Friedman E, Levinson D, Connell T A, Singh H
Department of Psychiatry, Medical College of Pennsylvania/EPPI, Philadelphia 19129.
Biol Psychiatry. 1993 Apr 1;33(7):520-5. doi: 10.1016/0006-3223(93)90006-y.
Protein kinase C (PKC) activity and PKC translocation in response to serotonin were investigated in platelets obtained from bipolar affective disorder subjects before and during lithium treatment. Ratios of platelet membrane-bound to cytosolic PKC activities were elevated in the manic subjects. In addition, serotonin-elicited platelet PKC translocation was found to be enhanced in those subjects. Lithium treatment for up to 2 weeks resulted in a reduction in cytosolic and membrane-associated PKC activities and in an attenuated PKC translocation in response to serotonin. These preliminary results suggest that alteration in platelet PKC is associated with the manic phase of bipolar illness. The results also suggest that lithium treatment reduces the sensitivity of platelets to PKC translocation induced by activation of serotonin-2 receptors.
研究了双相情感障碍患者在锂盐治疗前及治疗期间,血小板中蛋白激酶C(PKC)活性及PKC转位对血清素的反应。躁狂症患者血小板膜结合型与胞质型PKC活性之比升高。此外,发现这些患者中血清素诱导的血小板PKC转位增强。长达2周的锂盐治疗导致胞质型和膜相关PKC活性降低,以及血清素诱导的PKC转位减弱。这些初步结果表明,血小板PKC的改变与双相情感障碍的躁狂相有关。结果还表明,锂盐治疗降低了血小板对血清素-2受体激活诱导的PKC转位的敏感性。