Tadokoro C, Kiuchi Y, Yamazaki Y, Oguchi K, Kamijima K
Department of Psychiatry, School of Medicine, Showa University, Tokyo, Japan.
Eur J Pharmacol. 1998 Jan 19;342(1):51-4. doi: 10.1016/s0014-2999(97)01530-6.
Three-week administration of sertraline or imipramine to rats (10 mg/kg, intraperitoneally, twice a day) increased ex vivo cyclic AMP-dependent protein kinase activity in the soluble but not in the particulate fraction of the frontal cortex. However, cyclic AMP-dependent protein kinase activity was not affected in either fraction of the parietotemporal cortex and hippocampus. Neither antidepressant altered protein kinase C activity in the soluble and particulate fractions or Ca2+/calmodulin-dependent protein kinase II activity in the frontal cortex. Therefore, sertraline and imipramine both selectively enhance cyclic AMP-dependent protein kinase activity in the frontal cortex. This enhancement might be involved in their biochemical mechanisms.
给大鼠腹腔注射舍曲林或丙咪嗪三周(10毫克/千克,每天两次)可增加前额叶皮质可溶性部分而非颗粒部分的离体环磷酸腺苷依赖性蛋白激酶活性。然而,顶颞叶皮质和海马体的这两个部分的环磷酸腺苷依赖性蛋白激酶活性均未受影响。这两种抗抑郁药均未改变额叶皮质可溶性和颗粒部分的蛋白激酶C活性或钙调蛋白依赖性蛋白激酶II活性。因此,舍曲林和丙咪嗪均选择性增强前额叶皮质中环磷酸腺苷依赖性蛋白激酶活性。这种增强可能与其生化机制有关。