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Expression Profiles of Kidney Mitochondrial Proteome during the Progression of the Unilateral Ureteral Obstruction: Focus on Energy Metabolism Adaptions

Kidney diseases encompass many pathologies, including obstructive nephropathy (ON), a common clinical condition caused by different etiologies such as urolithiasis, prostatic hyperplasia in males, tumors, congenital stenosis, and others. Unilateral ureteral obstruction (UUO) in rodents is an experim...

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Autores principales: Ortega-Lozano, Ariadna Jazmín, Jiménez-Uribe, Alexis Paulina, Aranda-Rivera, Ana Karina, Gómez-Caudillo, Leopoldo, Ríos-Castro, Emmanuel, Tapia, Edilia, Bellido, Belen, Aparicio-Trejo, Omar Emiliano, Sánchez-Lozada, Laura Gabriela, Pedraza-Chaverri, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607257/
https://www.ncbi.nlm.nih.gov/pubmed/36295838
http://dx.doi.org/10.3390/metabo12100936
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author Ortega-Lozano, Ariadna Jazmín
Jiménez-Uribe, Alexis Paulina
Aranda-Rivera, Ana Karina
Gómez-Caudillo, Leopoldo
Ríos-Castro, Emmanuel
Tapia, Edilia
Bellido, Belen
Aparicio-Trejo, Omar Emiliano
Sánchez-Lozada, Laura Gabriela
Pedraza-Chaverri, José
author_facet Ortega-Lozano, Ariadna Jazmín
Jiménez-Uribe, Alexis Paulina
Aranda-Rivera, Ana Karina
Gómez-Caudillo, Leopoldo
Ríos-Castro, Emmanuel
Tapia, Edilia
Bellido, Belen
Aparicio-Trejo, Omar Emiliano
Sánchez-Lozada, Laura Gabriela
Pedraza-Chaverri, José
author_sort Ortega-Lozano, Ariadna Jazmín
collection PubMed
description Kidney diseases encompass many pathologies, including obstructive nephropathy (ON), a common clinical condition caused by different etiologies such as urolithiasis, prostatic hyperplasia in males, tumors, congenital stenosis, and others. Unilateral ureteral obstruction (UUO) in rodents is an experimental model widely used to explore the pathophysiology of ON, replicating vascular alterations, tubular atrophy, inflammation, and fibrosis development. In addition, due to the kidney’s high energetic demand, mitochondrial function has gained great attention, as morphological and functional alterations have been demonstrated in kidney diseases. Here we explore the kidney mitochondrial proteome differences during a time course of 7, 14, and 21 days after the UUO in rats, revealing changes in proteins involved in three main metabolic pathways, oxidative phosphorylation (OXPHOS), the tricarboxylic acid cycle (TCA), and the fatty acid (FA) metabolism, all of them related to bioenergetics. Our results provide new insight into the mechanisms involved in metabolic adaptations triggered by the alterations in kidney mitochondrial proteome during the ON.
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spelling pubmed-96072572022-10-28 Expression Profiles of Kidney Mitochondrial Proteome during the Progression of the Unilateral Ureteral Obstruction: Focus on Energy Metabolism Adaptions Ortega-Lozano, Ariadna Jazmín Jiménez-Uribe, Alexis Paulina Aranda-Rivera, Ana Karina Gómez-Caudillo, Leopoldo Ríos-Castro, Emmanuel Tapia, Edilia Bellido, Belen Aparicio-Trejo, Omar Emiliano Sánchez-Lozada, Laura Gabriela Pedraza-Chaverri, José Metabolites Article Kidney diseases encompass many pathologies, including obstructive nephropathy (ON), a common clinical condition caused by different etiologies such as urolithiasis, prostatic hyperplasia in males, tumors, congenital stenosis, and others. Unilateral ureteral obstruction (UUO) in rodents is an experimental model widely used to explore the pathophysiology of ON, replicating vascular alterations, tubular atrophy, inflammation, and fibrosis development. In addition, due to the kidney’s high energetic demand, mitochondrial function has gained great attention, as morphological and functional alterations have been demonstrated in kidney diseases. Here we explore the kidney mitochondrial proteome differences during a time course of 7, 14, and 21 days after the UUO in rats, revealing changes in proteins involved in three main metabolic pathways, oxidative phosphorylation (OXPHOS), the tricarboxylic acid cycle (TCA), and the fatty acid (FA) metabolism, all of them related to bioenergetics. Our results provide new insight into the mechanisms involved in metabolic adaptations triggered by the alterations in kidney mitochondrial proteome during the ON. MDPI 2022-10-02 /pmc/articles/PMC9607257/ /pubmed/36295838 http://dx.doi.org/10.3390/metabo12100936 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
Ortega-Lozano, Ariadna Jazmín
Jiménez-Uribe, Alexis Paulina
Aranda-Rivera, Ana Karina
Gómez-Caudillo, Leopoldo
Ríos-Castro, Emmanuel
Tapia, Edilia
Bellido, Belen
Aparicio-Trejo, Omar Emiliano
Sánchez-Lozada, Laura Gabriela
Pedraza-Chaverri, José
Expression Profiles of Kidney Mitochondrial Proteome during the Progression of the Unilateral Ureteral Obstruction: Focus on Energy Metabolism Adaptions
title Expression Profiles of Kidney Mitochondrial Proteome during the Progression of the Unilateral Ureteral Obstruction: Focus on Energy Metabolism Adaptions
title_full Expression Profiles of Kidney Mitochondrial Proteome during the Progression of the Unilateral Ureteral Obstruction: Focus on Energy Metabolism Adaptions
title_fullStr Expression Profiles of Kidney Mitochondrial Proteome during the Progression of the Unilateral Ureteral Obstruction: Focus on Energy Metabolism Adaptions
title_full_unstemmed Expression Profiles of Kidney Mitochondrial Proteome during the Progression of the Unilateral Ureteral Obstruction: Focus on Energy Metabolism Adaptions
title_short Expression Profiles of Kidney Mitochondrial Proteome during the Progression of the Unilateral Ureteral Obstruction: Focus on Energy Metabolism Adaptions
title_sort expression profiles of kidney mitochondrial proteome during the progression of the unilateral ureteral obstruction: focus on energy metabolism adaptions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607257/
https://www.ncbi.nlm.nih.gov/pubmed/36295838
http://dx.doi.org/10.3390/metabo12100936
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