Sukapiriya Chawin, Chanpalakorn Niramol, Chalermsanyakorn Panas, Leungwattanakij Somboon
Division of Urology, Department of Surgery, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Int J Androl. 2005 Aug;28(4):230-3. doi: 10.1111/j.1365-2605.2005.00533.x.
We have previously reported that irrigation of the distal vas deferens using a normal saline solution (NSS) is successful in removing a large amount of spermatozoa from the tract. However, this technique does not completely remove all the motile spermatozoa from the ejaculate. The aim of the present study is to evaluate the location of the residual spermatozoa after distally irrigating the vas deferens. Twenty male Sprague-Dawley rats (400-450 g) constitute our study population. The animals were divided into two groups: group 1, control group (n = 10), rats that undergo only vasectomy and group 2, experimented group (n = 10), rats that undergo vasectomy and distal irrigation of the vas deferens using 3 mL of NSS. In both groups, the middle and terminal parts of the vas deferens including the seminal vesicles are removed and sent for spermatozoa count. The post-vasectomy urine samples containing spermatozoa are obtained by mid-ventral cystocentesis and the concentration is determined using a haemocytometer. More spermatozoa was found in the urine samples of the experimented group than the control (21.3 +/- 10.61 vs. 0.2 +/- 0.20 million/ml, p-value = 0.068), and lesser residual sperms reside at both the middle and the terminal parts of the vas deferens (0.5 +/- 0.31 vs. 3.0 +/- 0.00; p = 0.008 and 1.1 +/- 0.99 vs. 2.0 +/- 0.00; p = 0.036 respectively). No sperms were present in the seminal vesicles of the control group, but two of 10 rats in the experimented group had few to moderate amount of sperms in their seminal vesicles (p = 0.180). After the distal irrigation of the vas deferens using NSS, some residual sperms resided in the middle and more at the distal part of the vas with a few that escaped into the seminal vesicles.
我们之前曾报道,使用生理盐水(NSS)冲洗输精管远端能成功从管道中清除大量精子。然而,该技术并不能完全清除射精中的所有活动精子。本研究的目的是评估输精管远端冲洗后残留精子的位置。20只雄性Sprague-Dawley大鼠(400-450克)构成我们的研究群体。动物被分为两组:第1组,对照组(n = 10),仅接受输精管切除术的大鼠;第2组,实验组(n = 10),接受输精管切除术并使用3毫升NSS冲洗输精管远端的大鼠。在两组中,包括精囊在内的输精管中部和末端部分被切除并送去进行精子计数。通过腹中部膀胱穿刺获取输精管切除术后含精子的尿液样本,并使用血细胞计数器测定浓度。实验组尿液样本中的精子比对照组多(21.3±10.61对0.2±0.20百万/毫升,p值 = 0.068),输精管中部和末端的残留精子较少(分别为0.5±0.31对3.0±0.00;p = 0.008和1.1±0.99对2.0±0.00;p = 0.036)。对照组精囊中无精子,但实验组10只大鼠中有2只精囊中有少量至中等数量的精子(p = 0.180)。使用NSS对输精管远端进行冲洗后,一些残留精子位于输精管中部,更多位于输精管远端,少数进入了精囊。