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三七总皂苷通过调节 IRS1-PI3K-AKT 信号通路和 GLUT4 表达来减轻骨骼肌胰岛素抵抗。

Panax notoginseng saponins alleviate skeletal muscle insulin resistance by regulating the IRS1-PI3K-AKT signaling pathway and GLUT4 expression.

机构信息

Dongfang Hospital of Beijing University of Chinese Medicine, China.

Key Laboratory of Health Cultivation of the Ministry of Education, Beijing University of Chinese Medicine, China.

出版信息

FEBS Open Bio. 2019 May;9(5):1008-1019. doi: 10.1002/2211-5463.12635. Epub 2019 Apr 26.

Abstract

Panax notoginseng saponins (PNS) are a commonly used traditional medicine to treat diabetes in China. Recent studies have confirmed their anti-diabetic effects, but the underlying mechanisms have remained unclear. The present study was designed to explore whether PNS decrease hyperglycemia by improving insulin sensitivity in skeletal muscle and to elucidate the molecular mechanisms. The anti-diabetic effects of PNS were analyzed in a skeletal myoblast cell line, C2C12, and in high fat diet-induced diabetic KKAy mice. C2C12 cells were treated with PNS (50, 100, and 200 μg·L ) and examined for glucose uptake, cell viability and expression of components of the phosphoinositide 3-kinase (PI3K)-protein kinase B (AKT) signaling pathway. KKAy mice were intraperitoneally injected with PNS (200 mg·kg ) for 6 weeks. Body weight, blood glucose, serum insulin, serum lipid, glucose and insulin tolerance were measured to evaluate the anti-diabetic effects of PNS. Pathological changes, apoptosis and the PI3K-AKT signaling pathway were analyzed in KKAy skeletal muscle. PNS significantly increased insulin-induced glucose uptake, but did not affect the cell viability of C2C12 cells. In addition, PNS reduced blood glucose and serum insulin levels and improved glucose tolerance and insulin tolerance of KKAy mice. Pathological changes and apoptosis of skeletal muscle were relieved by PNS treatment. Moreover, PNS treatment enhanced expression of mRNA encoding IRS1 and GLUT4, as well as the protein expression of phosphorylated (p) -insulin receptor substrate 1 (IRS1), p-PI3K, p-AKT and glucose transporter type 4 (GLUT4) in C2C12 and KKAy mouse muscle. Collectively, these data indicate that PNS reduces hyperglycemia and insulin resistance through up-regulating GLUT4 expression and the IRS1-PI3K-AKT signaling pathway. Furthermore, PNS alleviated diabetes skeletal muscle pathological damage. Thus, our data suggest that PNS may be promising anti-diabetic compounds.

摘要

三七总皂苷(PNS)是一种常用的传统医学药物,用于治疗中国的糖尿病。最近的研究证实了其抗糖尿病作用,但作用机制仍不清楚。本研究旨在探讨 PNS 是否通过改善骨骼肌胰岛素敏感性来降低高血糖,并阐明其分子机制。在骨骼肌成肌细胞系 C2C12 和高脂肪饮食诱导的糖尿病 KKAy 小鼠中分析了 PNS 的抗糖尿病作用。用 PNS(50、100 和 200μg·L-1)处理 C2C12 细胞,并检测葡萄糖摄取、细胞活力和磷酸肌醇 3-激酶(PI3K)-蛋白激酶 B(AKT)信号通路组成成分的表达。用 PNS(200mg·kg-1)对 KKAy 小鼠进行腹腔注射,持续 6 周。测量体重、血糖、血清胰岛素、血脂、葡萄糖和胰岛素耐量,以评估 PNS 的抗糖尿病作用。分析 KKAy 骨骼肌的病理变化、细胞凋亡和 PI3K-AKT 信号通路。PNS 显著增加胰岛素诱导的葡萄糖摄取,但不影响 C2C12 细胞的细胞活力。此外,PNS 降低了 KKAy 小鼠的血糖和血清胰岛素水平,并改善了葡萄糖耐量和胰岛素耐量。PNS 治疗缓解了骨骼肌的病理变化和细胞凋亡。此外,PNS 治疗增强了 C2C12 和 KKAy 鼠肌肉中 IRS1 和 GLUT4 编码 mRNA 的表达,以及胰岛素受体底物 1(IRS1)、PI3K、AKT 和葡萄糖转运蛋白 4(GLUT4)的磷酸化(p)蛋白表达。总之,这些数据表明,PNS 通过上调 GLUT4 表达和 IRS1-PI3K-AKT 信号通路来降低高血糖和胰岛素抵抗。此外,PNS 缓解了糖尿病骨骼肌的病理损伤。因此,我们的数据表明 PNS 可能是有前途的抗糖尿病化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e83/6487711/d6a273711531/FEB4-9-1008-g001.jpg

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