A Comparative Study on the Ameliorating Role of Flavonoids Rich Fraction Versus Zinc Oxide Nanoparticles in Spinal Cord of Multiple Sclerosis Rat Model Targeting PINK-1/PARKIN; A Biochemical, Histological and Immunohistochemical study | ||||
Egyptian Journal of Histology | ||||
Articles in Press, Accepted Manuscript, Available Online from 08 September 2024 | ||||
Document Type: Original Article | ||||
DOI: 10.21608/ejh.2024.311160.2121 | ||||
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Authors | ||||
Radwa Ismail![]() ![]() ![]() ![]() ![]() ![]() ![]() | ||||
1Anatomy and Embryology department, Faculty of Medicine, Tanta University | ||||
2Department of Pharmacognosy, Faculty of Pharmacy, Tanta University | ||||
3Pharmacology Department, Faculty of Medicine, Tanta University | ||||
4Physiology Department, Faculty of Medicine, Tanta University | ||||
5Medical Biochemistry Department, Faculty of Medicine, Tanta University | ||||
6Pharmaceutical Microbiology Department, Faculty of Pharmacy, Tanta University | ||||
7Rheumatology, Rehabilitation and Physical Medicine Department, Faculty of Medicine, Tanta University | ||||
8Anatomy and embryology department, Faculty of Medicine, Tanta university | ||||
Abstract | ||||
Introduction: Multiple sclerosis (MS) as an autoimmune condition causes demyelination and neuronal loss. Materials and methods: Forty-eight male adult dark agouti rats divided into six equal groups, group I functioned as control group. EAE was induced in rats of group II, III and IV; Flavonoids rich fraction (FRF) used as treatment of rats in group III; zinc oxide nanoparticles (ZnO-NPs) used as treatment of rats in group IV; Group V received Flavonoids rich fraction; Group VI received zinc oxide nanoparticles. The lumbar spinal cord was divided into three parts. The first part was for enzyme-linked immunosorbent assay (ELISA) and quantitative reverse transcription polymerase chain reaction (qRT-PCR) techniques. The second part of the spinal cord was for histopathological and immunohistochemical studies (H&E – MBP). The third part was for electron microscopic study. Results: This study demonstrates, for the first time, the beneficial effects of ZnO-NPs over FRF in ameliorating oxidative stress, modulating immune responses, reducing inflammation, and promoting neurodegenerative changes in a rat model of MS. Both FRF, and ZnO-NPs significantly suppressed the inflammatory activity detected in EAE model, through increasing IL-10 and decreasing lL-17 and TNF-α compared to the EAE group. H&E of sections of Group IV (ZnO-NPs treated group) revealed nearly normal architecture of lumbar section of spinal cord with myelinated nerve fibers and normal blood vessels. TEM examination of Flavonoids treated group (group III) showed less affected axons with little irregularity of myelin sheath. Group IV (ZnO-NPs treated group) TEM examination showed nearly normal nerve fibers axons with normal compact myelin sheath and normally arranged mitochondria with normal cristae. Conclusion: These outcomes might lessen symptoms, reduce the rate at which the illness progresses, enhance the quality of life for MS patients, and the potential intervention of ZnO-NPs as a therapeutic strategy for MS. | ||||
Keywords | ||||
Flavonoids; zinc oxide nanoparticles; spinal cord; multiple sclerosis; rats | ||||
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