Cryoprotective effect of L-carnitine on motility, vitality and DNA oxidation of human spermatozoa.

Citation data:

Andrologia, ISSN: 1439-0272, Vol: 46, Issue: 6, Page: 637-41

Publication Year:
2014
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Citations 28
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Repository URL:
https://engagedscholarship.csuohio.edu/scichem_facpub/306
PMID:
23822772
DOI:
10.1111/and.12130
Author(s):
Banihani, S.; Agarwal, A.; Sharma, R.; Bayachou, Mekki
Publisher(s):
Wiley-Blackwell
Tags:
Biochemistry, Genetics and Molecular Biology; Medicine; DNA oxidation—L-carnitine—motility—sperm cryopreservation—vitality; Chemistry
article description
Successful cryopreservation for human spermatozoa markedly influences the reproductive outcomes of assisted reproductive technologies. But in spite of its usefulness, cryopreservation significantly decreases sperm quality. l-carnitine has been found to improve the quality of spermatozoa in selected cases with male infertility. Here, we examined the efficacy of l-carnitine in improving sperm motility and vitality and reducing sperm DNA oxidation during cryopreservation. Semen samples from infertile patients (n = 22) were collected and analysed. Cryopreservation medium supplemented with l-carnitine was mixed with the semen at a ratio of 1 : 1 (v/v). The final l-carnitine concentration in each cryovial was 0.5 mg ml(-1) per 5 × 10(6) cell ml(-1) . Controls were cryopreserved without addition of l-carnitine. After 24 h of cryopreservation, thawed sperm samples were analysed for motility, vitality and DNA oxidation. Sperm vitality was assessed by the eosin-nigrosin test, while sperm DNA oxidation was measured by flow cytometry. Addition of l-carnitine significantly improved sperm motility and vitality (P < 0.05) compared with the control. The flow cytometry experiment showed no statistical difference (P > 0.05) in the levels of DNA oxidation between samples and controls. In conclusion, l-carnitine improves human sperm motility and vitality, but has no effect on sperm DNA oxidation after cryopreservation.