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首页> 外文期刊>Journal of pharmacological sciences. >Ranirestat (AS-3201), a potent aldose reductase inhibitor, reduces sorbitol levels and improves motor nerve conduction velocity in streptozotocin-diabetic rats
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Ranirestat (AS-3201), a potent aldose reductase inhibitor, reduces sorbitol levels and improves motor nerve conduction velocity in streptozotocin-diabetic rats

机译:Ranirestat(AS-3201)是有效的醛糖还原酶抑制剂,可降低链脲佐菌素-糖尿病大鼠的山梨醇水平并提高运动神经传导速度

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Ranirestat (AS-3201) is a novel aldose reductase (AR) inhibitor with potentially beneficial effects on diabetic sensorimotor polyneuropathy. In this study, we performed a kinetic analysis to determine the mode of inhibition of ranirestat on AR and investigated the effects of ranirestat on sorbitol levels in the sciatic nerves and lens of streptozotocin (STZ)-diabetic rats. We also evaluated the effects on motor nerve conduction velocity (MNCV) in STZ-diabetic rats. Kinetic analyses revealed that the ranirestat inhibition of AR is uncompetitive and reversible. In the sciatic nerve and lens of STZ-diabetic rats, single oral administration of ranirestat slightly reduced sorbitol levels. However, repeated oral administration of ranirestat for 5, 21, or 60 days enhanced the reducing effect of the ranirestat on sorbitol levels in the sciatic nerves and lens of STZ-diabetic rats with maximum effects after 21 days of treatment. Finally, repeated oral administration of ranirestat for 21 or 42 days dose-dependently improved the STZ-induced decrease in MNCV in STZ-diabetic rats. These findings demonstrate that repeated oral administration of ranirestat reduces sorbitol accumulation and improves MNCV in STZ-diabetic rats, indicating that ranirestat is an agent for the management of diabetic sensorimotor polyneuropathy.
机译:Ranirestat(AS-3201)是一种新型的醛糖还原酶(AR)抑制剂,对糖尿病感觉运动性多发性神经病具有潜在的有益作用。在这项研究中,我们进行了动力学分析,以确定雷尼司他对AR的抑制模式,并研究了雷尼司他对链脲佐菌素(STZ)糖尿病大鼠坐骨神经和晶状体中山梨醇水平的影响。我们还评估了STZ糖尿病大鼠对运动神经传导速度(MNCV)的影响。动力学分析表明,雷尼司他对AR的抑制是无竞争性且可逆的。在STZ糖尿病大鼠的坐骨神经和晶状体中,单次口服ranirestat可以降低山梨醇的水平。但是,重复口服雷那司他5、21或60天可增强雷那司他对STZ糖尿病大鼠坐骨神经和晶状体中山梨醇水平的降低作用,在治疗21天后效果最大。最后,重复口服雷兰司他21天或42天剂量依赖性地改善了STZ糖尿病大鼠中STZ诱导的MNCV降低。这些发现表明,反复口服雷那司他可减少STZ糖尿病大鼠的山梨糖醇积累并改善MNCV,这表明雷那司他是糖尿病感觉运动性多神经病的治疗剂。

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