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通过调节胰岛素信号传导、维持糖脂稳态以及减轻2型糖尿病小鼠的炎症反应来改善肝脏胰岛素抵抗。

ameliorates hepatic insulin resistance by modulating insulin signalling, maintaining glycolipid homeostasis and reducing inflammation in type 2 diabetic mice.

作者信息

Dong Xuan, Zhao Shu-Xiang, Xu Bing-Qing, Zhang Yu-Qing

机构信息

National Engineering Laboratory for Modern Silk , School of Biology and Basic Medical Sciences , Soochow University , RM702-2303 , No. 199 , Renai Road , Dushuhu Higher Edu. Town , Suzhou , P R China . Email:

出版信息

Toxicol Res (Camb). 2019 Sep 27;8(6):928-938. doi: 10.1039/c9tx00191c. eCollection 2019 Nov 1.

Abstract

Diabetes mellitus, one of the fastest growing epidemics worldwide, has become a serious health problem in modern society. (GD), an edible medicinal plant, has been shown to have hypoglycaemic effects. The molecular mechanisms by which GD improves hepatic insulin resistance (IR) in mice with type 2 diabetes (T2D) remain largely unknown. The aerial parts of GD were prepared in a lyophilized powder, which was added into the diet of T2D mice for 4 weeks. GD could result in an obvious decrease in fasting blood glucose and insulin levels in T2D mice. Meanwhile, the underlying mechanisms involved in the insulin-signalling pathway, glucose metabolism, lipid metabolism and inflammatory reaction in the liver tissue were also investigated by western blot, which indicated that GD further ameliorated hepatic IR by activating the PI3K/p-AKT pathway, decreasing the levels of hepatic phosphoenolpyruvate carboxykinase and glucose-6-phosphatase and increasing the levels of glucokinase and peroxisome proliferator-activated receptor-γ in the livers of T2D mice. GD has the potential to alleviate both hyperglycaemia and hepatic IR in T2D mice. Therefore, GD might be a promising functional food or medicine for T2D treatment.

摘要

糖尿病是全球增长最快的流行病之一,已成为现代社会中一个严重的健康问题。绞股蓝(GD)是一种可食用的药用植物,已被证明具有降血糖作用。GD改善2型糖尿病(T2D)小鼠肝脏胰岛素抵抗(IR)的分子机制在很大程度上仍不清楚。将GD的地上部分制成冻干粉,添加到T2D小鼠的饮食中4周。GD可使T2D小鼠的空腹血糖和胰岛素水平明显降低。同时,还通过蛋白质印迹法研究了肝组织中胰岛素信号通路、糖代谢、脂代谢和炎症反应的潜在机制,结果表明GD通过激活PI3K/p-AKT通路、降低肝组织中磷酸烯醇式丙酮酸羧激酶和葡萄糖-6-磷酸酶的水平以及提高T2D小鼠肝脏中葡萄糖激酶和过氧化物酶体增殖物激活受体-γ的水平,进一步改善了肝脏IR。GD有减轻T2D小鼠高血糖和肝脏IR的潜力。因此,GD可能是一种有前途的用于治疗T2D的功能性食品或药物。

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