Pacanis A, Strzelecki T, Rogulski J
J Biol Chem. 1981 Dec 25;256(24):13035-8.
Effects of maleate on the content of CoA derivatives in isolated mitochondria and in the tissues of maleate-intoxicated rats have been studied. The addition of maleate to kidney mitochondria incubated with 2-oxo-glutarate decreased CoA-SH and acid-soluble acyl-CoA concentrations while acid insoluble acyl-CoA content remained unchanged. As a result, a substantial loss (depletion) of the total CoA occurred. Similar changes in CoA content were found in vivo in the kidneys of maleate-treated rats. Neither in the isolated liver mitochondria nor in the liver of intoxicated animals have such changes been observed before. Acetoacetate, the substrate for CoA transferase, added to kidney mitochondria before maleate, abolished its inhibitory effect on oxidation of 2-oxoglutarate and prevented the decrease of CoA content. The data are in accord with the previous findings indicating that maleate can bind and sequester CoA in the form of a stable and metabolically inert compound.
已研究了马来酸盐对离体线粒体及马来酸盐中毒大鼠组织中辅酶A(CoA)衍生物含量的影响。向与2-氧代戊二酸一起孵育的肾线粒体中添加马来酸盐,会降低辅酶A-巯基(CoA-SH)和酸溶性酰基辅酶A的浓度,而酸不溶性酰基辅酶A的含量保持不变。结果,总辅酶A大量损失(耗竭)。在经马来酸盐处理的大鼠肾脏中,体内也发现了类似的辅酶A含量变化。在离体肝线粒体中以及中毒动物的肝脏中,均未观察到此类变化。在添加马来酸盐之前向肾线粒体中加入辅酶A转移酶的底物乙酰乙酸,可消除其对2-氧代戊二酸氧化的抑制作用,并防止辅酶A含量降低。这些数据与之前的研究结果一致,表明马来酸盐能够以稳定且代谢惰性的化合物形式结合并螯合辅酶A。