Cargando…

Dietary Metabolites and Chronic Kidney Disease

Dietary contents and their metabolites are closely related to chronic kidney disease (CKD) progression. Advanced glycated end products (AGEs) are a type of uremic toxin produced by glycation. AGE accumulation is not only the result of elevated glucose levels or reduced renal clearance capacity, but...

Descripción completa

Detalles Bibliográficos
Autores principales: Hasegawa, Sho, Jao, Tzu-Ming, Inagi, Reiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409697/
https://www.ncbi.nlm.nih.gov/pubmed/28375181
http://dx.doi.org/10.3390/nu9040358
_version_ 1783232525362003968
author Hasegawa, Sho
Jao, Tzu-Ming
Inagi, Reiko
author_facet Hasegawa, Sho
Jao, Tzu-Ming
Inagi, Reiko
author_sort Hasegawa, Sho
collection PubMed
description Dietary contents and their metabolites are closely related to chronic kidney disease (CKD) progression. Advanced glycated end products (AGEs) are a type of uremic toxin produced by glycation. AGE accumulation is not only the result of elevated glucose levels or reduced renal clearance capacity, but it also promotes CKD progression. Indoxyl sulfate, another uremic toxin derived from amino acid metabolism, accumulates as CKD progresses and induces tubulointerstitial fibrosis and glomerular sclerosis. Specific types of amino acids (d-serine) or fatty acids (palmitate) are reported to be closely associated with CKD progression. Promising therapeutic targets associated with nutrition include uremic toxin absorbents and inhibitors of AGEs or the receptor for AGEs (RAGE). Probiotics and prebiotics maintain gut flora balance and also prevent CKD progression by enhancing gut barriers and reducing uremic toxin formation. Nrf2 signaling not only ameliorates oxidative stress but also reduces elevated AGE levels. Bardoxolone methyl, an Nrf2 activator and NF-κB suppressor, has been tested as a therapeutic agent, but the phase 3 clinical trial was terminated owing to the high rate of cardiovascular events. However, a phase 2 trial has been initiated in Japan, and the preliminary analysis reveals promising results without an increase in cardiovascular events.
format Online
Article
Text
id pubmed-5409697
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-54096972017-05-03 Dietary Metabolites and Chronic Kidney Disease Hasegawa, Sho Jao, Tzu-Ming Inagi, Reiko Nutrients Review Dietary contents and their metabolites are closely related to chronic kidney disease (CKD) progression. Advanced glycated end products (AGEs) are a type of uremic toxin produced by glycation. AGE accumulation is not only the result of elevated glucose levels or reduced renal clearance capacity, but it also promotes CKD progression. Indoxyl sulfate, another uremic toxin derived from amino acid metabolism, accumulates as CKD progresses and induces tubulointerstitial fibrosis and glomerular sclerosis. Specific types of amino acids (d-serine) or fatty acids (palmitate) are reported to be closely associated with CKD progression. Promising therapeutic targets associated with nutrition include uremic toxin absorbents and inhibitors of AGEs or the receptor for AGEs (RAGE). Probiotics and prebiotics maintain gut flora balance and also prevent CKD progression by enhancing gut barriers and reducing uremic toxin formation. Nrf2 signaling not only ameliorates oxidative stress but also reduces elevated AGE levels. Bardoxolone methyl, an Nrf2 activator and NF-κB suppressor, has been tested as a therapeutic agent, but the phase 3 clinical trial was terminated owing to the high rate of cardiovascular events. However, a phase 2 trial has been initiated in Japan, and the preliminary analysis reveals promising results without an increase in cardiovascular events. MDPI 2017-04-04 /pmc/articles/PMC5409697/ /pubmed/28375181 http://dx.doi.org/10.3390/nu9040358 Text en © 2017 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Hasegawa, Sho
Jao, Tzu-Ming
Inagi, Reiko
Dietary Metabolites and Chronic Kidney Disease
title Dietary Metabolites and Chronic Kidney Disease
title_full Dietary Metabolites and Chronic Kidney Disease
title_fullStr Dietary Metabolites and Chronic Kidney Disease
title_full_unstemmed Dietary Metabolites and Chronic Kidney Disease
title_short Dietary Metabolites and Chronic Kidney Disease
title_sort dietary metabolites and chronic kidney disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409697/
https://www.ncbi.nlm.nih.gov/pubmed/28375181
http://dx.doi.org/10.3390/nu9040358
work_keys_str_mv AT hasegawasho dietarymetabolitesandchronickidneydisease
AT jaotzuming dietarymetabolitesandchronickidneydisease
AT inagireiko dietarymetabolitesandchronickidneydisease