Vaccinium bracteatum Thunb. Leaves' polysaccharide alleviates hepatic gluconeogenesis via the downregulation of miR-137.

IF 7.5
Hai-Feng Qian, Yan Li, Li Wang
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引用次数: 18

Abstract

Vaccinium bracteatum Thunb.(VBT) is a traditional Chinese herb that recorded has an effect of hypoglycemic. We previous discovered a dose-dependent anti-diabetic function of VBT. leaves' polysaccharide (VBTLP), but little is known about its underlying molecular mechanism. Therefore, we hypothesized that VBTLP would decrease hepatic gluconeogenesis to improve glucose metabolism in mice. To test this hypothesis, glucose tolerance test was performed to evaluate the effect of VBTLP on mice hepatic gluconeogenesis. Western blot and RT-PCR were performed to measure both in vivo and in vitro gene regulation under VBTLP treatment. Online bioinformatic analysis was performed to discover a target candidate, miR-137 of LKB1 and AMPK under VBTLP treatment, and the luciferase assay was conducted to validate it. Here we found that VBT. leaves' polysaccharide (VBTLP) decreased hepatic gluconeogenesis via activation of LKB1/AMPK axis in vivo and in vitro. Mechanistic studies reveal that miR-137 regulates hepatic glucose homeostasis by directly targeting AMPK and LKB1. Furthermore, we shown that VBTLP decreased hepatic miR-137 level, which might contribute to activation of LKB1/AMPK and downregulation of gluconeogenesis. Taken together, our study shown that the mechanisms might involve in VBTLP hypoglycemic effect, alleviates hepatic gluconeogenesis via the downregulation of miR-137. Our findings provide guidance in developing novel, safe and effective therapies for T2DM.

苞片苞片叶多糖通过下调miR-137来缓解肝脏糖异生。
牛蒡子(VBT)是一种有降血糖作用的中药。我们之前发现VBT具有剂量依赖性的抗糖尿病功能。叶多糖(VBTLP),但对其潜在的分子机制知之甚少。因此,我们假设VBTLP可以减少肝脏糖异生,改善小鼠的糖代谢。为了验证这一假设,我们通过糖耐量试验来评价VBTLP对小鼠肝脏糖异生的影响。采用Western blot和RT-PCR检测VBTLP处理下的体内和体外基因调控情况。通过在线生物信息学分析发现VBTLP处理下LKB1和AMPK的miR-137靶点候选物,并进行荧光素酶测定验证。这里我们发现VBT。叶多糖(VBTLP)通过激活LKB1/AMPK轴在体内外抑制肝脏糖异生。机制研究表明,miR-137通过直接靶向AMPK和LKB1调节肝脏葡萄糖稳态。此外,我们发现VBTLP降低肝脏miR-137水平,这可能有助于激活LKB1/AMPK和下调糖异生。综上所述,我们的研究表明其机制可能涉及VBTLP的降糖作用,通过下调miR-137缓解肝脏糖异生。我们的研究结果为开发新型、安全、有效的T2DM治疗方法提供了指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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