Umemoto S, Kawai Y, Ueyama T, Senba E
Department of Anatomy and Neurobiology, Wakayama Medical College, Wakayama City, Japan.
Neuroscience. 1997 Oct;80(3):763-73. doi: 10.1016/s0306-4522(97)00050-x.
We reported that repeated immobilization for six days attenuates the subsequent acute immobilization stress-induced expression of the immediate early genes c-fos, fos B, jun B and nerve growth factor-induced gene-B (NGFI-B), but not of NGFI-A, in the rat paraventricular hypothalamic nucleus. In this study, we confirmed these findings by means of a time-course study, and further investigated whether the elevated plasma basal glucocorticoid level induced by repeated stress underlies the attenuated response of immediate early genes and the preserved reactivity of NGFI-A. Rats implanted with 100, 200 or 400 mg corticosterone or placebo pellets (control), were immobilized for 1 h and decapitated seven days later. In control rats acute immobilization induced c-fos, fos B, jun B, NGFI-A and NGFI-B messenger RNA in the paraventricular hypothalamic nucleus, whereas all of them except NGFI-A, were significantly reduced in rats given 200 and 400 mg corticosterone implants. The similarity of the results from the two procedures suggests that glucocorticoid is involved in regulating immediate early genes in the paraventricular 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 of rats implanted with 100 mg corticosterone, suggesting that a repetitive stress-induced corticosterone surge also contributes to this mechanism.
我们曾报道,连续六天反复制动会减弱随后急性制动应激诱导的大鼠下丘脑室旁核中即早基因c-fos、fos B、jun B和神经生长因子诱导基因B(NGFI-B)的表达,但不会减弱NGFI-A的表达。在本研究中,我们通过一项时间进程研究证实了这些发现,并进一步研究了反复应激诱导的血浆基础糖皮质激素水平升高是否是即早基因反应减弱和NGFI-A反应性保留的基础。给植入了100、200或400mg皮质酮或安慰剂药丸(对照)的大鼠进行1小时制动,七天后断头。在对照大鼠中,急性制动诱导下丘脑室旁核中的c-fos、fos B、jun B、NGFI-A和NGFI-B信使核糖核酸表达,而在植入200和400mg皮质酮药丸的大鼠中,除NGFI-A外,所有这些基因的表达均显著降低。两种实验方法结果的相似性表明,糖皮质激素参与反复应激下下丘脑室旁核即早基因的调节,且NGFI-A基因不受此机制调节。然而,反复应激大鼠的血浆基础皮质酮水平低于植入100mg皮质酮的大鼠,这表明反复应激诱导的皮质酮激增也参与了这一机制。