Suarez S S, Katz D F, Overstreet J W
Biol Reprod. 1983 Dec;29(5):1277-87. doi: 10.1095/biolreprod29.5.1277.
Rabbit spermatozoa were recovered from the oviductal ampullae 11 h postcoitus by an oil microflush technique. Their movement was evaluated in the ampullar fluid, or in ampullar fluid diluted with in vitro fertilization medium, in slide preparations which were approximately 25 micron or 100 micron deep. The movement of these sperm was compared with the movement of ejaculated sperm in diluted semen. Movement parameters measured from videotapes recorded by a high-speed camera were coded according to treatment and entered into a microcomputer for statistical analysis. A total of 157 spermatozoa were recovered from the oviducts of 16 does: 152 were motile and 126 were free-swimming. Nearly all of the free-swimming sperm swam in trajectories whose average paths were circular. The flagellar beat pattern of the circular swimmers was asymmetric and nearly planar, and the sperm did not roll. Spermatozoa observed in 25-micron slide preparations produced smaller flagellar bends than sperm swimming in 100-micron preparations and tended to swim in larger circles which were oriented in the plane of the slide. Spermatozoa observed within the cumulus matrix moved in a slow, erratic, sinuous manner, but resumed rapid circling upon leaving the matrix. It was concluded that the ampullar sperm were hyperactivated, retaining this physiological condition as they entered the cumulus. The movement qualitatively resembled that of hyperactivated guinea pig and hamster spermatozoa because these species effectively swim in circles. In contrast, 80% of the ejaculated spermatozoa swam in linear trajectories, resulting from relatively symmetrical, flagellar beat patterns. The percentage of rolling spermatozoa and the rolling frequencies were less in the 25-micron than the 100-micron slide preparations. Thus, the movement parameters of both ampullar and ejaculated spermatozoa were affected by the geometry of their observation chambers. This influence should be taken into account when observing sperm motility in vitro. It could also be important in vivo, where changes in sperm movement in response to epithelial surfaces might provide an advantage for reaching the cumulus mass. Ninety-eight percent of the motile ampullar sperm were observed to have acrosomes, including all spermatozoa found within the cumulus matrix.
在交配后11小时,通过油微冲洗技术从输卵管壶腹部回收兔精子。在约25微米或100微米深的载玻片制剂中,于壶腹液或用体外受精培养基稀释的壶腹液中评估其运动。将这些精子的运动与稀释精液中射出精子的运动进行比较。从高速摄像机记录的录像带中测量的运动参数根据处理进行编码,并输入微型计算机进行统计分析。从16只母兔的输卵管中总共回收了157个精子:152个有活力,126个自由游动。几乎所有自由游动的精子都沿平均路径为圆形的轨迹游动。做圆周运动的精子的鞭毛摆动模式不对称且几乎呈平面状,精子不翻滚。在25微米载玻片制剂中观察到的精子产生的鞭毛弯曲比在100微米制剂中游泳的精子小,并且倾向于在载玻片平面内沿更大的圆圈游动。在卵丘基质内观察到的精子以缓慢、不规则、蜿蜒的方式移动,但离开基质后恢复快速圆周运动。得出的结论是,壶腹精子处于超激活状态,进入卵丘时保持这种生理状态。其运动在质量上类似于超激活的豚鼠和仓鼠精子,因为这些物种有效地做圆周运动。相比之下,80%的射出精子沿直线轨迹游动,这是由相对对称的鞭毛摆动模式导致的。25微米载玻片制剂中翻滚精子的百分比和翻滚频率低于100微米载玻片制剂。因此,壶腹精子和射出精子的运动参数都受到其观察室几何形状的影响。在体外观察精子活力时应考虑这种影响。在体内也可能很重要,精子运动对上皮表面的反应变化可能为到达卵丘团提供优势。观察到98%有活力的壶腹精子有顶体,包括在卵丘基质内发现的所有精子。