The Second Clinical Medical School, Henan University of Chinese Medicine, Zhengzhou, China.
The First Affiliated Hospital of Henan University of Chinese Medicine, Zhengzhou, China.
Pharm Biol. 2022 Dec;60(1):1286-1302. doi: 10.1080/13880209.2022.2089694.
Di-2-ethylhexyl phthalate (DEHP), a known persistent organic pollutant, can increase the sperm DNA fragmentation index (DFI).
To investigate the mechanism underlying the repair of DEHP-induced sperm DNA damage in mice by Wuwei Fuzheng Yijing (WFY) formula.
The potential targets of WFY and sperm DNA fragment (SDF) were obtained from the TCMSP, BATMAN-TCM, OMIM and GeneCards. The protein-protein interaction (PPI) network, GO and KEGG pathway analyses of WFY-SDF were constructed. An animal model of DEHP-induced sperm DNA damage was replicated by gavage of SPF ICR (CD1) mice DEHP at 1 g/kg/d and treated with WFY at 8.92, 17.84 and 35.67 g/kg, respectively, for 60 d. Sperm DFI of each group was detected and compared. The target genes of WFY identified by transcriptomic and proteomic analyses were validated by qRT-PCR and Western blotting.
Network pharmacology pathway analysis indicated that PI3K/Akt was the potential target of WFY on SDF. The DFI of the DEHP group (25.48%) was significantly higher than that of the control group (4.02%). The high-dose WFY group (19.05%) exhibited the most significant repairing effect. The related pathways were PI3K/Akt and metabolic. Aass, Aldh1a7, GSTA3, betaine homocysteine -methyltransferase (Bhmt), Mug2 and Svs1 were screened and Bhmt was validated.
WFY can repair sperm DNA damage caused by DEHP, and the mechanism may be related to PI3K/Akt and metabolic pathways, and Bhmt. This provides a new direction for using traditional Chinese medicine to prevent and repair reproductive system injury caused by pollutants.
邻苯二甲酸二(2-乙基)己酯(DEHP)是一种已知的持久性有机污染物,可增加精子 DNA 碎片化指数(DFI)。
研究五味扶正益精方(WFY)对 DEHP 致小鼠精子 DNA 损伤的修复机制。
从 TCMSP、BATMAN-TCM、OMIM 和 GeneCards 中获取 WFY 和精子 DNA 片段(SDF)的潜在靶点。构建 WFY-SDF 的蛋白质-蛋白质相互作用(PPI)网络、GO 和 KEGG 通路分析。采用灌胃方式给予 SPF ICR(CD1)小鼠 DEHP(1g/kg/d),复制 DEHP 致精子 DNA 损伤的动物模型,同时分别给予 WFY 8.92、17.84 和 35.67g/kg,连续给药 60d。检测各组精子 DFI 并进行比较。采用转录组学和蛋白质组学分析鉴定 WFY 的靶基因,并通过 qRT-PCR 和 Western blot 进行验证。
网络药理学通路分析表明,PI3K/Akt 是 WFY 作用于 SDF 的潜在靶点。DEHP 组(25.48%)的 DFI 明显高于对照组(4.02%),高剂量 WFY 组(19.05%)修复效果最显著。相关通路为 PI3K/Akt 和代谢。筛选出 Aass、Aldh1a7、GSTA3、betaine homocysteine-methyltransferase(Bhmt)、Mug2 和 Svs1,并验证了 Bhmt。
WFY 能修复 DEHP 所致的精子 DNA 损伤,其机制可能与 PI3K/Akt 和代谢通路及 Bhmt 有关。这为利用中药预防和修复污染物引起的生殖系统损伤提供了新方向。