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Gut Microbiota as a Source of Uremic Toxins

Uremic retention solutes are the compounds that accumulate in the blood when kidney excretory function is impaired. Some of these compounds are toxic at high concentrations and are usually known as “uremic toxins”. The cumulative detrimental effect of uremic toxins results in numerous health problem...

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Autores principales: Popkov, Vasily A., Zharikova, Anastasia A., Demchenko, Evgenia A., Andrianova, Nadezda V., Zorov, Dmitry B., Plotnikov, Egor Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745165/
https://www.ncbi.nlm.nih.gov/pubmed/35008909
http://dx.doi.org/10.3390/ijms23010483
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author Popkov, Vasily A.
Zharikova, Anastasia A.
Demchenko, Evgenia A.
Andrianova, Nadezda V.
Zorov, Dmitry B.
Plotnikov, Egor Y.
author_facet Popkov, Vasily A.
Zharikova, Anastasia A.
Demchenko, Evgenia A.
Andrianova, Nadezda V.
Zorov, Dmitry B.
Plotnikov, Egor Y.
author_sort Popkov, Vasily A.
collection PubMed
description Uremic retention solutes are the compounds that accumulate in the blood when kidney excretory function is impaired. Some of these compounds are toxic at high concentrations and are usually known as “uremic toxins”. The cumulative detrimental effect of uremic toxins results in numerous health problems and eventually mortality during acute or chronic uremia, especially in end-stage renal disease. More than 100 different solutes increase during uremia; however, the exact origin for most of them is still debatable. There are three main sources for such compounds: exogenous ones are consumed with food, whereas endogenous ones are produced by the host metabolism or by symbiotic microbiota metabolism. In this article, we identify uremic retention solutes presumably of gut microbiota origin. We used database analysis to obtain data on the enzymatic reactions in bacteria and human organisms that potentially yield uremic retention solutes and hence to determine what toxins could be synthesized in bacteria residing in the human gut. We selected biochemical pathways resulting in uremic retention solutes synthesis related to specific bacterial strains and revealed links between toxin concentration in uremia and the proportion of different bacteria species which can synthesize the toxin. The detected bacterial species essential for the synthesis of uremic retention solutes were then verified using the Human Microbiome Project database. Moreover, we defined the relative abundance of human toxin-generating enzymes as well as the possibility of the synthesis of a particular toxin by the human metabolism. Our study presents a novel bioinformatics approach for the elucidation of the origin of both uremic retention solutes and uremic toxins and for searching for the most likely human microbiome producers of toxins that can be targeted and used for the therapy of adverse consequences of uremia.
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spelling pubmed-87451652022-01-11 Gut Microbiota as a Source of Uremic Toxins Popkov, Vasily A. Zharikova, Anastasia A. Demchenko, Evgenia A. Andrianova, Nadezda V. Zorov, Dmitry B. Plotnikov, Egor Y. Int J Mol Sci Article Uremic retention solutes are the compounds that accumulate in the blood when kidney excretory function is impaired. Some of these compounds are toxic at high concentrations and are usually known as “uremic toxins”. The cumulative detrimental effect of uremic toxins results in numerous health problems and eventually mortality during acute or chronic uremia, especially in end-stage renal disease. More than 100 different solutes increase during uremia; however, the exact origin for most of them is still debatable. There are three main sources for such compounds: exogenous ones are consumed with food, whereas endogenous ones are produced by the host metabolism or by symbiotic microbiota metabolism. In this article, we identify uremic retention solutes presumably of gut microbiota origin. We used database analysis to obtain data on the enzymatic reactions in bacteria and human organisms that potentially yield uremic retention solutes and hence to determine what toxins could be synthesized in bacteria residing in the human gut. We selected biochemical pathways resulting in uremic retention solutes synthesis related to specific bacterial strains and revealed links between toxin concentration in uremia and the proportion of different bacteria species which can synthesize the toxin. The detected bacterial species essential for the synthesis of uremic retention solutes were then verified using the Human Microbiome Project database. Moreover, we defined the relative abundance of human toxin-generating enzymes as well as the possibility of the synthesis of a particular toxin by the human metabolism. Our study presents a novel bioinformatics approach for the elucidation of the origin of both uremic retention solutes and uremic toxins and for searching for the most likely human microbiome producers of toxins that can be targeted and used for the therapy of adverse consequences of uremia. MDPI 2022-01-01 /pmc/articles/PMC8745165/ /pubmed/35008909 http://dx.doi.org/10.3390/ijms23010483 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
Popkov, Vasily A.
Zharikova, Anastasia A.
Demchenko, Evgenia A.
Andrianova, Nadezda V.
Zorov, Dmitry B.
Plotnikov, Egor Y.
Gut Microbiota as a Source of Uremic Toxins
title Gut Microbiota as a Source of Uremic Toxins
title_full Gut Microbiota as a Source of Uremic Toxins
title_fullStr Gut Microbiota as a Source of Uremic Toxins
title_full_unstemmed Gut Microbiota as a Source of Uremic Toxins
title_short Gut Microbiota as a Source of Uremic Toxins
title_sort gut microbiota as a source of uremic toxins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745165/
https://www.ncbi.nlm.nih.gov/pubmed/35008909
http://dx.doi.org/10.3390/ijms23010483
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