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黄芪多糖对3T3-L1前脂肪细胞增殖与分化的影响

[Effects of Astragalus polysaccharides on proliferation and differentiation of 3T3-L1 preadipocytes].

作者信息

Liu Yi, Wang Wen-jian, Chen Wei-hua, Yin Jian

机构信息

Institute of Chinese Integrative Medicine, Fudan University, Shanghai 200040, China.

出版信息

Zhong Xi Yi Jie He Xue Bao. 2007 Jul;5(4):421-6. doi: 10.3736/jcim20070412.

Abstract

OBJECTIVE

To observe the effects of Astragalus polysaccharides (APS) on the proliferation and differentiation of 3T3-L1 preadipocytes and to elucidate its possible mechanism.

METHODS

The proliferation of 3T3-L1 preadipocytes was detected by XTT method. Lipid droplets accumulated in cytoplasm of the differentiated preadipocytes were observed by using red O staining and quantified by colorimetry. The expressions of peroxisome proliferation activated receptor gamma (PPAR gamma) and CAAT/enhancer binding protein (C/EBP alpha) mRNAs and proteins were detected by real-time polymerase chain reaction (RT-PCR) and Western blotting respectively.

RESULTS

APS at different concentrations (0.025-0.8 g/L) affected 3T3-L1 preadipocyte proliferation and differentiation dose-dependently. 3T3-L1 preadipocytes treated with 0.4 g/L APS had lots of lipid droplets in the cytoplasma, which were similar to cells treated with rosiglitazone (ROS). APS significantly increased the mRNA and protein expressions of PPAR gamma and C/EBP alpha (P<0.05, P<0.01, compared with the normal control group) in the course of 3T3-LI preadipocyte differentiation.

CONCLUSION

APS can promote the proliferation of 3T3-L1 preadipocytes, enhance the accumulation of lipid drops, and increase the terminal differentiation of preadipocytes, which may be associated with its effects in increasing the expressions of PPAR gamma and C/EBP alpha mRNAs and proteins. The study suggests that APS has potential in the treatment of metabolic syndrome.

摘要

目的

观察黄芪多糖(APS)对3T3-L1前脂肪细胞增殖与分化的影响,并阐明其可能机制。

方法

采用XTT法检测3T3-L1前脂肪细胞的增殖情况。用油红O染色观察分化的前脂肪细胞胞质内脂滴的积聚情况,并通过比色法进行定量分析。分别采用实时聚合酶链反应(RT-PCR)和蛋白质印迹法检测过氧化物酶体增殖物激活受体γ(PPARγ)和CCAAT/增强子结合蛋白(C/EBPα)mRNA及蛋白的表达。

结果

不同浓度(0.025 - 0.8 g/L)的APS对3T3-L1前脂肪细胞的增殖和分化具有剂量依赖性影响。用0.4 g/L APS处理的3T3-L1前脂肪细胞胞质内有大量脂滴,与用罗格列酮(ROS)处理的细胞相似。在3T3-L1前脂肪细胞分化过程中,APS显著增加了PPARγ和C/EBPα的mRNA及蛋白表达(与正常对照组相比,P<0.05,P<0.01)。

结论

APS可促进3T3-L1前脂肪细胞的增殖,增强脂滴的积累,并增加前脂肪细胞的终末分化,这可能与其增加PPARγ和C/EBPα mRNA及蛋白表达的作用有关。该研究提示APS在代谢综合征的治疗中具有潜在应用价值。

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