首页|原花青素减轻热应激诱导的牛卵母细胞氧化应激

原花青素减轻热应激诱导的牛卵母细胞氧化应激

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[目的]旨在探究体外成熟液中添加原花青素B2(PB2)对热应激牛卵母细胞的保护机制,为揭示热应激对牛卵母细胞质量和胚胎体外培养发育能力的影响提供科学依据。[方法]以6~8岁淘汰荷斯坦牛为试验对象,屠宰场共采集牛卵巢103对。实验室抽吸卵巢表面卵泡内卵丘-卵母细胞复合体(COCs),将COCs随机分成3组进行体外成熟:对照组(38。5℃培养24 h);热应激组(41℃培养8 h转入38。5℃培养箱继续培养16 h);原花青素组(25 µmol/L PB2、41℃培养8 h转入38。5℃培养箱继续培养16 h)。体外成熟培养24 h,COCs经透明质酸酶消化后,在体视显微镜下统计各组卵母细胞成熟率;使用化学试剂对卵母细胞进行孤雌激活,体外培养48 h统计卵裂率,168 h统计囊胚率;利用荧光染色法检测卵母细胞活性氧(ROS)、还原型谷胱甘肽(GSH)活性,以及囊胚细胞总数;利用实时荧光定量PCR(qPCR)检测各组卵母细胞抗氧化基因(SOD1、SOD2、CAT)和成熟相关基因(GSS、GPX1、CAS6)相对表达量。[结果](1)COCs体外成熟24 h,与热应激组相比,原花青素组提高了卵母细胞成熟率,但两者之间差异不显著(P>0。05);(2)孤雌激活后,与热应激组相比,原花青素组卵裂率和囊胚细胞总数显著提高(P<0。05),囊胚率差异不显著(P>0。05);(3)与热应激组相比,原花青素组ROS活性极显著降低(P<0。01),GSH活性显著提高、成熟基因和抗氧化基因表达量显著升高(P<0。05)。[结论]在体外成熟培养液中添加25 µmol/L原花青素B2,可以有效缓解热应激对牛卵母细胞造成的氧化应激,增强胚胎发育潜力,并提高其质量。
Reduction of heat stress-induced oxidative stress in bovine oocytes by Proanthocyanidins
[Objective]The objective of this study is to explore the protective mechanisms of proanthocyanidin B2(PB2)when incorporated into the maturation medium of bovine oocytes under heat stress conditions.This investigation aims to provide a scientific foundation for enhancing the quality of bovine oocytes exposed to high temperatures and improving their capacity for embryonic development in vitro.[Method]A total of 103 pairs of ovaries were collected from 6-8 years old Holstein cattle.The cumulus oocyte complex(COCs)in ovarian follicles were aspirated in the laboratory and randomly divided into 3 groups for in vitro maturation:control group(cultured at 38.5℃for 24 h);heat stress group(cultured at 41℃for 8h and transferred to 38.5℃incubator for 16 h);proanthocyanidin group(25 µmol/L PB2,cultured at 41℃for 8h and transferred to 38.5℃incubator for 16 h).After the oocytes were treated by hyaluronidase,the oocyte maturation rate of each group was measured under stereomicroscope.After parthenogenetic activation of oocytes by chemical agent,the cleavage rate and blastocyst rate were recorded at 48 h and 168 h,respectively.The ROS and GSH of oocytes and the total number of blastocysts were measured by fluorescence staining.The expression levels of antioxidant genes(SOD1,SOD2,CAT)and maturation genes(GSS,GPX1,CAS6)were detected by quantitative real-time PCR(qPCR).[Result](1)COCs matured in vitro for 24 h.Compared with the heat stress group,the proanthocyanidin group increased the oocyte maturation rate,but there was no significant difference between the two groups(P>0.05);(2)After parthenogenesis activation,compared with heat stress group,the cleavage rate of proanthocyanidin group was significantly increased(P<0.05),the blastocyst rate was not significantly different(P>0.05),but the total number of blastocyst cells was significantly increased(P<0.05);(3)After 24h maturation in vitro,compared with heat stress group,ROS content in proanthocyanidins group was significantly decreased(P<0.01),GSH content was significantly increased(P<0.05),the expression levels of maturation genes and antioxidant genes were significantly increased(P<0.05).[Conclusion]By adding proanthocyanidin B2 to in vitro maturation medium,oxidative stress of bovine oocytes induced by heat stress can be effectively alleviated,thus improving the maturation process of oocytes in vitro and enhancing the development potential of embryos as well as embryo quality.

proanthocyanidinoocytesheat stressoxidative stress

朱肖亭、闵佳、张志浩、施巧婷、王香南、楚秋霞、张子敬、陈付英、赵彩艳、乔智慧、李静、王二耀

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河南省农业科学院 畜牧研究所,河南 郑州 45000

河南农业大学 动物科技学院,河南 郑州 450002

河南省泌阳县夏南牛研究推广中心,河南 驻马店 463700

原花青素 卵母细胞 热应激 氧化应激

2024

江西农业大学学报
江西农业大学

江西农业大学学报

CSTPCD北大核心
影响因子:0.748
ISSN:1000-2286
年,卷(期):2024.46(6)