Barbu V, Mazière J C, Maindrault F, Mazière C, Rampini C, Roux C, Polonovski J
Biochem Pharmacol. 1987 Feb 1;36(3):353-6. doi: 10.1016/0006-2952(87)90293-0.
Amphiphilic molecules AY 9944 and chlorpromazine (CPZ) inhibited DNA synthesis in Concanavalin A-stimulated lymphocytes in a dose-dependent manner. While AY 9944 strongly decreased 7-dehydrocholesterol conversion to cholesterol, CPZ did not significantly affect this reaction. Moreover, the inhibitory effect of AY 9944 and CPZ on DNA synthesis took place in the presence of cholesterol in the culture medium. These findings suggest that the mechanism of inhibition of DNA synthesis by AY 9944 or CPZ is not related to endogenous cholesterol synthesis or exogenous cholesterol supply. Results are discussed in relation to the amphiphilic properties of AY 9944 and CPZ and to the interaction of these drugs with membranes or other intracellular targets such as calmodulin.
两亲性分子AY 9944和氯丙嗪(CPZ)以剂量依赖性方式抑制伴刀豆球蛋白A刺激的淋巴细胞中的DNA合成。虽然AY 9944强烈降低了7-脱氢胆固醇向胆固醇的转化,但CPZ对该反应没有显著影响。此外,AY 9944和CPZ对DNA合成的抑制作用在培养基中存在胆固醇的情况下发生。这些发现表明,AY 9944或CPZ抑制DNA合成的机制与内源性胆固醇合成或外源性胆固醇供应无关。结合AY 9944和CPZ的两亲性特性以及这些药物与膜或其他细胞内靶点(如钙调蛋白)的相互作用对结果进行了讨论。