Engle C E, Foley C W, Witherspoon D M, Scarth R D, Goetsch D D
Am J Vet Res. 1975 Aug;36(08):1149-52.
Three experiments were conducted on the metabolism of stallion sperm. In experiment 1, whole and washed sperm were incubated under aerobic and anaerobic enviroments and analyzed before and after controlled incubation for motility, pH, lactic acid, glucose, fructose, and O2 comsumption. In experiment 2, whole and washed sperm were incubated aerobically and anaerobically with and without uterine tubal fluids. Experiment 3 was the same as experiment 2, except added substrates of glucose and lactic acid were studied. The same examinations were made in experiments 2 and 3 as for experiment 1. Motility decreased significantly during incubation for all treatments, with the greatest decrease occurring for whole semen where only trace amounts of substrate (fructose) were present. Exogenous glucose plus uterine tubal fluid maintained sperm motility better than did added lactate. However, sperm respiration rates were highest when exogenous lactate was the only substrate in the incubation medium. The mean pH values for gel-free stallion semen at the start of controlled aerobic and anaerobic incubation were 7.08 and 7.34. Lactic acid accummulation for 1 hour increased from 0.05 mg to 0.09 mg/10(9) sperm when uterine tubal fluid was added to the incubation medium. Washed spermatozoa incubated in 0.03 M glucose plus uterine tubal fluid utilized less glucose than did sperm incubated in the glucose medium. These results, along with the increased oxygen utilization (ZO2) values produced by adding uterine tubal fluid to the incubation mediums, might indicate utilization of a uterine tubal substrate. Added uterine tubal fluid resulted in increased ZO2 values (expressed in mul of O2 utilized by 10(8) sperm in 1 hour at 37 C) for whole semen from 10.45 to 12.63. Washed spermatozoa also respired at a significantly greater rate than whole sperm. Respiration rates were greater for sperm incubated with 0.01 M lactic acid than for any other substrate or experiment.
进行了三项关于种马精子代谢的实验。在实验1中,将完整精子和洗涤后的精子在有氧和无氧环境下孵育,并在控制孵育前后分析其活力、pH值、乳酸、葡萄糖、果糖和氧气消耗。在实验2中,将完整精子和洗涤后的精子在有氧和无氧条件下分别与有无输卵管液一起孵育。实验3与实验2相同,只是研究了添加葡萄糖和乳酸底物的情况。实验2和实验3与实验1进行相同的检测。所有处理在孵育过程中活力均显著下降,其中完整精液下降幅度最大,因为完整精液中仅存在微量底物(果糖)。外源性葡萄糖加输卵管液比添加乳酸能更好地维持精子活力。然而,当外源性乳酸是孵育培养基中唯一底物时,精子呼吸速率最高。在有氧和无氧控制孵育开始时,无凝胶种马精液的平均pH值分别为7.08和7.34。当向孵育培养基中添加输卵管液时,1小时内乳酸积累量从0.05毫克增加到0.09毫克/10⁹精子。在0.03M葡萄糖加输卵管液中孵育的洗涤精子比在葡萄糖培养基中孵育的精子消耗的葡萄糖更少。这些结果,连同向孵育培养基中添加输卵管液所产生的氧气利用率(ZO₂)值增加,可能表明利用了输卵管底物。添加输卵管液使完整精液的ZO₂值(以37℃下10⁸精子1小时消耗的O₂微摩尔数表示)从10.45增加到12.63。洗涤后的精子呼吸速率也明显高于完整精子。与0.01M乳酸一起孵育的精子的呼吸速率高于任何其他底物或实验。