TY - JOUR
T1 - APS could potentially activate hepatic insulin signaling in HFD-induced IR mice
AU - Sun, Jie
AU - Liu, Yan
AU - Yu, Jinhui
AU - Wu, Jin
AU - Gao, Wenting
AU - Ran, Liyuan
AU - Jiang, Rujiao
AU - Guo, Meihua
AU - Han, Dongyu
AU - Liu, Bo
AU - Wang, Ning
AU - Li, Youwei
AU - Huang, He
AU - Zeng, Li
AU - Gao, Ying
AU - Li, Xin
AU - Wu, Yingjie
N1 - Funding Information:
This work was supported by the Ministry of Science and Technology of China (Grant No. 2014DFA32120), the National Science Foundation of China (Grant No. 81471000, 31871163) and the Natural Science Foundation of Liaoning (Grant No. 2014023042) to Y W, the National Science Foundation of China (Grant No. 81600668) to L R.
Publisher Copyright:
© 2019 Society for Endocrinology Published by Bioscientifica Ltd. Printed in Great Britain.
PY - 2019/7
Y1 - 2019/7
N2 - Astragalus polysaccharide (APS) is the main component of Astragalus membranaceus, an anti-diabetic herb being used for thousands of years in Traditional Chinese medicine (TCM). In this study, we aimed to evaluate the impact of APS on hepatic insulin signaling, autophagy and ER stress response in high-fat-diet (HFD)-induced insulin resistance (IR) mice. APS was intra-gastrically administrated and metformin was used as a control medicine. Apart from monitoring the changes in the important parameters of IR progression, the gene and protein expression of the key factors marking the state of hepatic ER stress and autophagic flux were examined. We found th at, largely comparable to the metformin regime, APS treatment resulted in an overall i mprovement of IR, as indicated by better control of body weight and blood glucose/lipid levels, recovery of liver functions and regained insulin sensitivity. In particular, the excessive and proapoptotic ER stress response and inhibition of autophagy, as a result of prolonged HFD exposure, were significantly corrected by APS administration, indicating a switch of the cellular fate in favor of cell survival. Using the HepG2/IR cel l model, we demonstrated that APS modulated the insulin-initiated phosphorylation cascades in a similar manner to metformin. This study provides a rationale for exploiting the insulin-sensitizing potential of APS, which has a therapeutic performance almost equivalent to metformin, to enrich our options in the treatment of IR.
AB - Astragalus polysaccharide (APS) is the main component of Astragalus membranaceus, an anti-diabetic herb being used for thousands of years in Traditional Chinese medicine (TCM). In this study, we aimed to evaluate the impact of APS on hepatic insulin signaling, autophagy and ER stress response in high-fat-diet (HFD)-induced insulin resistance (IR) mice. APS was intra-gastrically administrated and metformin was used as a control medicine. Apart from monitoring the changes in the important parameters of IR progression, the gene and protein expression of the key factors marking the state of hepatic ER stress and autophagic flux were examined. We found th at, largely comparable to the metformin regime, APS treatment resulted in an overall i mprovement of IR, as indicated by better control of body weight and blood glucose/lipid levels, recovery of liver functions and regained insulin sensitivity. In particular, the excessive and proapoptotic ER stress response and inhibition of autophagy, as a result of prolonged HFD exposure, were significantly corrected by APS administration, indicating a switch of the cellular fate in favor of cell survival. Using the HepG2/IR cel l model, we demonstrated that APS modulated the insulin-initiated phosphorylation cascades in a similar manner to metformin. This study provides a rationale for exploiting the insulin-sensitizing potential of APS, which has a therapeutic performance almost equivalent to metformin, to enrich our options in the treatment of IR.
KW - Astragalus polysaccharide
KW - Autophagy
KW - Endoplasmic reticulum stress
KW - Insulin resistance
KW - Liver
KW - Traditional Chinese medicine
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U2 - 10.1530/JME-19-0035
DO - 10.1530/JME-19-0035
M3 - Article
C2 - 31137008
AN - SCOPUS:85073340628
SN - 0952-5041
VL - 63
SP - 77
EP - 91
JO - Journal of Molecular Endocrinology
JF - Journal of Molecular Endocrinology
IS - 1
ER -