中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Anti-diabetic effect and mechanism of Kursi Wufarikun Ziyabit in L6 rat skeletal muscle cells

文献类型:期刊论文

作者Edirs, S (Edirs, Salamet)[ 1,3 ]; Jiang, L (Jiang, Lan)[ 1,2 ]; Xin, XL (Xin, XueLei)[ 1,2 ]; Aisa, HA (Aisa, Haji Akber)[ 1,2 ]
刊名JOURNAL OF PHARMACOLOGICAL SCIENCES
出版日期2018
卷号137期号:2页码:212-219
关键词Type 2 Diabetes Kursi Wufarikun Ziyabit Anti-diabetic Activity Insulin Signaling Pathway Endoplasmic Reticulum Stress
ISSN号1347-8613
DOI10.1016/j.jphs.2018.06.011
英文摘要

Kursi Wufarikun Ziyabit (KWZ) is a traditional prescription that used in folk tea drinking for its health care effect in treatment of type 2 diabetes mellitus (T2DM) in central Asia. However, the underlying mechanism of KWZ in T2DM has not been investigated extensively. This study designed to observe the effect of KWZ on glucose consumption and assess the molecular mechanism on associated proteins in insulin signaling and ER stress pathway in L6 rat skeletal muscle cells. The results showed that, KWZ exhibited proteins of PTP-1B and alpha-glycosidase inhibitory activity in vitro. No cytotoxicity of KWZ was found on L6 cell line. The best effect of glucose consumption of cells was shown at 6.25 mu g/mL after KWZ treatment for 12 h. Expression of PTP-1B protein was inhibited by KWZ in L6 moytubes. PI3K-dependent Akt phosphorylation was found to be activated by KWZ. Moreover, the insulin-mediated induction of IRS-1 and GSK-3 were also activated by KWZ. Western blot results indicated that KWZ significantly improved the levels of ER stress proteins, which reduced the expression of GRP78, enhanced the expression of the PERK, eIF2 alpha and XBP1s. The activation of PERK/eIF2 alpha was likely consequence of GRP78 inhibition, and this might be beneficial for improving the stability of ER and alleviating insulin resistance. These results suggest that KWZ might be serving as the potential drug for the prevention and treatment of T2DM.

WOS记录号WOS:000440452000015
源URL[http://ir.xjipc.cas.cn/handle/365002/5575]  
专题新疆理化技术研究所_省部共建新疆特有药用资源利用重点实验室
新疆理化技术研究所_资源化学研究室
通讯作者Xin, XL (Xin, XueLei)[ 1,2 ]; Aisa, HA (Aisa, Haji Akber)[ 1,2 ]
作者单位1.Chinese Acad Sci, Xinjiang Tech Inst Phys & Chem, Key Lab Plant Resources & Chem Arid Zone, 40-1 Beijing Rd, Urumqi 830011, Xinjiang, Peoples R China
2.Chinese Acad Sci, Xinjiang Tech Inst Phys & Chem, State Key Lab Basis Xinjiang Indigenous Med Plant, 40-1 Beijing Rd, Urumqi 830011, Xinjiang, Peoples R China
3.Univ Chinese Acad Sci, 19 A Yuquan Rd, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Edirs, S ,Jiang, L ,Xin, XL ,et al. Anti-diabetic effect and mechanism of Kursi Wufarikun Ziyabit in L6 rat skeletal muscle cells[J]. JOURNAL OF PHARMACOLOGICAL SCIENCES,2018,137(2):212-219.
APA Edirs, S ,Jiang, L ,Xin, XL ,&Aisa, HA .(2018).Anti-diabetic effect and mechanism of Kursi Wufarikun Ziyabit in L6 rat skeletal muscle cells.JOURNAL OF PHARMACOLOGICAL SCIENCES,137(2),212-219.
MLA Edirs, S ,et al."Anti-diabetic effect and mechanism of Kursi Wufarikun Ziyabit in L6 rat skeletal muscle cells".JOURNAL OF PHARMACOLOGICAL SCIENCES 137.2(2018):212-219.

入库方式: OAI收割

来源:新疆理化技术研究所

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