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首页> 外文期刊>The Journal of general physiology >OBSERVATIONS ON THE MOTILITY OF RABBIT SPERMATOZOA IN DILUTE SUSPENSION
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OBSERVATIONS ON THE MOTILITY OF RABBIT SPERMATOZOA IN DILUTE SUSPENSION

机译:稀悬液中兔精子活动性的观察

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1. Rabbit spermatozoa suspended in Baker's solution rapidly lose motility at relatively high dilutions. At a concentration of 0.4 million per ml., the spermatozoa from most ejaculates are completely immotile within 2 or 3 hours. The same phenomenon occurs with chloride-free diluents and is therefore not due to the toxic action of chlorides.2. This rapid immobilisation may be prevented by suspension in cell-free supernatants from other more concentrated suspensions of rabbit semen and by the accessory secretions from a vasectomised buck. The most effective supernatants are those prepared from suspensions of spermatozoa which have been left overnight before centrifuging. Immobilisation may also be prevented by many other agents, the most effective of which are gum arabic, starch, glycogen, and serum proteins (carbohydrate-containing or carbohydrate-free). Yet, in no case is the action of these substances as effective as more concentrated suspension in Baker's solution.3. The immobilisation is not prevented by catalase, gelatin, agar, or sodium silicate. It is almost certainly not due to the toxic action of traces of heavy metals and is not affected by the use of water doubly distilled over glass in the preparation of the diluent, or by treating the diluent with activated charcoal.4. Washing with Baker's solution does not cause immobilisation of spermatozoa suspended at 20 million per ml. at a stage at which the concentration of seminal plasma has been reduced to that equivalent to dilution to 0.4 million per ml. Further washing (six repeated centrifugings of 0.2 ml. semen in 4 ml. of Baker's solution) immobilises them. This confirms the opinion that loss of intracellular, or perhaps rather paracellular, material is a responsible agent in the dilution phenomenon.
机译:1.悬浮在贝克溶液中的兔精子在较高稀释度下迅速失去活力。在每毫升40万的浓度下,大多数射精产生的精子在2或3个小时内完全无法活动。不含氯化物的稀释剂也会发生同样的现象,因此不是由于氯化物的毒性作用引起的。2。这种快速固定可以通过以下方法来防止:将其悬浮在来自其他更浓缩的兔精液的无细胞上清液中,以及通过输精管切块术的辅助分泌物。最有效的上清液是由精子悬浮液制备的,上清液在离心前已放置过夜。许多其他试剂也可以防止固定化,其中最有效的是阿拉伯胶,淀粉,糖原和血清蛋白(含碳水化合物或不含碳水化合物)。然而,这些物质的作用绝不像贝克溶液中更浓的悬浮液一样有效。3。过氧化氢酶,明胶,琼脂或硅酸钠不会阻止固定化。几乎可以肯定,这不是由于痕量重金属的毒性作用,并且不受稀释剂制备中使用在玻璃上加倍蒸馏的水或用活性炭处理稀释剂的影响。4。用贝克溶液洗涤不会导致悬浮在每毫升2000万个精子上。在精浆浓度已降低至相当于稀释至每毫升40万的阶段。进一步洗涤(在4mL贝克溶液中重复0.2次离心0.2mL精液)使其固定。这证实了以下观点,即细胞内物质或细胞外物质的损失是稀释现象中的负责任因素。

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