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Retracted : Salidroside from Rhodiola wallichiana var. cholaensis reverses insulin resistance and stimulates the GLP‐1 secretion by alleviating ROS‐mediated activation of MAPKs signaling pathway and mitigating apoptosis
Author(s) -
Yan Tingxu,
Nian Tingting,
Li Fuyuan,
He Bosai,
Jia Ying,
Bi Kaishun,
Wang Zhenzhong
Publication year - 2020
Publication title -
journal of food biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.507
H-Index - 47
eISSN - 1745-4514
pISSN - 0145-8884
DOI - 10.1111/jfbc.13446
Subject(s) - salidroside , p38 mitogen activated protein kinases , pi3k/akt/mtor pathway , mapk/erk pathway , insulin resistance , signal transduction , chemistry , reactive oxygen species , phosphorylation , apoptosis , microbiology and biotechnology , insulin , biochemistry , biology , endocrinology , chromatography
The present study was aimed to investigate the mechanisms of salidroside (SAL) from Rhodiola wallichiana var. cholaensis on hypoglycemic and oxidative stress responses. The palmitate (PA)‐induced GLUTag cells model and the glucosamine‐induced insulin resistance model in HepG2 cells were built. SAL led to the up‐regulation of the serum glucagon‐like peptide 1 (GLP‐1) level by facilitating the SCFAs production, the promotion of GLP‐1 synthesis by improving p38 MAPK phosphorylation and regulating insulin resistance. Moreover, the production of reactive oxygen species (ROS) and the expression of MAPKs were down‐regulated. Furthermore, SAL was found to be able to inhibit PA‐induced apoptosis that down‐regulates cleaved caspase‐3 and Bax expressions, while up‐regulating Bcl‐2 expression and up‐regulates the Bcl‐2/Bax ratio in glucosamine induced insulin resistance model. Besides, SAL can also up‐regulate the mTOR/p70S6k signaling pathway in the PA‐induced GLUTag cells model. Our data demonstrated that SAL could reverse insulin resistance and stimulates the GLP‐1 secretion by alleviating ROS‐mediated activation of MAPKs signaling pathway and mitigating apoptosis. Practical applications Our data showed that SAL could increase the GLP‐1 level by stimulating the SCFAs production and p38 phosphorylation and facilitate the IR and GLP‐1 synthesis by alleviating ROS‐mediated activation of MAPKs signaling pathway and mitigating apoptosis. Furthermore, the SAL has also stimulated the mTOR/p70S6k signaling pathway in PA‐induced GLUTag cells model. The results provided a possibility to employ SAL for diabetes treatment.