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Sulforaphane Protects against Unilateral Ureteral Obstruction-Induced Renal Damage in Rats by Alleviating Mitochondrial and Lipid Metabolism Impairment

Unilateral ureteral obstruction (UUO) is an animal rodent model that allows the study of obstructive nephropathy in an accelerated manner. During UUO, tubular damage is induced, and alterations such as oxidative stress, inflammation, lipid metabolism, and mitochondrial impairment favor fibrosis deve...

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Autores principales: Aranda-Rivera, Ana Karina, Cruz-Gregorio, Alfredo, Aparicio-Trejo, Omar Emiliano, Tapia, Edilia, Sánchez-Lozada, Laura Gabriela, García-Arroyo, Fernando Enrique, Amador-Martínez, Isabel, Orozco-Ibarra, Marisol, Fernández-Valverde, Francisca, Pedraza-Chaverri, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598813/
https://www.ncbi.nlm.nih.gov/pubmed/36290577
http://dx.doi.org/10.3390/antiox11101854
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author Aranda-Rivera, Ana Karina
Cruz-Gregorio, Alfredo
Aparicio-Trejo, Omar Emiliano
Tapia, Edilia
Sánchez-Lozada, Laura Gabriela
García-Arroyo, Fernando Enrique
Amador-Martínez, Isabel
Orozco-Ibarra, Marisol
Fernández-Valverde, Francisca
Pedraza-Chaverri, José
author_facet Aranda-Rivera, Ana Karina
Cruz-Gregorio, Alfredo
Aparicio-Trejo, Omar Emiliano
Tapia, Edilia
Sánchez-Lozada, Laura Gabriela
García-Arroyo, Fernando Enrique
Amador-Martínez, Isabel
Orozco-Ibarra, Marisol
Fernández-Valverde, Francisca
Pedraza-Chaverri, José
author_sort Aranda-Rivera, Ana Karina
collection PubMed
description Unilateral ureteral obstruction (UUO) is an animal rodent model that allows the study of obstructive nephropathy in an accelerated manner. During UUO, tubular damage is induced, and alterations such as oxidative stress, inflammation, lipid metabolism, and mitochondrial impairment favor fibrosis development, leading to chronic kidney disease progression. Sulforaphane (SFN), an isothiocyanate derived from green cruciferous vegetables, might improve mitochondrial functions and lipid metabolism; however, its role in UUO has been poorly explored. Therefore, we aimed to determine the protective effect of SFN related to mitochondria and lipid metabolism in UUO. Our results showed that in UUO SFN decreased renal damage, attributed to increased mitochondrial biogenesis. We showed that SFN augmented peroxisome proliferator-activated receptor γ co-activator 1α (PGC-1α) and nuclear respiratory factor 1 (NRF1). The increase in biogenesis augmented the mitochondrial mass marker voltage-dependent anion channel (VDAC) and improved mitochondrial structure, as well as complex III (CIII), aconitase 2 (ACO2) and citrate synthase activities in UUO. In addition, lipid metabolism was improved, observed by the downregulation of cluster of differentiation 36 (CD36), sterol regulatory-element binding protein 1 (SREBP1), fatty acid synthase (FASN), and diacylglycerol O-acyltransferase 1 (DGAT1), which reduces triglyceride (TG) accumulation. Finally, restoring the mitochondrial structure reduced excessive fission by decreasing the fission protein dynamin-related protein-1 (DRP1). Autophagy flux was further restored by reducing beclin and sequestosome (p62) and increasing B-cell lymphoma 2 (Bcl2) and the ratio of microtubule-associated proteins 1A/1B light chain 3 II and I (LC3II/LC3I). These results reveal that SFN confers protection against UUO-induced kidney injury by targeting mitochondrial biogenesis, which also improves lipid metabolism.
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spelling pubmed-95988132022-10-27 Sulforaphane Protects against Unilateral Ureteral Obstruction-Induced Renal Damage in Rats by Alleviating Mitochondrial and Lipid Metabolism Impairment Aranda-Rivera, Ana Karina Cruz-Gregorio, Alfredo Aparicio-Trejo, Omar Emiliano Tapia, Edilia Sánchez-Lozada, Laura Gabriela García-Arroyo, Fernando Enrique Amador-Martínez, Isabel Orozco-Ibarra, Marisol Fernández-Valverde, Francisca Pedraza-Chaverri, José Antioxidants (Basel) Article Unilateral ureteral obstruction (UUO) is an animal rodent model that allows the study of obstructive nephropathy in an accelerated manner. During UUO, tubular damage is induced, and alterations such as oxidative stress, inflammation, lipid metabolism, and mitochondrial impairment favor fibrosis development, leading to chronic kidney disease progression. Sulforaphane (SFN), an isothiocyanate derived from green cruciferous vegetables, might improve mitochondrial functions and lipid metabolism; however, its role in UUO has been poorly explored. Therefore, we aimed to determine the protective effect of SFN related to mitochondria and lipid metabolism in UUO. Our results showed that in UUO SFN decreased renal damage, attributed to increased mitochondrial biogenesis. We showed that SFN augmented peroxisome proliferator-activated receptor γ co-activator 1α (PGC-1α) and nuclear respiratory factor 1 (NRF1). The increase in biogenesis augmented the mitochondrial mass marker voltage-dependent anion channel (VDAC) and improved mitochondrial structure, as well as complex III (CIII), aconitase 2 (ACO2) and citrate synthase activities in UUO. In addition, lipid metabolism was improved, observed by the downregulation of cluster of differentiation 36 (CD36), sterol regulatory-element binding protein 1 (SREBP1), fatty acid synthase (FASN), and diacylglycerol O-acyltransferase 1 (DGAT1), which reduces triglyceride (TG) accumulation. Finally, restoring the mitochondrial structure reduced excessive fission by decreasing the fission protein dynamin-related protein-1 (DRP1). Autophagy flux was further restored by reducing beclin and sequestosome (p62) and increasing B-cell lymphoma 2 (Bcl2) and the ratio of microtubule-associated proteins 1A/1B light chain 3 II and I (LC3II/LC3I). These results reveal that SFN confers protection against UUO-induced kidney injury by targeting mitochondrial biogenesis, which also improves lipid metabolism. MDPI 2022-09-20 /pmc/articles/PMC9598813/ /pubmed/36290577 http://dx.doi.org/10.3390/antiox11101854 Text en © 2022 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
Aranda-Rivera, Ana Karina
Cruz-Gregorio, Alfredo
Aparicio-Trejo, Omar Emiliano
Tapia, Edilia
Sánchez-Lozada, Laura Gabriela
García-Arroyo, Fernando Enrique
Amador-Martínez, Isabel
Orozco-Ibarra, Marisol
Fernández-Valverde, Francisca
Pedraza-Chaverri, José
Sulforaphane Protects against Unilateral Ureteral Obstruction-Induced Renal Damage in Rats by Alleviating Mitochondrial and Lipid Metabolism Impairment
title Sulforaphane Protects against Unilateral Ureteral Obstruction-Induced Renal Damage in Rats by Alleviating Mitochondrial and Lipid Metabolism Impairment
title_full Sulforaphane Protects against Unilateral Ureteral Obstruction-Induced Renal Damage in Rats by Alleviating Mitochondrial and Lipid Metabolism Impairment
title_fullStr Sulforaphane Protects against Unilateral Ureteral Obstruction-Induced Renal Damage in Rats by Alleviating Mitochondrial and Lipid Metabolism Impairment
title_full_unstemmed Sulforaphane Protects against Unilateral Ureteral Obstruction-Induced Renal Damage in Rats by Alleviating Mitochondrial and Lipid Metabolism Impairment
title_short Sulforaphane Protects against Unilateral Ureteral Obstruction-Induced Renal Damage in Rats by Alleviating Mitochondrial and Lipid Metabolism Impairment
title_sort sulforaphane protects against unilateral ureteral obstruction-induced renal damage in rats by alleviating mitochondrial and lipid metabolism impairment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598813/
https://www.ncbi.nlm.nih.gov/pubmed/36290577
http://dx.doi.org/10.3390/antiox11101854
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