Viring S, Einarsson S
Acta Vet Scand. 1980;21(4):598-606. doi: 10.1186/BF03546847.
The main purpose of the present study was to investigate whether boar seminal plasma affects the transport of spermatozoa in the genital tract of oestrous pigs or not, with special reference to the sperm transport into the oviducts. Altogether 17 gilts were used in three experiments. Experiment I. In nine gilts one uterine horn was injected surgically with 10 spermatozoa suspended in seminal plasma and the other uterine horn with 10 spermatozoa suspended in TESNaK-glucose buffer solution. The sperm deposition was performed under general anaesthesia. The gilts were slaughtered 1–2 or 4–6 h after insemination. The genital tract was removed and the numbers of spermatozoa determined in oviducts and in uterine horns. Experiment II. The insemination doses were prepared exactly as in Experiment I. Approx. 24 h before insemination Polyvinylchloride cannulas were inserted into the uterine lumen of the horns, drawn via the midventral incision at linea alba subcutaneously to cutaneous incisions ventral to the vulva opening. One cannula was placed in each uterine horn. At standing heat the insemination doses were slowly injected through the cannulas. The gilts were slaughtered 1 h after insemination and the numbers of spermatozoa within the genital tract were counted. Experiment III. In three gilts under general anaesthesia the uterine horns were ligated 10 cm from the uterotubal junction. The semen doses (containing 2 × 10 spermatozoa), prepared as in Experiment I, were deposited into the uterine horns anterior to the ligatures through a cannula. The gilts were slaughtered 1 h after insemination, and the numbers of spermatozoa within the oviducts and ligated part of the uterine horns were counted. In all three experiments more spermatozoa were, on average, recovered in the oviducts connected to uterine horns inseminated with spermatozoa suspended in seminal plasma. In Experiments I and II this was the case for 10 of 14 gilts and in Experiment III for all the three gilts. It is therefore suggested that boar seminal plasma pro¬motes sperm transport into the oviduct of oestrous pigs. The back¬ground mechanism for this is discussed.
本研究的主要目的是探讨公猪精液血浆是否会影响发情母猪生殖道内精子的运输,特别是精子向输卵管的运输。在三个实验中总共使用了17头后备母猪。实验一:在9头后备母猪中,通过手术向一个子宫角注射悬浮于精液血浆中的10个精子,向另一个子宫角注射悬浮于TESNaK - 葡萄糖缓冲液中的10个精子。精子接种在全身麻醉下进行。在授精后1 - 2小时或4 - 6小时屠宰母猪。取出生殖道,测定输卵管和子宫角中的精子数量。实验二:授精剂量的制备与实验一完全相同。在授精前约24小时,将聚氯乙烯套管插入子宫角的子宫腔,经白线处的腹中线切口皮下引出至外阴开口腹侧的皮肤切口。每个子宫角放置一个套管。在静立发情时,将授精剂量缓慢通过套管注入。在授精后1小时屠宰母猪,计数生殖道内的精子数量。实验三:在3头处于全身麻醉状态的后备母猪中,在距子宫输卵管连接处10厘米处结扎子宫角。将按实验一制备的精液剂量(含有2×10个精子)通过套管注入结扎部位前方的子宫角。在授精后1小时屠宰母猪,计数输卵管和结扎部位子宫角内的精子数量。在所有三个实验中,平均而言,与用悬浮于精液血浆中的精子授精的子宫角相连的输卵管中回收的精子更多。在实验一和实验二中,14头后备母猪中有10头是这种情况,在实验三中,所有3头后备母猪都是这种情况。因此,表明公猪精液血浆促进精子向发情母猪的输卵管运输。并讨论了其背后的机制。