TY - JOUR
T1 - Histaminergic activation of the hypothalamic-pituitary-adrenal axis
AU - Kjaer, A
AU - Larsen, P J
AU - Knigge, U
AU - Warberg, J
PY - 1994/9
Y1 - 1994/9
N2 - Centrally administered histamine (HA) stimulates the secretion of adenohypophysial POMC-derived peptides, which subsequently cause release of corticosterone. The effect of HA on POMC-derived peptide release is indirect, and it is possible that hypothalamic neurons containing corticotropin-releasing hormone (CRH), arginine vasopressin (AVP), or oxytocin (OT) are involved in the mediation of this response. We studied the effect of HA on: 1) expression of CRH, AVP, and OT messenger RNA (mRNA) at the hypothalamic level; 2) expression of c-fos and POMC mRNA at the pituitary level; and 3) peripheral plasma levels of AVP, OT, ACTH, beta-endorphin (beta-END), and corticosterone. HA (270 nmol) infused intracerebroventricularly increased the expression of CRH, AVP, and OT mRNA in the paraventricular nucleus as well as that of OT mRNA in the supraoptic nucleus of the hypothalamus. At the pituitary level the expression of mRNA for c-fos and POMC increased in the anterior but not in the intermediate lobe in response to HA. Plasma levels of AVP, OT, ACTH, beta-END, and corticosterone all increased in response to central HA administration. Circulating levels of AVP and OT peaked after 5 min, ACTH and beta-END after 15 min, whereas corticosterone levels were highest after 30 min. In concert with our earlier discoveries, the present data support the hypothesis that HA-induced secretion of ACTH and beta-END is mediated via central activation of hypothalamic neuroendocrine neurons containing CRH, AVP, and/or OT.
AB - Centrally administered histamine (HA) stimulates the secretion of adenohypophysial POMC-derived peptides, which subsequently cause release of corticosterone. The effect of HA on POMC-derived peptide release is indirect, and it is possible that hypothalamic neurons containing corticotropin-releasing hormone (CRH), arginine vasopressin (AVP), or oxytocin (OT) are involved in the mediation of this response. We studied the effect of HA on: 1) expression of CRH, AVP, and OT messenger RNA (mRNA) at the hypothalamic level; 2) expression of c-fos and POMC mRNA at the pituitary level; and 3) peripheral plasma levels of AVP, OT, ACTH, beta-endorphin (beta-END), and corticosterone. HA (270 nmol) infused intracerebroventricularly increased the expression of CRH, AVP, and OT mRNA in the paraventricular nucleus as well as that of OT mRNA in the supraoptic nucleus of the hypothalamus. At the pituitary level the expression of mRNA for c-fos and POMC increased in the anterior but not in the intermediate lobe in response to HA. Plasma levels of AVP, OT, ACTH, beta-END, and corticosterone all increased in response to central HA administration. Circulating levels of AVP and OT peaked after 5 min, ACTH and beta-END after 15 min, whereas corticosterone levels were highest after 30 min. In concert with our earlier discoveries, the present data support the hypothesis that HA-induced secretion of ACTH and beta-END is mediated via central activation of hypothalamic neuroendocrine neurons containing CRH, AVP, and/or OT.
KW - Animals
KW - Arginine Vasopressin/genetics
KW - Corticotropin-Releasing Hormone/genetics
KW - Histamine/pharmacology
KW - Hormones/blood
KW - Hypothalamo-Hypophyseal System/drug effects
KW - In Situ Hybridization
KW - Male
KW - Oxytocin/genetics
KW - Paraventricular Hypothalamic Nucleus/metabolism
KW - Pituitary Gland/metabolism
KW - Pituitary-Adrenal System/drug effects
KW - Pro-Opiomelanocortin/genetics
KW - Proto-Oncogene Proteins c-fos/genetics
KW - RNA, Messenger/metabolism
KW - Rats
KW - Rats, Wistar
KW - Supraoptic Nucleus/metabolism
U2 - 10.1210/endo.135.3.8070360
DO - 10.1210/endo.135.3.8070360
M3 - Journal article
C2 - 8070360
SN - 0013-7227
VL - 135
SP - 1171
EP - 1177
JO - Endocrinology
JF - Endocrinology
IS - 3
ER -