Hypothalamic and amygdaloid corticotropin-releasing hormone (CRH) and CRH receptor-1 mRNA expression in the stress-hyporesponsive late pregnant and early lactating rat

Citation
Apc. Da Costa et al., Hypothalamic and amygdaloid corticotropin-releasing hormone (CRH) and CRH receptor-1 mRNA expression in the stress-hyporesponsive late pregnant and early lactating rat, MOL BRAIN R, 91(1-2), 2001, pp. 119-130
Citations number
61
Categorie Soggetti
Neurosciences & Behavoir
Journal title
MOLECULAR BRAIN RESEARCH
ISSN journal
0169328X → ACNP
Volume
91
Issue
1-2
Year of publication
2001
Pages
119 - 130
Database
ISI
SICI code
0169-328X(20010713)91:1-2<119:HAACH(>2.0.ZU;2-#
Abstract
This study investigated the expression of corticotropin releasing hormone ( CRH) and its receptor CRHR-1, and arginine vasopressin (AVP) mRNAs during t he stress hyporesponsive periods of late pregnancy and lactation (day-3) an d in virgin stress-responsive females. In situ hybridization histochemistry showed that basal CRH mRNA in the paraventricular nucleus (PVN) decreased in pregnant and increased in lactating rats (compared with virgin controls) , whereas it increased after restraint stress only in virgin rats. Basal PV N CRHR-1 mRNA increased markedly in all groups but reached lower levels in pregnant rats. Basal AVP mRNA in the parvocellular PVN was higher in lactat ing rats, and in contrast to CRH mRNA, it increased after stress in all gro ups. In medial preoptic area (MPOA) CRH mRNA levels were higher in lactatin g females compared with virgin and pregnant rats, and unexpectedly they dec reased markedly after stress only in virgin rats. CRH mRNA levels in the ce ntral and medial nuclei of the amygdala were higher in lactating rats than in virgin or pregnant ones, and stress had no effect in either group. These data suggest that these stress hyporesponsive periods: (1)do not depend on basal CRH mRNA expression in the PVN; (2) appear to have intact stress-act ivated afferent pathways to the PVN, as shown by preservation of CRHR-1 and AVP responses to stress, but the information may be differently processed; (3) are associated with an alteration in a CRH mediated pathway from the M POA. (C) 2001 Published by Elsevier Science B.V.