Department of Gastroenterology, Institute of Surgery Research, Daping Hospital, Third Military Medical University, Chongqing 400042, China.
Toxicol Lett. 2013 Oct 24;222(2):224-32. doi: 10.1016/j.toxlet.2013.05.644. Epub 2013 Jun 7.
Non-alcoholic fatty liver disease (NAFLD) is closely associated with reduced levels of testosterone, which may affect fertility. Herein, we investigated whether NAFLD impairs the reproductive function of male rats. Male Sprague-Dawley rats were fed a high fat diet (HFD) until they developed NAFLD. N-3 polyunsaturated fatty acid (PUFA) was then given for 4 weeks to prevent hepatic steatosis. Testes weight and serum and testicular testosterone were significantly lower in rats with NAFLD compared with healthy controls. Testicular pathological changes in NAFLD rats included markedly reduced sperm number and motility, and the number of apoptotic spermatogenic cells was higher, which was consistent with a reduction in the number of tetraploid cells. Breeding experiments indicated that paternal NAFLD affected neither the sperm morphology nor the development of fetuses and offspring, but did prolong the days required for insemination. However, administration of N-3 PUFA alleviated the impairment of reproductive function. These results suggest that NAFLD impairs reproductive function in male rats by decreasing testicular testosterone synthesis, and N-3 PUFA treatment may have a beneficial therapeutic effect.
非酒精性脂肪性肝病(NAFLD)与睾丸酮水平降低密切相关,而睾丸酮可能会影响生育能力。本研究旨在探讨 NAFLD 是否会损害雄性大鼠的生殖功能。雄性 Sprague-Dawley 大鼠给予高脂肪饮食(HFD)直至发生 NAFLD。然后给予 N-3 多不饱和脂肪酸(PUFA)治疗 4 周以预防肝脂肪变性。与健康对照组相比,NAFLD 大鼠的睾丸重量和血清及睾丸睾丸酮明显降低。NAFLD 大鼠的睾丸组织学变化包括精子数量和活力显著减少,且凋亡性精原细胞数量增加,这与四倍体细胞数量减少一致。繁殖实验表明,父代 NAFLD 既不影响精子形态,也不影响胚胎和后代的发育,但确实延长了授精所需的天数。然而,N-3 PUFA 的给药可减轻生殖功能障碍。这些结果表明,NAFLD 通过降低睾丸睾丸酮合成来损害雄性大鼠的生殖功能,而 N-3 PUFA 治疗可能具有有益的治疗作用。