依米霉素对胰岛素分泌和胰岛素抵抗双重机制的药理特性

Iwatsuki N, B. H, O. M
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引用次数: 5

摘要

最新的糖尿病医疗保健标准于2022年1月提出。在口服降糖药(OHAs)中,伊美霉素已成为治疗2型糖尿病(T2DM)的一种新型药物。在药理学上,伊米霉素是一种含三嗪环的环状分子。它具有增加胰岛素作用和升高葡萄糖刺激胰岛素分泌(GSIS)的药理机制。临床结果显示,单药治疗HbA1c降低0.46%,联合其他oha治疗HbA1c降低0.56-0.92%。比较500mg, 1000mg和1500mg的剂量,1000mg两次剂量是足够的。未发现伊米霉素治疗中出现的显著不良事件(teae)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological Characteristic of Imeglimin (Twymeeg) For Dual Mechanism to Insulin Secretion and Resistance
Latest Standards of Medical Care in Diabetes was presented in January 2022. Among oral hypoglycemic agents (OHAs), imeglimin has been topic for a novel agent for type 2 diabetes mellitus (T2DM). Pharmacologically, imeglimin is a cyclic molecule including triazine ring. It has both pharmacological mechanism of increased insulin action and elevation of glucose-stimulated insulin secretion (GSIS). Clinically, it showed HbA1c reduction for 0.46% by monotherapy and 0.56-0.92% by combined therapy with other OHAs. From compared administration of 500mg, 1000mg and 1500mg, 1000mg twice doses would be adequate. No remarkable treatment-emergent adverse events (TEAEs) were found for treatment of imeglimin.
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