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  6. Comparative Neuroprotective Potential Of Nanoformulated And Free Resveratrol Against Cuprizone-induced Demyelination In Rats

Comparative Neuroprotective Potential of Nanoformulated and Free Resveratrol Against Cuprizone-Induced Demyelination in Rats

Sara A M El-Sayed1, Ghadha Ibrahim Fouad2, Maha Z Rizk2

  • 1Refractories, Ceramics and Building Materials Department, National Research Centre, 33 El Bohouth St., Dokki, PO Box 12622, Cairo, Egypt. sarali_87@yahoo.com.

Molecular Neurobiology
|August 16, 2024

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View abstract on PubMed

Summary
This summary is machine-generated.

Resveratrol-loaded iron oxide nanoparticles (IONP-RESV) effectively reduced demyelination and neuroinflammation in a rat model. IONP-RESV demonstrated superior neuroprotection compared to free resveratrol, showing promise for treating neurological diseases like multiple sclerosis.

Area of Science:

  • Neuroscience
  • Biomedical Engineering
  • Pharmacology

Background:

  • Demyelination, a hallmark of multiple sclerosis (MS), causes significant neurological impairment.
  • The cuprizone (CZ) model is widely used to study demyelination induced by oxidative stress and neuroinflammation.
  • Resveratrol (RESV), a polyphenol, exhibits neuroprotective properties.

Purpose of the Study:

  • To investigate the therapeutic efficacy of resveratrol-loaded iron oxide nanoparticles (IONP-RESV) against CZ-induced demyelination and neuroinflammation in a rat model.
  • To compare the neuroprotective effects of IONP-RESV with free RESV.

Main Methods:

  • Induction of demyelination using cuprizone (CZ) in a rat model.
  • Administration of free resveratrol (RESV) and resveratrol-loaded iron oxide nanoparticles (IONP-RESV).
Keywords:
CuprizoneDemyelinationMagnetite nanoparticlesMultiple sclerosis

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  • Molecular analysis of myelin proteolipid protein (PLP), tumor necrosis factor-α (TNF-α), and S100β expression.
  • Histopathological examination of cerebral cortices.
  • Main Results:

    • CZ exposure led to decreased PLP expression and increased TNF-α and S100β levels, indicating demyelination and neuroinflammation.
    • Both RESV and IONP-RESV treatments reversed CZ-induced alterations.
    • IONP-RESV exhibited enhanced anti-inflammatory activity, with greater downregulation of TNF-α and S100β compared to RESV alone.
    • Histopathology confirmed the neuroprotective effects of both treatments, with IONP-RESV showing superior results.

    Conclusions:

    • RESV-loaded IONPs offer enhanced neuroprotective benefits over free RESV in mitigating demyelination and neuroinflammation.
    • IONP-RESV demonstrates significant pro-remyelinating, anti-inflammatory, and antioxidant properties.
    • IONP-RESV holds promise as a future neurotherapeutic intervention for neurological disorders such as MS.
    Resveratrol