Department of Morphology, Institute of Biosciences, UNESP-Univ Estadual Paulista, Botucatu, São Paulo, Brazil.
PLoS One. 2013 Jun 12;8(6):e66091. doi: 10.1371/journal.pone.0066091. Print 2013.
Sperm acquire motility and fertility capacity during epididymal transit, under the control of androgens and sympathetic innervations. It is already known that the acceleration of epididymal sperm transit time can lead to lower sperm quality. In a previous work we showed that rats exposed to the anorexigen sibutramine, a non-selective serotonin-norepinephrine reuptake inhibitor, presented faster sperm transit time, lower epididymal sperm reserves and potentiation of the tension of epididymal duct to norepinephrine exposed acutely in vitro to sibutramine. In the present work we aimed to further investigate pharmacological mechanisms involved in these alterations and the impact on rat sperm quality. For this, adult male Wistar rats were treated with sibutramine (10 mg/kg/day) or vehicle for 30 days. Sibutramine decreased final body, seminal vesicle, ventral prostate and epididymal weights, as well as sperm transit time in the epididymal cauda. On the contrary of the in vitro pharmacological assays, in which sibutramine was added directly to the bath containing strips of distal epididymal cauda, the ductal tension was not altered after in vivo sub-chronic exposure to sibutramine. However, there is pharmacological evidence that the endogenous epididymal norepinephrine reserves were reduced in these animals. It was also shown that the decrease in prostate weight can be related to increased tension developed of the gland, due to sibutramine sympathomimetic effects. In addition, our results showed reduced sperm quality after in utero artificial insemination, a more sensitive procedure to assess fertility in rodents. The epididymal norepinephrine depletion exerted by sibutramine, associated with decreases in sperm transit time, quantity and quality, leading to reduced fertility in this experimental model, reinforces the concerns about the possible impact on fertility of man taking sibutramine as well as other non-selective serotonin-norepinephrine reuptake inhibitors, especially considering the lower reproductive efficiency of humans compared to males of other species.
精子在附睾转运过程中获得运动能力和生育能力,受雄激素和交感神经支配。已知附睾精子转运时间的加速会导致精子质量下降。在之前的一项工作中,我们发现暴露于厌食药西布曲明(一种非选择性 5-羟色胺去甲肾上腺素再摄取抑制剂)的大鼠附睾精子转运时间更快,附睾精子储备减少,并且在体外急性暴露于西布曲明时,附睾管对去甲肾上腺素的张力增强。在本工作中,我们旨在进一步研究这些变化涉及的药理学机制及其对大鼠精子质量的影响。为此,成年雄性 Wistar 大鼠用西布曲明(10mg/kg/天)或载体处理 30 天。西布曲明降低了终体重、精囊、腹侧前列腺和附睾重量,以及附睾尾部的精子转运时间。与在体外药理学测定相反,在体外药理学测定中,西布曲明直接添加到含有远端附睾尾部条带的浴中,而在体内亚慢性暴露于西布曲明后,管腔张力并未改变。然而,有药理学证据表明,这些动物的内源性附睾去甲肾上腺素储备减少。还表明,由于西布曲明的拟交感作用,前列腺重量的减少可能与腺体张力的增加有关。此外,我们的结果显示,宫内人工授精后精子质量下降,这是一种更敏感的评估啮齿动物生育力的方法。西布曲明引起的附睾去甲肾上腺素耗竭,与精子转运时间、数量和质量的减少有关,导致该实验模型生育力下降,这加剧了人们对服用西布曲明和其他非选择性 5-羟色胺去甲肾上腺素再摄取抑制剂的人可能对生育能力产生影响的担忧,尤其是考虑到与其他物种的雄性相比,人类的生殖效率较低。