Our previous data have shown that restraint (RT), a mild nonpainful stresso
r, acutely impairs nonsocial and social behavior in male rats. Corticotropi
n-releasing hormone (CRH) is a regulator of these behavioral responses. To
evaluate whether CRH mediates the neuroendocrine and behavioral alterations
present 24 h after restraint stress, we administered the CRH antagonist ct
-helical CRH9-41, (alpha-hCRH) intracerebroventricularly to male rats and w
e compared its effects with those of saline. Twenty-four hours after treatm
ent, nonsocial behaviors were significantly decreased by alpha-hCRH, this e
ffect being independent of RT. Among social behaviors, only introductory ac
tivity showed significant differences as a result of both RT and alpha-hCRH
. The concentrations of ACTH in the plasma and those of beta-endorphin in t
he anterior and neurointermediate lobes of the pituitary were affected by a
lpha-hCRH treatment. The effect on ACTH was simply related to the administr
ation of the alpha-hCRH, while for beta-endorphin, significant interactions
between alpha-hCRH and RT were found. On the whole, these results point to
the role played by CRH in the control of neuronal mechanisms involved in t
he stress-induced effects. (C) 1999 Elsevier Science Inc.