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邻苯二甲酸二(2-乙基)己酯通过基因甲基化途径诱导睾丸损伤及大豆异黄酮对 Sprague-Dawley 大鼠的保护作用。

DEHP-induced testicular injury through gene methylation pathway and the protective effect of soybean isoflavones in Sprague-Dawley rats.

机构信息

Department of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, PR China.

Department of Urology, Institute of Urology, West China Hospital, Sichuan University, Chengdu, 610041, Sichuan, PR China; Department of Urology, Shenzheng Hospital, Southern Medical University, Shenzheng, 518110, PR China.

出版信息

Chem Biol Interact. 2021 Oct 1;348:109569. doi: 10.1016/j.cbi.2021.109569. Epub 2021 Jun 29.

Abstract

As one of the most important members of Phthalate esters (PAEs), di-(2-ethylhexyl) phthalate (DEHP) is widely used in plastics and known as a male reproductive toxicant. Many studies have shown that soybean isoflavones (SI) can rescue the testicular injury caused by DEHP, but the underlying mechanism is unknown. Because methylation is one of the most important mechanisms for maintaining normal biological functions, we studied whether methylation is involved in testicular injury induced by DEHP and whether SI could counter testicular impairment in peripubertal male Sprague Dawley rats. Compared with the control group, we found that the mRNA levels of testicular Sod2, Gpx1, and Igf-1 significantly decreased in the 900 mg/kg DEHP group (DEHP' group) (P < 0.01); however, in the DEHP + SI group, the mRNA levels of the genes obviously increased compared with the DEHP' group (P < 0.01). Simultaneously, the methylation level changes of testicular Sod2, Gpx1, and Igf-1 were similar to the mRNA levels (P < 0.01). Therefore, DEHP may affect testis and leydig cells via inducing methylation of Sod2, Gpx1, and Igf-1, and SI may rescue the impairments at the methylation level. In summary, SI is supposed to be used in DEHP-induced testicular injury treatment.

摘要

作为邻苯二甲酸酯(PAEs)中最重要的成员之一,邻苯二甲酸二(2-乙基己基)酯(DEHP)广泛应用于塑料行业,被认为是一种雄性生殖毒物。许多研究表明,大豆异黄酮(SI)可以挽救 DEHP 引起的睾丸损伤,但具体机制尚不清楚。因为甲基化是维持正常生物功能的最重要机制之一,所以我们研究了 DEHP 引起的睾丸损伤是否涉及甲基化,以及 SI 是否可以拮抗青春期前雄性 Sprague Dawley 大鼠的睾丸损伤。与对照组相比,我们发现 900mg/kg DEHP 组(DEHP'组)睾丸 Sod2、Gpx1 和 Igf-1 的 mRNA 水平明显降低(P<0.01);然而,在 DEHP+SI 组中,与 DEHP'组相比,这些基因的 mRNA 水平明显增加(P<0.01)。同时,睾丸 Sod2、Gpx1 和 Igf-1 的甲基化水平变化与 mRNA 水平相似(P<0.01)。因此,DEHP 可能通过诱导 Sod2、Gpx1 和 Igf-1 的甲基化来影响睾丸和 Leydig 细胞,SI 可能在甲基化水平上挽救损伤。总之,SI 有望用于 DEHP 诱导的睾丸损伤治疗。

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