Possible mechanisms involved in the protective effect of lutein against cyclosporine-induced testicular damage in rats
- 1Department of Human Physiology, Adeleke University, Ede, Osun State, Nigeria.
- 2Department of Pharmacology, Faculty of Basic Medical Science, Delta State University, Abraka, Delta State, Nigeria.
- 3Department of Science Laboratory Technology, Delta State Polytechnic, Ogwashi-Uku, Delta State, Nigeria.
- 4Department of Human Physiology, University of Medical Sciences, Ondo, Ondo State, Nigeria.
- 5Department of Human Physiology, University of Ibadan, Ibadan, Oyo State, Nigeria.
- 6Department of Pharmacology and Therapeutics, Faculty of Basic Clinical Science, Delta State University, Abraka, Delta State, Nigeria.
- 7Department of Human Physiology, Faculty of Basic Medical Science, Delta State University, Abraka, Delta State, Nigeria.
- 0Department of Human Physiology, Adeleke University, Ede, Osun State, Nigeria.
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View abstract on PubMed
Summary
This summary is machine-generated.Lutein protects against cyclosporine-induced reproductive damage by reducing oxidative stress and inflammation. This study highlights lutein
Area Of Science
- Reproductive Biology
- Toxicology
- Biochemistry
Background
- Cyclosporine impairs reproductive function via oxidative stress and inflammation.
- Antioxidant and anti-inflammatory agents may counteract cyclosporine's adverse effects.
- Lutein possesses antioxidant and anti-inflammatory properties, but its protective role in cyclosporine-induced reproductive impairment is not fully understood.
Purpose Of The Study
- To investigate the protective effects of lutein against cyclosporine-induced reproductive impairment in male Wistar rats.
- To elucidate the role of the nuclear factor erythroid 2 related factor-2 (Nrf2)/heme-oxygenase-1 (HO-1)/connexin-43 (Cx-43) signaling pathway in lutein's protective mechanism.
Main Methods
- Male Wistar rats were administered cyclosporine (40 mg/kg) and/or lutein (30 mg/kg) daily for four weeks.
- Assays were performed to measure testicular antioxidant markers, inflammatory cytokines, apoptotic proteins, and other relevant biochemical parameters.
- Specific focus was placed on evaluating the Nrf2/HO-1/Cx-43 and NOX-1 signaling pathways.
Main Results
- Cyclosporine significantly increased oxidative stress markers (e.g., TBARS, MPO) and pro-inflammatory cytokines (e.g., TNF-α, IL-1β).
- Lutein treatment reversed cyclosporine-induced increases in oxidative stress and inflammation, and reduced apoptosis (caspase-3, -9).
- Lutein upregulated the Nrf2/HO-1/Cx-43 pathway and downregulated NOX-1 signaling, restoring antioxidant enzyme levels (SOD, CAT, GSH) and testicular function.
Conclusions
- Lutein demonstrates significant protective effects against cyclosporine-induced reproductive impairment.
- These protective mechanisms involve lutein's antioxidant, anti-apoptotic, and anti-inflammatory properties.
- Upregulation of the Nrf2/HO-1/Cx-43 pathway and downregulation of NOX-1 signaling are key to lutein's beneficial effects.
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