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Protective Effects of Auraptene against Free Radical-Induced Erythrocytes Damage

OBJECTIVES: Auraptene is the most abundant natural prenyloxycoumarin. Recent studies have shown that it has multiple biological and therapeutic properties, including antioxidant properties. Erythrocytes are constantly subjected to oxidative damage that can affect proteins and lipids within the eryth...

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Autores principales: Jamialahmadi, Khadijeh, Amiri, Amir Hossein, Zahedipour, Fatemeh, Faraji, Fahimeh, Karimi, Gholamreza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Pharmacopuncture Institute (KPI) 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806157/
https://www.ncbi.nlm.nih.gov/pubmed/36628343
http://dx.doi.org/10.3831/KPI.2022.25.4.344
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author Jamialahmadi, Khadijeh
Amiri, Amir Hossein
Zahedipour, Fatemeh
Faraji, Fahimeh
Karimi, Gholamreza
author_facet Jamialahmadi, Khadijeh
Amiri, Amir Hossein
Zahedipour, Fatemeh
Faraji, Fahimeh
Karimi, Gholamreza
author_sort Jamialahmadi, Khadijeh
collection PubMed
description OBJECTIVES: Auraptene is the most abundant natural prenyloxycoumarin. Recent studies have shown that it has multiple biological and therapeutic properties, including antioxidant properties. Erythrocytes are constantly subjected to oxidative damage that can affect proteins and lipids within the erythrocyte membrane and lead to some hemoglobinopathies. Due to the lack of sufficient information about the antioxidant effects of auraptene on erythrocytes, this study intended to evaluate the potential of this compound in protecting radical-induced erythrocytes damages. METHODS: The antioxidant activity of auraptene was measured based on DPPH and FRAP assays. Notably, oxidative hemolysis of human erythrocytes was used as a model to study the ability of auraptene to protect biological membranes from free radical-induced damage. Also, the effects of auraptene in different concentrations (25-400 µM) on AAPH-induced lipid/protein peroxidation, glutathione (GSH) content and morphological changes of erythrocytes were determined. RESULTS: Oxidative hemolysis and lipid/protein peroxidation of erythrocytes were significantly suppressed by auraptene in a time and concentration-dependent manner. Auraptene prevented the depletion of the cytosolic antioxidant GSH in erythrocytes. Furthermore, it inhibited lipid and protein peroxidation in a time and concentration-dependent manner. Likewise, FESEM results demonstrated that auraptene reduced AAPH-induced morphological changes in erythrocytes. CONCLUSION: Auraptene efficiently protects human erythrocytes against free radicals. Therefore, it can be a potent candidate for treating oxidative stress-related diseases.
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spelling pubmed-98061572023-01-09 Protective Effects of Auraptene against Free Radical-Induced Erythrocytes Damage Jamialahmadi, Khadijeh Amiri, Amir Hossein Zahedipour, Fatemeh Faraji, Fahimeh Karimi, Gholamreza J Pharmacopuncture Original Article OBJECTIVES: Auraptene is the most abundant natural prenyloxycoumarin. Recent studies have shown that it has multiple biological and therapeutic properties, including antioxidant properties. Erythrocytes are constantly subjected to oxidative damage that can affect proteins and lipids within the erythrocyte membrane and lead to some hemoglobinopathies. Due to the lack of sufficient information about the antioxidant effects of auraptene on erythrocytes, this study intended to evaluate the potential of this compound in protecting radical-induced erythrocytes damages. METHODS: The antioxidant activity of auraptene was measured based on DPPH and FRAP assays. Notably, oxidative hemolysis of human erythrocytes was used as a model to study the ability of auraptene to protect biological membranes from free radical-induced damage. Also, the effects of auraptene in different concentrations (25-400 µM) on AAPH-induced lipid/protein peroxidation, glutathione (GSH) content and morphological changes of erythrocytes were determined. RESULTS: Oxidative hemolysis and lipid/protein peroxidation of erythrocytes were significantly suppressed by auraptene in a time and concentration-dependent manner. Auraptene prevented the depletion of the cytosolic antioxidant GSH in erythrocytes. Furthermore, it inhibited lipid and protein peroxidation in a time and concentration-dependent manner. Likewise, FESEM results demonstrated that auraptene reduced AAPH-induced morphological changes in erythrocytes. CONCLUSION: Auraptene efficiently protects human erythrocytes against free radicals. Therefore, it can be a potent candidate for treating oxidative stress-related diseases. The Korean Pharmacopuncture Institute (KPI) 2022-12-31 2022-12-31 /pmc/articles/PMC9806157/ /pubmed/36628343 http://dx.doi.org/10.3831/KPI.2022.25.4.344 Text en © 2022 Korean Pharmacopuncture Institute https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jamialahmadi, Khadijeh
Amiri, Amir Hossein
Zahedipour, Fatemeh
Faraji, Fahimeh
Karimi, Gholamreza
Protective Effects of Auraptene against Free Radical-Induced Erythrocytes Damage
title Protective Effects of Auraptene against Free Radical-Induced Erythrocytes Damage
title_full Protective Effects of Auraptene against Free Radical-Induced Erythrocytes Damage
title_fullStr Protective Effects of Auraptene against Free Radical-Induced Erythrocytes Damage
title_full_unstemmed Protective Effects of Auraptene against Free Radical-Induced Erythrocytes Damage
title_short Protective Effects of Auraptene against Free Radical-Induced Erythrocytes Damage
title_sort protective effects of auraptene against free radical-induced erythrocytes damage
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9806157/
https://www.ncbi.nlm.nih.gov/pubmed/36628343
http://dx.doi.org/10.3831/KPI.2022.25.4.344
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