The role of corticotrophin-releasing hormone receptors in the calcitonin gene-related peptide-induced suppression of pulsatile luteinising hormone secretion in the female rat.

Corticotrophin-releasing hormone (CRH) plays a pivotal role in the suppression of the gonadotrophin-releaning hormone (GRH) pulse generator in response to stress and intracerebroventricular (icv) administration of calcitonin gene-related peptide (CGRP). We have previously shown both CRH receptor subtypes, CRH-R1 and CRH-R2, are involved in the stress-induced suppression of LH pulses. The aims of the present study were to examine the role of CRH-R1 and CRH-R2 in CGRP-induced suppression of LH pulses, and to investigate the effects of CGRP on CRH expression in the paraventricular nucleus (PVN) and central nucleus of the amygdala (CeA), which have prominent CRH neurone populations that receive dense CGRP innervations. The suppression of LH pulses by CGRP (1.5 mu g icv) was completely prevented by intravenous administration of the CRH-R1 antagonist SSR125543Q (7.5 mg/ rat iv, 30 min before CGRP), but was not affected by the CRH-R2 antagonist, astressin(2)-B (100 mu g icv, 10 min before CGRP). CGRP increased the CRH mRNA expression in PVN and CeA. These results provide evidence of a role for CRH-R1 in mediating the suppressive effects of CGRP on pulsatile LH secretion in the female rat, and additionally raise the possibility of an involvement of PVN and CeA CRH neuronal populations in this suppression.