Sener A, Herberg L, Malaisse W J
Laboratory of Experimental Medicine, Brussels Free University, Belgium.
FEBS Lett. 1993 Feb 1;316(3):224-7. doi: 10.1016/0014-5793(93)81297-d.
The mitochondrial enzyme FAD-linked glycerophosphate dehydrogenase plays a key role in the glucose-sensing device of the insulin-producing pancreatic B-cell. Its activity was found to be decreased in islet, but not liver, homogenates of BL/Ks-db/db mice, in which diabetes mellitus represents an inherited disease. The decreased activity of FAD-linked glycerophosphate dehydrogenase contrasted with a normal activity of glutamate dehydrogenase and 2-ketoglutarate dehydrogenase in the islets of db/db mice. It is proposed that a site-specific defect of FAD-linked glycerophosphate dehydrogenase in the pancreatic B-cell might represent a far-from-uncommon causal or contributing factor in the pathogenesis of non-insulin-dependent diabetes mellitus.
线粒体酶黄素腺嘌呤二核苷酸(FAD)连接的甘油磷酸脱氢酶在产生胰岛素的胰腺β细胞的葡萄糖传感装置中起关键作用。在遗传性糖尿病的BL/Ks-db/db小鼠的胰岛匀浆中,发现该酶活性降低,但在肝脏匀浆中未降低。FAD连接的甘油磷酸脱氢酶活性降低与db/db小鼠胰岛中谷氨酸脱氢酶和2-酮戊二酸脱氢酶的正常活性形成对比。有人提出,胰腺β细胞中FAD连接的甘油磷酸脱氢酶的位点特异性缺陷可能是非胰岛素依赖型糖尿病发病机制中一个相当常见的致病或促成因素。