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首页> 外文期刊>International journal of molecular medicine >Genistein attenuates di-(2-ethylhexyl) phthalate-induced testicular injuries via activation of Nrf2/HO-1 following prepubertal exposure
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Genistein attenuates di-(2-ethylhexyl) phthalate-induced testicular injuries via activation of Nrf2/HO-1 following prepubertal exposure

机译:Genistein通过预先暴露后的NRF2 / HO-1激活衰减二甲酸酯诱导的睾丸损伤

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摘要

Di-(2-ethylhexyl) phthalate (DEHP) and genistein (GEN) are of the most common endocrine disrupting chemicals (EDCs) present in the environment or the diet. However, investigation of the effects of acute exposure to these two EDCs during prepuberty has been lacking. In this study, DEHP and GEN were administrated to prepubertal male Sprague-Dawley rats by gavage from PND22 to PND35 with vehicle control, GEN 50 mg/kg body weight (bw)/day, DEHP50, 150 and 450 mg/kg bw/day, and combined treatment. Reproductive parameters including testis weight, anogenital distance and organ coefficient were evaluated on PND36. Enzyme activity involved in the regulation of testicular redox state as well as expression of genes and proteins related to anti-oxidative ability and apoptosis were also investigated. The results revealed that by PND36, DEHP treatment had significantly decreased the testis weight, organ coefficient, testicular anti-oxidative enzyme activities and caused tubular vacuolation; however, co-administration of GEN partially alleviated DEHP-induced testicular injuries and enhanced testicular anti-oxidative enzyme activities and upregulated the expression of NF-E2 related factor 2 and heme oxygenase-1, which indicated that GEN partially attenuated DEHP-induced male reproductive system damage through anti-oxidative action following acute prepubertal exposure to DEHP. Thus, GEN may have use in attenuating the damaging effects of other EDCs that lead to reproductive disorders.
机译:邻苯二甲酸二(2-乙基己基)和Genistein(Gen)是在环境或饮食中存在的最常见的内分泌破坏化学物质(EDC)。然而,缺乏对急性暴露对这两种EDC的影响的调查。在本研究中,DeHP和Gen通过从PND22到PND35的PND22给予Phubbertal雄性Sprague-Dawley大鼠,载体控制,Gen 50mg / kg体重(BW)/日,DEHP50,150和450 mg / kg BW /天和组合治疗。在PND36中评估了包括睾丸重量,胃部距离和器官系数的生殖参数。还研究了参与睾丸氧化还原状态的调节的酶活性以及与抗氧化能力和凋亡相关的基因和蛋白质的表达。结果表明,通过PND36,DEHP处理显着降低了睾丸重量,器官系数,睾丸抗氧化酶活性并引起管状真空;但是,共同施用基因部分缓解了Dehp诱导的睾丸损伤和增强的睾丸抗氧化酶活性,并上调了NF-E2相关因子2和血红素氧酶-1的表达,这表明Gen部分减弱了Dehp诱导的雄性生殖通过急性预接种暴露在DeHP后通过抗氧化作用造成的系统损伤。因此,Gen可用于衰减导致生殖障碍的其他EDC的破坏性效果。

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