SGLT2抑制剂:来自两栖动物世界的建议

S. Michelassi
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引用次数: 0

摘要

钠-葡萄糖共转运蛋白2抑制剂是一类抑制近端肾小管葡萄糖重吸收的降糖药物。在许多试验中,这些药物显示出不可预测的主要心脏和肾保护特性。已经提出了多种假设来阐明最后影响的机制。一些作者认为,这可能是由于当代尿中能量(如葡萄糖)和水分(通过渗透性利尿)的损失。这种特殊的情况可以诱导代谢变化,从而在心脏和肾脏水平上产生更有效的能量,并减少氧化应激。这些变化可能真的是一系列进化上保守的代谢开关的一部分,这些开关允许生物体在营养和水供应有限的干旱栖息地生存,在两栖动物身上得到了很好的研究,统称为“estivation”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SGLT2 inhibitors: suggestions from the amphibian world
Sodium-glucose cotransporter 2 inhibitors are a class of antidiabetic drugs that inhibit glucose reabsorption in the proximal renal tubules. In many trials these drugs have shown unpredictable major cardio- and nephroprotective properties. Multiple hypotheses have been raised to elucidate the mechanisms underlying the last effects. Some authors suggest they may be due to the contemporary urinary loss of energy (as glucose) and water (by osmotic diuresis). This particular condition could induce metabolic changes resulting in more efficient energetics at cardiac and renal levels and in less oxidative stress. These changes might really be part of a series of evolutionarily conserved metabolic switches that allow organisms to survive in arid habitats with restricted nutrients and water availability, well studied in amphibians and collectively named “estivation”.
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