The Effect of Adding Antioxidants on Cooled Zarabi Buck Semen During Different Seasons

Ahmed Hadary, Iman Bawab, Kamal Metwaly, Samia Rheem
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Abstract

Semen preservation by cooling or freezing is an essential artificial insemination (AI) step. AI is affected by many factors, such as semen quality. The aim of this study was to evaluate the effect of adding different concentrations of different antioxidants such as selenium, zinc oxide and Vitamin C to the diluted buck semen during cooling in both summer and winter. Eight mature healthy Zaraibi bucks were used in the study. semen was collected twice weekly during summer 2021 (august and September) and winter 2022 (January and February). Semen samples were collected by an electro- ejaculator device. Samples of good quality semen were pooled and diluted by extender and divided according to experimental groups: Group 1 Vitamin C: 50 mg /100 ml, 1oo mg /100 ml, 150 mg /100 ml. Group 2 Zinc oxide: 0.5 mg /100 ml, 1 mg /100 ml, 1.5 mg /100 ml. Group 3 Selenium: 100 μL/100 ml, 200 μL / 100, 300 μL / 100. After cooling by 1 hr. semen parameters were examined as motility, livability, acrosome integrity and cell membrane integrity and at 8 hours from cooling then every 8 hr till 64 hr. Seminal antioxidant activities as SOD and catalase were estimated at 0 hr, 24 hr and 48 hr. The results indicated that selenium 200 μL / 100 ml diluent has a favorable effect on cooled diluted buck semen during summer and winter more than selenium 100 μL and 300 μL. Selenium is better than Zinc oxide and Vitamin C for improving the semen quality as with minimum cost. In conclusion adding selenium as antioxidant to buck semen during cooling preservation with 200 μL concentration per 100 diluents is preferred for buck semen during cooling preservation.
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不同季节添加抗氧化剂对冷却扎比鹿精液的影响
通过冷却或冷冻保存精液是人工授精(AI)的重要步骤。人工智能受到许多因素的影响,比如精液质量。本研究的目的是评价在夏季和冬季冷却过程中,在稀释后的雄鹿精液中添加不同浓度的硒、氧化锌和维生素C等不同抗氧化剂的效果。研究中使用了8只成熟健康的宰来比雄鹿。在2021年夏季(8月和9月)和2022年冬季(1月和2月)每周采集两次精液。精液样本由电射精器采集。取优质精液,取浓缩器稀释后按实验组进行分组:1组维生素C: 50 mg /100 ml、100 mg /100 ml、150 mg /100 ml, 2组氧化锌:0.5 mg /100 ml、1 mg /100 ml、1.5 mg /100 ml, 3组硒:100 μL/100 ml、200 μL/100、300 μL/100。冷却1小时后。在冷却后8小时,每隔8小时检测一次精液的活力、存活率、顶体完整性和细胞膜完整性。在0小时、24小时和48小时测定种子SOD和过氧化氢酶的抗氧化活性。结果表明,在夏季和冬季,200 μL / 100 ml的硒比100 μL和300 μL的硒更有利于冷却稀释雄鹿精液。硒比氧化锌和维生素C更能以最低的成本提高精液质量。综上所述,在雄鹿精液冷却保存过程中,以200 μL / 100稀释剂的浓度添加硒作为抗氧化剂对雄鹿精液的冷却保存效果较好。
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