chrysin and Infertility--Male

chrysin has been researched along with Infertility--Male* in 2 studies

Other Studies

2 other study(ies) available for chrysin and Infertility--Male

ArticleYear
Improvement in colistin-induced reproductive damage, apoptosis, and autophagy in testes via reducing oxidative stress by chrysin.
    Journal of biochemical and molecular toxicology, 2018, Volume: 32, Issue:11

    This study aimed to investigate the effect of chrysin on colistin-induced reproductive toxicity. Twenty-eight adult male Sprague-Dawley rats were divided into four groups of seven rats each. Group I received physiological saline for 7 days. Group II received 50 mg/kg/day chrysin for 7 days. Group III received a total dose of 73 mg/kg colistin for 7 days. Group IV received 50 mg/kg/day chrysin by an oral gavage after the colistin treatment. Colistin causes an increase in oxidative stress (OS) in the testis. Chrysin treatment significantly decreased the OS in the chrysin + colistin group compared with the colistin group. The highest caspase-3 and LC3B expression levels were found in the colistin group and these levels were statistically lower in the chrysin + colistin group. Colistin treatment caused a decrease in sperm motility and an increase in sperm abnormality. Chrysin treatment mitigated these side effects significantly. In conclusion, chrysin treatment can be beneficial against colistin-induced reproductive toxicity.

    Topics: Animals; Anti-Bacterial Agents; Antioxidants; Apoptosis; Autophagy; Caspase 3; Colistin; Dietary Supplements; Epididymis; Flavonoids; Infertility, Male; Injections, Intramuscular; Male; Microtubule-Associated Proteins; Organ Size; Oxidative Stress; Rats, Sprague-Dawley; Sperm Motility; Spermatogenesis; Testis

2018
Chrysin Administration Protects against Oxidative Damage in Varicocele-Induced Adult Rats.
    Oxidative medicine and cellular longevity, 2017, Volume: 2017

    Oxidative stress is known as the leading factor responsible for varicocele-related infertility and for that reason, many antioxidant therapies have been proposed. Considering that, we evaluated the reproductive outcomes and fertility of varicocelized rats and the impact of chrysin within these parameters. The animals were allocated into three groups: sham (control), varicocele treated via gavage with 50 mg/kg/day of chrysin (V1), or vehicle (V2) for 56 days. Chrysin treatment prevented oxidative damage resulting from varicocele by decreasing testicular concentrations of malondialdehyde and sperm DNA fragmentation. It also improved histological aspect of the testis and maintained morphometric parameters similar to the sham group. Furthermore, there were no differences in body and reproductive organ weights, histopathological analysis of epididymis, sperm counts and morphology, testosterone levels, sexual behavior, and fertility parameters among experimental groups. Our results reinforce the idea that injuries provoked by experimental varicocele are related, at least in part, to oxidative stress. Moreover, varicocele showed bilateral deleterious effects without interfering with fertility. Chrysin administration significantly ameliorated sperm parameters, protecting the reproductive system against varicocele damages. For that reason, chrysin might be an alternative adjuvant therapy to improve sperm quality in men presenting this condition.

    Topics: Animals; Female; Flavonoids; Humans; Infertility, Male; Male; Oxidative Stress; Rats; Rats, Wistar; Sperm Motility; Testis; Varicocele

2017