see citing works

Insulin-Induced Hypoglycemia Increases Corticotropin- Releasing Factor Messenger Ribonucleic Acid Levels in Rat Hypothalamus*

Suda, T., TOZAWA, F., YAMADA, M., USHIYAMA, T., Tomori, N., Sumitomo, T., NAKAGAMI, Y., Demura, H., & SHIZUME, K. (1988) · Endocrinology · doi:10.1210/endo-123-3-1371 · Cited by 82 · see citing works

Corticotropin-Releasing Factor Differentially Regulates Anterior and Intermediate Pituitary Lobe Proopiomelanocortin Gene Transcription, Nuclear Precursor RNA and Mature mRNA in vivo

Autelitano, D. J., Blum, M., Lopingco, M. C., Allen, R. G., & Roberts, J. L. (2008) · Neuroendocrinology · doi:10.1159/000125327 · Cited by 76 · see citing works

Secretion of Corticotropin-Releasing Factor from Cultured Rat Hypothalamic Cells: Effects of Catecholamines*

Widmaier, E. P., LIM, A. T. W., & Vale, W. (1989) · Endocrinology · doi:10.1210/endo-124-2-583 · Cited by 73 · see citing works

Distributions of pro‐vasopressin expressing and pro‐vasopressin deficient CRH neurons in the paraventricular hypothalamic nucleus of colchicine‐treated normal and adrenalectomized rats

Whitnall, M. H. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902750103 · Cited by 72 · see citing works

Secretion of corticotropin releasing factor (CRF) and vasopressin (AVP) into the hypophysial portal blood of conscious, unrestrained rams

Caraty, A., Grino, M., Locatelli, A., & Oliver, C. (1988) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(88)80572-2 · Cited by 70 · see citing works

Second Messengers Involved in the Regulation of Corticotropin-Releasing Hormone mRNA and Peptide in Cultured Rat Fetal Hypothalamic Primary Cultures

Emanuel, R. L., Girard, D. M., Thull, D. L., & Majzoub, J. A. (1990) · Endocrinology · doi:10.1210/endo-126-6-3016 · Cited by 65 · see citing works

Corticotrophin-releasing peptides in rat hypophysial portal blood after paraventricular lesions: a marked reduction in the concentration of corticotrophin-releasing factor-41, but no change in vasopressin

Antoni, F. A., Fink, G., & Sheward, W. J. (1990) · Journal of Endocrinology · doi:10.1677/joe.0.1250175 · Cited by 63 · see citing works

Central catecholaminergic system stimulates secretion of CRH at different sites

SZAFARCZYK, A., Guillaume, V., Conte‐Devolx, B., Alonso, G., Malaval, F., Parés-Herbute, N., Oliver, C., & ASSENMACHER, I. (1988) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1988.255.4.e463 · Cited by 57 · see citing works

Dissociation of the Adrenocorticotropin Secretory Responses to Corticotropin-Releasing Factor (CRF) and Vasopressin or Oxytocin by Using a Specific Cytotoxic Analog of CRF*

Schwartz, J., & Vale, W. (1988) · Endocrinology · doi:10.1210/endo-122-4-1695 · Cited by 55 · see citing works

Vasopressin Concentrations in Hypophysial Portal Plasma: Insignificant Reduction following Removal of the Posterior Pituitary Gland

Recht, L. D., Hoffman, D. L., Haldar, J., Silverman, A., & Zimmerman, E. A. (2008) · Neuroendocrinology · doi:10.1159/000123208 · Cited by 51 · see citing works

Ultrastructural characterization of exocytotic release sites in different layers of the median eminence of the rat

Buma, P., & Nienwenhuys, R. (1988) · Cell and Tissue Research · doi:10.1007/bf00213831 · Cited by 47 · see citing works

Plasma adrenocorticotrophin, cortisol and aldosterone responses to ovine corticotrophin-releasing factor and vasopressin in sheep

Pradier, P., Davicco, M. J., Safwate, A., Tournaire, C., Dalle, M., Barler, J. P., & Delost, P. (1986) · European Journal of Endocrinology · doi:10.1530/acta.0.1110093 · Cited by 45 · see citing works

Regulation of corticotropin-releasing factor secretion in vitro by glucose

Widmaier, E. P., Plotsky, P. M., Sutton, S. W., & Vale, W. (1988) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1988.255.3.e287 · Cited by 45 · see citing works

Evidence for an Ultradian Secretion of Adrenocorticotropin, β-Endorphin and α-Melanocyte-Stimulating Hormone by the Ovine Anterior and Intermediate Pituitary

Engler, D., Pham, T., Fullerton, M. J., Clarke, I. J., & Funder, J. W. (2008) · Neuroendocrinology · doi:10.1159/000125139 · Cited by 44 · see citing works

Effect of Metyrapone on the Pituitary-Adrenal Axis in Depression Relation to Dexamethasone Suppressor Status

Ur, E., Dinan, T. G., O’Keane, V., Clare, A. W., McLoughlin, L., REES, L. H., Turner, T. H., Grossman, A. B., & Besser, M. (2008) · Neuroendocrinology · doi:10.1159/000126271 · Cited by 39 · see citing works

Evidence That the Central Noradrenergic and Adrenergic Pathways Activate the Hypothalamic- Pituitary-Adrenal Axis in the Sheep*

Liu, J., Clarke, I. J., Funder, J. W., & Engler, D. (1991) · Endocrinology · doi:10.1210/endo-129-1-200 · Cited by 37 · see citing works

Comparison of Adrenocorticotropin Control in Brattleboro, Long-Evans, and Wistar Rats

Tannahill, L. A., Dow, R. C., Fairhall, K. M., Robinson, I. C. A. F., & Fink, G. (2008) · Neuroendocrinology · doi:10.1159/000125077 · Cited by 30 · see citing works

Adrenergic neurons in sheep brain demonstrated by immunohistochemistry with antibodies to phenylethanolamine N-methyltransferase (PNMT) and dopamine-β-hydroxylase (DBH): Absence of the C1 cell group in the sheep brain

Tillet, Y. (1988) · Neuroscience Letters · doi:10.1016/0304-3940(88)90641-6 · Cited by 30 · see citing works

Brain neuropeptide Y in the control of adrenocorticotropic hormone secretion in the dog

Inui, A., Inoue, T., Nakajima, M., Okita, M., Sakatani, N., Okimura, Y., Chihara, K., & Baba, S. (1990) · Brain Research · doi:10.1016/0006-8993(90)91369-r · Cited by 27 · see citing works

Ultrastructural demonstration of neurohaemal contacts in the internal zone of the median eminence of the Mongolian gerbil (Meriones unguiculatus): correlation with synaptophysin immunohistochemistry

Redecker, P. (1991) · Histochemistry and Cell Biology · doi:10.1007/bf00315747 · Cited by 8 · see citing works

Anatomy of Vasopressin-Producing Cells

Zimmerman, E. A. (2015) · Frontiers of hormone research · doi:10.1159/000410094 · Cited by 7 · see citing works

Salivary cortisol as a biomarker in stress research

Hellhammer, D. H., Wüst, S., & Kudielka, B. M. (2009) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2008.10.026 · Cited by 1,925 · see citing works

Endocrinology of the stress response

Charmandari, E., Tsigos, C., & Chrousos, G. (2005) · Annual Review of Physiology · doi:10.1146/annurev.physiol.67.040403.120816 · Cited by 1,799 · see citing works

Endocrine and Paracrine Regulation of Birth at Term and Preterm*

Challis, J. R. G., Matthews, S. G., Gibb, W., & Lye, S. J. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.5.0407 · Cited by 995 · see citing works

Interactions between the Hypothalamic-Pituitary-Adrenal Axis and the Female Reproductive System: Clinical Implications

Chrousos, G. P., Torpy, D. J., & Gold, P. W. (1998) · Annals of Internal Medicine · doi:10.7326/0003-4819-129-3-199808010-00012 · Cited by 707 · see citing works

What’s in a Name? In Search of Leptin’s Physiologic Role1

Flier, J. S. (1998) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.83.5.4779 · Cited by 518 · see citing works

Pediatric Stress: Hormonal Mediators and Human Development

Charmandari, E., Kino, T., Souvatzoglou, E., & Chrousos, G. P. (2003) · Hormone Research in Paediatrics · doi:10.1159/000069325 · Cited by 364 · see citing works

Toxic Stress in Children and Adolescents

Bucci, M., Marques, S. S., Oh, D., & Harris, N. B. (2016) · Advances in Pediatrics · doi:10.1016/j.yapd.2016.04.002 · Cited by 295 · see citing works

Ultradian rhythm of basal corticosterone release in the female rat: dynamic interaction with the response to acute stress

Windle, R. J., Wood, S. A., Shanks, N., Lightman, S. L., & Ingram, C. D. (1998) · Endocrinology · doi:10.1210/en.139.2.443 · Cited by 276 · see citing works

A neurodevelopmental model for anorexia nervosa

Connan, F., Campbell, I. C., Katzman, M. A., Lightman, S. L., & Treasure, J. L. (2003) · Physiology & Behavior · doi:10.1016/s0031-9384(03)00101-x · Cited by 255 · see citing works

Central Administration of Leptin to Ovariectomized Ewes Inhibits Food Intake without Affecting the Secretion of Hormones from the Pituitary Gland: Evidence for a Dissociation of Effects on Appetite and Neuroendocrine Function

Henry, B. A., Goding, J. W., Alexander, W. S., Tilbrook, A. J., Canny, B. J., Dunshea, F. R., Rao, A., Mansell, A. S., & Clarke, I. J. (1999) · Endocrinology · doi:10.1210/en.140.3.1175 · Cited by 238 · see citing works

The Pulsatile Characteristics of Hypothalamo-Pituitary-Adrenal Activity in Female Lewis and Fischer 344 Rats and Its Relationship to Differential Stress Responses*

Windle, R. J., Wood, S. A., Lightman, S. L., & Ingram, C. D. (1998) · Endocrinology · doi:10.1210/endo.139.10.6238 · Cited by 201 · see citing works

Comparative distribution of neuropeptide Y Y1 and Y5 receptors in the rat brain by using immunohistochemistry

Wolak, M. L., DeJoseph, M. R., Cator, A. D., Mokashi, A. S., Brownfield, M. S., & Urban, J. H. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10823 · Cited by 199 · see citing works

Gestational Hypoxia and Developmental Plasticity

Ducsay, C. A., Goyal, R., Pearce, W. J., Wilson, S. M., Hu, X., & Zhang, L. (2018) · Physiological Reviews · doi:10.1152/physrev.00043.2017 · Cited by 203 · see citing works

Neuroendocrine Responses to Starvation and Weight Loss

Schwartz, M. W., & Seeley, R. J. (1997) · New England Journal of Medicine · doi:10.1056/nejm199706193362507 · Cited by 265 · see citing works

A review of endocrine changes in anorexia nervosa

Støving, R. K., Hangaard, J., Hansen‐Nord, M., & Hagen, C. (1999) · Journal of Psychiatric Research · doi:10.1016/s0022-3956(98)00049-1 · Cited by 151 · see citing works

Anorexia nervosa, self–starvation and the reward of stress

Bergh, C. E. K., & Södersten, P. (1996) · Nature Medicine · doi:10.1038/nm0196-21 · Cited by 135 · see citing works

The Central Effects of Orexin‐A in the Hypothalamic‐Pituitary‐Adrenal Axis In Vivo and In Vitro in Male Rats

Russell, S. H., Small, C. J., Dakin, C. L., Abbott, C. R., Morgan, D. G. A., Ghatei, M. A., & Bloom, S. R. (2001) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2001.00672.x · Cited by 128 · see citing works

Chronic central neuropeptide Y infusion in normal rats: status of the hypothalamo-pituitary-adrenal axis, and vagal mediation of hyperinsulinaemia

Sainsbury, A., Rohner-Jeanrenaud, F., Cusin, I., Zakrzewska, K. E., Halban, P. A., Gaillard, R. C., & Jeanrenaud, B. (1997) · Diabetologia · doi:10.1007/s001250050820 · Cited by 115 · see citing works

Anatomy of melancholia: focus on hypothalamic–pituitary–adrenal axis overactivity and the role of vasopressin

Dinan, T. G., & Scott, L. V. (2005) · Journal of Anatomy · doi:10.1111/j.1469-7580.2005.00443.x · Cited by 110 · see citing works

Organization and Integration of the Endocrine System: The Arousal and Sleep Perspective

Chrousos, G. P. (2007) · Sleep Medicine Clinics · doi:10.1016/j.jsmc.2007.04.004 · Cited by 103 · see citing works

New model for the regulation of energy balance and adiposity by the central nervous system

Kaiyala, K., Woods, S. C., & Schwartz, M. (1995) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/62.5.1123s · Cited by 98 · see citing works

Arginine Vasopressin Is Associated with Hypercortisolemia and Suicide Attempts in Depression

Inder, W. J., Donald, R. A., Prickett, T. C. R., FRAMPTON, C. M. A., Sullivan, P. F., Mulder, R., & Joyce, P. R. (1997) · Biological Psychiatry · doi:10.1016/s0006-3223(97)00301-6 · Cited by 88 · see citing works

Hypothalamus as an Endocrine Organ

Clarke, I. J. (2014) · Comprehensive physiology · doi:10.1002/cphy.c140019 · Cited by 104 · see citing works

Long-Term Alterations in Adiposity Affect the Expression of Melanin-Concentrating Hormone and Enkephalin But Not Proopiomelanocortin in the Hypothalamus of Ovariectomized Ewes1

Henry, B. A., Tilbrook, A. J., Dunshea, F. R., Rao, A., Blache, D., Martin, G. B., & Clarke, I. J. (2000) · Endocrinology · doi:10.1210/endo.141.4.7434 · Cited by 83 · see citing works

Hypothalamic-pituitary-adrenal axis activity and its relationship to the autonomic nervous system in women with visceral and subcutaneous obesity: Effects of the corticotropin-releasing factor/arginine-vasopressin test and of stress

Pasquali, R., Anconetani, B., Chattat, R., Biscotti, M., Spinucci, G., Casimirri, F., Vicennati, V., Carcello, A., & Labate, A. M. M. (1996) · Metabolism · doi:10.1016/s0026-0495(96)90290-5 · Cited by 109 · see citing works

Prolonged exercise increases peripheral plasma ACTH, CRH, and AVP in male athletes

Inder, W. J., Hellemans, J., Swanney, M. P., Prickett, T. C. R., & Donald, R. A. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.85.3.835 · Cited by 82 · see citing works

The corticotropin–release inhibitory factor hypothesis: a review of the evidence for the existence of inhibitory as well as stimulatory hypophysiotropic regulation of adrenocorticotropin secretion and biosynthesis

Engler, D., Redei, E., & Kola, I. (1999) · Endocrine Reviews · doi:10.1210/edrv.20.4.0376 · Cited by 79 · see citing works

Vasopressin as a target for antidepressant development: an assessment of the available evidence

Scott, L. V., & Dinan, T. G. (2002) · Journal of Affective Disorders · doi:10.1016/s0165-0327(02)00026-5 · Cited by 78 · see citing works

Regulation of the hypothalamo-pituitary-adrenocortical axis in fetal sheep

Matthews, S. G., & Challis, J. R. G. (1996) · Trends in Endocrinology and Metabolism · doi:10.1016/s1043-2760(96)00126-9 · Cited by 79 · see citing works

Effects of Increasing Gestation, Cortisol and Maternal Undernutrition on Hypothalamic Neuropeptide Y Expression in the Sheep Fetus

Warnes, K. E., Morris, M. J., Symonds, M. E., Phillips, I., Clarke, I. J., Owens, J. A., & McMillen, I. C. (1998) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1998.00172.x · Cited by 69 · see citing works

Plasma Leptin Levels Do not Change in Patients with Cushing's Disease Shortly after Correction of Hypercortisolism

Cizza, G., Lotsikas, A. J., Licinio, J., Gold, P. W., & Chrousos, G. P. (1997) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.82.8.4139 · Cited by 64 · see citing works

Update on Endocrine Disturbances in Anorexia Nervosa

Støving, R. K., Hangaard, J., & Hagen, C. (2001) · Journal of Pediatric Endocrinology and Metabolism · doi:10.1515/jpem.2001.14.5.459 · Cited by 64 · see citing works

Evidence that elevated plasma corticosterone levels are the cause of reduced hypothalamic corticotrophin-releasing hormone gene expression in diabetes.

Schwartz, M. W., Strack, A. M., & Dallman, M. F. (1997) · Regulatory Peptides · doi:10.1016/s0167-0115(97)01043-4 · Cited by 57 · see citing works

Leptin downregulates heat shock protein-70 (HSP-70) gene expression in chicken liver and hypothalamus

Figueiredo, D. F., Gertler, A., Cabello, G., Decuypere, E. M. P., Buyse, J. G., & Dridi, S. (2007) · Cell and Tissue Research · doi:10.1007/s00441-007-0414-6 · Cited by 57 · see citing works

Centrally Administered Murine-Leptin Stimulates the Hypothalamus-Pituitary- Adrenal Axis through Arginine-Vasopressin

Morimoto, I., Yamamoto, S., Kai, K., Fujihira, T., Morita, E., & Eto, S. (2000) · Neuroendocrinology · doi:10.1159/000054557 · Cited by 53 · see citing works

Complementary Role of Oxytocin and Vasopressin in Cardiovascular Regulation

Szczepanska‐Sadowska, E. K., Wsół, A., Cudnoch‐Jędrzejewska, A., & Żera, T. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111465 · Cited by 53 · see citing works

Decreased central and peripheral catecholaminergic activation in obese Zucker rats

Pacák, K., McCarty, R. C., Palkovits, M., Cizza, G., Kopin, I. J., Goldstein, D. S., & Chrousos, G. P. (1995) · Endocrinology · doi:10.1210/endo.136.10.7664655 · Cited by 51 · see citing works

The Neuroendocrinology of Stress

Kaltsas, G., Chrousos, G. P., & Sternberg, E. M. (2009) · Cambridge University Press eBooks · doi:10.1017/cbo9780511546396.013 · Cited by 50 · see citing works

Neuropeptides Amplify and Focus the Monoaminergic Inhibition of Nociception in Caenorhabditis elegans

Hapiak, V., Summers, P., Ortega, A., Law, W. J., Stein, A., & Komuniecki, R. W. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1324-13.2013 · Cited by 49 · see citing works

Cells of the Arcuate Nucleus and Ventromedial Nucleus of the Ovariectomized Ewe that Respond to Oestrogen: A Study Using Fos Immunohistochemistry

Clarke, I. J., Pompolo, S., Scott, C., Rawson, J. A., Caddy, D. J., Jakubowska, A. E., & Pereira, A. (2001) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2001.00694.x · Cited by 46 · see citing works

Constitutional Thinness and Anorexia Nervosa: A Possible Misdiagnosis?

Estour, B., Galusca, B., & Germain, N. (2014) · Frontiers in Endocrinology · doi:10.3389/fendo.2014.00175 · Cited by 41 · see citing works

Long-term hypoxia increases leptin receptors and plasma leptin concentrations in the late-gestation ovine fetus

Ducsay, C. A., Hyatt, K., Młynarczyk, M., Kaushal, K. M., & Myers, D. A. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00077.2006 · Cited by 38 · see citing works

Effects of Leptin on Fetal Plasma Adrenocorticotropic Hormone and Cortisol Concentrations and the Timing of Parturition in the Sheep1

Yuen, B. S. J., Owens, P. C., Symonds, M. E., Keisler, D. H., McFarlane, J. R., Kauter, K., & McMillen, I. C. (2004) · Biology of Reproduction · doi:10.1095/biolreprod.103.025254 · Cited by 37 · see citing works

NPY Y1 receptors exert opposite effects on corticotropin releasing factor and noradrenaline overflow from the rat hypothalamus in vitro

Hastings, J. A., McClure-Sharp, J. M., & Morris, M. J. (2001) · Brain Research · doi:10.1016/s0006-8993(00)02874-2 · Cited by 33 · see citing works

Elevated corticosterone and inhibition of ACTH responses to CRH and ether in the neonatal rat: effect of hypoxia from birth

Raff, H., Jacobson, L., & Cullinan, W. E. (2003) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00259.2003 · Cited by 29 · see citing works

Effect of Season on Neuropeptide Y and Galanin within the Hypothalamus of the Ewe in Relation to Plasma Luteinizing Hormone Concentrations and the Breeding Season: An Immunohistochemical Analysis

Barker‐Gibb, & Clarke, I. J. (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00514.x · Cited by 29 · see citing works

Hypothalamus as an Endocrine Organ

Clarke, I. J. (2015) · Comprehensive physiology · doi:10.1002/j.2040-4603.2015.tb00605.x · Cited by 28 · see citing works

The Effect of the Alpha‐2‐Adrenergic Agonist, Clonidine, on Secretion Patterns and Rates of Adrenocorticotropic Hormone and its Secretagogues in the Horse

Alexander, S. L., & IRVINE, C. H. G. (2000) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.2000.00542.x · Cited by 28 · see citing works

Altered levels of neuropeptides characterize the brain of lupus prone mice

Bracci‐Laudiero, L., Aloe, L., Lundeberg, T., Theodorsson, E., & Stenfors, C. (1999) · Neuroscience Letters · doi:10.1016/s0304-3940(99)00737-5 · Cited by 27 · see citing works

Regulation and adaptation of endocrine axes at high altitude

Keenan, D. M., Hefti, J. P., Veldhuis, J. D., & von Wolff, M. (2019) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00243.2019 · Cited by 22 · see citing works

Effects of Restraint Stress and Spontaneous Hypertension on Neuropeptide Y Neurones in the Brainstem and Arcuate Nucleus

Krukoff, MacTavish, & Jhamandas, V. (1999) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1999.00391.x · Cited by 22 · see citing works

Corticosteroid receptors and the central nervous system

Funder, J. W. (1994) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(94)90283-6 · Cited by 21 · see citing works

Regulation of corticosteroid receptors in patients with anorexia nervosa and Cushing's syndrome.

Armanini, D., Spinella, P., Simoncini, M., Basso, A., Zovato, S., Pozzan, G., Palo, C. D., Bucciante, G., & Karbowiak, I. (1998) · Journal of Endocrinology · doi:10.1677/joe.0.1580435 · Cited by 19 · see citing works

Central noradrenaline transporter availability is linked with HPA axis responsiveness and copeptin in human obesity and non-obese controls

Schinke, C., Hesse, S., Rullmann, M., Becker, G., Luthardt, J., Zientek, F., Patt, M., Stoppe, M., Schmidt, E., Meyer, K., et al. (2018) · Stress · doi:10.1080/10253890.2018.1511698 · Cited by 17 · see citing works

Metabolismo en el ayuno

Albero, R., Sanz, A., & Playán, J. (2004) · Endocrinología y Nutrición · doi:10.1016/s1575-0922(04)74599-4 · Cited by 14 · see citing works

Do Working Hours and Type of Work Affect Obesity in South Korean Female Workers? Analysis of the Korean Community Health Survey

Yoon, C., Kang, M., Bae, K.-J., & Yoon, J. (2015) · Journal of Women s Health · doi:10.1089/jwh.2014.5161 · Cited by 16 · see citing works

High Cortisol Response to Adrenocorticotrophic Hormone Identifies Ewes with Reduced Melanocortin Signalling and Increased Propensity to Obesity

Hewagalamulage, S. D., Clarke, I. J., Young, I. R., Rao, A., & Henry, B. A. (2014) · Journal of Neuroendocrinology · doi:10.1111/jne.12233 · Cited by 15 · see citing works

Fasting as a metabolic stress paradigm selectively amplifies cortisol secretory burst mass and delays the time of maximal nyctohemeral cortisol concentrations in healthy men

Bergendahl, M., Vance, M. L., Iranmanesh, A., Thorner, M. O., & Veldhuis, J. D. (1996) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.81.2.8636290 · Cited by 126 · see citing works

Ewes With Divergent Cortisol Responses to ACTH Exhibit Functional Differences in the Hypothalamo-Pituitary-Adrenal (HPA) Axis

Hewagalamulage, S. D., Clarke, I. J., Rao, A., & Henry, B. A. (2016) · Endocrinology · doi:10.1210/en.2016-1287 · Cited by 14 · see citing works

Noradrenaline, but Not Neuropeptide Y, Is Elevated in Cerebrospinal Fluid from the Third Cerebral Ventricle following Audiovisual Stress in Gonadectomised Rams and Ewes

Turner, A. I., Rivalland, E. T. A., Clarke, I. J., Lambert, G. W., Morris, M. J., & Tilbrook, A. J. (2002) · Neuroendocrinology · doi:10.1159/000067584 · Cited by 14 · see citing works

[Family support and quality of life of pregnant women during pregnancy and after birth].

野原, 真., & 宮城, 重. (2009) · PubMed · Cited by 14 · see citing works

Changes in Fetal Plasma Corticotropin-Releasing Hormone during Androstenedione-Induced Labor in the Rhesus Monkey: Lack of an Effect on the Fetal Hypothalamo-Pituitary-Adrenal Axis

Giussani, D. A., Winter, J. A., Jenkins, S. L., Tame, J. D., Abrams, L. M., Ding, X. Y., & Nathanielsz, P. W. (1998) · Endocrinology · doi:10.1210/endo.139.6.6044 · Cited by 15 · see citing works

The effects of ghrelin/GHSs on AVP mRNA expression and release in cultured hypothalamic cells in rats

Nemoto, T., Sugihara, H., Mano, A., Kano, T., & Shibasaki, T. (2011) · Peptides · doi:10.1016/j.peptides.2011.04.007 · Cited by 12 · see citing works

Plasma Levels of Corticotropin-Releasing Hormone in the Inferior Petrosal Sinuses of Healthy Volunteers, Patients with Cushing's Syndrome, and Patients with Pseudo-Cushing States

Yanovski, J. A., Nieman, L. K., Doppman, J. L., Chrousos, G. P., Wilder, R. L., Gold, P. W., & Kalogeras, K. T. (1998) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.83.5.1485 · Cited by 12 · see citing works

CRH mRNA expression in the hypothalamic paraventricular nucleus is inhibited despite the activation of the hypothalamo-pituitary-adrenal axis during starvation

Nishiyama, M., Makino, S., Iwasaki, Y., Tanaka, Y., Pournajafi‐Nazarloo, H., Kaneda, T., Asaba, K., & Hashimoto, K. (2008) · Brain Research · doi:10.1016/j.brainres.2008.06.065 · Cited by 11 · see citing works

Salsolinol: a potential modulator of the activity of the hypothalamic–pituitary–adrenal axis in nursing and postweaning sheep

Hasiec, M., Herman, A. P., & Misztal, T. (2015) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2015.04.004 · Cited by 10 · see citing works

Neurochemical Systems Regulating the Hypothalamo-Pituitary-Adrenocortical Axis

Herman, J. P., Figueiredo, H. F., Mueller, N. K., Ostrander, M. M., Zhang, R., Tauchi, M., Choi, D. C., Furay, A. R., Evanson, N. K., Nelson, E., et al. (2006) · Springer eBooks · doi:10.1007/978-0-387-30405-2_13 · Cited by 9 · see citing works

Corticotropin-release inhibitory factor

Engler, D., Liu, J., Clarke, I. J., & Funder, J. W. (1994) · Trends in Endocrinology and Metabolism · doi:10.1016/1043-2760(94)p3202-i · Cited by 9 · see citing works

Influence of arginine vasopressin on the ultradian dynamics of Hypothalamic-Pituitary-Adrenal axis

Stojiljković, A. S., Čupić, Ž., Maćešić, S., Ivanović-Šašić, A., & Kolar-Anić, L. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.976323 · Cited by 9 · see citing works

Neuropeptide Y (NPY) actions on the corticotroph cell of the anterior pituitary gland are not mediated by a direct effect

Small, C. J., Todd, J. F., Ghatei, M., Smith, D. M., & Bloom, S. R. (1998) · Regulatory Peptides · doi:10.1016/s0167-0115(98)00082-2 · Cited by 8 · see citing works

Regulation of Pulsatile and Entropic ACTH Secretion Under Fixed Exogenous Secretagogue Clamps

Roelfsema, F., Aoun, P., Takahashi, P. Y., Erickson, D., Yang, R., & Veldhuis, J. D. (2017) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2017-00115 · Cited by 7 · see citing works

Pituitary Function

Mol, J. A., & Rijnberk, A. (1997) · Elsevier eBooks · doi:10.1016/b978-012396305-5/50020-8 · Cited by 7 · see citing works

Neuroendocrine Actions Of Neuropeptide Y

Crowley, W. R. (2004) · Handbook of experimental pharmacology · doi:10.1007/978-3-642-18764-3_7 · Cited by 5 · see citing works

Chronic exposure to multiple stressors alters the salivary proteome of piglets

Prims, S., Ostade, X. V., Ayuso, M., Dom, M., Raemdonck, G. V., Cruchten, S. J. M. V., Casteleyn, C. R., & Ginneken, C. J. V. (2023) · PLoS ONE · doi:10.1371/journal.pone.0286455 · Cited by 4 · see citing works

A obesidade estaria relacionada ao aumento do volume das adrenais?

Matos, A. F. D. G., Vieira, A. R., Coutinho, W. F., Madeira, D. M., Carraro, L., Rodrigues, R., Bastos, G., Cabral, M. D., Pantaleão, A., Oliveira, J., et al. (2000) · Arquivos Brasileiros de Endocrinologia & Metabologia · doi:10.1590/s0004-27302000000100005 · Cited by 4 · see citing works

Posttraumatic stress disorder as psychiatric injury in civil litigation

Mendelson, G. (1995) · Psychiatry Psychology and Law · doi:10.1080/13218719509524850 · Cited by 3 · see citing works

Differences in serum neuropeptide Y levels and appetite changes in patients with major depressive disorder stratified by sex and reproductive aging

Yuan, Q., Wang, L., Zhuang, Y., Lin, D., Xu, Z., Wen, C., Su, W., Huang, Z., & Qiu, Y. (2026) · BMC Psychiatry · doi:10.1186/s12888-025-07753-9 · Cited by 1 · see citing works

NeUROpepTIDe Y-1 ReCepTORs meDIa Te The sUppRessION Of Lh seCReTION bY NpY IN CasTRa TeD maLe sheep

Hileman, S. M., Nestor, C. C., Bogusz, A. L., Billings, H. J., Alent, V., & Goodman, R. L. (2009) · Slovak Journal of Animal Science

CORTICOTROPHIN RELEASING HORMONE MODULATION OF FEED INTAKE, GASTRIC MOTILITY, AND BEHAVIOR IN LOW AND HIGH BODY WEIGHT SELECTED LINES OF CHICKENS

Cline, M. A. (2005) · VTechWorks (Virginia Tech)

Saliva as a biological matrix to assess piglet’s welfare

Prims, S. (2024) · doi:10.63028/10067/2049080151162165141

Communication in the Depressed Brain

Sunzeri, F. (2026) · Springer eBooks · doi:10.1007/978-3-032-14465-2_7

Direct Evidence that Stimulation of Neuropeptide Y Y5 Receptor Activates Hypothalamo-Pituitary-Adrenal Axis in Conscious Rats via both Corticotropin-Releasing Factor- and Arginine Vasopressin-Dependent Pathway

Kakui, N., & KITAMURA, K. (2007) · Endocrinology · doi:10.1210/en.2007-0189 · Cited by 31 · see citing works

Effect of neuropeptide Y on the hypothalamic-pituitary-adrenal axis in the dog

Inoue, T., Inui, A., Okita, M., Sakatani, N., Oya, M., Morioka, H., Mizuno, N., Oimoni, M., & Baba, S. (1989) · Life Sciences · doi:10.1016/0024-3205(89)90556-0 · Cited by 55 · see citing works

The Effect of Neuropeptide Y on the Hypothalamic-pituitary-adrenal Axis in the Dog

Inoue, T., Inui, A., Okita, M., Sakatani, N., Oya, M., Morioka, H., Mizuno, N., Oimomi, M., & Baba, S. (1990) · Folia Endocrinologica Japonica · doi:10.1507/endocrine1927.66.6_607 · Cited by 1 · see citing works

Evidence That the Central Noradrenergic and Adrenergic Pathways Activate the Hypothalamic- Pituitary-Adrenal Axis in the Sheep*

Liu, J., Clarke, I. J., Funder, J. W., & Engler, D. (1991) · Endocrinology · doi:10.1210/endo-129-1-200 · Cited by 37 · see citing works

Neuropeptide Y (NPY) in the area of the hypothalamic paraventricular nucleus activates the pituitary-adrenocortical axis in the rat

Wahlestedt, C., Skagerberg, G., Ekman, R., Heilig, M. A., Sundler, F., & Håkanson, R. (1987) · Brain Research · doi:10.1016/0006-8993(87)90176-4 · Cited by 285 · see citing works