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This version published online on December 9, 2004
Endocrinology, doi:10.1210/en.2004-1368
A more recent version of this article appeared on March 1, 2005
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Submitted on October 18, 2004
Accepted on December 1, 2004

Reduced hypothalamic vasopressin secretion underlies attenuated ACTH stress responses in pregnant rats

Shuaike Ma, Michael J Shipston, David Morilak, and John A Russell*

Division of Biomedical Sciences, School of Biomedical and Clinical Laboratory, Sciences, College of Medicine and Veterinary Medicine, University of Edinburgh, Hugh Robson Building, George Square, Edinburgh, EH8 9XD, UK; Present address:, Department of Pharmacology, University of Texas Health Science Center at San, Antonio, 7703 Floyd Curl Drive, San Antonio, Texas 78229-3900, USA

* To whom correspondence should be addressed. E-mail: j.a.russell{at}ed.ac.uk.

We sought to explain decreased ACTH secretory responses to stress in pregnant rats by investigating hypothalamic CRH and vasopressin secretion and actions on anterior pituitary corticotrophs. In late pregnancy median eminence CRH content was reduced (by 12%). Anterior pituitary POMC mRNA expression measured by in situ hybridization, but not radioimmunoassayed ACTH content, was also reduced (by 45% on day 21); CRH receptor 1 (CRHR1) mRNA expression was unaltered in pregnancy, but V1b receptor mRNA expression was reduced (by 19%). ACTH secretory responses, measured in jugular blood, to CRH (200ng/kg i.v.) or vasopressin (1.7 µg/kg, i.v.) were reduced on day 21 vs. virgins (49% and 44%), but the response to combined CRH and vasopressin injection was intact. Either antalarmin (CRHR1 antagonist; 20 mg/kg i.p.) or dP(Tyr(Me)2, Arg-NH2 9)AVP (V1a/b antagonist; 10 µg/kg, i.v.) pre-treatment reduced the ACTH secretory response to forced swimming (90s) in virgin rats (by 57% and 40%), but only antalarmin was effective in pregnant rats (53% decrease).

In vitro, measuring ACTH secretion from acutely dispersed anterior pituitary cells showed increased corticotroph sensitivity in pregnancy to CRH and to CRH augmentation by vasopressin, attributable to increased intracellular cAMP action. Hence, in late pregnancy reduced anterior pituitary CRHR1 or V1b receptor expression did not impair corticotroph responses to CRH or vasopressin. Rather, diminished secretagogue secretion in vivo accounts for reduced action of stress levels of exogenous CRH or vasopressin alone; the late pregnancy attenuated ACTH secretory response to swim stress is deduced to be due to reduced vasopressin release by parvocellular PVN neurones.


Key words: antalarmin • cAMP • corticotroph • corticotropin releasing hormone • CRHR1 mRNA • forced swimming • pituitary • pregnancy • V1a/b receptor antagonist • V1b receptor mRNA




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