Bilodeau J F, Blanchette S, Gagnon C, Sirard M A
Département des Sciences Animales, Université Laval, Quebec, Canada.
Theriogenology. 2001 Jul 15;56(2):275-86. doi: 10.1016/s0093-691x(01)00562-3.
We previously showed that cryopreservation of bull spermatozoa in egg yolk Tris extender (EYTG) significantly reduced the intracellular level of thiols. Other studies showed the beneficial effects of adding antioxidants to cryopreserved bull spermatozoa. These studies led us to investigate the effects of various thiols, an important class of antioxidants, on sperm motility of cryopreserved bull semen in a commonly used extender, EYTG. Sperm motility was analyzed by computer-assisted semen analysis (CASA). After thawing, a diluted pool of bull semen was incubated at 38.5 degrees C in airtight tubes with the following thiols for 6 hours: glutathione (GSH/GSSG), cysteine, N-acetyl-L-cysteine (NAC) and 2-mercaptoethanol in the presence or absence of oxidative stress. The oxidative stress was caused by adding H2O2 (100 microM) to diluted semen. Incubation of diluted bull semen in EYTG at 38.5 degrees C over a period of 6 h decreased sperm motility by approximately 9 fold from the start (72 +/- 3, mean +/- SEM, n=4) to the end (9 +/- 4, n=4) of the incubation. We found that all thiols to a concentration above 0.5 mM maintained high sperm motility for 6 h in the absence of an external source of oxidative stress (52 +/- 4, for 4 thiols). However, one mM of each thiol was required to efficiently protect sperm motility in the presence of 100 microM of H2O2 for 6 h. We also found that the GSH concentration in diluted semen was too low (microM) to adequately supply exogenous addition of 72 U/mL of glutathione peroxidase (GPx), an enzyme that detoxifies H2O2 and hydroperoxides using GSH as a cofactor. In fact, a better protection of sperm motility could be achieved with only 5 U/mL of GPx and 0.1 mM of GSH added to diluted semen. Our results also demonstrated that added GSSG (0.5 mM) in diluted semen was not regenerated efficiently to GSH over 6 h. The latter result indicated in the extender that the glutathione redox-cycle was deficient. Therefore, deleterious effects sperm motility after cryopreservation in EYTG can be counteracted by adding various thiols at mM concentration.
我们之前的研究表明,在卵黄Tris稀释液(EYTG)中冷冻保存公牛精子会显著降低细胞内的硫醇水平。其他研究表明,向冷冻保存的公牛精子中添加抗氧化剂具有有益效果。这些研究促使我们在常用的稀释液EYTG中,研究各类重要抗氧化剂硫醇对冷冻保存的公牛精液精子活力的影响。通过计算机辅助精液分析(CASA)对精子活力进行分析。解冻后,将稀释的公牛精液池在38.5摄氏度下于密封管中与以下硫醇一起孵育6小时:谷胱甘肽(GSH/GSSG)、半胱氨酸、N-乙酰-L-半胱氨酸(NAC)和2-巯基乙醇,同时设置有无氧化应激的条件。氧化应激通过向稀释精液中添加H2O2(100微摩尔)来引发。在EYTG中于38.5摄氏度下将稀释的公牛精液孵育6小时,精子活力从孵育开始时(72±3,平均值±标准误,n = 4)到结束时(9±4,n = 4)下降了约9倍。我们发现,在不存在外部氧化应激源的情况下,所有硫醇浓度高于0.5毫摩尔时能在6小时内维持较高的精子活力(4种硫醇时为52±4)。然而,在存在100微摩尔H2O2的情况下有效保护精子活力6小时,每种硫醇需要1毫摩尔。我们还发现,稀释精液中的GSH浓度过低(微摩尔),无法充分提供外源添加的72单位/毫升谷胱甘肽过氧化物酶(GPx),该酶以GSH作为辅助因子来解毒H2O2和氢过氧化物。实际上,向稀释精液中仅添加5单位/毫升的GPx和0.1毫摩尔的GSH就能更好地保护精子活力。我们的结果还表明,在稀释精液中添加的GSSG(0.5毫摩尔)在6小时内不能有效地再生为GSH。后一结果表明在稀释液中谷胱甘肽氧化还原循环存在缺陷。因此,在EYTG中冷冻保存后对精子活力的有害影响可通过添加毫摩尔浓度的各类硫醇来抵消。