Evaluating Neurotherapeutic Potential of Myricetin by In-Vivo research models

Authors

  • Marryum Dilshad Khanum IMCH, Karachi
  • Amber  Mekran Medical College, Turbat, Balochistan
  • Binish Anwar Continental Medical College. Lahore. Pakistan
  • Shumaila Kanwel Abu Umara medical and dental college Lahore, Pakistan
  • Pashmina Shaikh Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan
  • Pirya Liaquat university of Medical and Health Sciences Jamshoro, Sindh, Pakistan

DOI:

https://doi.org/10.36283/ziun-pjmd14-4/034

Keywords:

Nerve Growth Factor, Flavonoids, Rats, Wistar, Neurodegenerative Diseases

Abstract

Background: Oxidative stress, neuroinflammation, and poor neurotrophic signaling are associated with neurological diseases. Myricetin is a bioflavonoid present in berries, vegetables, and medicinal herbs, with strong anti-inflammatory, antioxidant, and neurotrophic properties in animal studies. The objective of the present in-vivo research was to assess the neuroprotective potential of myricetin on nerve growth factor (NGF) expression and neuroinflammation in chemically induced neural injury. Materials and Methods: Thirty healthy male adult Wistar rats (180-220g, 8 weeks old) were randomly divided into five groups (n=6 per group). Group I was used as a control, with no intervention. Groups II to V were exposed to a standard propionic acid (PPA) to induce neuroinflammation. Groups III-V were induced and subsequently administered with oral myricetin of 50 mg/kg, 100 mg/kg, and 200 mg/kg for 28 days. Serum levels of NGF were measured with Enzyme-linked Immunosorbent assay (ELISA). One-way ANOVA was performed for statistical analysis using SPSS. Results: PPA decreased NGF to 4.3 ± 0.5 pg/ml (p< 0.001). Myricetin restored NGF to 9.3, 7.6, and 9.8 pg/mL via 50, 100, and 200 mg/kg doses, respectively. At 200 mg/kg, C-reactive protein (CRP), tumor necrosis factor (TNF), and malondialdehyde (MDA) were decreased to 1.7 ± 0.2 mg/L, 26 ± 3 pg/mL, and 2.9 ± 0.3 nmol/mg, compared to 4.9 ± 0.4, 58 ± 4, and 6.7 ± 0.4. (p < 0.001). Conclusion: Myricetin exhibits promising neurotherapeutic potential, evidenced by its ability to upregulate NGF and mitigate neuroinflammatory damage, making it a potential therapeutic option for the treatment of neurological disorders.

Author Biographies

  • Marryum Dilshad Khanum, IMCH, Karachi

    Department of Pathology

  • Amber , Mekran Medical College, Turbat, Balochistan


    Department of Anatomy

  • Binish Anwar, Continental Medical College. Lahore. Pakistan

    Department of Pharmacology 


  • Shumaila Kanwel, Abu Umara medical and dental college Lahore, Pakistan

    Department of Pharmacology


  • Pashmina Shaikh, Liaquat University of Medical & Health Sciences, Jamshoro, Pakistan


    Department of Anatomy

  • Pirya , Liaquat university of Medical and Health Sciences Jamshoro, Sindh, Pakistan

    Department of Anatomy 

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Published

2025-09-29

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How to Cite

1.
Khanum MD, Amber , Anwar B, Kanwel S, Shaikh P, Pirya. Evaluating Neurotherapeutic Potential of Myricetin by In-Vivo research models. PJMD [Internet]. 2025 Sep. 29 [cited 2026 Jun. 4];14(4). Available from: https://ojs.zu.edu.pk/pjmd/article/view/4230

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