安普克
蛋白激酶A
一磷酸腺苷
二甲双胍
糖尿病
AMP活化蛋白激酶
药理学
腺苷
自噬
葡萄糖转运蛋白
非酒精性脂肪肝
医学
生物
化学
脂肪肝
激酶
内分泌学
内科学
细胞生物学
疾病
生物化学
胰岛素
细胞凋亡
作者
Naser Safaie,Shahab Masoumi,Shaban Alizadeh,Pourya Mirzajanzadeh,Hamid Reza Nejabati,Mobasher Hajiabbasi,Vahid Alivirdiloo,Neda Chobdari Basmenji,Aysan Derakhshi Radvar,Ziba Majidi,Yousef Faridvand
摘要
Abstract Sodium‐glucose co‐transporter‐2 (SGLT2) inhibitors, known as Gliflozins, are a class of Glucose‐lowering drugs in adults with type 2 diabetes (T2D) that induce glucosuria by blocking SGLT2 co‐transporters in the proximal tubules. Several lines of evidence suggest that SGLT2 inhibitors regulate multiple mechanisms associated with the regulation of varying cellular pathways. The 5′‐adenosine monophosphate‐activated protein kinase (AMPK) pathway plays an important role in metabolic homeostasis by influencing cellular processes. Recently, it has been shown that SGLT2 inhibitors can affect the AMPK pathway in differing physiological and pathological ways, resulting in kidney, intestinal, cardiovascular, and liver protective effects. Additionally, they have therapeutic effects on nonalcoholic fatty liver disease and diabetes mellitus‐associated complications. In this review, we summarize the results of studies of AMPK‐associated therapeutic effects of SGLT2 inhibitors in different organelle functions.
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