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Histaminergic activation of the hypothalamic-pituitary-adrenal axis

A Kjaer, P J Larsen, U Knigge, J Warberg

60 Citations (Scopus)

Abstract

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.

Original languageEnglish
JournalEndocrinology
Volume135
Issue number3
Pages (from-to)1171-7
Number of pages7
ISSN0013-7227
DOIs
Publication statusPublished - Sept 1994
Externally publishedYes

Keywords

  • Animals
  • Arginine Vasopressin/genetics
  • Corticotropin-Releasing Hormone/genetics
  • Histamine/pharmacology
  • Hormones/blood
  • Hypothalamo-Hypophyseal System/drug effects
  • In Situ Hybridization
  • Male
  • Oxytocin/genetics
  • Paraventricular Hypothalamic Nucleus/metabolism
  • Pituitary Gland/metabolism
  • Pituitary-Adrenal System/drug effects
  • Pro-Opiomelanocortin/genetics
  • Proto-Oncogene Proteins c-fos/genetics
  • RNA, Messenger/metabolism
  • Rats
  • Rats, Wistar
  • Supraoptic Nucleus/metabolism

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