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首页> 外文期刊>Japanese Journal of Pharmacology >Effects of ONO-2235, an Aldose Reductase Inhibitor, on Muscarinic Receptors and Contractile Response of the Urinary Bladder in Rats with Streotozotocin-Induced Diabetes
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Effects of ONO-2235, an Aldose Reductase Inhibitor, on Muscarinic Receptors and Contractile Response of the Urinary Bladder in Rats with Streotozotocin-Induced Diabetes

机译:醛糖还原酶抑制剂ONO-2235对链脲佐菌素诱导的糖尿病大鼠毒蕈碱受体和膀胱的收缩反应的影响

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摘要

References(39) Cited-By(12) This study was conducted to evaluate effects of the aldose reductase inhibitor ONO-2235 on the contractile response to acetylcholine of the urinary bladder dome of streptozotocin-induced diabetes mellitus (DM)rats and simultaneously observe the changes in the function and number of muscarinic receptors and the sorbitol content of the bladder. The contractile response to acetylcholine increased 51 % in the DM rat bladder dome compared to the normal rats; however, this was attenuated to a 10% increase by administration of 100 mg/kg ONO-2235 for 2 weeks. Treatment with ONO-2235 significantly decreased the specific [3H]quinuclidinyl benzilate binding in DM rats. However there was no significant dose-dependency among the ONO-2235-treated groups. The sorbitol levels of the sciatic nerve and the bladder were higher in the DM rats compared to the control rats; ONO-2235 decreased the level, although it did not completely reverse them to the control level. These results suggest that an aldose reductase inhibitor attenuates the increase of the muscarinic receptor number and normalizes the enhanced contractile response to acetylcholine caused by hyperglycemia and diuresis, probably through suppression of the polyol-pathway in the DM rat bladder dome.
机译:参考文献(39)Cited-By(12)这项研究旨在评估醛糖还原酶抑制剂ONO-2235对链脲佐菌素诱发的糖尿病(DM)大鼠膀胱穹顶对乙酰胆碱的收缩反应的影响,并同时观察毒蕈碱受体的功能和数量以及膀胱中山梨醇含量的变化。与正常大鼠相比,DM大鼠膀胱穹顶对乙酰胆碱的收缩反应增加了51%。但是,通过施用100 mg / kg ONO-2235持续2周,这种作用减弱了10%。用ONO-2235处理可显着降低DM大鼠中的[3H]奎宁环烷基苯甲酸酯特异性结合。然而,在ONO-2235治疗组之间没有明显的剂量依赖性。 DM大鼠的坐骨神经和膀胱的山梨醇水平高于对照组。 ONO-2235降低了水平,尽管它没有完全将它们恢复到控制水平。这些结果表明,醛糖还原酶抑制剂可以减轻由高血糖症和利尿引起的对毒蕈碱受体数目的增加,并使归因于乙酰胆碱的增强收缩反应正常化,这可能是通过抑制DM大鼠膀胱穹顶中的多元醇途径来实现的。

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