替卡西林-克拉维酸在INRA 96增效剂中用于种马精液冷却。

C J Dean, A M Hobgood, G P Blodgett, C C Love, T L Blanchard, D D Varner
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引用次数: 11

摘要

进行研究的原因:一种常用的商业扩展剂(即INRA 96)含有可能具有有限效力的抗菌剂。因此,在这种增种剂中加入替卡西林-克拉维酸是美国马养殖业的一种普遍做法。然而,这种做法并没有得到严格的评价。目的:评价在INRA 96中添加替卡西林-克拉维酸、不同增剂条件和不同抑菌保存条件对精子功能和抑菌效果的影响。方法:将14匹成熟的四分之一种马42份无凝胶精液用INRA 96进行扩展,并在Equitainer II中保存24 h。采用方差分析和卡方统计方法评估添加替卡西林-克拉维酸和不同扩展剂储存方式对精子运动特性(通过计算机辅助分析)、精子膜完整性(通过荧光测量)和细菌生长抑制(通过好氧和厌氧培养方法)的影响。P值为< 0.05。结果:在用于种马精液之前,冷冻和解冻改性或未改性的扩展剂会导致精子质量下降,冷却24小时后,精子活力(即总活力和渐进式活力)和精子膜完整性显著降低。在填充剂中加入替卡西林-克拉维酸后,与冷冻储存相比,在使用前将重组抗菌剂冷却储存时,精子速度更快。42次射精中只有28次(67%)在纯精液中产生细菌,但在INRA 96中添加替卡西林-克拉维酸与单独使用INRA 96在抑制细菌生长方面没有区别(分别为98%和94%)。结论:在INRA 96中加入替卡西林-克拉维酸(1mg /ml)对冷藏后延长精液的精子质量无不良影响。延长剂在使用前的冷冻和解冻对精子质量有不利影响。潜在相关性:这些数据表明INRA 96在使用前不应冷冻和解冻。在INRA 96中添加替卡西林-克拉维酸对精子质量没有影响。与纯精液相比,所有延长剂处理均能有效控制细菌的生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The addition of ticarcillin-clavulanic acid to INRA 96 extender for stallion semen cooling.

Reasons for performing study: A commonly used commercial extender (i.e. INRA 96) contains antimicrobials that may have limited effectiveness. Therefore, addition of ticarcillin-clavulanic acid to this extender is a widespread procedure in the equine breeding industry in the United States. However, such practice has not been critically evaluated.

Objectives: To evaluate the addition of ticarcillin-clavulanic acid to INRA 96 and different extender and antimicrobial storage conditions on sperm function and antimicrobial effectiveness.

Methods: Gel-free semen (42 ejaculates from 14 mature Quarter Horse stallions) was extended with INRA 96 and stored for 24 h in an Equitainer II. The effects of added ticarcillin-clavulanic acid and different extender storage procedures on sperm motion characteristics (by computer-assisted analysis), sperm membrane integrity (by fluorescence-based measurement) and suppression of bacterial growth (by aerobic and anaerobic culture methods) were evaluated using analysis-of-variance and Chi-square statistical methods. The P value for significance was set at < 0.05.

Results: Freezing and thawing of modified or unmodified extender prior to use for stallion semen resulted in reduced sperm quality post cooling for 24 h, as evidenced by a significant reduction in sperm motility (i.e. total and progressive) and sperm membrane integrity. Addition of ticarcillin-clavulanic acid to extender resulted in higher sperm velocity when the reconstituted antimicrobial was subjected to cooled storage, as compared with frozen storage, prior to use. Only 28 of 42 ejaculates (67%) yielded presence of bacteria in neat semen but addition of ticarcillin-clavulanic acid to INRA 96 was not different than INRA 96 alone for inhibiting growth of bacteria (98 vs. 94%, respectively).

Conclusions: Addition of ticarcillin-clavulanic acid (1 mg/ml) to INRA 96 did not adversely affect sperm quality in extended semen after cooled storage. Extender freezing and thawing prior to use had detrimental effects on sperm quality.

Potential relevance: These data suggest that INRA 96 should not be frozen and thawed prior to use. Addition of ticarcillin-clavulanic acid to INRA 96 did not impair sperm quality. All extender treatments effectively controlled the bacterial growth compared with neat semen.

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