Mergner W J, Marzella L, Mergner C, Kahng M W, Smith M W, Trump B F
Beitr Pathol. 1977 Nov;161(3):230-43. doi: 10.1016/s0005-8165(77)80079-6.
Electron transport in tissue cubes, isolated mitochondria and submitochondria particles were examined as a function of ischemic time. It was found that electron transport remains active in all systems beyond the 2 hour ischemic time interval. The NADH stimulated respiration, however, declined after 2 hours of ischemia in ASU (Ammonia-Sephadex-Urea) particles followed by respiration with matrix-located dehydrogenases tested by substrates such as glutamate, alpha-ketoglutarate and pyruvate plus malate. Succinate dependent respiration remains active at control levels. In contrast proton gradient reveals changes in two phases: Phase A is characterized by gradually increasing gradient without valinomycin and by a rapidly declining gradient with valinomycin in the medium. Phase B is characterized by a declining proton gradient with or without valinomycin. It is suggested that the alteration of the proton gradient between 1 and 2 hours ischemia is an important factor contributing to irreversible cell injury.
研究了组织块、分离的线粒体和亚线粒体颗粒中的电子传递作为缺血时间的函数。结果发现,在2小时缺血时间间隔之后,所有系统中的电子传递仍保持活跃。然而,在ASU(氨-葡聚糖-尿素)颗粒中,缺血2小时后,NADH刺激的呼吸作用下降,随后用谷氨酸、α-酮戊二酸和丙酮酸加苹果酸等底物测试基质定位脱氢酶的呼吸作用也下降。琥珀酸依赖性呼吸作用在对照水平保持活跃。相比之下,质子梯度显示出两个阶段的变化:A阶段的特征是在无缬氨霉素时梯度逐渐增加,而在培养基中有缬氨霉素时梯度迅速下降。B阶段的特征是无论有无缬氨霉素,质子梯度都在下降。有人提出,缺血1至2小时之间质子梯度的改变是导致不可逆细胞损伤的一个重要因素。