首页> 外文期刊>Bulletin of experimental biology and medicine >Effect of Nitric Oxide Synthesis Blockade on the Morphology of Langerhans Islets in August and Wistar Rats with Acute Alloxan Diabetes
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Effect of Nitric Oxide Synthesis Blockade on the Morphology of Langerhans Islets in August and Wistar Rats with Acute Alloxan Diabetes

机译:一氧化氮合成阻滞对八月份朗格汉斯胰岛和急性四氧嘧啶糖尿病Wistar大鼠形态的影响

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摘要

Alloxan diabetes was modeled in August rats with high activity of the NO system and in Wistar rats, and the effects of NO system blockade (by a course treatment with L-NNA) on Langerhans islet beta cells were studied in 15 days. The toxic effects of diabetes on the rat beta cells and islets were similar: the content of active beta cells in the islets decreased to 15-20%, the number of islets to 24-29% of control. A course of L-NNA reduced the beta cell and islet death, in August cells greater than in Wistar: the number of islets in August rats was restored to 81%, in Wistar rats to 60% of initial level; the activity of beta cells remained at the control level in the former and 2-fold lower than in the control in the latter. It seems that a less pronounced protective effect of L-NNA in Wistar rats was explained by excessive reduction of NO level essential for beta cell regeneration.
机译:在具有高NO系统活性的8月大鼠和Wistar大鼠中建立了四氧嘧啶糖尿病模型,并在15天之内研究了NO系统封锁(通过L-NNA进行疗程治疗)对Langerhans胰岛β细胞的影响。糖尿病对大鼠β细胞和胰岛的毒性作用相似:胰岛中活性β细胞的含量降至对照组的15-20%,胰岛数量降至对照组的24-29%。一疗程的L-NNA减少了β细胞和胰岛的死亡,八月的细胞比Wistar的多:八月的大鼠的胰岛数恢复到81%,Wistar的大鼠恢复到初始水平的60%; β细胞的活性在前者中保持在对照水平,比后者中的对照低2倍。看来,Wistar大鼠中L-NNA的保护作用不太明显,可以通过过度降低β细胞再生所必需的NO水平来解释。

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