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谭清, 姜雪霞, 贺真, 李耀福, 杨守林, 李丹, 白剑英. 邻苯二甲酸单乙基己基酯对HepG2细胞胆固醇代谢影响[J]. 中国公共卫生, 2021, 37(2): 298-302. DOI: 10.11847/zgggws1125827
引用本文: 谭清, 姜雪霞, 贺真, 李耀福, 杨守林, 李丹, 白剑英. 邻苯二甲酸单乙基己基酯对HepG2细胞胆固醇代谢影响[J]. 中国公共卫生, 2021, 37(2): 298-302. DOI: 10.11847/zgggws1125827
TAN Qing, JIANG Xue-xia, HE Zhen, . Effects of mono (2-ethylhexyl) phthalate on cholesterol metabolism in HepG2 cells[J]. Chinese Journal of Public Health, 2021, 37(2): 298-302. DOI: 10.11847/zgggws1125827
Citation: TAN Qing, JIANG Xue-xia, HE Zhen, . Effects of mono (2-ethylhexyl) phthalate on cholesterol metabolism in HepG2 cells[J]. Chinese Journal of Public Health, 2021, 37(2): 298-302. DOI: 10.11847/zgggws1125827

邻苯二甲酸单乙基己基酯对HepG2细胞胆固醇代谢影响

Effects of mono (2-ethylhexyl) phthalate on cholesterol metabolism in HepG2 cells

  • 摘要:
      目的  探讨邻苯二甲酸单乙基己基酯(MEHP)对肝细胞胆固醇代谢的影响,为了解MEHP的肝脏毒性作用机制提供依据。
      方法  分别以不同浓度MEHP、1 mmol/L油酸(OA)及完全培养基(阴性对照组)处理HepG2细胞24和48 h;用CHOD-PAP-POD法测定HepG2细胞内和培养上清中总胆固醇(TC)和游离胆固醇(FC)含量;采用免疫细胞化学法检测细胞核内固醇调节元件结合蛋白2(nSREBP-2)表达量;采用Western blot检测胆固醇代谢相关蛋白羟甲基戊二酸单酰辅酶A还原酶(HMGCR)、低密度脂蛋白受体(LDLR)和胆固醇酰基转移酶1(ACAT1)表达水平。
      结果  MEHP染毒24 h,与阴性对照组比较,100 μmol/L MEHP组细胞内FC含量(0.508 ± 0.069)mmol/g明显高于对照组(P < 0.05);与阴性对照组比较,各MEHP剂量组HepG2细胞中表征nSREBP-2蛋白表达水平的绿色荧光强度明显增加,阳性对照组HepG2细胞核内绿色荧光强度也明显增加。MEHP染毒48 h,细胞内FC含量恢复至正常水平(P > 0.05);免疫细胞化学结果显示,与阴性对照组比较,各MEHP剂量组HepG2细胞中nSREBP-2、HMGCR蛋白表达水平均明显降低(P < 0.05)。
      结论  MEHP对肝细胞胆固醇代谢具有一定的干扰作用,该作用是可逆的。

     

    Abstract:
      Objective  To investigate the effect of mono (2-ethylhexyl) phthalate (MEHP) on cholesterol content in hepatocytes and to provide evidences to researches on the mechanism of hepatic toxicity of MEHP.
      Methods  HepG2 cells were treated with MEHP at various dosages (0.8, 4.0, 20.0, and 100.0 μmol/L for intra-hepacellular and extra-hepacellular total cholesterol TC and free cholesterol FC test; 0.01, 1.00, 10.00, and 100.00 μmol/L for tests of endonuclear sterol regulatory element binding protein 2 SREBP-2 and cellular cholesterol metabolism-related proteins), Dulbecco′s modified Eagle′s medium (DMEM) as negative control and 1 mmol/L oleic acid (OA) for 24 and 48 hours, respectively. CHOD-PAP-POD enzymatic method was used to detect intra-hepacellular and extra-hepacellular TC and FC; the expression of SREBP-2 was measured with immunocytochemistry; protein expressions of hydroxymethylglutaryl coenzyme A reductase (HMGCR), low density lipoprotein receptor (LDLR) and cholesterol acyltransferase (ACAT1) were determined with Western blot.
      Results  After 24 hours′ treatment of 100 μmol/L MEHP, the intracellular FC (0.508 ± 0.069 mmol/g) was significantly higher than that of the negative control cells (P < 0.05); the endonuclear nSREBP-2 expressions increased obviously in all MEHP-treated cells and in positive control cells compared with that of the negative control cells. After 48 hours′ treatment, the intracellular FC returned to normal levels (P > 0.05); while, the intra-hepacellular expressions of nSREBP-2 and HMGCR decreased significantly in all MEHP exposed HepG2 cells in comparison with those in the negative control cells (all P < 0.05).
      Conclusion  MEHP has a certain interference effect on cholesterol metabolism in hepatocytes, but the effect is reversible.

     

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