Effects of long-term in vitro exposure of ejaculated boar sperm to zearalenone and α-zearalenol in sperm liquid storage medium
Effects of long-term in vitro exposure of ejaculated boar sperm to zearalenone and α-zearalenol in sperm liquid storage medium
复制标题
精子液体储存介质中玉米赤霉烯酮和α-玉米赤霉烯醇对射精公猪精子长期体外暴露的影响
DOI:
10.1111/j.1740-0929.2012.01033.x
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发表时间:
2013
影响因子:
2
通讯作者:
J. Fink-Gremmels and T. Otoi
中科院分区:
文献类型:
--
作者:
R. Sambuu;M. Takagi;Z. Namula;M. Nii;M. Taniguchi;S. Uno;E. Kokushi;C. Tshering;R. Rodrigues dos Santos;J. Fink-Gremmels and T. Otoi
The effects ofin vitroexposure of porcine spermatozoa to zearalenone (ZEN) and α‐zearalenol (α‐ZOL) were studied by evaluating several parameters of anin vitrofertilization (IVF) system. For this purpose, boar spermatozoa cultured with semen storage medium containing 0 (control), 10 and 1000 µg/L of ZEN and α‐ZOL for 1 week at 5°C were used for IVF ofin vitromatured oocytes. Overall, there were no significant differences in the rates of total penetration, monospermic fertilization, and polyspermic fertilization of oocytes inseminated with spermatozoa from the different groups. Similarly, ZEN and α‐ZOL at 10 and 1000 µg/L did not have detrimental effects on the cleavage and development to blastocysts of oocytes afterin vitrofertilization. Although the motility, viability, and plasma membrane integrity of spermatozoa significantly decreased after 3 weeks of storage compared to non‐stored spermatozoa (P< 0.05), ZEN and α‐ZOL at the evaluated concentrations did not exert detrimental effects on the above parameters, even after 3 weeks of storage. These results indicate that prolonged exposure of boar spermatozoa to ZEN and α‐ZOL up to 1000 µg/L under reduced metabolic conditions does not affect theirin vitrofunction.