FAD-Linked Glycerophosphate Dehydrogenase Activity in Islets, Liver, and Splenocytes of NOD Mice

Anak O., Malaisselagae F., Leclercqmeyer V., Sener A., Malaisse W.J.
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引用次数: 5

Abstract

The activity of FAD-linked glycerophosphate dehydrogenase (m-GDH), as well as that of glutamate dehydrogenase and both glutamate-oxalacetate and glutamate-pyruvate transaminases, were measured in islet, liver, and splenocyte homogenates from 6- to 7-week-old female nonobese diabetic mice (NOD) and age- and sex-matched control mice. Despite incipient insulitis and euglycemia, the NOD mice displayed both high islet insulin content and elevated insulinemia. The activity of m-GDH, expressed relative to protein content, was not decreased in islets of NOD mice, despite the fact that such a specific activity is lower in splenic lymphocytes than islet cells. In liver homogenates, the activity of m-GDH was even higher in NOD than control mice. It is proposed, therefore, that in this model of insulin-dependent diabetes no primary decrease in islet m-GDH activity occurs, at variance with the situation recently documented in several animal models of non-insulin-dependent diabetes.

FAD-Linked glycerophospdehydrogenase在NOD小鼠胰岛、肝脏和脾细胞中的活性
在6- 7周龄的雌性非肥胖糖尿病小鼠(NOD)和年龄和性别匹配的对照小鼠的胰岛、肝脏和脾细胞匀浆中,测量了fad连接的甘油磷酸脱氢酶(m-GDH)、谷氨酸脱氢酶、谷氨酸-草酸酯和谷氨酸-丙酮酸转氨酶的活性。尽管有早期的胰岛素炎和血糖升高,NOD小鼠显示出高胰岛胰岛素含量和胰岛素血症升高。在NOD小鼠的胰岛中,相对于蛋白质含量表达的m-GDH活性并未降低,尽管脾淋巴细胞的这种特异性活性低于胰岛细胞。在肝脏匀浆中,NOD中m-GDH的活性甚至高于对照小鼠。因此,我们提出,在这种胰岛素依赖型糖尿病模型中,胰岛m-GDH活性没有发生原发性降低,这与最近在几种非胰岛素依赖型糖尿病动物模型中记录的情况不同。
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