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Cryopreservation of Bangladeshi ram semen using different diluents and manual freezing techniques

机译:使用不同稀释剂和手动冻结技术的孟加拉国RAM精液的冷冻保存

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A study was conducted to establish a sustainable and effective manual freezing technique for cryopreservation of Bangladeshi ram semen. Three diluents and freezing techniques were tested, both as treatment combinations (diluent x freezing technique) and fixed effects (diluent or freezing technique) on post-thaw sperm motility (SM), viability (SV), plasma membrane integrity (SPMI) and acrosome integrity (SAI). Ten rams were selected, based on semen evaluation. Eight ejaculates were used for each treatment combination. Semen samples were diluted using a two-step protocol for home-made Tris-based egg yolk (20%, v/v) diluents: D1 (7% glycerol, v/v) and D2 (5% glycerol, v/v), and one-step for commercial diluent: D3 (Triladyl (R), consists of bi-distilled water, glycerol, tris, citric acid, fructose, spectinomycin, lincomycin, tylosin and gentamycin) at 35 degrees C. Fraction-A (without glycerol) was added at 35 degrees C, and following cooling of sample to 5 degrees C (-0.30 C/min), Fraction-B (with glycerol) was added. The diluted semen samples were aspirated into 0.25 ml French straws, sealed, and equilibrated at 5 degrees C for 2 h. The straws were frozen in liquid nitrogen (LN) vapour, in a Styrofoam box. The freezing techniques were; One-step (Fl): at -15.26 degrees C/min from + 5 degrees C to -140 degrees C; Two-step (F2): at -11.33 degrees C/min from +5 degrees C to 80 degrees C, and 30 degrees C/min from 80 degrees C-140 degrees C; and Three-step (F3): at 11.33 degrees C/min from + 5 degrees C to -80 degrees C, at -26.66 degrees C/min from to -80 degrees C to -120 degrees C, and at -13.33 degrees C/min from -120 degrees C to -140 degrees C. Two semen straws from each batch were evaluated before and after freezing. The group F3D3 exhibited significantly higher (p < 0.05) post-thaw SM 63.1 +/- 2.5%, SV 79.0 +/- 2.1% and SPMI 72.9 +/- 1.7%, whereas SAI 72.9 +/- 1.7% was significantly higher (p < 0.05) in group F3D2. The freezing technique F2 and F3 had significantly higher (p < 0.05) post-thaw sperm values compared to Fl. The post-thaw SM and SV were above 50% and 65% with the freezing technique F2 and F3 but differed non-significant. The SPMI 67.6 +/- 2.0% and SAI 76.1 1.4% were significantly higher (p < 0.05) with F3. Likewise, the diluent D2 and D3 had significantly higher (p < 0.05) post-thaw sperm values compared to Dl. The post-thaw SM, SV and SPMI were above 50%, 65% and 55% with the diluents D2 and D3 but differed non-significant. The SAI 76.1 +/- 1.1% was significantly higher (p < 0.05) with D3. We concluded that the use of a simple home-made Tris-based diluent containing 20% (v/v) egg yolk and 5% glycerol (v/v), two-step dilution and a three-step freezing technique is a sustainable and effective method for freezing ram semen. For further validation, the fertility of ewes artificially inseminated with the frozen semen will be observed.
机译:进行了一项研究,以建立一种可持续和有效的手动冻结技术,用于孟加拉国RAM精液的冷冻保存。测试了三种稀释剂和冷冻技术,作为治疗组合(稀释剂x冷冻技术)和固定效果(稀释剂或冷冻技术)在解冻后的精子运动(SM),活力(SV),质膜完整性(SPMI)和肌肤诚信(SAI)。根据精液评估选择了十个RAM。每种治疗组合使用八个射精。使用两步方案用于自制的Tris基蛋黄(20%,v / v)稀释剂的两步方案稀释:D1(7%甘油,v / v)和d2(5%甘油,v / v) ,以及商业稀释剂的一步:D3(三烷基(R),由35摄氏度-A(无在35℃下加入甘油,并在将样品冷却至5℃(-0.30℃/ min)后,加入馏分-b(用甘油)。将稀释的精液样品吸入0.25ml的法国秸秆,密封,并在5℃下平衡2小时。将吸管在液氮(LN)蒸气中冷冻,在聚苯乙烯泡沫塑料盒中。冷冻技术是;一步(FL):在-15.26摄氏度下,从+ 5°C到-140度C;两步(F2):在-11.33°C / min,从+ 5°C至80℃,30摄氏度,从80度C-140摄氏度C / min;和三步(F3):从+ 5℃/ min的11.33度至-80摄氏度,从-26.66摄氏度到-80°C至-120摄氏度,在-13.33摄氏度下/ min -120℃至-140℃。在冷冻之前和之后评估来自每批的两种精液吸管。综合增长率明显高(P <0.05)解冻后SM 63.1 + / -2.5%,SV 79.0 +/- 2.1%和SPMI 72.9 +/- 1.7%,而SAI 72.9 +/- 1.7%显着高( F3D2组中P <0.05)。与F1相比,冷冻技术F2和F3显着更高(P <0.05)后解冻精子值。冻乳后解冻SM和SV均高于50%和65%,冻结技术F2和F3但不同的非显着性。 SPMI 67.6 +/- 2.0%和SAI 76.1 1.4%明显高(P <0.05),F3。同样,与D1相比,稀释剂D2和D3显着更高(P <0.05)后解冻精子值。解冻后SM,SV和SPMI高于50%,65%和55%,稀释剂D2和D3但不同的非显着性。 SAI 76.1 +/- 1.1%明显高(P <0.05),D3。我们得出结论,使用含有20%(v / v)蛋黄和5%甘油(v / v),两步稀释和三步冷冻技术的简单自制的Tris基稀释剂是可持续的冷冻Ram精液的有效方法。为了进一步验证,将观察到与冷冻精液人工苗中的母羊的生育能力。

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