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Effects of spermatozoal concentration and post-thaw dilution rate on survival after thawing of dog spermatozoa

机译:精子浓度和解冻后稀释率对狗精子解冻后存活的影响

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The objectives of this study were to evaluate the effects and interactions of freezing dog semen using 4 different sperm concentrations (50 x 10~6, 100 x 10~6, 200 x 10~6 and 400 x 10~6 spermatozoa/mL) in 0.5-mL straws and diluting the thawed semen at 4 different rates (1:0, 1:1, 1:2 and 1:4) on post-thaw survival and longevity of dog spermatozoa during incubation at 38oc. Fifteen ejaculates were collected from 12 dogs and pooled. The semen pool was divided into 4 aliquots containing respectively 4200 x 10~6, 2100 x 10~6, 1050 x 10~6 and 525 x 10~6 spermatozoa, which were centrifuged, Sperm pellets were rediluted with TRiS-glucose-egg yolk extender containing 5% glycerol and 0.5% of Equex STM Paste to obtain the designated sperm concentrations. The semen was frozen in 0.5-mL straws 4 cm above liquid nitrogen (LN_2). The straws were thawed at 70 deg C for 8 sec and the contents of each straw were divided into 4 aliquots and diluted with TRIS buffer at 38 deg C at rates of 1:0, 1:1, 1:2 and 1:4 (semen:buffer), respectively, making a total of 16 treatments. Sperm motility was subjectively evaluated after thawing and at l-h intervals during 8 h of incubation at 38 deg C. Plasma membrane integrity and acrosomal status were evaluated at 1, 3, 6, 12 and 18 h post-thaw using a triple-staining procedure and flow cytometry. For data pooled across the post-thaw dilution rate, motility was higher (P<0.001) in samples frozen with 200 x 10~6 spermatozoa/mL. The integrity of sperm plasma membranes after 18 h incubation was higher (P<0.05) in samples frozen with 200 x 10~6 and 400 x 10~6 spermatozoa/mL. For data pooled across sperm concentration, samples diluted at a rate of 1:2 or 1:4 had better (P<0.001) motilities after 8 h of incubation than undiluted samples or those diluted at 1:l. The integrity of the sperm plasma membranes was higher (P<0.001) at increasing dilution rates. When the 16 treatments were compared, the best longevity was obtained when semen packaged at a concentration of 200 x 10~6 spermatozoa/mL was diluted immediately after thawing at 1:4 dilution rate.
机译:本研究的目的是使用4种不同精子浓度(50 x 10〜6、100 x 10〜6、200 x 10〜6和400 x 10〜6精子/ mL)评估冷冻狗精液的作用和相互作用。 0.5mL的吸管和以4种不同的比率(1:0、1:1、1:2和1:4)稀释融化的精液对38oc孵育的狗精子的解冻后存活率和寿命。从12只狗中收集15个射精并汇集。将精液池分成4个等分试样,分别包含4200 x 10〜6、2100 x 10〜6、1050 x 10〜6和525 x 10〜6精子,将其离心,用TRiS-葡萄糖-蛋黄重新稀释精子沉淀。含有5%甘油和0.5%Equex STM Paste的填充剂以获得指定的精子浓度。将精液冷冻在液氮(LN_2)上方4厘米处的0.5 mL吸管中。将秸秆在70摄氏度下融化8秒钟,将每种秸秆的内容分成4等份,并在38摄氏度下用TRIS缓冲液以1:0、1:1、1:2和1:4的比例稀释(精液:缓冲液),总共进行16次治疗。在融解后和在38摄氏度孵育8小时的过程中以1h间隔主观评估精子运动能力。解冻后1、3、6、12和18 h使用三重染色程序评估质膜完整性和顶体状态流式细胞仪。对于融化后稀释率收集的数据,以200 x 10〜6精子/ mL冷冻的样品的运动性更高(P <0.001)。在用200 x 10〜6和400 x 10〜6精子/ mL冷冻的样品中,经过18 h孵育后,精子质膜的完整性更高(P <0.05)。对于跨精子浓度收集的数据,孵育8小时后,以1:2或1:4的比例稀释的样品比未稀释的样品或以1:1的样品具有更好的(P <0.001)流动性。随着稀释率的增加,精子质膜的完整性更高(P <0.001)。比较这16种处理方法,将以200 x 10〜6精子/ mL浓度包装的精液在以1:4的稀释比例解冻后立即稀释,可获得最佳的寿命。

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