Evans O B, Stacpoole P W
Biochem Pharmacol. 1982 Apr 1;31(7):1295-300. doi: 10.1016/0006-2952(82)90019-3.
Dichloroacetate (DCA) given gastrically as a single dose to healthy, fed rats caused transient lowering of blood glucose, lactate, and pyruvate. Chronic daily dosing caused lowering of these metabolites and a delay in the return of lactate to basal levels for 48 hr after the final dose. DCA caused activation of the pyruvate dehydrogenase complex (PDHC), with acute multiple dosing or chronic daily dosing. The elevated active PDHC persisted for 12 hr following the final dose. In addition, total PDHC activity was increased with chronic dosing and persisted for 48 hr following the final dose. This increase was not blocked by protein synthesis inhibitors. DCA increased isolated hepatocyte [14C-1]pyruvate oxidation and activated hepatocyte PDHC. Glyoxylate and oxalate, hepatic metabolites of DCA, were inhibitory at similar concentrations.
给健康的、已进食的大鼠经胃单次给予二氯乙酸(DCA)会导致血糖、乳酸和丙酮酸短暂降低。每日长期给药会使这些代谢物降低,且在末次给药后48小时内乳酸恢复至基础水平的时间延迟。无论是急性多次给药还是每日长期给药,DCA都会导致丙酮酸脱氢酶复合体(PDHC)激活。末次给药后,升高的活性PDHC持续12小时。此外,长期给药会使总PDHC活性增加,且在末次给药后持续48小时。这种增加不受蛋白质合成抑制剂的阻断。DCA增加了分离的肝细胞中[14C-1]丙酮酸的氧化,并激活了肝细胞PDHC。DCA的肝脏代谢产物乙醛酸和草酸在相似浓度下具有抑制作用。