基础医学与临床 ›› 2016, Vol. 36 ›› Issue (2): 232-236.

• 研究论文 • 上一篇    下一篇

硫化氢抑制小鼠胰岛素抵抗3T3-L1脂肪细胞株抵抗素的分泌

郝丹丹1,张垒2,刘俊3,张凤宁4,瑞云4   

  1. 1. 赤峰学院
    2. 赤峰学院医学院附属医院
    3. 复旦大学 上海医学院
    4. 赤峰学院医学院
  • 收稿日期:2015-09-21 修回日期:2015-12-07 出版日期:2016-02-05 发布日期:2016-01-21
  • 通讯作者: 郝丹丹 E-mail:hdd2011yx@163.com

H2S inhibits resistin secretion in mouse insulin-resistant 3T3-L1 adipocytes

  • Received:2015-09-21 Revised:2015-12-07 Online:2016-02-05 Published:2016-01-21

摘要: 目的 观察硫化氢(H2S)是否通过AMPK信号通路影响小鼠胰岛素抵抗3T3-L1脂肪细胞株抵抗素的分泌。方法 将细胞分为对照组、胰岛素抵抗3T3-L1组和50 μmol/L NaHS组,利用ELISA法检测抵抗素(resistin)的分泌,Western blot检测AMP激活的蛋白激酶(AMPK)及乙酰辅酶A羧化酶(ACC)磷酸化蛋白的表达,实时荧光定量PCR(RT-PCR)检测resistin及AMPK mRNA表达。结果 与对照组比较,给予NaHS后抵抗素分泌明显降低(P<0.05)。正常和胰岛素抵抗细胞中AMPK和ACC磷酸化蛋白表达显著增加(P<0.05)。AMPK通路特异性阻断剂compound C可减弱NaHS对AMPK及ACC蛋白磷酸化的作用,且降低正常和胰岛素抵抗细胞抵抗素的分泌。结论 H2S可能通过激活AMPK通路来抑制小鼠正常和胰岛素抵抗3T3-L1脂肪细胞的抵抗素分泌。

关键词: 硫化氢, AMP蛋白激酶, 3T3-L1脂肪细胞, 抵抗素

Abstract: Objective To investigate whether H2S can inhibit resistin secretion in mouse insulin-resistant 3T3-L1 adipocytes via activation of amp-activated protein kinase. Methods The cells were divided into the normal groups, the insulin resistance groups and the 50 umol/L NaHS treatmen tgroups. The ELISA method was used to analyze the level of resistin secretion, Western blot was used to analyze the expression of activated protein kinase (AMPK) and acetyl coenzyme A carboxylase enzyme (ACC) phosphorylation protein and RT-PCR was performed to analyzed the expression of resistin mRNA and AMPK mRNA. Results The effects of NaHS significantly decreased the secretion level of resistin compared with the control group(P<0.05). The expression of AMPK and ACC protein phosphorylation in normal and insulin resistant cells significantly increased(P<0.05). The AMPK pathway inhibitor compound C markly weakened the effects on AMPK and ACC protein phosphorylation. At the same time, the secretion level of resistin was inhibited. Conclusion Hydrogen sulflide may inhibits resistin secretion in mouse insulin-resistant 3T3-L1 adipocytes via activation of AMP-activated protein kinase.

Key words: hydrogen sulfide, amp-activated protein kinase, 3T3-L1 adipocytes, resistin

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