Effect of Astragalus polysaccharides and berberine on carbohydrate metabolism and cell differentiation in 3T3-L1 adipocytes.
- Author:
Shu-hai WANG
1
;
Wen-jian WANG
;
Xue-feng WANG
;
Weihua CHEN
Author Information
- Publication Type:Journal Article
- MeSH: 3T3-L1 Cells; Adipocytes; cytology; metabolism; Animals; Astragalus Plant; chemistry; Berberine; pharmacology; CCAAT-Enhancer-Binding Protein-alpha; biosynthesis; genetics; Cell Differentiation; drug effects; Cell Division; drug effects; Drugs, Chinese Herbal; chemistry; pharmacology; Glucose; metabolism; Mice; PPAR gamma; biosynthesis; genetics; Polysaccharides; pharmacology; RNA, Messenger; genetics; metabolism
- From: Chinese Journal of Integrated Traditional and Western Medicine 2004;24(10):926-928
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo compare the effects of Astragalus polysaccharides (AP) and berberine (BB) on the adipocyte's carbohydrate metabolism and cell differentiation, for assessing the possible mechanism of them in improving carbohydrate metabolism.
METHODSAdipocytes were treated with AP or BE, the 3H-glucose up-take rate in them was investigated, those of differentiation phase were stained by oil red O to analyze the degree of cell differentiation by spectrophotography quantitatively. The adipocyte differentiation related expression of PPARgamma mRNA and C/EBPalpha mRNA were determined by RT-PCR.
RESULTSThe 3H-glucose up-take rate in the AP group and BE group were 109.3% and 182.7% of that in the blank control group respectively. AP obviously promoted the cell differentiation and up-regulated expression of PPARgamma mRNA, while BE suppressed the differentiation and expression of PPARgamma and C/EBPalpha mRNA distinctly, all showing significant difference as compared with that in the blank control (P<0.01).
CONCLUSIONAP could promote glucose up-take, cell differentiation and PPARgamma mRNA expression, BB also promote glucose up-take, but suppress the cell differentiation, and inhibit expressions of PPARgamma and C/EBPalpha mRNA in 3T3-L1 adipocytes.