Saito N, Guitart X, Hayward M, Tallman J F, Duman R S, Nestler E J
Laboratory of Molecular Psychiatry, Yale University School of Medicine, New Haven, CT.
Proc Natl Acad Sci U S A. 1989 May;86(10):3906-10. doi: 10.1073/pnas.86.10.3906.
The possibility that glucocorticoids regulate specific guanine nucleotide binding regulatory proteins (G proteins) was investigated in rat cerebral cortex. Corticosterone was administered to normal and bilaterally adrenalectomized rats, and hormone regulation of individual G-protein subunits was investigated in cerebral cortex in three ways: (i) immunoblot analysis of subunit protein, (ii) hybridization blot analysis of subunit mRNA, and (iii) ADP-ribosylation analysis of stimulatory G protein (Gs alpha) subunits. Chronic (7 days) corticosterone administration to normal rats increased levels of Gs alpha immunoreactivity, mRNA, and ADP-ribosylation but decreased levels of inhibitory G protein (Gi alpha) mRNA and tended to decrease levels of Gi alpha immunoreactivity. In contrast, levels of Go alpha and G beta immunoreactivity and mRNA were not influenced by corticosterone treatment. In adrenalectomized rats, corticosterone treatment produced a 25-50% increase in the levels of Gs alpha immunoreactivity, mRNA, and ADP-ribosylation, whereas the hormone produced a 20-35% decrease in the levels of Gi alpha immunoreactivity and mRNA. Adrenalectomy, without corticosterone replacement, produced the opposite effects on Gs alpha and Gi alpha compared to sham-operated controls, indicating that these G proteins are regulated by this class of steroid hormone under physiological conditions in vivo. The results indicate that specific G-protein subunits--namely, Gs alpha and Gi alpha--are under the coordinated control of glucocorticoids in rat brain and demonstrate that G proteins are physiological targets of glucocorticoids in vivo. Possible roles played by these G-protein responses in mediating the effects of glucocorticoids on brain function are discussed.
在大鼠大脑皮层中研究了糖皮质激素调节特定鸟嘌呤核苷酸结合调节蛋白(G蛋白)的可能性。对正常大鼠和双侧肾上腺切除的大鼠给予皮质酮,并通过三种方式研究大脑皮层中单个G蛋白亚基的激素调节:(i)亚基蛋白的免疫印迹分析,(ii)亚基mRNA的杂交印迹分析,以及(iii)刺激性G蛋白(Gsα)亚基的ADP核糖基化分析。对正常大鼠长期(7天)给予皮质酮可增加Gsα免疫反应性、mRNA和ADP核糖基化水平,但降低抑制性G蛋白(Giα)mRNA水平,并倾向于降低Giα免疫反应性水平。相比之下,Goα和Gβ免疫反应性及mRNA水平不受皮质酮处理的影响。在肾上腺切除的大鼠中,皮质酮处理使Gsα免疫反应性、mRNA和ADP核糖基化水平增加25 - 50%,而该激素使Giα免疫反应性和mRNA水平降低20 - 35%。与假手术对照组相比,未进行皮质酮替代的肾上腺切除术对Gsα和Giα产生相反的影响,表明在体内生理条件下,这些G蛋白受这类甾体激素调节。结果表明,特定的G蛋白亚基——即Gsα和Giα——在大鼠脑中受糖皮质激素的协同控制,并证明G蛋白是体内糖皮质激素的生理靶点。讨论了这些G蛋白反应在介导糖皮质激素对脑功能影响中可能发挥的作用。