Corticotropin-releasing factor (CRF) functions as one of the major mediators of the mammalian stress response and appears to play a key role in the pathophysiology of mood and
anxiety disorders. Small molecule CRF₁ receptor antagonists may represent a novel form of
pharmacotherapy for these disorders. The therapeutic success of CRF₁ receptor antagonists will depend, in part, upon whether tolerance develops to the actions of these compounds and whether appropriate patterns of HPA axis function is maintained. This study evaluated the effects of long term (~4 week) treatment with the CRF₁ receptor antagonist
R121919, on
CRF receptor function, HPA axis activity, behavioral measures, adrenal gland size, and
body weight gain. Animals treated with 20 mg/kg/day of
R121919 spent significantly more time in the open field in a defensive withdrawal test (138±36s for
R121919 vs 52±12s for vehicle, p=0.01). No significant effect of chronic CRF₁ receptor blockade on basal
ACTH or
corticosterone concentrations were detected, nor were significant changes detected in an elevated plus maze test. Both vehicle- and R121919- treated rats showed increases in AUC and peak
ACTH and
corticosterone concentrations following air puff startle stress, without any overall group differences, although a clear but non-significant attenuation in HPA axis response was observable in
R121919 treated animals. Chronic CRF₁ receptor blockade increased CRF
peptide mRNA expression in the PVN and decreased CRF
peptide mRNA expression in the central nucleus of the amygdala. Overall our results suggest that
anxiolytic effects of chronic CRF₁ receptor antagonism persist following chronic administration without significant attenuation of the HPA axis's ability to mount a stress response. This article is part of a Special Issue entitled 'Trends in neuropharmacology: in memory of Erminio Costa'.