CHRONIC GLUCOCORTICOID ADMINISTRATION AS WELL AS REPEATED STRESS AFFECTS THE SUBSEQUENT ACUTE IMMOBILIZATION STRESS-INDUCED EXPRESSION OF IMMEDIATE-EARLY GENES BUT NOT THAT OF NGFI-A
S. Umemoto et al., CHRONIC GLUCOCORTICOID ADMINISTRATION AS WELL AS REPEATED STRESS AFFECTS THE SUBSEQUENT ACUTE IMMOBILIZATION STRESS-INDUCED EXPRESSION OF IMMEDIATE-EARLY GENES BUT NOT THAT OF NGFI-A, Neuroscience, 80(3), 1997, pp. 763-773
We reported that repeated immobilization for six days attenuates the s
ubsequent acute immobilization stress-induced expression of the immedi
ate early genes c-fos, fos B, jun B and nerve growth factor-induced ge
ne-B (NGFI-B), but not of NGFI-A, in the rat paraventricular hypothala
mic nucleus. In this study, we confirmed these findings by means of a
time-course study, and further investigated whether the elevated plasm
a basal glucocorticoid level induced by repeated stress underlies the
attenuated response of immediate early genes and the preserved reactiv
ity of NGFI-A. Rats implanted with 100, 200 or 400 mg corticosterone o
r placebo pellets (control), were immobilized for Ih and decapitated s
even days later. In control rats acute immobilization induced c-fos, f
os B, jun B, NGFI-A and NGFI-B messenger RNA in the paraventricular hy
pothalamic nucleus, whereas all of them except NGFI-A, were significan
tly reduced in rats given 200 and 400 mg corticosterone implants. The
similarity of the results from the two procedures suggests that glucoc
orticoid is involved in regulating immediate early genes in the parave
ntricular hypothalamic nucleus under repeated stress and that the NGFI
-A gene is not regulated by this mechanism. However, the plasma basal
corticosterone level in repeatedly stressed rats was lower than that o
f rats implanted with 100 mg corticosterone, suggesting that a repetit
ive stress-induced corticosterone surge also contributes to this mecha
nism. (C) 1997 IBRO. Published by Elsevier Science Ltd.