ROLE OF ENDOGENOUS CORTICOTROPIN-RELEASING FACTOR IN MEDIATION OF NEUROENDOCRINE AND BEHAVIORAL-RESPONSES TO CHOLECYSTOKININ OCTAPEPTIDE SULFATE ESTER IN RATS
E. Biro et al., ROLE OF ENDOGENOUS CORTICOTROPIN-RELEASING FACTOR IN MEDIATION OF NEUROENDOCRINE AND BEHAVIORAL-RESPONSES TO CHOLECYSTOKININ OCTAPEPTIDE SULFATE ESTER IN RATS, Neuroendocrinology, 57(2), 1993, pp. 340-345
The possible involvement of endogenous corticotropin-releasing factor
(CRF) in the anxiogenic and pituitary-adrenal-axis-activating effects
of cholecystokinin octapeptide sulfate ester (CCK 8) was investigated
in rats. Intracerebroventricularly (i.c.v.) administered CCK 8 induced
an anxiogenic response in an elevated plus-maze test, and enhanced th
e plasma corticosterone level. Pretreatment with different dilutions (
1:10, 1:20 and 1:100, i.c.v.) of CRF antiserum and different doses of
a CRF receptor antagonist, alpha-helical CRF (ahCRF, 0.001-1.0 mug, i.
c.v.) prevented the anxiogenic response to CCK 8 in a dose-dependent m
anner. None of the doses of CRF antiserum or ahCRF alone produced any
alteration in either the elevated plus-maze paradigm or corticosterone
level in saline-treated control rats. The results strongly suggest th
at the anxiogenic and hypothalamo-pituitary-adrenal-activating effects
of CCK 8 are mediated via CRF.