MacDonald M J
Biochem Int. 1984 Jun;8(6):771-8.
The net uptake of 45Ca into mitochondria from pancreatic islets is stimulated by substrates that transfer reducing equivalents to various sites of the respiratory chain, such as succinate or glycerol 3-phosphate (site II), malate plus pyruvate (site I) or ascorbate plus TMPD (site III). Diazoxide, a known inhibitor of insulin release in vivo and in vitro, strongly inhibited net 45Ca uptake supported by glycerol phosphate and succinate and weakly inhibited 45Ca uptake supported by the other substrates. These results suggest that diazoxide, although not completely specific, is predominately an inhibitor at site II of the respiratory chain. This result is consistent with previous work that showed diazoxide inhibits the enzyme activity of the mitochondrial glycerol phosphate dehydrogenase in islets. Sodium ion inhibited the net accumulation of 45Ca by islet mitochondria suggesting a similarity between islet mitochondria and those of heart and some other endocrine tissues.
胰岛线粒体对45Ca的净摄取受到将还原当量转移至呼吸链不同位点的底物的刺激,例如琥珀酸或3-磷酸甘油(位点II)、苹果酸加丙酮酸(位点I)或抗坏血酸加TMPD(位点III)。二氮嗪是一种已知的体内和体外胰岛素释放抑制剂,它强烈抑制由磷酸甘油和琥珀酸支持的45Ca净摄取,并微弱抑制由其他底物支持的45Ca摄取。这些结果表明,二氮嗪虽然并非完全特异性,但主要是呼吸链位点II的抑制剂。这一结果与先前的研究一致,先前研究表明二氮嗪抑制胰岛中线粒体磷酸甘油脱氢酶的酶活性。钠离子抑制胰岛线粒体对45Ca的净积累,这表明胰岛线粒体与心脏及其他一些内分泌组织的线粒体存在相似性。