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Aim: To examine the potential effects of Astragalus polysaccharide (APS) on hepatic endoplasmic reticulum (ER) stress in vivo and in vitro and its link with hypoglycemia activity, thus establishing the mechanism underlying the hypogly- cemic action of APS. Methods: The obese and type 2 diabetic KKAy mouse model, which is the yellow offspring of the KK mice expressed Ay2 gene (700 mg·kg-12-d-12, 8 weeks) and a high glucose-induced HepG2 cell model (200 μg/mL, 24 h) were treated with APS. The oral glucose tolerance test was measured to reflex insulin sensitivity with the calculated homeostasis model assessment (HOMA- IR) index. XBP1 (Xho1 site-binding protein 1) transcription and splicing, an indica- tor of ER stress, was analyzed by RT-PCR and real-time PCR. The expression and activation of glycogen synthase kinase 3 beta (GSK3β), an insulin signaling protein, was measured by Weste blotting. Results: APS can alleviate ER stress in cul- tured cells in vivo. The hyperglycemia status, systemic insulin sensitivity, fatty liver disease, and insulin action in the liver of diabetic mice were partly normalized or improved in response to APSadministration. Conclusion: Our results indicate that APS enables insulin-sensitizing and hypoglycemic activity at least in part by enhancing the adaptive capacity of the ER, which can further promote insulin signal transduction. Thus, APS has promising application in the treatment of type 2 diabetes.