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Antidiabetic effect of SN158 through PPAR alpha/gamma dual activation in ob/ob mice

机译:SN158通过OB / OB小鼠PPARα/γ双激活的抗抛配效应

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In this study, we aimed to demonstrate the antidiabetic potential of (E)-N-(4-(3-(5-bromo-4-hydroxy-2-methoxyphenyl) acryloyl) phenyl)-4-tert-butylbenzamide (SN158) through peroxisome proliferator-activated receptor (PPAR)-alpha/gamma dual activation. SN158 interacted with both PPAR alpha and PPAR gamma, and increased their transcriptional activities. Simultaneously, SN158 treatment led to an increase in adipogenic differentiation of 3T3-L1 preadipocytes and fatty acid oxidation in hepatocytes. In addition, glucose uptake in myotubes was significantly increased by SN158 treatment. Finally, SN158 significantly lowered the plasma levels of glucose, triglycerides, and free fatty acids in ob/ob mice without severe weight gain and hepatomegaly. These results suggest that SN158 can be useful as a potential therapeutic agent against type 2 diabetes and related metabolic disorders by alleviating glucose and lipid abnormalities. (C) 2017 Elsevier B.V. All rights reserved.
机译:在这项研究中,我们旨在证明(E)-N-(4-(3-(5-溴-4-羟基-2-甲氧基苯基)丙烯酰基)苯基)-4-叔丁基苯甲酰胺(SN158)的抗糖尿病潜力(SN158) 通过过氧化物体增殖物激活受体(PPAR) - alpha /γ双激活。 SN158与PPAR alpha和PPAR伽玛共同互动,并增加了转录活动。 同时,SN158治疗导致肝细胞中3T3-L1前脂肪细胞和脂肪酸氧化的脂肪发生分化的增加。 此外,SN158治疗,肌管中的葡萄糖摄取显着增加。 最后,SN158显着降低了OB / OB小鼠中的葡萄糖,甘油三酯和游离脂肪酸的血浆水平,而没有严重的体重增加和肝肿大。 这些结果表明,通过减轻葡萄糖和脂质异常,SN158可用作针对2型糖尿病和相关代谢障碍的潜在治疗剂。 (c)2017 Elsevier B.v.保留所有权利。

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