Vercesi A E
Arch Biochem Biophys. 1984 Jul;232(1):86-91. doi: 10.1016/0003-9861(84)90523-x.
NAD(P)+-stimulated Ca2+ efflux from mitochondria in a high-sucrose medium is irreversible and is accompanied by large-amplitude mitochondrial swelling and membrane damage. If sucrose is partially replaced by polyethylene glycol (Mr approximately equal to 1000) as osmolar supporting medium, Ca2+ efflux is still stimulated by NAD(P)+ but mitochondrial swelling is eliminated. Other experiments in a high-sucrose medium showed that the lag phase between NAD(P)H oxidation and the beginning of net Ca2+ efflux decreases with increasing temperature. At 37 degrees C Ca2+ efflux precedes mitochondrial swelling, even in a high-sucrose medium, showing that the mitochondrial damage, as reflected by large-amplitude swelling, is not obligatory for Ca2+ efflux induced by the oxidized state of mitochondrial NAD(P)+. If a high-sucrose medium is supplemented with 20 mM potassium acetate, longer periods of Ca2+ release can be observed before the appearance of swelling. Under these experimental conditions the release of Ca2+ can be completely reversed if the rereduction of NAD(P)+ is brought about by the addition of the reductants beta-hydroxybutyrate and isocitrate.
在高糖培养基中,NAD(P)+刺激的线粒体Ca2+外流是不可逆的,且伴有大幅度的线粒体肿胀和膜损伤。如果用聚乙二醇(分子量约为1000)部分替代蔗糖作为渗透压支持介质,NAD(P)+仍能刺激Ca2+外流,但线粒体肿胀消失。在高糖培养基中的其他实验表明,NAD(P)H氧化与净Ca2+外流开始之间的延迟期随温度升高而缩短。在37℃时,即使在高糖培养基中,Ca2+外流也先于线粒体肿胀出现,这表明由线粒体NAD(P)+氧化态诱导的Ca2+外流并不一定伴随着如大幅度肿胀所反映的线粒体损伤。如果在高糖培养基中添加20 mM醋酸钾,在肿胀出现之前可以观察到更长时间的Ca2+释放。在这些实验条件下,如果通过添加还原剂β-羟基丁酸和异柠檬酸使NAD(P)+重新还原,Ca2+的释放可以完全逆转。