[Sulfonylurea].

R. Usuda
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引用次数: 3

Abstract

SU drug promotes insulin secretion by acting on pancreatic β cell. The hypoglycemic effect is the most powerful among oral diabetic drugs with high cost-effectiveness. Particularly for the Japanese with type 2 diabetes caused by a decrease in insulin secretion as a main pathological condition, it was widely used until the present since 1957 and largely contributed for the sickness. On the other hand, it is true that a number of issues such as a prolonged hypoglycemic coma or obesity due to a neglect of proper usage, patient education, and a possibility of second failure have been discussed so far. After a structure of K(ATP) channel on pancreatic β cell as playing an important role with insulin secretion is clarified recently and neonatal diabetes mellitus by the genetic defect is reported, a new possibility for SU drug receives attention. Furthermore, a receptor of SU drug on β cell membrane was solely known as a target molecule for SU drug, but since a binding to Epac2 as a protein to detect a part of SU drug's cAMP signal within β cell is determined, a relation with an enhancing mechanism of insulin secretion by incretin is being clarified at present. As understanding a new potential for SU drug, we consider a positioning and proper usage for SU drug again.
(磺酰脲类)。
SU药物通过作用于胰腺β细胞促进胰岛素分泌。降糖效果是口服降糖药物中最强的,成本效益高。特别是对于以胰岛素分泌减少为主要病理状态的2型糖尿病患者,自1957年以来,它一直被广泛使用,直到现在,这在很大程度上是造成糖尿病的原因。另一方面,由于忽视正确使用、患者教育和二次失败的可能性而导致的长期低血糖昏迷或肥胖等问题,到目前为止确实已经讨论过。近年来,胰腺β细胞K(ATP)通道在胰岛素分泌中起重要作用的结构被阐明,新生儿糖尿病的遗传缺陷被报道,SU药物的新可能性受到关注。此外,SU药物在β细胞膜上的受体是唯一已知的SU药物的靶分子,但由于在β细胞内确定了与Epac2结合作为检测部分SU药物cAMP信号的蛋白,因此目前正在阐明肠促胰岛素增强胰岛素分泌机制的关系。在认识到磺胺类药物的新潜力的基础上,重新考虑磺胺类药物的定位和合理使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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