Sulfonylureas can Stimulate Insulin Release by Flip-Flop across Phospholipid Membranes

J. Alruwaili
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引用次数: 2

Abstract

The design of new drugs and drug-delivery systems requires insight about how a drug interacts with the phospholipid bilayer. Sulfonylureas are used to treat type 2 diabetes mellitus because they stimulate insulin secretion from pancreatic β-cells. Two generations of Sulfonylurea drugs have been marketed to treat type II diabetes mellitus. Tolbutamide was chosen to represent the first generation of these drugs, whereas Glibenclamide was from the second generation. This study investigated how the Sulfonylureas cross the phospholipid membrane and it found that these drugs are transported by non-energy dependent flip-flop mechanism. A u-shaped conformation for both Tolbutamide and Glibenclamide is being proposed to explain the binding of these drugs to the phospholipid membrane.
磺脲类化合物可以通过磷脂膜的翻转来刺激胰岛素释放
新药物和药物传递系统的设计需要了解药物如何与磷脂双分子层相互作用。磺脲类药物用于治疗2型糖尿病,因为它们能刺激胰腺β细胞分泌胰岛素。两代磺脲类药物已经上市用于治疗II型糖尿病。Tolbutamide被选为这些药物的第一代代表,而格列本脲是第二代。本研究考察了磺脲类药物是如何穿过磷脂膜的,发现这些药物是通过非能量依赖的触发器机制运输的。甲苯丁酰胺和格列本脲的u形构象被提出来解释这些药物与磷脂膜的结合。
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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