Bucak Mustafa Numan, Keskin Nazan, Bodu Mustafa, Bülbül Bülent, Kırbaş Mesut, Öztürk Ali Erdem, Frootan Fateme, İli Pınar, Özkan Hüseyin, Başpınar Nuri, Dursun Şükrü
Department of Reproduction and Artificial Insemination, Faculty of Veterinary Sciences, Selçuk University, Konya, Turkey.
Department of Histology and Embryology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Andrology. 2022 Mar;10(3):585-594. doi: 10.1111/andr.13130. Epub 2021 Nov 30.
Sperm cryopreservation has been widely used in the field of reproductive biotechnology. It applies to certain males of economic and scientific values, including livestock breeds or endangered animal species. The development of a semen extender with a low cryoprotectant concentration and an appropriate amount of trehalose and boron can prevent the deterioration of sperm parameters.
The main goal of this study is to establish a suitable ram extender model, by examining different combinations of high (5%) and low (3%) glycerol concentrations (to reduce its toxic effects on sperm freezing), a fixed amount of trehalose and an increased dose of boron to prevent the deterioration of sperm parameters, and investigate the levels of gene expressions.
The Merino ram ejaculates were collected. The collected ejaculates providing the defined criteria were pooled. The pooled ejaculates were divided into eight aliquots and diluted with the Tris extender including different combinations of glycerol (5% and 3%) and boron (0.25, 0.5, and 1 mm) concentrations and a fixed amount of trehalose, then frozen. After freeze-thawing process, sperm motility, mitochondrial membrane activity, plasma membrane integrity, acrosomal membrane integrity, DNA damage (single cell gel electrophoresis (COMET) and TUNEL assays) as well as NAD(P)H quinone oxyreductase (NQO1), glutamate-cycteine ligase (GCLC), and glutathione S-transferase (GSTP1) for molecular mechanisms of sperm cell response to oxidative stress were assessed for different extender groups following freeze-thawing process: 5% glycerol + 0 mm boron (G5B0.00), 5% glycerol + 0.25 mm boron (G5B0.25), 5% glycerol + 0.5 mm boron (G5B0.50), 5% glycerol + 1 mm boron (G5B1.00), 3% glycerol + 0 mm boron (G3B.00), 3% glycerol + 0.25 mm boron (G3B0.25), 3% glycerol + 0.5 mm boron (G3B0.50), and 3% glycerol + 1 mm boron (G3B1.00).
G3B0.25 presented higher percentages of subjective motility, mitochondrial activity, and viability of spermatozoa comparing with G5B0.00 and groups with boron. Supplementation of 0.25 mm boron with and without trehalose (G3B0.25 and G5B0.25) showed higher acrosome integrity, compared with G5B0.00, G5B1.00, G3B0.50, and G3B1.00. For TUNEL analysis, G3B1.00 showed the highest DNA integrity among the experimental groups which was statistically significant only with G5B0.50 (p < 0.05). The mRNA levels of NQO1 were significantly decreased in G5B1.00, G3B0.50, and G3B1.00, when compared to G5B0.00. In comparison with G5B0.00, supplementation of 1 mm boron with and without trehalose had significantly lower expression of GCLC. The level of GSTP1 gene was significantly lower (approximately threefold) in G3B1.00, compared to G5B0.00 (p < 0.05).
It can be assumed that the increase of the boron concentration in the extender may have important adverse effects on sperm parameters and antioxidant gene expression after thawing. The results obtained from this study will help to understand the toxicity limits of boron and eliminate the toxicity of glycerol in studies of gametes and tissue freezing. Therefore, it can be concluded that the use of sufficient boron can decrease cryodamages of cryopreservation of mammalian spermatozoa as well tissue engineering.
精子冷冻保存已在生殖生物技术领域广泛应用。它适用于具有经济和科学价值的某些雄性动物,包括家畜品种或濒危动物物种。开发一种具有低冷冻保护剂浓度以及适量海藻糖和硼的精液稀释剂,可以防止精子参数恶化。
本研究的主要目标是通过检测高(5%)和低(3%)甘油浓度(以降低其对精子冷冻的毒性作用)的不同组合、固定量的海藻糖以及增加硼剂量以防止精子参数恶化,建立一个合适的公羊稀释剂模型,并研究基因表达水平。
采集美利奴公羊的射精精液。将符合既定标准的采集精液汇集。将汇集的精液分成八等份,并用含有甘油(5%和3%)和硼(0.25、0.5和1毫摩尔)浓度不同组合以及固定量海藻糖的Tris稀释剂进行稀释,然后冷冻。在冻融过程后,对不同稀释剂组在冻融过程后的精子活力、线粒体膜活性、质膜完整性、顶体膜完整性、DNA损伤(单细胞凝胶电泳(彗星试验)和TUNEL检测)以及用于精子细胞对氧化应激反应分子机制的NAD(P)H醌氧化还原酶(NQO1)、谷氨酸 - 半胱氨酸连接酶(GCLC)和谷胱甘肽S - 转移酶(GSTP1)进行评估:5%甘油 + 0毫摩尔硼(G5B0.00)、5%甘油 + 0.25毫摩尔硼(G5B0.25)、5%甘油 + 0.5毫摩尔硼(G5B0.50)、5%甘油 + 1毫摩尔硼(G5B1.00)、3%甘油 + 0毫摩尔硼(G3B.00)、3%甘油 + 0.25毫摩尔硼(G3B0.25)、3%甘油 + 0.5毫摩尔硼(G3B0.50)和3%甘油 + 1毫摩尔硼(G3B1.00)。
与G5B0.00和含硼组相比,G3B0.25组的主观活力、线粒体活性和精子活力百分比更高。与G5B0.00、G5B1.00、G3B0.50和G3B1.00相比,添加0.25毫摩尔硼(无论有无海藻糖)的G3B0.25和G5B0.25组显示出更高的顶体完整性。对于TUNEL分析,G3B1.00组在实验组中显示出最高的DNA完整性,仅与G5B0.50组有统计学差异(p < 0.05)。与G5B0.00相比,G5B1.00、G3B0.50和G3B1.00组中NQO1的mRNA水平显著降低。与G5B0.00相比,添加1毫摩尔硼(无论有无海藻糖)的组GCLC表达显著降低。与G5B0.00相比,G3B1.00组中GSTP1基因水平显著降低(约三倍)(p < 0.05)。
可以推测,稀释剂中硼浓度的增加可能对解冻后的精子参数和抗氧化基因表达产生重要的不利影响。本研究获得的结果将有助于了解硼的毒性限度,并在配子和组织冷冻研究中消除甘油的毒性。因此,可以得出结论,使用适量的硼可以减少哺乳动物精子冷冻保存以及组织工程中的冷冻损伤。