...
首页> 外文期刊>Pakistan Veterinary Journal >Effects of storage duration on the quality and DNA integrity of Nili-Ravi bull spermatozoa frozen and stored in liquid nitrogen.
【24h】

Effects of storage duration on the quality and DNA integrity of Nili-Ravi bull spermatozoa frozen and stored in liquid nitrogen.

机译:储存时间对冷冻和储存在液氮中的Nili-Ravi公牛精子质量和DNA完整性的影响。

获取原文
获取原文并翻译 | 示例
           

摘要

In the present study, effects of storage duration on the quality and DNA integrity of Nili-Ravi buffalo bull spermatozoa frozen and stored in liquid nitrogen for up to three years were investigated. According to duration of storage, the semen samples were categorized into 10 groups, viz. (i) 0 day, (ii) one day, (iii) two weeks, (iv) one month, (v) three months, (vi) six months, (vii) nine months, (viii) one year, (ix) two years and (x) three years. A total of 50 straws, with 5 straws for each of the 10 groups were used. After thawing for 30 seconds at 37 degrees C, these samples were evaluated for sperm motility, livability, livability index, plasma membrane integrity, acrosome damage and DNA damage. At 0 day, mean values for sperm motility (%), livability (hrs), livability index, plasma membrane integrity (%), acrosome damage (%) and DNA damage (%) were 53+or-1.22, 6.0+or-0.0, 130+or-5.2, 45.4+or-1.6, 3.8+or-0.6 and 2.2+or-0.4. After 3 years of storage, the corresponding values were 39+or-3.32, 4.4+or-0.2, 78.5+or-5.7, 28.2+or-2.2, 12.0+or-0.7 and 5.8+or-0.6. Sperm motility and livability remained unaffected up to 3 months of storage, followed by a decrease at 6th month, while absolute index of livability and membrane integrity started decreasing at 1 month (P<0.05). Sperm with damaged acrosome increased at 6th month (P<0.05). Similarly, sperm with damaged DNA increased after one year of storage (P<0.05). Thus, post-thaw motility, livability and acrosome integrity of spermatozoa of Nili-Ravi bulls started decreasing at 6th month of storage, while sperm DNA integrity remained unaffected for one year of storage in liquid nitrogen.
机译:在本研究中,研究了保存时间对冷冻并保存在液氮中长达三年的Nili-Ravi水牛牛精子质量和DNA完整性的影响。根据保存时间长短,将精液样本分为10组。 (i)0天,(ii)一天,(iii)两周,(iv)一个月,(v)三个月,(vi)六个月,(vii)九个月,(viii)一年,(ix )两年和(x)三年。总共使用了50根吸管,每10组中有5根吸管。在37℃融化30秒后,评估这些样品的精子活动性,存活率,存活率指数,质膜完整性,顶体损伤和DNA损伤。在第0天,精子活动度(%),存活率(小时),存活率指数,质膜完整性(%),顶体损伤(%)和DNA损伤(%)的平均值为53+或-1.22、6.0+或- 0.0、130+或-5.2、45.4+或-1.6、3.8+或-0.6和2.2+或-0.4。储存3年后,相应的值为39+或-3.32、4.4+或-0.2、78.5+或-5.7、28.2+或-2.2、12.0+或-0.7和5.8+或-0.6。精子活力和存活率在储存3个月后仍未受影响,随后在第6个月下降,而存活率和膜完整性的绝对指数在1个月时开始下降(P <0.05)。顶体受损的精子在第6个月增加(P <0.05)。同样,DNA受损的精子在储存一年后增加(P <0.05)。因此,Nili-Ravi公牛的精子在解冻后的运动能力,活力和顶体完整性在储存的第6个月开始下降,而精子DNA的完整性在液氮中储存1年仍不受影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号