低温保存
DNA断裂
精子
男科
扩展器
生物
精子活力
表观遗传学
精液
顶体
DNA甲基化
化学
细胞生物学
生物化学
细胞凋亡
医学
胚胎
基因表达
基因
有机化学
程序性细胞死亡
聚氨酯
作者
Razieh Fouladvandi,Ali Akbar Masoudi,Mehdi Totonchi,Maryam Hezavehei,Mohsen Sharafi
摘要
Abstract The cryopreservation process induces alterations in cellular parameters and epigenetic patterns in bull sperm, which can be prevented by adding cryoprotectants in the freezing extenders. The purpose of this study was to compare the protective effects of two extenders based on soybean lecithin (SLE) and egg yolk (EYE) on epigenetic patterns and quality parameters of sperm such as motility parameters, mitochondrial membrane integrity, DNA fragmentation, viability, and apoptotic‐like changes of bull sperm after cryopreservation. Results demonstrated that cryopreservation significantly ( p < .05) reduced the level of DNA global methylation, H3K9 histone acetylation, and H3K4 histone methylation in both frozen groups compared to the fresh sperm. Also, the level of H3K9 acetylation was lower in the frozen SLE group (21.2 ± 1.86) compared to EYE group (15.2 ± 1.86). In addition, the SLE frozen group had a higher percentage of viability, progressive motility, and linearity (LIN) in SLE frozen group compared to EYE frozen group. However, no difference was observed in mitochondrial membrane integrity and DNA fragmentation between SLE and EYE frozen groups. While soybean‐lecithin‐based extender showed some initial positive impacts of epigenetics and semen parameters, further investigations can provide useful information for better freezing.
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