Murase Tetsuma, Imaeda Noriaki, Yamada Hiroto, Takasu Masaki, Taguchi Kazuo, Katoh Tsutomu
Laboratory of Theriogenology, Division of Veterinary Medicine, Faculty of Applied Biological Sciences, Gifu University, Gifu, Japan.
J Reprod Dev. 2010 Jun;56(3):309-14. doi: 10.1262/jrd.09-157n. Epub 2010 Mar 3.
The present study investigated whether substitution of HEPES for bicarbonate in BTS (BTS-H) used to dilute boar ejaculates immediately after ejaculation could reduce the increased inducibility of the acrosome reaction by calcium and calcium ionophore A23187. When an ejaculate was split, diluted 5-fold with regular BTS (BTS-B) and BTS-H and stored at 17 C for 12 h or 60 h, the extender or storage time had no significant influence on sperm motility or viability measured by the eosin-nigrosin method. When spermatozoa diluted serially with BTS-B and stored (36 h) were stimulated with Ca2+ (3 mM) and A23187 (0.3 microM), the proportion of spermatozoa that underwent the acrosome reaction (% acrosome reactions) significantly increased as the magnifications of dilution increased (bicarbonate content almost unchanged by dilution). By contrast, the % acrosome reactions in spermatozoa similarly diluted and stored with BTS-H decreased with the increasing magnifications of dilution (bicarbonate decreased). Sperm motility immediately after the end of incubation without A23178 tended to be lower for BTS-H than BTS-B, and the ejaculates for BTS-H had a tendency to have a lower total protein in seminal plasma than those for BTS-B. These results implied that the samples for BTS-H could be used as a model for ejaculates possibly collected during summer and showing subfertility. When an ejaculate was split, diluted serially with BTS-B and BTS-H and stored, viability measured by staining with propidium iodide was extremely similar between the 2 extenders and among the different dilution magnifications, regardless of whether spermatozoa were washed (stored for 36-66 h) or not (stored for 66-72 h). These results suggest that boar ejaculate can be stored with BTS-H at least according to the results for sperm motility and viability and that hypersensitivity of spermatozoa to Ca2+ and A23187 potentially associated with boar subfertility could be lessened by diluting ejaculates with BTS-H.
本研究调查了在射精后立即用于稀释公猪精液的BTS(BTS-H)中,用HEPES替代碳酸氢盐是否可以降低钙和钙离子载体A23187诱导顶体反应的增加。当一份精液被分成两份,分别用常规BTS(BTS-B)和BTS-H稀释5倍,并在17℃下储存12小时或60小时时,稀释剂或储存时间对通过伊红-黑色素法测量的精子活力或生存力没有显著影响。当用BTS-B连续稀释并储存(36小时)的精子用Ca2+(3 mM)和A23187(0.3 microM)刺激时,发生顶体反应的精子比例(顶体反应百分比)随着稀释倍数的增加而显著增加(碳酸氢盐含量几乎不因稀释而改变)。相比之下,用BTS-H类似稀释并储存的精子中的顶体反应百分比随着稀释倍数的增加而降低(碳酸氢盐减少)。在没有A23178的孵育结束后,BTS-H处理的精子活力立即往往低于BTS-B处理的精子,并且BTS-H处理的精液在精浆中的总蛋白含量往往低于BTS-B处理的精液。这些结果表明,BTS-H处理的样本可以用作可能在夏季采集且表现出生育力低下的精液的模型。当一份精液被分成两份,分别用BTS-B和BTS-H连续稀释并储存时,无论精子是否洗涤(储存36-66小时)或未洗涤(储存66-72小时),通过碘化丙啶染色测量的生存力在两种稀释剂之间以及不同稀释倍数之间都极其相似。这些结果表明,至少根据精子活力和生存力的结果,公猪精液可以用BTS-H储存,并且用BTS-H稀释精液可以减轻精子对Ca2+和A23187的超敏反应,而这种超敏反应可能与公猪生育力低下有关。