Tissue & cell · 2026
Astaxanthin-loaded chitosan nanoparticles attenuate chlorpyrifos-induced nephrotoxicity via activation of the Nrf2/HO-1 axis and suppression of oxidative, inflammatory, and apoptotic pathways.
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Obaid Ahmad A, Ghaith Mazen M, Alshammari Ahmad Najem, Elmorsy Ekramy M, Fawzy Manal S, Ebrahim Neven A, Salem Hamada S, Hussein Nashwa Mostafa
Аннотация
BACKGROUND: Chlorpyrifos was shown to cause oxidative, inflammatory, and apoptotic renal damage. The natural Astaxanthin (ASX) exhibits nephroprotective effects, however its limited bioavailability hinders its therapeutic potential. Chitosan nanoparticles were shown to enhance bioavailability and therapeutic delivery of the natural compounds.
OBJECTIVE: This study investigated the renoprotective effects of astaxanthin-loaded chitosan nanoparticles (ASX-CNPs) compared with crude astaxanthin (ASX) against chlorpyrifos (CPF)-induced nephrotoxicity in male Wistar rats.
METHODS: Ninety rats (235 g) were randomly assigned into six groups (n = 15) and orally treated for 60 days with saline, ASX (40 mg/kg), ASX-CNPs (40 mg/kg), CPF (10 mg/kg), or combinations of CPF with ASX or ASX-CNPs. ASX-CNPs were characterized by transmission electron microscopy and dynamic light scattering, revealing uniform spherical nanoparticles with high stability and an encapsulation efficiency of 84.72 %. Oxidative, inflammatory, and apoptotic pathways were evaluated via different assays RESULTS: CPF exposure significantly impaired renal function, elevating blood urea, creatinine, uric acid, cystatin C, and NGAL levels, while promoting oxidative stress, lipid peroxidation, and DNA damage. CPF also suppressed the Nrf2/HO-1 antioxidant pathway, triggered inflammation and nitrosative stress, and disrupted apoptotic balance by increasing Bax and Caspase-3 while decreasing Bcl-2 expression. Histopathological and ultra-structural analysis confirmed severe renal alterations, including glomerular contraction, structurally disrupted mitochondria, vascular congestion, and tubular degeneration. Co-treatment with ASX-CNPs markedly ameliorated biochemical, oxidative, inflammatory, nitrosative, and apoptotic disturbances, restoring renal morphology close to normal. In contrast, crude ASX provided partial protection, with less pronounced effects on antioxidant enzyme activities, cytokine levels, and tissue architecture. The superior efficacy of ASX-CNPs highlights the advantages of nanoparticle delivery in enhancing bioavailability, stability, and cellular uptake compared with the conventional form.
CONCLUSION: These findings indicate that ASX-CNPs represent a promising nanotherapeutic strategy for preventing CPF-induced kidney injury and demonstrate the enhanced protective potential of nanoformulations over their crude counterparts.
OBJECTIVE: This study investigated the renoprotective effects of astaxanthin-loaded chitosan nanoparticles (ASX-CNPs) compared with crude astaxanthin (ASX) against chlorpyrifos (CPF)-induced nephrotoxicity in male Wistar rats.
METHODS: Ninety rats (235 g) were randomly assigned into six groups (n = 15) and orally treated for 60 days with saline, ASX (40 mg/kg), ASX-CNPs (40 mg/kg), CPF (10 mg/kg), or combinations of CPF with ASX or ASX-CNPs. ASX-CNPs were characterized by transmission electron microscopy and dynamic light scattering, revealing uniform spherical nanoparticles with high stability and an encapsulation efficiency of 84.72 %. Oxidative, inflammatory, and apoptotic pathways were evaluated via different assays RESULTS: CPF exposure significantly impaired renal function, elevating blood urea, creatinine, uric acid, cystatin C, and NGAL levels, while promoting oxidative stress, lipid peroxidation, and DNA damage. CPF also suppressed the Nrf2/HO-1 antioxidant pathway, triggered inflammation and nitrosative stress, and disrupted apoptotic balance by increasing Bax and Caspase-3 while decreasing Bcl-2 expression. Histopathological and ultra-structural analysis confirmed severe renal alterations, including glomerular contraction, structurally disrupted mitochondria, vascular congestion, and tubular degeneration. Co-treatment with ASX-CNPs markedly ameliorated biochemical, oxidative, inflammatory, nitrosative, and apoptotic disturbances, restoring renal morphology close to normal. In contrast, crude ASX provided partial protection, with less pronounced effects on antioxidant enzyme activities, cytokine levels, and tissue architecture. The superior efficacy of ASX-CNPs highlights the advantages of nanoparticle delivery in enhancing bioavailability, stability, and cellular uptake compared with the conventional form.
CONCLUSION: These findings indicate that ASX-CNPs represent a promising nanotherapeutic strategy for preventing CPF-induced kidney injury and demonstrate the enhanced protective potential of nanoformulations over their crude counterparts.