Astragalus Polysaccharide Improves Insulin Sensitivity via AMPK Activation in 3T3-L1 Adipocytes

polysaccharide (APS) is an important bioactive component of which is used as an anti-diabetes herb in traditional Chinese medicine. The objective of this study was to investigate the effects and mechanisms of APS on insulin-sensitizing of adipocytes. Mouse 3T3-L1 preadipocytes were used as a model....

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2018-10, Vol.23 (10), p.2711
Hauptverfasser: Zhang, Ruixin, Qin, Xuze, Zhang, Ting, Li, Qian, Zhang, Jianxin, Zhao, Junxing
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Sprache:eng
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Zusammenfassung:polysaccharide (APS) is an important bioactive component of which is used as an anti-diabetes herb in traditional Chinese medicine. The objective of this study was to investigate the effects and mechanisms of APS on insulin-sensitizing of adipocytes. Mouse 3T3-L1 preadipocytes were used as a model. The results showed that APS increased preadipocytes proliferation in a dose dependent manner, and 0.1 μg/mL APS sufficiently increased Proliferating Cell Nuclear Antigen (PCNA) content ( < 0.01). Moreover, APS enhanced intracellular lipid accumulation and mRNA expression of proliferator-activated receptor γ (PPARγ, < 0.01), CCAAT/enhancer binding protein α (C/EBPα, < 0.01) and fatty acid binding protein ( P2, < 0.01). As expected, corresponding protein contents were elevated. Importantly, APS increased 2-( -(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)Amino)-2-Deoxyglucose (2-NBDG) uptake ( < 0.01). Meanwhile, both mRNA and protein content of glucose transporter 4 (Glut4) were elevated by APS ( < 0.01). The APS treatment enhanced tyrosine phosphorylation of insulin receptor substrate 1 (IRS1, < 0.05) and phosphor-Akt content ( < 0.01). Besides, phosphorylated AMP-activated protein kinase (AMPK) content was increased in the APS treated cells ( < 0.01). Taken together, APS improved insulin sensitivity by enhancing glucose uptake, possibly through AMPK activation. These results suggested that APS might be a therapeutic candidate for insulin resistance.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules23102711