Lesch K P, Aulakh C S, Tolliver T J, Hill J L, Wolozin B L, Murphy D L
Laboratory of Clinical Science, National Institute of Mental Health, Bethesda, MD 20892.
Eur J Pharmacol. 1991 Aug 14;207(4):355-9. doi: 10.1016/0922-4106(91)90011-6.
The G protein subunits, Gs alpha, Gi alpha, and Go alpha, have been quantitated in various rat brain regions using enzyme-linked immunosorbent assay (ELISA) techniques. Chronic (3-week) treatment with carbamazepine decreased Gs alpha in several brain regions reaching significance in the neostriatum, while chronic lithium treatment had no unequivocal effect. Lithium significantly increased Gi alpha in the hypothalamus and hippocampus, whereas carbamazepine decreased Gi alpha in the frontal cortex. Both treatments had no consistent effects on Go alpha. We conclude that long-term treatment with lithium and carbamazepine exerts differential effects on G protein alpha subunits, and that this modification of signal transduction represents a potential mechanism of antibipolar drug-induced neural plasticity.
利用酶联免疫吸附测定(ELISA)技术,对不同大鼠脑区的G蛋白亚基Gsα、Giα和Goα进行了定量分析。卡马西平慢性(3周)治疗使几个脑区的Gsα减少,在新纹状体中达到显著水平,而慢性锂治疗没有明确的效果。锂显著增加了下丘脑和海马体中的Giα,而卡马西平降低了额叶皮质中的Giα。两种治疗对Goα均无一致影响。我们得出结论,锂和卡马西平的长期治疗对G蛋白α亚基有不同的影响,这种信号转导的改变代表了抗双相情感障碍药物诱导神经可塑性的潜在机制。