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Diosmin protects the testicles from doxorubicin-induced damage by increasing steroidogenesis and suppressing
Mega O Oyovwi1,2, Benneth Ben-Azu3, Edesiri P Tesi4
1Department of Physiology, Adeleke University Ede, Osun State, Nigeria.
Background:
Cancer chemotherapy with doxorubicin (DOX) has been linked to serious testicular damage and spermatotoxicity due to the induction of oxidative stress, inflammation, and apoptosis. Thus, the current study was carried out to assess the potential ameliorative impact of diosmin, an antioxidant drug, against DOX-mediated spermatoxicity and testicular injury in rats.
Material And Methods:
In the experimental protocol, rats were grouped into 4: Group 1 received vehicle and saline for 8 weeks while group 2 received diosmin and saline concomitantly for 8 weeks. Group 3 was given 3 mg/kg intraperitoneal DOX once every 7 days for 8 weeks. Group 4 was given 40 mg/kg of diosmin orally for 56 days followed by DOX diosmin administration after one hour. After 56 days of treatment, sperm quality, hormonal testing, biochemical parameters, and histological alterations in the testes were evaluated.
Results:
DOX-induced reduce spermatogenic function, testicular 3- and 17β-Hydroxysteroid dehydrogenases, and serum follicle stimulating hormone, luteinizing hormone, and testosterone. It also enhanced inflammation, testicular oxidative damage, and apoptosis. The histopathologic examinations corroborated the biochemical results obtained. Significantly, diosmin treatment reduced DOX-induced injury, as evidenced by restored testicular architecture, increased steroidogenesis, preservation of spermatogenesis, suppression of oxide-inflammatory response, and apoptosis.
Conclusion:
It was found that through diosmin antioxidant, anti-apoptotic, and anti-oxido-inflammatory it presents a possible therapeutic alternative for protecting testicular tissue against DOX's harmful effects.
Insights
Diosmin, an antioxidant, protects against doxorubicin-induced testicular damage and spermatotoxicity by reducing oxidative stress, inflammation, and apoptosis. This study suggests diosmin as a potential therapeutic agent for mitigating chemotherapy side effects.
Area of Science:
- Reproductive Toxicology
- Pharmacology
- Biochemistry
Background:
- Doxorubicin (DOX) chemotherapy causes testicular damage and spermatotoxicity via oxidative stress, inflammation, and apoptosis.
- This study investigates the protective effects of diosmin against DOX-induced testicular injury in rats.
Purpose of the Study:
- To evaluate the ameliorative impact of diosmin on doxorubicin-mediated spermatotoxicity.
- To assess diosmin's potential as a protective agent against chemotherapy-induced testicular damage.
Main Methods:
- Rats were divided into four groups: control, diosmin only, doxorubicin only, and doxorubicin with diosmin.
- Treatments were administered over 8 weeks, followed by evaluation of sperm quality, hormone levels, biochemical markers, and testicular histology.
- Key parameters assessed included steroidogenic enzymes, oxidative stress markers, inflammatory markers, and apoptosis.
Main Results:
- Doxorubicin significantly reduced sperm quality, steroidogenic enzyme activity, and hormone levels (FSH, LH, testosterone).
- DOX treatment increased testicular oxidative damage, inflammation, and apoptosis, confirmed by histopathological findings.
- Diosmin administration counteracted DOX-induced testicular injury, restoring architecture, preserving spermatogenesis, and reducing inflammation and apoptosis.
Conclusions:
- Diosmin exhibits antioxidant, anti-apoptotic, and anti-inflammatory properties.
- Diosmin demonstrates significant potential as a therapeutic agent to protect testicular tissue from doxorubicin-induced toxicity.
- Diosmin may offer a protective strategy against the adverse reproductive effects of doxorubicin chemotherapy.
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