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大豆异黄酮对HepG2细胞胆固醇代谢的作用及其机制 被引量:3

Effect and Mechanism of Soy Isoflavones in Improving Cholesterol Metabolism in HepG2 Cells
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摘要 目的:对大豆异黄酮降低胆固醇作用及其机制进行探讨,并比较金雀异黄素(Gen),大豆素(Dai)和雌马酚(Eq)的作用强弱。方法:采用MTT检测细胞增殖状况,采用试剂盒检测LDL-C、TC和apoA-I的表达,采用实时定量PCR检测mRNA的表达。结果:大豆异黄酮可以增加细胞内胆固醇含量,增加LDL-C的摄取量和apoA-I的分泌量,其中Gen的作用最为明显,Eq的作用较弱。PPARγ和LXRα的mRNA表达量增多。结论:大豆异黄酮能够调节细胞胆固醇代谢,其作用可能是通过调节PPARγ/LXRα通路实现的。 【Objective】To explore the effect of soy isoflavones on cholesterol metabolism in HepG2 cells and the possible mechanism of it and to compare the strength of Gen,Dai,and Eq.【Method】The proliferation of HepG2 cell was by MTT,the measurement of LDL-C and TC content was by the kit,the apoA-I content was by Elisa kit,and the measurement of mRNA was by real time PCR.【Result】Soy isoflavones could increase the cellular cholesterol content,LDL-C uptake and apoA-I secretion.Gen had the strongest effect and Eq had the weakest.The mRNA expression of PPARγ and LXRα was increased.【Conclusion】Soy isoflavones could affect cholesterol metabolism and it was maybe through the PPARγ/LXRα pathway.
出处 《中国食物与营养》 2011年第11期66-69,共4页 Food and Nutrition in China
基金 国家自然科学基金(项目编号:30671759 30872114 30872115)
关键词 大豆异黄酮 胆固醇 PPARΓ LXRΑ soy isoflavones cholesterol metabolism PPARγ LXRα
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  • 1张玉梅,季莉莉.高含量大豆异黄酮对高脂大鼠的降血脂作用[J].中国预防医学杂志,2005,6(1):1-4. 被引量:18
  • 2杨功焕,王俊芳,万霞,王黎君,陈爱平.影响中国人群疾病死亡因素的定量分析[J].中华流行病学杂志,2005,26(12):934-938. 被引量:83
  • 3毛光明,陈江,夏勇,华炜,鹿伟.大豆异黄酮对大鼠脂质的影响及减肥作用研究[J].浙江预防医学,2007,19(7):10-11. 被引量:9
  • 4Hampl R,Ostatnikova D,Celec P,et al.Short-term effect of soyconsumption on thyroid hormone levels and correlation with phytoestrogen level in healthy subjects [J] .Endocr Regul, 2008, 42(2-3) :53-61.
  • 5Lu LJ, Anderson KE, Grady JJ, et al.Decreased ovarian hormones during a soya diet:implications for breast cancer prevention [ J ] .Cancer Res, 2000,60( 15 ) : 4112-4121.
  • 6Horton JD,Shah NA,Warrington JA,et al.Combined analysis of oligonucleotide microarray data from transgenic and knockout mice identifies direct SREBP target genes [J].Proc Natl Acad Sci, 2003,100(21 ) : 12027-12032.
  • 7Gomez-Lechon MJ, Donato MT, Martinez-Romero A, et al.A human hepatocellular in vitro model to investigate steatosis [J]. Chem Biol Interact, 2007,165 (2) : 106-116.
  • 8Karaskov E,Scott C,Zhang L,et al.Chronic palmitate but not oleate exposure induces endoplasmic reticulum stress, which may contribute to INS-1 pancreatic beta-cell apoptosis [J]. Endocrinology, 2006,147 ( 7 ) : 3398-3407.
  • 9Cui W,Chen SL,Hu KQ.Quantification and mechanisms of oleic acid-induced steatosis in HepG2 cells[J]. Am J Transl Res, 2010,2( 1 ) : 95-104.
  • 10Cousin SP,Htlgl SR,Wrede CE,et al.Free fatty acid-induced inhibition of glucose and insulin-like growth factor I-induced deoxyribonucleic acid synthesis in the pancreatic beta-cell line INS- 1 [ J ] .Endocrinology, 2001,142 ( 1 ) : 229-240.

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