Davis M H, Jung D W, Brierley G P
Department of Physiological Chemistry, Ohio State University Medical Center, Columbus 43210.
J Bioenerg Biomembr. 1987 Oct;19(5):515-24. doi: 10.1007/BF00770034.
Diethylpyrocarbonate inhibits Na+/Ca2+ antiport activity in isolated heart mitochondria. The inhibition is time-dependent with maximum activity developed after 5 min at 25 degrees C. The reaction of diethylpyrocarbonate with the mitochondrial membrane is biphasic with 25-30 nmol mg-1 reacting rapidly and an additional 30 nmol mg-1 taken up slowly over a 30-min incubation. Inhibition of mitochondrial Na+/Ca2+ antiport by diethylpyrocarbonate decreases the Vmax of the reaction, and the inhibition cannot be reversed by washing the mitochondria or addition of excess histidine. The inhibition occurs at levels of inhibitor that have little or no effect on Ca2+ uptake, Na+/H+ antiport, or succinate respiration. A portion of the Na+-dependent efflux of Ca2+ is insensitive to diethylpyrocarbonate and this component is abolished by diltiazem. The mechanism by which diethylpyrocarbonate inactivates Na+/Ca2+ antiport is still uncertain, but may involve the modification of an unprotonated histidine residue in the transporter.
焦碳酸二乙酯抑制离体心脏线粒体中的Na⁺/Ca²⁺反向转运活性。这种抑制作用具有时间依赖性,在25℃下5分钟后达到最大活性。焦碳酸二乙酯与线粒体膜的反应是双相的,25 - 30 nmol/mg迅速反应,在30分钟的孵育过程中,另外30 nmol/mg缓慢摄取。焦碳酸二乙酯对线粒体Na⁺/Ca²⁺反向转运的抑制作用降低了反应的Vmax,并且通过洗涤线粒体或添加过量组氨酸不能逆转这种抑制作用。抑制作用发生在对Ca²⁺摄取、Na⁺/H⁺反向转运或琥珀酸呼吸作用几乎没有影响的抑制剂水平。一部分依赖Na⁺的Ca²⁺外流对焦碳酸二乙酯不敏感,并且该成分被地尔硫卓消除。焦碳酸二乙酯使Na⁺/Ca²⁺反向转运失活的机制仍不确定,但可能涉及转运体中未质子化组氨酸残基的修饰。