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Kidney metabolism and acid–base control: back to the basics

Kidneys are central in the regulation of multiple physiological functions, such as removal of metabolic wastes and toxins, maintenance of electrolyte and fluid balance, and control of pH homeostasis. In addition, kidneys participate in systemic gluconeogenesis and in the production or activation of...

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Autores principales: Imenez Silva, Pedro Henrique, Mohebbi, Nilufar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338915/
https://www.ncbi.nlm.nih.gov/pubmed/35513635
http://dx.doi.org/10.1007/s00424-022-02696-6
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author Imenez Silva, Pedro Henrique
Mohebbi, Nilufar
author_facet Imenez Silva, Pedro Henrique
Mohebbi, Nilufar
author_sort Imenez Silva, Pedro Henrique
collection PubMed
description Kidneys are central in the regulation of multiple physiological functions, such as removal of metabolic wastes and toxins, maintenance of electrolyte and fluid balance, and control of pH homeostasis. In addition, kidneys participate in systemic gluconeogenesis and in the production or activation of hormones. Acid–base conditions influence all these functions concomitantly. Healthy kidneys properly coordinate a series of physiological responses in the face of acute and chronic acid–base disorders. However, injured kidneys have a reduced capacity to adapt to such challenges. Chronic kidney disease patients are an example of individuals typically exposed to chronic and progressive metabolic acidosis. Their organisms undergo a series of alterations that brake large detrimental changes in the homeostasis of several parameters, but these alterations may also operate as further drivers of kidney damage. Acid–base disorders lead not only to changes in mechanisms involved in acid–base balance maintenance, but they also affect multiple other mechanisms tightly wired to it. In this review article, we explore the basic renal activities involved in the maintenance of acid–base balance and show how they are interconnected to cell energy metabolism and other important intracellular activities. These intertwined relationships have been investigated for more than a century, but a modern conceptual organization of these events is lacking. We propose that pH homeostasis indissociably interacts with central pathways that drive progression of chronic kidney disease, such as inflammation and metabolism, independent of etiology.
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spelling pubmed-93389152022-08-01 Kidney metabolism and acid–base control: back to the basics Imenez Silva, Pedro Henrique Mohebbi, Nilufar Pflugers Arch Invited Review Kidneys are central in the regulation of multiple physiological functions, such as removal of metabolic wastes and toxins, maintenance of electrolyte and fluid balance, and control of pH homeostasis. In addition, kidneys participate in systemic gluconeogenesis and in the production or activation of hormones. Acid–base conditions influence all these functions concomitantly. Healthy kidneys properly coordinate a series of physiological responses in the face of acute and chronic acid–base disorders. However, injured kidneys have a reduced capacity to adapt to such challenges. Chronic kidney disease patients are an example of individuals typically exposed to chronic and progressive metabolic acidosis. Their organisms undergo a series of alterations that brake large detrimental changes in the homeostasis of several parameters, but these alterations may also operate as further drivers of kidney damage. Acid–base disorders lead not only to changes in mechanisms involved in acid–base balance maintenance, but they also affect multiple other mechanisms tightly wired to it. In this review article, we explore the basic renal activities involved in the maintenance of acid–base balance and show how they are interconnected to cell energy metabolism and other important intracellular activities. These intertwined relationships have been investigated for more than a century, but a modern conceptual organization of these events is lacking. We propose that pH homeostasis indissociably interacts with central pathways that drive progression of chronic kidney disease, such as inflammation and metabolism, independent of etiology. Springer Berlin Heidelberg 2022-05-05 2022 /pmc/articles/PMC9338915/ /pubmed/35513635 http://dx.doi.org/10.1007/s00424-022-02696-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Invited Review
Imenez Silva, Pedro Henrique
Mohebbi, Nilufar
Kidney metabolism and acid–base control: back to the basics
title Kidney metabolism and acid–base control: back to the basics
title_full Kidney metabolism and acid–base control: back to the basics
title_fullStr Kidney metabolism and acid–base control: back to the basics
title_full_unstemmed Kidney metabolism and acid–base control: back to the basics
title_short Kidney metabolism and acid–base control: back to the basics
title_sort kidney metabolism and acid–base control: back to the basics
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338915/
https://www.ncbi.nlm.nih.gov/pubmed/35513635
http://dx.doi.org/10.1007/s00424-022-02696-6
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