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The effect of swim-up purification and incubation of cells on sperm viability in dogs of different ages

机译:游泳提纯和细胞温育对不同年龄犬精子活力的影响

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ABSTRACT: The influence of selected semen extenders on the motility of frozen-thawed dog spermatozoa has been clearly demonstrated in several studies, although there are no reports indicating the effect of swim-up purification on sperm viability in this species of mammals. Therefore, this study was aimed at investigating phosphatidylser- ine (PS) externalization and necrosis in sperm after variable lengths of time of in vitro incubation after swim-up purification. Dog semen samples were collected from (i) ten dogs aged six months to 1.5 year, (ii) ten dogs aged six to eight years, and (iii) ten dogs aged 11 to 13 years. A flow cytometric method was employed to evaluate dog sperm viability in animals of different age groups after employment of a swim-up (SU) purification technique. After SU spermatozoa were incubated for 15, 30, 45 and 60 min in Sperm-TALP medium. We observed an increase in the number of viable sperm (double negatives) after 15 min of incubation compared to sperm undergoing PS externalization and late necrotic sperms (P < 0.001) in each group of dogs. We also found a higher number of early necrotic sperm after 60 min of in vitro incubation (P < 0.001). The amounts of late necrotic sperm and cells with PS externalization were similar among animals of different age groups. We show for the first time that most viable sperm are recovered after an in vitro incubation step of 15 min (control samples in this study) because as the time of incubation increases so does the number of degenerated or damaged cells. The higher number of early necrotic cells after 60 min of in vitro incubation may be a special feature of this species and may result from the induction of necrosis in the sperm. This knowledge may be used in future experiments for the preparation of spermatozoa following in vitro fertilization in dogs.
机译:摘要:尽管没有报道表明提纯提纯对这种哺乳动物哺乳动物精子活力的影响,但在一些研究中已经清楚地证明了选定的精液补充剂对冻融狗精子活力的影响。因此,本研究的目的是研究在上清液纯化后的体外温育时间变化后,精子中的磷脂酰丝氨酸(PS)的外在化和坏死。从(i)十只六个月至1.5岁的狗,(ii)十只六至八岁的狗和(iii)十只十一至十三岁的狗收集狗精液样品。采用流式细胞仪(SU)纯化技术后,采用流式细胞术评估狗在不同年龄组动物中的精子活力。 SU后,将精子在Sperm-TALP培养基中孵育15、30、45和60分钟。我们观察到,在每组狗中,经过15分钟孵育的精子数量(双阴性)与经历PS外化作用的精子和晚期坏死精子相比有所增加(P <0.001)。在体外培养60分钟后,我们还发现了更多的早期坏死精子(P <0.001)。不同年龄组动物的晚期坏死精子和带有PS外在化作用的细胞数量相似。我们首次展示了在15分钟的体外温育步骤(本研究中的对照样品)后,大​​多数存活的精子得以恢复,因为随着温育时间的增加,变性或受损细胞的数量也会增加。体外培养60分钟后,早期坏死细胞数量增加,可能是该物种的特殊特征,可能是由于精子中坏死的诱导。该知识可用于狗体外受精后制备精子的未来实验中。

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