Impacts of Indoxyl Sulfate and p-Cresol Sulfate on Chronic Kidney Disease and Mitigating Effects of AST-120.
TLDR
Oral sorbent AST-120 reduces serum levels of uremic toxins in CKD patients by adsorbing the precursors of IS and PCS generated by amino acid metabolism in the intestine, and reduces the production of reactive oxygen species by endothelial cells, to impede the subsequent oxidative stress.Abstract:
Uremic toxins, such as indoxyl sulfate (IS) and p-cresol, or p-cresyl sulfate (PCS), are markedly accumulated in the organs of chronic kidney disease (CKD) patients These toxins can induce inflammatory reactions and enhance oxidative stress, prompting glomerular sclerosis and interstitial fibrosis, to aggravate the decline of renal function Consequently, uremic toxins play an important role in the worsening of renal and cardiovascular functions Furthermore, they destroy the quantity and quality of bone Oral sorbent AST-120 reduces serum levels of uremic toxins in CKD patients by adsorbing the precursors of IS and PCS generated by amino acid metabolism in the intestine Accordingly, AST-120 decreases the serum IS levels and reduces the production of reactive oxygen species by endothelial cells, to impede the subsequent oxidative stress This slows the progression of cardiovascular and renal diseases and improves bone metabolism in CKD patients Although large-scale studies showed no obvious benefits from adding AST-120 to the standard therapy for CKD patients, subsequent sporadic studies may support its use This article summarizes the mechanisms of the uremic toxins, IS, and PCS, and discusses the multiple effects of AST-120 in CKD patientsread more
Citations
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Oxidative Stress in the Pathogenesis and Evolution of Chronic Kidney Disease: Untangling Ariadne's Thread.
TL;DR: The scope of this review is to tackle the issue of oxidative stress in CKD in a holistic manner so as to provide a future framework for potential interventions.
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Diet posttranslationally modifies the mouse gut microbial proteome to modulate renal function.
Lior Lobel,Y. Grace Cao,Kathrin Fenn,Jonathan N. Glickman,Jonathan N. Glickman,Wendy S. Garrett +5 more
TL;DR: In a mouse model of CKD, it was found that a high sulfur amino acid–containing diet resulted in posttranslationally modified microbial tryptophanase activity that reduced uremic toxin–producing activity and ameliorated progression to CKD in the mice.
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Gut-organ axis: a microbial outreach and networking.
TL;DR: In this review, the bidirectional relationship between the gut and the vital human organs was envisaged and discussed under several headings and several disease symptoms were also revisited to redefine the communication network between the Gut microbes and the associated organs.
Journal ArticleDOI
Nutritional Therapy Modulates Intestinal Microbiota and Reduces Serum Levels of Total and Free Indoxyl Sulfate and P-Cresyl Sulfate in Chronic Kidney Disease (Medika Study)
Biagio Di Iorio,Maria Teresa Rocchetti,Maria De Angelis,Carmela Cosola,Stefania Marzocco,Lucia Di Micco,Ighli di Bari,Matteo Accetturo,Mirco Vacca,Marco Gobbetti,Mattia Di Iorio,Antonio Bellasi,Loreto Gesualdo +12 more
TL;DR: MD and, to a greater extent, VLPD are effective in the beneficial modulation of gut microbiota, reducing IS and PCS serum levels, and restoring intestinal permeability in CKD patients.
Journal ArticleDOI
Indoxyl Sulfate, a Uremic Endotheliotoxin.
TL;DR: Reducing IS endothelial toxicity appears to be necessary to improve cardiovascular health in CKD patients, and the various molecular pathways implicated are focused on.
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