Salidroside, A Natural Antioxidant, Improves β-Cell Survival and Function via Activating AMPK Pathway

被引:65
作者
Ju, Linjie [1 ,2 ]
Wen, Xiaohua [1 ,2 ]
Wang, Chunjun [1 ,2 ]
Wei, Yingjie [1 ,2 ]
Peng, Yunru [1 ]
Ding, Yongfang [1 ]
Feng, Liang [1 ,2 ]
Shu, Luan [1 ,2 ]
机构
[1] Nanjing Univ Chinese Med, Affiliated Hosp Integrated Tradit Chinese & Weste, Nanjing, Jiangsu, Peoples R China
[2] Jiangsu Prov Acad Chinese Med, Key Lab New Drug Delivery Syst Chinese Mat Med, Nanjing, Jiangsu, Peoples R China
关键词
type; 2; diabetes; beta-cells; salidroside; oxidative stress; AMPK; OXIDATIVE STRESS; NADPH OXIDASE; PROTEIN-KINASE; INDUCED APOPTOSIS; GLUCOSE TOXICITY; FASTING GLYCEMIA; DIABETIC MICE; ER STRESS; PI3K/AKT/FOXO1; MECHANISM;
D O I
10.3389/fphar.2017.00749
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim: The enhanced oxidative stress contributes to progression of type 2 diabetes mellitus (T2DM) and induces beta-cell failure. Salidroside is a natural antioxidant extracted from medicinal food plant Rhodiola rosea. This study was aimed to evaluate protective effects of salidroside on beta-cells against diabetes associated oxidative stress. Methods and Results: In diabetic db/db and high-fat diet-induced mice, we found salidroside ameliorated hyperglycemia and relieved oxidative stress. More importantly, salidroside increased beta-cell mass and beta-cell replication of diabetic mice. Mechanism study in Min6 cells revealed that, under diabetic stimuli, salidroside suppressed reactive oxygen species production and restore mitochondrial membrane potential (1 9 m) via reducing NOX2 expression and inhibiting JNK-caspase 3 apoptotic cascade subsequently to protect beta-cell survival. Simultaneously, diabetes associated oxidative stress also activated FOXO1 and triggered nuclear exclusion of PDX1 which resulted in beta-cell dysfunction. This deleterious result was reversed by salidroside by activating AMPK-AKT to inhibit FOXO1 and recover PDX1 nuclear localization. The efficacy of salidroside in improving beta-cell survival and function was further confirmed in isolated cultured mouse islets. Moreover, the protective effects of salidroside on beta-cells against diabetic stimuli can be abolished by an AMPK inhibitor compound C, which indicated functions of salidroside on beta-cells were AMPK activation dependent. Conclusion: These results confirmed beneficial metabolic effects of salidroside and identified a novel role for salidroside in preventing beta-cell failure via AMPK activation. Our finding highlights the potential value of Rhodiola rosea as a dietary supplement for diabetes control.
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页数:12
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