癌变·畸变·突变 ›› 2016, Vol. 28 ›› Issue (1): 46-50,55.doi: 10.3969/j.issn.1004-616x.2016.01.010

• 论著 • 上一篇    下一篇

高脂诱导BRL-3A细胞胰岛素抵抗模型的建立

金磊, 王帅, 王欣, 海春旭, 李文丽   

  1. 第四军医大学军事预防医学院毒理学教研室, 陕西省自由基生物学与医学重点实验室, 陕西 西安 710032
  • 收稿日期:2015-07-03 修回日期:2015-12-16 出版日期:2016-01-31 发布日期:2016-01-31
  • 通讯作者: 李文丽,E-mail:liwenli@fmmu.edu.cn E-mail:liwenli@fmmu.edu.cn
  • 作者简介:金磊,E-mail:kingleer001@163.com。
  • 基金资助:
    国家自然科学基金(31170807)

Induction of insulin resistance by palmitic acid in BRL-3A cells

JIN Lei, WANG Shuai, WANG Xin, HAI Chunxu, LI Wenli   

  1. Shaanxi Key Lab of Free Radical Biology and Medicine, Department of Toxicology, School of Preventive Medicine, Fourth Military Medical University, Xi'an 710032, Shaanxi, China
  • Received:2015-07-03 Revised:2015-12-16 Online:2016-01-31 Published:2016-01-31

摘要: 目的: 采用棕榈酸(PA)诱导BRL-3A细胞,建立肝细胞胰岛素抵抗体外模型。方法: 分别用不同浓度(0、50、100、200、300、400 μmol/L)棕榈酸处理BRL-3A细胞不同时间(6、12、24 h)后,检测细胞生存率、基础葡萄糖消耗及胰岛素刺激葡萄糖消耗的变化。结果: 高浓度PA(200、300、400 μmol/L)使细胞生存率显著降低(P<0.05);低浓度PA(50、100 μmol/L)短时间(6和12 h)作用对细胞生存率无明显影响(P>0.05);不同浓度PA短时间(6 h)作用于细胞,其基础葡萄糖消耗及胰岛素刺激葡萄糖消耗与正常组相比无显著变化(P>0.05),作用24 h后细胞葡萄糖消耗量均明显下降(P<0.05),100 μmol/L的PA处理12 h可降低细胞基础葡萄糖消耗及胰岛素刺激的葡萄糖消耗量(P<0.05),且在继续培养至72 h摄糖能力无明显改变。结论: 100 μmol/L的PA作用12 h可诱导BRL-3A细胞产生胰岛素抵抗。

关键词: 棕榈酸, 胰岛素抵抗, 葡萄糖消耗, 葡萄糖氧化酶法

Abstract: OBJECTIVE: To investigate an insulin resistance in BRL-3A cells after their exposure to palmitic acid (PA). METHODS: BRL-3A cells were incubated with PA (0,50,100,200,300,400 μmol/L) for 6,12 or 24 hours. After the exposure,cell viability,basic and insulin-stimulated glucose consumption were assayed. RESULTS: Incubation of cells with high concentrations of PA (200,300,400 μmol/L) significantly decreased survival of cells (P<0.05). Incubation of cells with low concentrations of PA (50,100 μmol/L) for 6 and 12 h had no significant effect on cell viability (P>0.05). The basic and insulin-stimulated glucose consumption in these cells were not altered by different concentration of PA incubation for 6 h (P>0.05). However,24 h after the exposure,all concentrations of PA decreased glucose consumption (P<0.05). At 12 h after the exposure,100 μmol/L of PA decreased basic and insulin-stimulated glucose consumption (P<0.05),and this ability remained unchanged after 72 h of continuing cultured. CONCLUSION: Incubation of BRL-3A cells with 100 μmol/L of PA for 12 h could induce insulin resistance in vitro.

Key words: palmitic acid, insulin resistance, glucose consumption, glucose oxidase peroxidase

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