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Open AccessJournal ArticleDOI

Impacts of Indoxyl Sulfate and p-Cresol Sulfate on Chronic Kidney Disease and Mitigating Effects of AST-120.

Wen-Chih Liu, +2 more
- 11 Sep 2018 - 
- Vol. 10, Iss: 9, pp 367
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 patients

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Citations
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Journal ArticleDOI

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.
Journal ArticleDOI

Diet posttranslationally modifies the mouse gut microbial proteome to modulate renal function.

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.
Journal ArticleDOI

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

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.
References
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Journal ArticleDOI

Intestinal mucosal barrier function in health and disease.

TL;DR: Recent advances have uncovered mechanisms by which the intestinal mucosal barrier is regulated in response to physiological and immunological stimuli, along with evidence that this regulation shapes mucosal immune responses in the gut and, when dysfunctional, may contribute to disease.
Journal Article

K/DOQI clinical practice guidelines for bone metabolism and disease in chronic kidney disease

Shaul G. Massry, +80 more
Journal ArticleDOI

Chronic kidney disease alters intestinal microbial flora

TL;DR: Uremia profoundly alters the composition of the gut microbiome and the biological impact of this phenomenon is unknown and awaits further investigation.
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