2017
DOI: 10.1186/s41110-017-0054-x
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The cross-talk between the kidney and the gut: implications for chronic kidney disease

Abstract: In recent decades, special attention has been given to the potential association between the gut ecosystem and chronic diseases. Several features and complications of chronic kidney disease (CKD) may induce an unbalanced gut environment, leading to unfavorable consequences for a patient's health. The first section of this review is dedicated to a description of some aspects of gut microbiota and intestinal barrier physiology. The following section explores the impact of CKD on the gut ecosystem and intestinal … Show more

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Cited by 21 publications
(21 citation statements)
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References 161 publications
(203 reference statements)
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“…(B) Gut–kidney crosstalk with decreased kidney function increasing gut permeability has been hypothesized to fuel systemic inflammation and thereby progressive renal damage both as a cause of CKD progression [ 56 , 57 ] and AKI in septic shock [ 58 ]; and…”
Section: The Theoretical Frameworkmentioning
confidence: 99%
“…(B) Gut–kidney crosstalk with decreased kidney function increasing gut permeability has been hypothesized to fuel systemic inflammation and thereby progressive renal damage both as a cause of CKD progression [ 56 , 57 ] and AKI in septic shock [ 58 ]; and…”
Section: The Theoretical Frameworkmentioning
confidence: 99%
“…In addition, Andrade et al . did not observe a significant difference in the production of reactive oxygen species (ROS) and expression of toll-like receptors (TLR), proteins that recognize bacterial components and are important for gut homeostasis7.…”
mentioning
confidence: 95%
“…However, these pathological processes have not yet been fully elucidated. The dysfunction of the intestinal epithelium can be explained, at least in part, by the effects induced by uremia resulting from CKD on intestinal epithelial cells, such as enterocytes and colonocytes1 - 7.…”
mentioning
confidence: 99%
See 1 more Smart Citation
“…2 ). Toxic metabolites such as trimethylamine N-oxide, D-amino acids, hippurate, phenylacetylglutamine, polyamines including putrescine, cadaverine, agmatine, and tyramine, acrolein, p -cresol sulfate, indoxyl sulfate, indole-3 acetic, phenol- and sulfur-containing compounds, as well as ammonia produced by the intestinal microbes can destroy the junctional complexes of the intestinal epithelial lining, thereby increasing the leakiness of the gut [, 151 , 152 , 153 , 154 , 155 , 156 , 157 , 158 , 159 , 160 , 161 , 162 , 163 , 164 , 165 ] (immune responses triggered by these microbial metabolites are integral to leaky gut [ 163 , 164 , 165 ]). This increases impairment in selective transport and paracellular shunt of substances between the gut and circulatory system, allowing for unregulated movement of biomolecules including toxins into the surrounding tissues and circulatory system from the luminal side of the gut (Fig.…”
Section: Dementia-dysbiome Repertoirementioning
confidence: 99%