۶-Gingerol Improves Human Freezing Thawing Process

سال انتشار: 1397
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 40

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شناسه ملی سند علمی:

SCROYAN14_225

تاریخ نمایه سازی: 14 آبان 1403

چکیده مقاله:

Background: Cryopreservation of human sperm associatedwith an increase in reactive oxygen species (ROS) which leadto lipid peroxidation of sperm membrane. Natural antioxidantsimprove the quality and metabolic activity of sperm during thecryopreservation. Ginger (Zingiberofficinale Roscoe, Zingiberaceae)contains volatile oil rich pungent principiesShogaols,zingerone, and gingerols) that exhibited substantial antioxidantactivities. In this study we evaluated the effect of gingerol asan antioxidant in sperm cryopreservation medium on differentsperm parameters during the freezing thawing process.Materials and Methods: Semen were collected from ۲۰ normospermicmen referring to the Royan Institute and dividedinto three groups; Fresh group, control freezing group andfreezing with ۶-gingerol (final concentration of ۱۰μM) group.Finally, sperm motility the levels of malondialdehyde (MDA)and acrosome intact were evaluated in all groups.Results: Evaluation of sperm motility was performed withcomputer-assisted-semen analysis (CASA). Total motility andprogressive motility was significantly Lowe in freezing group(۲۹.۹۰% ± ۲.۱۳% and ۳۰.۰۳% ± ۲.۸۲ resp) compared to freshgroup (۶۱.۲۷% ± ۲.۹۵). However, MDA levels in the freezinggroup were higher than fresh group (P<۰.۰۵).There was no significantdifference between freezing and freezing + Gingerol insperm motility and MDA levels. Acrosome intact were evaluatedby hypo osmotic swelling test (HOST). Acrosome intact infresh and freezing + Gingerol groups were significantly higher(۸۴.۴۵% ± ۱.۹۴% and ۶۳.۵۰% ± ۱.۴۱% respectively) than freezinggroup (۵۳.۲۵% ± ۱.۵۱).Conclusion: Accordingly, we concluded that although Gingerolimproved sperm viability, it did not show positive effecton MDA levels and motility. It seems that addition of Gingerolto freezing medium can improve sperm freezing condition.

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نویسندگان

R Bahiraei

Department of Biology, Faculty of Science and Research, Islamic Azad University, Tehran, Iran- Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran

P Maghami

Department of Biology, Faculty of Science and Research, Islamic Azad University, Tehran, Iran

B Ebrahimi

Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran

M Sabbaghian

Department of Andrology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran

V Esmaeili

Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran