Studies of the secretion of corticotropin-releasing factor and arginine vasopressin into the hypophysial-portal circulation of the conscious sheep. I. Effect of an audiovisual stimulus and insulin-induced hypoglycemia.

Studies were undertaken to characterize the secretion of corticotropin-releasing factor (CRF) and arginine vasopressin (AVP) into the hypophysial-portal circulation of the conscious sheep. In addition, we examined the temporal relationship between the secretion of these two hypothalamic peptides and the secretion of three pro-opiomelanocortin peptides--adrenocorticotropic hormone (ACTH), ir-beta-endorphin, and ir-alpha-melanocyte-stimulating hormone--and cortisol and determined the effects of an audiovisual emotional stimulus and insulin-induced hypoglycemia on the entire hypothalamic-pituitary-adrenal axis. In the basal state, the secretion of CRF, AVP, the three pro-opiomelanocortin peptides, and cortisol was pulsatile in nature, and three CRF and AVP pulse patterns were observed: a concordant increase in CRF and AVP, an isolated rise in CRF, and an isolated increase in AVP. In 4 of the 5 animals, a 3-min audiovisual stress (barking dog) rapidly increased the plasma levels of all the measured substances, although the magnitude and duration of the effect differed markedly between the animals. Insulin-induced hypoglycemia markedly increased AVP and, to a lesser extent, CRF concentrations in portal plasma and thereby altered the CRF:AVP molar ratio. Although pituitary-adrenal activation was closely correlated with the increased hypothalamic activity, a strict 1:1 concordance between CRF/AVP secretion and ACTH secretion was not seen. The anesthetic ketamine selectively increased portal AVP concentrations to levels which exceeded those attained during hypoglycemia and rapidly activated the pituitary-adrenal axis. We conclude the following: (1) CRF and AVP are secreted by the hypothalamus in a pulsatile fashion; (2) ACTH secretion can be stimulated by increases in either CRF or AVP; (3) the absence of a strict 1:1 concordance between hypothalamic CRF/AVP release and pituitary ACTH secretion during stress may be partly due to the release of additional hypothalamic ACTH secretagogues; (4) the ability of both audiovisual stimuli and insulin-induced hypoglycemia to augment CRF and AVP secretion indicates that the paraventricular hypothalamus may be activated by a variety of neural inputs, and (5) the marked alteration of the CRF:AVP molar ratio during stress suggests that AVP may be an important ACTH secretagogue in vivo in the sheep.

[1]  Y. Oomura,et al.  Glucose responding neurons in the nucleus tractus solitarius of the rat: In vitro study , 1984, Brain Research.

[2]  G. Chrousos,et al.  Catecholamine effects upon rat hypothalamic corticotropin-releasing hormone secretion in vitro. , 1988, The Journal of clinical investigation.

[3]  G. Gillies,et al.  Corticotropin releasing activity of the new CRF is potentiated several times by vasopressin , 1982, Nature.

[4]  I. Clarke,et al.  THE TEMPORAL RELATIONSHIP BETWEEN GONADOTROPIN RELEASING HORMONE (GnRH) AND LUTEINIZING HORMONE (LH) SECRETION IN OVARIECTOMIZED EWES1 , 1982 .

[5]  T. Suda,et al.  Insulin-induced hypoglycemia increases corticotropin-releasing factor messenger ribonucleic acid levels in rat hypothalamus. , 1988, Endocrinology.

[6]  T. O'donohue,et al.  The anatomy of neuropeptide-y-containing neurons in rat brain , 1985, Neuroscience.

[7]  Y. Tillet 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 , 1988, Neuroscience Letters.

[8]  W. Vale,et al.  Dissociation of the adrenocorticotropin secretory responses to corticotropin-releasing factor (CRF) and vasopressin or oxytocin by using a specific cytotoxic analog of CRF. , 1988, Endocrinology.

[9]  R. Sapolsky,et al.  Hypercortisolism and its possible neural bases , 1990, Biological Psychiatry.

[10]  L. Recht,et al.  Vasopressin concentrations in hypophysial portal plasma: insignificant reduction following removal of the posterior pituitary gland. , 1981, Neuroendocrinology.

[11]  M. Sugimori,et al.  Glucose Inhibition of the Glucose-sensitive Neurone in the Rat Lateral Hypothalamus , 1974, Nature.

[12]  I. Meredith,et al.  Overflow of catecholamine neurotransmitters to the circulation: source, fate, and functions. , 1990, Physiological reviews.

[13]  V. Mutt,et al.  Neuropeptide Y—a novel brain peptide with structural similarities to peptide YY and pancreatic polypeptide , 1982, Nature.

[14]  M. Dallman,et al.  Corticosteroid inhibition of ACTH secretion. , 1984, Endocrine reviews.

[15]  S. Leibowitz,et al.  Neuropeptide Y: stimulation of feeding and drinking by injection into the paraventricular nucleus. , 1984, Life sciences.

[16]  S. Kliewer,et al.  Functional antagonism between oncoprotein c-Jun and the glucocorticoid receptor , 1990, Cell.

[17]  I. Clarke,et al.  Evidence for an ultradian secretion of adrenocorticotropin, β-endorphin and α-melanocyte-stimulating hormone by the ovine anterior and intermediate pituitary , 1989 .

[18]  J. Calabrese,et al.  Responses to corticotropin-releasing hormone in the hypercortisolism of depression and Cushing's disease. Pathophysiologic and diagnostic implications. , 1986, The New England journal of medicine.

[19]  T. Crow,et al.  Neuropeptide Y distribution in the rat brain. , 1983, Science.

[20]  L. Swanson,et al.  The organization of noradrenergic pathways from the brainstem to the paraventricular and supraoptic nuclei in the rat , 1982, Brain Research Reviews.

[21]  Burger Hg,et al.  A generalized computer program for the treatment of data from competitive protein-binding assays including radioimmunoassays. , 1972 .

[22]  L. Swanson,et al.  Organization of ovine corticotropin-releasing factor immunoreactive cells and fibers in the rat brain: an immunohistochemical study. , 1983, Neuroendocrinology.

[23]  R. G. Allen,et al.  Corticotropin-releasing factor differentially regulates anterior and intermediate pituitary lobe proopiomelanocortin gene transcription, nuclear precursor RNA and mature mRNA in vivo. , 1990, Neuroendocrinology.

[24]  J. Morley,et al.  Effect of neuropeptide Y on ingestive behaviors in the rat. , 1987, The American journal of physiology.

[25]  J. Gillin,et al.  Pulsatile rhythms of adrenocorticotropin (ACTH) and cortisol in women with endogenous depression: evidence for increased ACTH pulse frequency. , 1987, The Journal of clinical endocrinology and metabolism.

[26]  M. Linnoila,et al.  Norepinephrine and its metabolites in cerebrospinal fluid, plasma, and urine. Relationship to hypothalamic-pituitary-adrenal axis function in depression. , 1988, Archives of general psychiatry.

[27]  M. Davicco,et al.  Plasma adrenocorticotrophin, cortisol and aldosterone responses to ovine corticotrophin-releasing factor and vasopressin in sheep. , 1986, Acta endocrinologica.

[28]  J. Vaughan,et al.  Effects of synthetic ovine corticotropin-releasing factor, glucocorticoids, catecholamines, neurohypophysial peptides, and other substances on cultured corticotropic cells. , 1983, Endocrinology.

[29]  E. Widmaier,et al.  Regulation of corticotropin-releasing factor secretion in vitro by glucose. , 1988, The American journal of physiology.

[30]  G. Fink,et al.  Comparison of adrenocorticotropin control in Brattleboro, Long-Evans, and Wistar rats. Measurement of corticotropin-releasing factor, arginine vasopressin, and oxytocin in hypophysial portal blood. , 1988, Neuroendocrinology.

[31]  P. Robinson,et al.  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. , 1990, The Journal of biological chemistry.

[32]  F. Antoni,et al.  Hypothalamic control of adrenocorticotropin secretion: advances since the discovery of 41-residue corticotropin-releasing factor. , 1986, Endocrine reviews.

[33]  T. O'donohue,et al.  Localization of neuropeptide Y messenger ribonucleic acid in rat and mouse brian by in situ hybridization , 1987, Synapse.

[34]  E. Widmaier,et al.  Secretion of corticotropin-releasing factor from cultured rat hypothalamic cells: effects of catecholamines. , 1989, Endocrinology.

[35]  J. Powell,et al.  An arcuato-paraventricular and -dorsomedial hypothalamic neuropeptide Y-containing system which lacks noradrenaline in the rat , 1985, Brain Research.

[36]  G. Fink,et al.  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. , 1990, The Journal of endocrinology.

[37]  T. Ono,et al.  Glucoresponsive neurons in rat ventromedial hypothalamic tissue slices in vitro , 1982, Brain Research.

[38]  S. Foote,et al.  Corticotropin-releasing factor activates noradrenergic neurons of the locus coeruleus , 1983, Brain Research.

[39]  C. Wahlestedt,et al.  Neuropeptide Y (NPY) in the area of the hypothalamic paraventricular nucleus activates the pituitary-adrenocortical axis in the rat , 1987, Brain Research.

[40]  A. Grossman,et al.  Acetylcholine and norepinephrine stimulate the release of corticotropin-releasing factor-41 from the rat hypothalamus in vitro. , 1988, Endocrinology.

[41]  W. Vale,et al.  Corticotropin-releasing factor regulates proopiomelanocortin messenger ribonucleic acid levels in vivo. , 1984, Neuroendocrinology.

[42]  J Levin,et al.  The production rate of cortisol declines during recovery from anorexia nervosa. , 1981, The Journal of clinical endocrinology and metabolism.

[43]  W. Vale,et al.  Presence of corticotropin releasing factor-like immunoreactivity in hypophysial portal blood. , 1982, Endocrinology.

[44]  C. Oliver,et al.  Secretion of corticotropin releasing factor (CRF) and vasopressin (AVP) into the hypophysial portal blood of conscious, unrestrained rams. , 1988, Biochemical and biophysical research communications.

[45]  P. Butler,et al.  Corticotropin-releasing factor produces fear-enhancing and behavioral activating effects following infusion into the locus coeruleus , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[46]  P. Plotsky,et al.  Hypophysiotropic regulation of adrenocorticotropin secretion in response to insulin-induced hypoglycemia. , 1985, Endocrinology.

[47]  G. Smythe,et al.  Relationships between brain noradrenergic activity and blood glucose , 1984, Nature.

[48]  M. Whitnall Distributions of pro‐vasopressin expressing and pro‐vasopressin deficient CRH neurons in the paraventricular hypothalamic nucleus of colchicine‐treated normal and adrenalectomized rats , 1988, The Journal of comparative neurology.

[49]  L. Swanson,et al.  Colocalization of neuropeptide Y immunoreactivity in brainstem catecholaminergic neurons that project to the paraventricular nucleus of the hypothalamus , 1985, The Journal of comparative neurology.

[50]  K. Fuxe,et al.  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 , 1985, Neuroscience Letters.

[51]  J. Funder,et al.  Arginine vasopressin is a much more potent stimulus to ACTH release from ovine anterior pituitary cells than ovine corticotropin-releasing factor. 1. In vitro studies. , 1989, Neuroendocrinology.

[52]  C. Oliver,et al.  Insulin-induced hypoglycemia stimulates corticotropin-releasing factor and arginine vasopressin secretion into hypophysial portal blood of conscious, unrestrained rams. , 1990, The Journal of clinical investigation.

[53]  N. Ling,et al.  The responses of plasma adrenocorticotropin and cortisol to corticotropin-releasing hormone (CRH) and cerebrospinal fluid immunoreactive CRH in anorexia nervosa patients. , 1986, The Journal of clinical endocrinology and metabolism.

[54]  M. Greenberg,et al.  The regulation and function of c-fos and other immediate early genes in the nervous system , 1990, Neuron.