Hansford R G, Hogue B, Prokopczuk A, Wasilewska E, Lewartowski B
Laboratory of Cardiovascular Science, National Institute on Aging, Baltimore, MD.
Biochim Biophys Acta. 1990 Jul 25;1018(2-3):282-6. doi: 10.1016/0005-2728(90)90268-9.
(1) Electrical stimulation (2 Hz) of guinea-pig hearts, perfused with medium containing 11 mM D-glucose plus 0.1 mM octanoate as substrate, resulted in an increase in the percentage of pyruvate dehydrogenase in the active form (PDHa) from 16 to 68%. (2) Rapid isolation of mitochondria by a technique designed to minimize net loss or gain of Ca2+ revealed an increase in mitochondrial Ca2+ content of the stimulated hearts, as measured with 45Ca (2.74 +/- 0.27 versus 1.37 +/- 0.11 nmol/mg protein; stimulated versus rested). (3) Perfusion of rested hearts with a medium containing a reduced Na+ concentration (20 mM, with the remainder replaced with Li+) also gave increased values of PDHa content (30.9% versus 16% for the normal, physiological medium). This procedure is known to raise cytosol Ca2+ concentrations and would be expected to give mitochondrial Ca2+ loading. (4) These results are consistent with a role of mitochondrial Ca2+ in activating pyruvate dehydrogenase in the intact heart.
(1) 用含有11 mM D-葡萄糖加0.1 mM辛酸作为底物的培养基灌注豚鼠心脏,并进行电刺激(2 Hz),结果显示活性形式的丙酮酸脱氢酶(PDHa)百分比从16%增加到68%。(2) 通过一种旨在尽量减少Ca2+净损失或净增加的技术快速分离线粒体,结果显示,用45Ca测量,受刺激心脏的线粒体Ca2+含量增加(2.74±0.27对1.37±0.11 nmol/mg蛋白质;受刺激与静息)。(3) 用含有降低的Na+浓度(20 mM,其余用Li+替代)的培养基灌注静息心脏,也会使PDHa含量增加(正常生理培养基为16%,此培养基为30.9%)。已知该操作会提高细胞质Ca2+浓度,并预期会导致线粒体Ca2+负载。(4) 这些结果与线粒体Ca2+在完整心脏中激活丙酮酸脱氢酶的作用一致。