Effect of L-carnosine on frozen ram-semen quality evaluated by CASA and flow-cytometry

IF 1.4 4区 农林科学 Q2 Agricultural and Biological Sciences
Ibrahim Halil Güngör, Seyfettin Gür, Edanur Güler Ekmen
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引用次数: 0

Abstract

Context

Successful freezing of ram semen has not yet reached the desired levels. The main reason for this situation could be due to the fact that the spermatozoa of this species have a lipid composition different from that of other species.

Aims

The objective of the study was to evaluate the effect of different concentrations of L-carnosine added to the extender on ram semen after being frozen and thawed.

Methods

Semen was collected from six Akkaraman rams twice a week for a period of 3 weeks. Pooling was performed at each time. The semen were reconstituted with a pre-prepared tris + egg yolk solution and different amounts of L-carnosine to form experimental groups (Group 1: 1 mM, Group 2: 5 mM, Group 3: 10 mM, Group 4: 20 mM, Group 5: control) and were drawn into 0.25 mL mini straws. Subsequently, the samples were subjected to freezing by using an automated freezing device. Following the freezing process, the straws were placed in containers containing liquid nitrogen and thawed after 24 h.

Key results

After thawing, it was found that the samples containing 5 mM L-carnosine had superior results in all analyses. This concentration exhibited significantly higher percentages of progressive, total, and rapid sperm motility, live spermatozoa, high mitochondrial membrane potential rate, and higher GSH-Px concentrations. In addition, it was determined that 5 mM L-carnosine group protected the membrane integrity and significantly decreased the rate of abnormal spermatozoa, acrosomal damage rate, low mitochondrial membrane potential and apoptotic cell rate.

Conclusions

As a result, It was determined that adding 5 mM of L-carnosine to the semen extender during the freezing of ram samples would be beneficial for successful freezing.

Implications

The addition of 5 mM L-carnosine to ram-semen extenders ensures the freezability of the semen of this species; thus, this protocol could be used to perform artificial insemination with frozen ram semen.

用 CASA 和流式细胞仪评估左旋肉碱对冷冻公羊脾质量的影响
背景公羊精液的成功冷冻尚未达到预期水平。造成这种情况的主要原因可能是该物种精子的脂质成分与其他物种不同。研究的目的是评估添加到扩增剂中的不同浓度的左旋肉碱对冷冻和解冻后的公羊精液的影响。方法在 3 周内每周两次从 6 只阿卡拉曼公羊身上采集精液。每次都进行汇集。精液用预先准备好的三酸+蛋黄溶液和不同量的左旋肉碱重新配制成实验组(第 1 组:1 毫摩尔;第 2 组:5 毫摩尔;第 3 组:10 毫摩尔;第 4 组:20 毫摩尔;第 5 组:对照组),并抽取到 0.25 毫升的迷你吸管中。随后,使用自动冷冻装置对样品进行冷冻。主要结果解冻后发现,含有 5 mM 左旋肉碱的样本在所有分析中的结果都更优。这种浓度的精子运动能力、总精子运动能力和快速精子运动能力、活精子、线粒体膜电位率和 GSH-Px 浓度都明显较高。此外,5 mM 左旋肉碱组还能保护精子膜的完整性,并显著降低畸形精子率、顶体损伤率、线粒体膜电位低和细胞凋亡率。结论因此,在冷冻公羊样本时,在精液扩展液中添加 5 毫摩尔的左旋肉碱有利于成功冷冻。意义在公羊精液扩展剂中添加 5 毫摩尔左旋肉碱可确保该物种精液的可冷冻性;因此,该方案可用于使用冷冻公羊精液进行人工授精。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Animal Production Science
Animal Production Science Agricultural and Biological Sciences-Food Science
CiteScore
3.00
自引率
7.10%
发文量
139
审稿时长
3-8 weeks
期刊介绍: Research papers in Animal Production Science focus on improving livestock and food production, and on the social and economic issues that influence primary producers. The journal (formerly known as Australian Journal of Experimental Agriculture) is predominantly concerned with domesticated animals (beef cattle, dairy cows, sheep, pigs, goats and poultry); however, contributions on horses and wild animals may be published where relevant. Animal Production Science is published with the endorsement of the Commonwealth Scientific and Industrial Research Organisation (CSIRO) and the Australian Academy of Science.
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