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Neuroprotective Effect of Propolis Polyphenol-Based Nanosheets in Cellular and Animal Models of Rotenone-Induced Parkinson’S Disease Publisher Pubmed



Mamashli F1 ; Meratan AA2 ; Ghasemi A1 ; Obeidi N3 ; Salmani B2 ; Atarod D1 ; Pirhaghi M1 ; Moosavimovahedi F1 ; Mohammadzaheri M1 ; Shahsavani MB4 ; Habibikelishomi Z1 ; Goliaei B1 ; Gholami M5 ; Saboury AA1
Authors
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Authors Affiliations
  1. 1. Institute of Biochemistry and Biophysics, University of Tehran, Tehran, 1417614335, Iran
  2. 2. Department of Biological Sciences, Institute for Advanced Studies in Basic Sciences (IASBS), Zanjan, 6673145137, Iran
  3. 3. Department of Clinical Sciences, Faculty of Veterinary Medicine, Islamic Azad University, Karaj Branch, Karaj, 3149968111, Iran
  4. 4. Protein Chemistry Laboratory (PCL), Department of Biology, College of Sciences, Shiraz University, Shiraz, 7196484334, Iran
  5. 5. Department of Toxicology & Pharmacology, Faculty of Pharmacy, Toxicology and Poisoning Research Centre, Tehran University of Medical Sciences, Tehran, 1417614411, Iran

Source: ACS Chemical Neuroscience Published:2023


Abstract

Considering the central role of oxidative stress in the onset and progress of Parkinson’s diseases (PD), search for compounds with antioxidant properties has attracted a growing body of attention. Here, we compare the neuroprotective effect of bulk and nano forms of the polyphenolic fraction of propolis (PFP) against rotenone-induced cellular and animal models of PD. Mass spectrometric analysis of PFP confirmed the presence of multiple polyphenols including kaempferol, naringenin, coumaric acid, vanillic acid, and ferulic acid. In vitro cellular experiments indicate the improved efficiency of the nano form, compared to the bulk form, of PFP in attenuating rotenone-induced cytotoxicity characterized by a decrease in cell viability, release of lactate dehydrogenase, increased ROS generation, depolarization of the mitochondrial membrane, decreased antioxidant enzyme activity, and apoptosis induction. In vivo experiments revealed that while no significant neuroprotection was observed relating to the bulk form, PFP nanosheets were very effective in protecting animals, as evidenced by the improved behavioral and neurochemical parameters, including decreased lipid peroxidation, increased GSH content, and antioxidant enzyme activity enhancement. We suggest that improved neuroprotective effects of PFP nanosheets may be attributed to their increased water solubility and enrichment with oxygen-containing functional groups (such as OH and COOH), leading to increased antioxidant activity of these compounds. © 2023 American Chemical Society.