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链脲佐菌素而非四氧嘧啶可在体外诱导小鼠胰岛中的DNA修复合成。

Streptozotocin, but not alloxan, induces DNA repair synthesis in mouse pancreatic islets in vitro.

作者信息

Sandler S, Swenne I

出版信息

Diabetologia. 1983 Nov;25(5):444-7. doi: 10.1007/BF00282526.

Abstract

In the present investigation, the abilities of streptozotocin and alloxan to induce DNA repair synthesis in isolated mouse pancreatic islets have been compared using an autoradiographic technique. Streptozotocin exposure in vitro induced a dose-dependent DNA repair synthesis, whereas no such effect was observed after alloxan treatment. The hydroxyl radical scavenger dimethyl urea and the poly(ADP-ribose) synthetase inhibitors nicotinamide and theophylline reduced the streptozotocin-induced DNA repair. The results suggest that the initial events in streptozotocin-induced B cell injury are DNA damage and repair and that alloxan exerts its major cytotoxic effect by a different mechanism.

摘要

在本研究中,已使用放射自显影技术比较了链脲佐菌素和四氧嘧啶在分离的小鼠胰岛中诱导DNA修复合成的能力。体外暴露于链脲佐菌素可诱导剂量依赖性的DNA修复合成,而四氧嘧啶处理后未观察到这种效应。羟基自由基清除剂二甲基脲以及聚(ADP - 核糖)合成酶抑制剂烟酰胺和茶碱可减少链脲佐菌素诱导的DNA修复。结果表明,链脲佐菌素诱导的B细胞损伤的初始事件是DNA损伤和修复,并且四氧嘧啶通过不同的机制发挥其主要细胞毒性作用。

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