癌变·畸变·突变 ›› 2010, Vol. 22 ›› Issue (2): 104-107.doi: 10.3969/j.issn.1004-616x.2010.02.006

• 论著 • 上一篇    下一篇

DEHP及MEHP对小鼠卵巢颗粒细胞分泌功能的影响

马明月;张玉敏;裴秀丛;段志文;王旭   

  1. 沈阳医学院毒理学教研室,辽宁 沈阳110034
  • 收稿日期:2009-10-19 修回日期:2009-11-18 出版日期:2010-03-30 发布日期:2010-03-30
  • 通讯作者: 马明月

Effects of di(2-ethylhexyl) phthalate and mono(2-ethyl- hexyl) phthalate on ovarian granulosa cells in mice

MA Ming-yue, ZHANG Yu-min, PEI Xiu-cong, DUAN Zhi-wen,WANG Xu   

  1. Department of Toxicology, Shenyang Medical College, Shenyang 110034, Liaoning, China
  • Received:2009-10-19 Revised:2009-11-18 Online:2010-03-30 Published:2010-03-30
  • Contact: MA Ming-yue

摘要: 目的: 研究邻苯二甲酸二(2-乙基)己酯(DEHP)及其活性中间产物邻苯二甲酸单(2-乙基)己酯(MEHP)对卵巢颗粒细胞及其激素合成、分泌功能的影响。 方法: 体外培养健康初断乳ICR小鼠的卵巢颗粒细胞,分别加入DEHP(10、 50、 250 nmol/L),MEHP (10、 50、 250 nmol/L)和溶剂对照 (DMSO),作用细胞24 h。用RT-PCR法测定原代小鼠颗粒细胞中类固醇激素合成急性调节蛋白(StAR)和P450侧链裂解酶 (P450scc)mRNA水平;用Real time-PCR法测定原代小鼠颗粒细胞中芳香化酶 (CYP19)和过氧化物酶体增殖剂激活受体(PPARα、PPARβ、PPARγ) mRNA水平;用酶联免疫法 (EIA)检测卵巢颗粒细胞上清液中雌二醇和孕酮的水平。 结果: 与对照组比较,250 nmol/L MEHP抑制StAR基因及P450scc基因表达(P均<0.05);250 nmol/L DEHP对CYP19基因表达有促进作用(P<0.05); 而10、50 nmol/L DEHP及50、250 nmol/L MEHP对CYP19基因表达均有抑制作用(P<0.05)。 除10 nmol/L DEHP外, DEHP及MEHP其它浓度组均能抑制PPARα、PPARβ基因的表达(P<0.05);10 nmol/L DEHP及MEHP对PPARγ基因表达有促进作用(P<0.05), 而250 nmol/L MEHP对PPARγ基因表达有抑制作用(P<0.05)。各剂量DEHP及MEHP均能使颗粒细胞分泌雌二醇增加(P<0.05),10 nmol/L DEHP、50及250 nmol/L MEHP抑制颗粒细胞分泌孕酮 (P<0.05)。 结论: DEHP及MEHP影响颗粒细胞类固醇激素合成酶、PPARs的基因表达及分泌功能。

关键词: 生殖毒性, 邻苯二甲酸二(2-乙基)己酯, 甲苯二甲酸单(2-乙基)己酯, 卵巢颗粒细胞

Abstract: OBJECTIVE: To investigate the effects of di(2-ethylhexyl) phthalate (DEHP) and its active metabolite, mono(2-ethylhexyl) phthalate (MEHP) on ovarian granulosa cells. METHODS: ICR mice ages at the 21 days were used by subcutaneous injection PMSG. The ovarian granulosa cells were collected and cultured in DMEM-F12. After the ovarian granulosa cells were prepared, cells were exposed to doses of 10, 50, 250 nmol/L DEHP and 10, 50, 250 nmol/L MEHP for 24 h. The mRNA levels of StAR, P450scc were determined by RT-PCR. The mRNA levels of CYP19, PPARα, PPARβ, PPARγ were determined by Real time RT-PCR. Estradiol and progesterone were measured by enzyme immunoassay (EIA) in ovarian granulosa cell. RESULTS: 250 nmol/L MEHP group decreased the gene expression of StAR and P450scc (P<0.05); 250 nmol/L DEHP group increased the gene expression of CYP19, but 10, 50 nmol/L DEHP and 50, 250 nmol/L MEHP groups decreased the gene expression of CYP19 (P<0.05). Except 10 nmol/L DEHP group, DEHP and MEHP decreased the gene expression of PPARα and PPARβ (P<0.05). 10 nmol/L DEHP and MEHP groups increased the gene expression of PPARγ, but 250 nmol/L MEHP group decreased the gene expression of PPARγ (P<0.05). DEHP and MEHP enhanced the concentration of estradiol at all dose groups, but 10 nmol/L DEHP, 50 and 250 nmol/L MEHP groups decreased the concentration of progesterone in ovarian granulosa cells (P<0.05). CONCLUSION: DEHP and MEHP could affect the gene expression of steroid biosynthesis enzymes, PPARs, and the secretory function in ovarian granulosa cells.

Key words: reproductive toxicity, di(2-ethylhexyl) phthalate, mono(2-ethylhexyl) phthalate, ovarian granulosa cells

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