Effect of chrysin on methotrexate‐induced testicular damage in rats

This study was conducted on 28 male Wistar albino rats to determine the effects of chrysin on methotrexate‐induced damage to testicular tissue. Rats were grouped into four groups of seven rats reach: Group 1 (n = 7) was the control group to which no drugs were administered; this group was only provi...

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Published in:Andrologia Vol. 51; no. 1; pp. e13145 - n/a
Main Authors: Belhan, Saadet, Çomaklı, Selim, Küçükler, Sefa, Gülyüz, Fetih, Yıldırım, Serkan, Yener, Zabit
Format: Journal Article
Language:English
Published: Germany Wiley Subscription Services, Inc 01-02-2019
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Summary:This study was conducted on 28 male Wistar albino rats to determine the effects of chrysin on methotrexate‐induced damage to testicular tissue. Rats were grouped into four groups of seven rats reach: Group 1 (n = 7) was the control group to which no drugs were administered; this group was only provided with food and water. Group 2 (n = 7) was administered 20 mg/kg of methotrexate once intraperitoneally. Group 3 (n = 7) was administered 50 mg/kg of chrysin for 7 days orally. Group 4 (n = 7) was administered 20 mg/kg of methotrexate once intraperitoneally, followed by oral administration of 50 mg/kg of chrysin for 7 days. At the end of the experiment, rats were anaesthetised, rat testes were removed, and spermatozoon was obtained from the cauda epididymis. It was determined that sperm count and motility, glutathione peroxidase, superoxide dismutase and catalase activities decreased in the methotrexate group, whereas malondialdehyde, tumour necrosis factor‐α, interleukin‐1β and nuclear kappa factor B expression levels increased. Furthermore, damage to tubulus seminiferus structures and affusion in germ cells was identified. In the methotrexate + chrysin administered group, sperm count improved, biochemical enzyme levels increased, and structural improvements were observed in testicular tubules. These findings demonstrated that chrysin plays a protective role in testicular damage in rats.
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ISSN:0303-4569
1439-0272
DOI:10.1111/and.13145