Mukherjee A, Wong T M, Templeton G, Buja L M, Willerson J T
Am J Physiol. 1979 Aug;237(2):H224-38. doi: 10.1152/ajpheart.1979.237.2.H224.
Oxidative phosphorylation of isolated canine myocardial mitochondria has been evaluated after exposure to different concentrations of phosphate (5--50 mM), lactate ion in excess (5--40 mM, pH 7.4), calcium (50--270 nmol/mg protein), to lactic acidosis (pH 6.3), and to mitochondrial protein dilution (in vitro volume expansion) for 10 min to 8 h. The influence of phosphate and lactate ion addition, lactic acidosis, and in vitro volume expansion on mitochondrial function were studied in the isolation medium (0.18 M KCl, 0.5% BSA (bovine serum albumin), with or without Tris-EDTA, pH 7.4) prior to evaluation of mitochondrial function in the assay medium (0.25 M sucrose, 10 mM Tris-HCl, and 10 mM inorganic phosphate, pH 7.4). The effect of calcium addition was assessed in the assay medium. The results of these studies demonstrate that each of these interventions detrimentally alters mitochondrial oxidative phosphorylative ability. The most severe mitochondrial functional impairment resulted from phosphate or calcium addition. The detrimental effect of phosphate and in vitro volume expansion was partially corrected by the addition of cytochrome c.
在分离的犬心肌线粒体暴露于不同浓度的磷酸盐(5 - 50 mM)、过量乳酸离子(5 - 40 mM,pH 7.4)、钙(50 - 270 nmol/mg蛋白质)、乳酸酸中毒(pH 6.3)以及线粒体蛋白稀释(体外体积膨胀)10分钟至8小时后,对其氧化磷酸化进行了评估。在测定介质(0.25 M蔗糖、10 mM Tris - HCl和10 mM无机磷酸盐,pH 7.4)中评估线粒体功能之前,先在分离介质(0.18 M KCl、0.5%牛血清白蛋白(BSA),含或不含Tris - EDTA,pH 7.4)中研究了磷酸盐和乳酸离子添加、乳酸酸中毒以及体外体积膨胀对线粒体功能的影响。在测定介质中评估了钙添加的效果。这些研究结果表明,这些干预措施中的每一种都会有害地改变线粒体的氧化磷酸化能力。磷酸盐或钙添加导致最严重的线粒体功能损害。添加细胞色素c可部分纠正磷酸盐和体外体积膨胀的有害作用。