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Integration of Ultrastructural and Computational Approaches Reveals the Protective Effect of Astaxanthin against BPA-Induced Nephrotoxicity

Background: Bisphenol A (BPA) is an environmental contaminant that can induce deleterious organ effects. Human Cytochrome P450 CYP2C9 enzyme belongs to the essential xenobiotic-metabolizing enzymes, producing ROS as a byproduct. Astaxanthin (ATX) is a powerful antioxidant that protects organs and ti...

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Autores principales: A. Eid, Refaat, Alaa Edeen, Muhammad, Soltan, Mohamed A., Al-Shraim, Mubarak, Samir A. Zaki, Mohamed, M. Al-Qahtani, Saleh, Fayad, Eman, T. Salem, Eman, K. Abdulsahib, Waleed, Emam, Hebatallah, M. Hassan, Hesham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953522/
https://www.ncbi.nlm.nih.gov/pubmed/36830956
http://dx.doi.org/10.3390/biomedicines11020421
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author A. Eid, Refaat
Alaa Edeen, Muhammad
Soltan, Mohamed A.
Al-Shraim, Mubarak
Samir A. Zaki, Mohamed
M. Al-Qahtani, Saleh
Fayad, Eman
T. Salem, Eman
K. Abdulsahib, Waleed
Emam, Hebatallah
M. Hassan, Hesham
author_facet A. Eid, Refaat
Alaa Edeen, Muhammad
Soltan, Mohamed A.
Al-Shraim, Mubarak
Samir A. Zaki, Mohamed
M. Al-Qahtani, Saleh
Fayad, Eman
T. Salem, Eman
K. Abdulsahib, Waleed
Emam, Hebatallah
M. Hassan, Hesham
author_sort A. Eid, Refaat
collection PubMed
description Background: Bisphenol A (BPA) is an environmental contaminant that can induce deleterious organ effects. Human Cytochrome P450 CYP2C9 enzyme belongs to the essential xenobiotic-metabolizing enzymes, producing ROS as a byproduct. Astaxanthin (ATX) is a powerful antioxidant that protects organs and tissues from the damaging effects of oxidative stress caused by various diseases. Aim of the study: This study investigated the possible protective impacts of ATX against BPA-induced nephrotoxicity and its underlying mechanism. Materials and methods: Kidney tissues were isolated and examined microscopically from control, protected, and unprotected groups of rats to examine the potential protective effect of ATX against nephrotoxicity. Moreover, a molecular dynamic (MD) simulation was conducted to predict the performance of ATX upon binding to the active site of P450 CYP2C9 protein receptor as a potential mechanism of ATX protective effect. Results: Implemented computational methods revealed the possible underlying mechanism of ATX protection; the protective impact of ATX is mediated by inhibiting P450 CYP2C9 through binding to its dimeric state where the RMSF value for apo-protein and ATX-complex system were 5.720.57 and 1.040.41, respectively, implicating the ATX-complex system to have lesser variance in its residues, leading to the prevention of ROS excess production, maintaining the oxidant-antioxidant balance and re-establishing the proper mitochondrial functionality. Furthermore, the experimental methods validated in silico outcomes and revealed that ATX therapy effectively restored the typical histological architecture of pathological kidney tissues. Conclusions: ATX prevents BPA-induced nephrotoxicity by controlling oxidative imbalance and reversing mitochondrial dysfunction. These outcomes shed new light on the appropriate use of ATX as a treatment or prophylactic agent for these severe conditions.
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spelling pubmed-99535222023-02-25 Integration of Ultrastructural and Computational Approaches Reveals the Protective Effect of Astaxanthin against BPA-Induced Nephrotoxicity A. Eid, Refaat Alaa Edeen, Muhammad Soltan, Mohamed A. Al-Shraim, Mubarak Samir A. Zaki, Mohamed M. Al-Qahtani, Saleh Fayad, Eman T. Salem, Eman K. Abdulsahib, Waleed Emam, Hebatallah M. Hassan, Hesham Biomedicines Article Background: Bisphenol A (BPA) is an environmental contaminant that can induce deleterious organ effects. Human Cytochrome P450 CYP2C9 enzyme belongs to the essential xenobiotic-metabolizing enzymes, producing ROS as a byproduct. Astaxanthin (ATX) is a powerful antioxidant that protects organs and tissues from the damaging effects of oxidative stress caused by various diseases. Aim of the study: This study investigated the possible protective impacts of ATX against BPA-induced nephrotoxicity and its underlying mechanism. Materials and methods: Kidney tissues were isolated and examined microscopically from control, protected, and unprotected groups of rats to examine the potential protective effect of ATX against nephrotoxicity. Moreover, a molecular dynamic (MD) simulation was conducted to predict the performance of ATX upon binding to the active site of P450 CYP2C9 protein receptor as a potential mechanism of ATX protective effect. Results: Implemented computational methods revealed the possible underlying mechanism of ATX protection; the protective impact of ATX is mediated by inhibiting P450 CYP2C9 through binding to its dimeric state where the RMSF value for apo-protein and ATX-complex system were 5.720.57 and 1.040.41, respectively, implicating the ATX-complex system to have lesser variance in its residues, leading to the prevention of ROS excess production, maintaining the oxidant-antioxidant balance and re-establishing the proper mitochondrial functionality. Furthermore, the experimental methods validated in silico outcomes and revealed that ATX therapy effectively restored the typical histological architecture of pathological kidney tissues. Conclusions: ATX prevents BPA-induced nephrotoxicity by controlling oxidative imbalance and reversing mitochondrial dysfunction. These outcomes shed new light on the appropriate use of ATX as a treatment or prophylactic agent for these severe conditions. MDPI 2023-02-01 /pmc/articles/PMC9953522/ /pubmed/36830956 http://dx.doi.org/10.3390/biomedicines11020421 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
A. Eid, Refaat
Alaa Edeen, Muhammad
Soltan, Mohamed A.
Al-Shraim, Mubarak
Samir A. Zaki, Mohamed
M. Al-Qahtani, Saleh
Fayad, Eman
T. Salem, Eman
K. Abdulsahib, Waleed
Emam, Hebatallah
M. Hassan, Hesham
Integration of Ultrastructural and Computational Approaches Reveals the Protective Effect of Astaxanthin against BPA-Induced Nephrotoxicity
title Integration of Ultrastructural and Computational Approaches Reveals the Protective Effect of Astaxanthin against BPA-Induced Nephrotoxicity
title_full Integration of Ultrastructural and Computational Approaches Reveals the Protective Effect of Astaxanthin against BPA-Induced Nephrotoxicity
title_fullStr Integration of Ultrastructural and Computational Approaches Reveals the Protective Effect of Astaxanthin against BPA-Induced Nephrotoxicity
title_full_unstemmed Integration of Ultrastructural and Computational Approaches Reveals the Protective Effect of Astaxanthin against BPA-Induced Nephrotoxicity
title_short Integration of Ultrastructural and Computational Approaches Reveals the Protective Effect of Astaxanthin against BPA-Induced Nephrotoxicity
title_sort integration of ultrastructural and computational approaches reveals the protective effect of astaxanthin against bpa-induced nephrotoxicity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953522/
https://www.ncbi.nlm.nih.gov/pubmed/36830956
http://dx.doi.org/10.3390/biomedicines11020421
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