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Luteolin-Loaded Chitosan Nanoparticles Attenuate Fenvalerate-Induced Nephrotoxicity and Humoral Immune Suppression
Ahmed M S Hegazy1, Ayat B Al-Ghafari2,3,4, Huda A Al Doghaither2
1Department of Anatomy, Faculty of Medicine, Northern Border University, Arar, Saudi Arabia.
Abstract:
Fenvalerate (FEV), a widely used pyrethroid, induces renal toxicity and suppresses humoral immunity. This study evaluated the protective effects of crude luteolin (LUT) and LUT-loaded chitosan nanoparticles (LUT-CHNPs) in male Wistar rats. The research included 60 rats divided into six groups: control, LUT, LUT-CHNPs, FEV, FEV + LUT, and FEV + LUT-CHNPs and administered oral treatment for a duration of 30 days. Exposure to FEV elevated levels of renal biomarkers, oxidative stress markers, pro-inflammatory cytokines, apoptotic proteins, and complement C3. It also reduced levels of antioxidant enzymes, GSH, NRF2/HO-1 expression, Bcl-2, and immunoglobulins (IgG, IgM). The concurrent administration of LUT-CHNPs significantly enhanced these alterations, restoring renal function, oxidative balance, anti-inflammatory and anti-apoptotic mechanisms, and humoral immunity. Histopathological and ultrastructural analyses confirmed the preservation of glomerular and tubular architecture, mitochondrial integrity, and organization of apical microvilli with LUT-CHNPs, indicating superior efficacy relative to crude LUT. The findings indicate that LUT-CHNPs enhance drug bioavailability and safeguard the kidneys and immune system against FEV-induced nephrotoxicity and immune suppression.
Insights
Fenvalerate causes kidney damage and immune suppression. LUT-loaded chitosan nanoparticles protected rats by restoring kidney function, reducing oxidative stress, and boosting immunity, showing superior effects to crude luteolin.
Area of Science:
- Toxicology
- Nanotechnology
- Immunology
Background:
- Fenvalerate (FEV), a pyrethroid insecticide, is known to cause nephrotoxicity and immune suppression.
- Luteolin (LUT), a natural flavonoid, possesses antioxidant and anti-inflammatory properties.
- Chitosan nanoparticles (CHNPs) can enhance the bioavailability and delivery of therapeutic agents.
Purpose of the Study:
- To evaluate the protective effects of crude luteolin (LUT) and LUT-loaded chitosan nanoparticles (LUT-CHNPs) against Fenvalerate (FEV)-induced nephrotoxicity and immune suppression in male Wistar rats.
- To compare the efficacy of LUT-CHNPs with crude LUT in mitigating FEV toxicity.
Main Methods:
- Sixty male Wistar rats were divided into six groups and treated orally for 30 days.
- Groups included: control, LUT, LUT-CHNPs, FEV, FEV + LUT, and FEV + LUT-CHNPs.
- Biochemical, oxidative stress, inflammatory, apoptotic, and immunological parameters were assessed. Histopathological and ultrastructural analyses were performed.
Main Results:
- FEV exposure increased renal biomarkers, oxidative stress, pro-inflammatory cytokines, and apoptotic proteins, while decreasing antioxidant enzymes, GSH, NRF2/HO-1, Bcl-2, and immunoglobulins (IgG, IgM).
- LUT-CHNPs significantly ameliorated FEV-induced alterations, restoring renal function, oxidative balance, and humoral immunity.
- Histopathology confirmed LUT-CHNPs preserved kidney architecture and mitochondrial integrity, demonstrating superior efficacy over crude LUT.
Conclusions:
- LUT-loaded chitosan nanoparticles effectively protect against Fenvalerate-induced nephrotoxicity and immune suppression.
- LUT-CHNPs demonstrate enhanced bioavailability and therapeutic efficacy compared to crude luteolin.
- This study highlights the potential of nano-formulated luteolin as a protective agent against pesticide-induced organ damage and immune dysfunction.
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