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Silver Nanoparticles Loaded with Oleuropein Reduce Doxorubicin-Induced Testicular Damage by Regulating Endoplasmic
Elif Erbaş1, Volkan Gelen2, Hülya Kara3
1Department of Histology and Embryology, Faculty of Veterinary Medicine, Atatürk University, Erzurum, Turkey.
Abstract:
Doxorubicin (DOX) is the most used chemotherapeutic agent for treating solid tumors. DOX treatment may lead to testicular damage using oxidative stress, resulting in infertility. These adverse effects may be prevented by the activation of antioxidant systems. Oleuropein (OLE) is a powerful flavonoid with several ameliorative effects, including antioxidative, antiproliferative, and anti-inflammatory. It would be more efficient and applicable in treating chronic human diseases if its poor bioavailability improves with a nano-delivery system. The current study aims to assess the histopathological changes and antioxidative effects of OLE loaded with silver nanoparticles oleuropein (OLE-AgNP) on the testicular injury triggered by DOX in rats. Forty-eight male albino rats were randomly divided into six groups as follows: the control, DOX (2.5 mg/kg), OLE (50 mg/kg), AgNP (100 mg/kg), OLE + AgNP (50 mg/kg), OLE (50 mg/kg) + DOX (2.5 mg/kg), AgNP (100 mg/kg) + DOX (2.5 mg/kg), and OLE-AgNP (50 mg/kg) + DOX (2.5 mg/kg) for 11 days. Oxidative stress, inflammation, apoptosis, endoplasmic reticulum stress markers, sperm analysis, and histopathological analyses were performed on testicular tissues taken from rats decapitated after the applications and compared between the experimental groups. The tissue MDA level was lower in the OLE and OLE+AgNP-treated groups than in the DOX-treated group. In addition, SOD and GSH levels significantly increased in both the OLE and OLE+AgNP-treated groups compared to the DOX group. Both OLE and OLE+AgNP, particularly OLE+AgNP, ameliorated DOX-induced testicular tissue injury, as evidenced by reduced injury and improved seminiferous tubules and spermatocyte area. In addition, OLE and OLE+AgNP, especially OLE+AgNP, inhibited DOX-induced testicular tissue inflammation, apoptosis, and endoplasmic reticulum stress. The findings suggest that nanotechnology and the production of OLE+AgNP can ameliorate DOX-induced testicular damage.
Insights
Doxorubicin causes testicular damage, but oleuropein loaded silver nanoparticles (OLE-AgNP) show protective effects. OLE-AgNP treatment reduced oxidative stress and inflammation, preserving testicular health against chemotherapy damage.
Area of Science:
- Biomedical Science
- Toxicology
- Nanotechnology
Background:
- Doxorubicin (DOX) is a widely used chemotherapy drug for solid tumors.
- DOX treatment can induce testicular damage via oxidative stress, leading to infertility.
- Oleuropein (OLE), a potent antioxidant flavonoid, has therapeutic potential but suffers from poor bioavailability.
Purpose of the Study:
- To evaluate the protective effects of oleuropein loaded with silver nanoparticles (OLE-AgNP) against Doxorubicin-induced testicular injury in rats.
- To assess the histopathological changes and antioxidative impacts of OLE-AgNP on testicular tissue.
Main Methods:
- Forty-eight male rats were divided into eight groups, receiving treatments including DOX, OLE, AgNP, and OLE-AgNP.
- Key markers of oxidative stress, inflammation, apoptosis, and endoplasmic reticulum stress were analyzed in testicular tissues.
- Sperm analysis and histopathological examinations were conducted to assess testicular damage and recovery.
Main Results:
- OLE and OLE-AgNP treatments significantly reduced malondialdehyde (MDA) levels and increased superoxide dismutase (SOD) and glutathione (GSH) levels compared to the DOX group.
- OLE-AgNP notably ameliorated DOX-induced testicular injury, improving seminiferous tubules and spermatocyte areas.
- OLE and OLE-AgNP, particularly OLE-AgNP, inhibited DOX-induced inflammation, apoptosis, and endoplasmic reticulum stress in testicular tissues.
Conclusions:
- Nanotechnology-based delivery of oleuropein (OLE-AgNP) effectively mitigates Doxorubicin-induced testicular damage.
- OLE-AgNP demonstrates significant antioxidative, anti-inflammatory, and anti-apoptotic effects, protecting testicular function.
- The findings highlight the therapeutic potential of OLE-AgNP for preventing chemotherapy-induced male infertility.
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