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知母提取物通过激活糖尿病啮齿动物的AMP活化蛋白激酶改善高血糖和胰岛素抵抗。

Rhizoma Anemarrhenae extract ameliorates hyperglycemia and insulin resistance via activation of AMP-activated protein kinase in diabetic rodents.

作者信息

Han Jun, Yang Na, Zhang Feng, Zhang Chuan, Liang Fengying, Xie WeiFen, Chen Wansheng

机构信息

Department of Gastroenterology, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai 200003, PR China.

Department of Pharmacy, Changzheng Hospital, Second Military Medical University, 415 Fengyang Road, Shanghai 200003, PR China.

出版信息

J Ethnopharmacol. 2015 Aug 22;172:368-76. doi: 10.1016/j.jep.2015.05.016. Epub 2015 Jul 7.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Rhizoma Anemarrhenae has been used in Asian countries for thousands of years to treat diabetes. Insulin resistance (IR) is the primary cause responsible for type 2 diabetes. The aim of this study was to to assess the hypoglycemic and insulin sensitizing properties of Rhizoma Anemarrhenae extract (TFA) in animal models of insulin resistance and/or diabetes and to delineate modes of action.

MATERIALS AND METHODS

In-vivo studies were performed on STZ-induced diabetic mice and KK-Ay mice, the former of which were given the extract alone or in combination with insulin for 7 days, and the latter of which were given the extract for 8 consecutive weeks. Fasting blood glucose and serum insulin levels were measured. Pancreatic tissue sections were examined using transmission electron micrographs. Further, hyperinsulinemic-euglycemic clamping study was conducted in BCG vaccine-induced insulin resistance rats, and glucose infusion rate was examined. Mechanisms of action were investigated in 3T3-L1 and Hela cells using Western blot analysis.

RESULTS

Our study showed that TFA enhanced the glucose-lowering effects of exogenous insulin administration in STZ-induced diabetic mice. Therapeutic administration of TFA significantly reduced fasting blood glucose, and serum insulin levels, and markedly increased the size and the number of insulin-producing beta cells in KK-Ay mice. Further, hyperinsulinemic-euglycemic clamping study showed that glucose infusion rate was significantly improved in TFA-treated BCG vaccine-induced insulin resistance rats. Study of mechanism of action revealed that TFA increased phosphorylation of AMPK and its downstream target, acetyl-CoA carboxylase (ACC) in 3T3-L1 cells. It activates AMPK in a LKB1-independent manner, providing a unified explanation for the beneficial effects of TFA.

CONCLUSIONS

This study that TFA mediates activation of AMPK and improves overall glucose and lipid metabolism in diabetic rodents, highlights the potential utility of TFA for the management of type 2 diabetes.

摘要

民族药理学相关性

知母在亚洲国家已被用于治疗糖尿病数千年。胰岛素抵抗(IR)是2型糖尿病的主要病因。本研究的目的是评估知母提取物(TFA)在胰岛素抵抗和/或糖尿病动物模型中的降血糖和胰岛素增敏特性,并阐明其作用模式。

材料与方法

对链脲佐菌素诱导的糖尿病小鼠和KK-Ay小鼠进行体内研究,前者单独给予提取物或与胰岛素联合给药7天,后者连续8周给予提取物。测量空腹血糖和血清胰岛素水平。使用透射电子显微镜检查胰腺组织切片。此外,在卡介苗诱导的胰岛素抵抗大鼠中进行高胰岛素-正常血糖钳夹研究,并检测葡萄糖输注速率。使用蛋白质免疫印迹分析在3T3-L1和Hela细胞中研究作用机制。

结果

我们的研究表明,TFA增强了链脲佐菌素诱导的糖尿病小鼠中外源性胰岛素给药的降糖效果。TFA的治疗性给药显著降低了空腹血糖和血清胰岛素水平,并显著增加了KK-Ay小鼠中产生胰岛素的β细胞的大小和数量。此外,高胰岛素-正常血糖钳夹研究表明,在TFA治疗的卡介苗诱导的胰岛素抵抗大鼠中,葡萄糖输注速率显著提高。作用机制研究表明,TFA增加了3T3-L1细胞中AMPK及其下游靶点乙酰辅酶A羧化酶(ACC)的磷酸化。它以不依赖LKB1的方式激活AMPK,为TFA的有益作用提供了统一的解释。

结论

本研究表明TFA介导AMPK的激活并改善糖尿病啮齿动物的整体葡萄糖和脂质代谢,突出了TFA在2型糖尿病管理中的潜在效用。

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