Gut-Derived Protein-Bound Uremic Toxins

Chronic kidney disease (CKD) afflicts more than 500 million people worldwide and is one of the fastest growing global causes of mortality. When glomerular filtration rate begins to fall, uremic toxins accumulate in the serum and significantly increase the risk of death from cardiovascular disease an...

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Main Authors: Amanda L. Graboski, Matthew R. Redinbo
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Toxins
Subjects:
Online Access:https://www.mdpi.com/2072-6651/12/9/590
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spelling doaj-355754d47245419eb27a2bbc75b33dd22020-11-25T03:06:06ZengMDPI AGToxins2072-66512020-09-011259059010.3390/toxins12090590Gut-Derived Protein-Bound Uremic ToxinsAmanda L. Graboski0Matthew R. Redinbo1Department of Pharmacology, University of North Carolina, Chapel Hill, NC 27599-7365, USADepartments of Chemistry, Biochemistry, Microbiology and Genomics, University of North Carolina, Chapel Hill, NC 27599-3290, USAChronic kidney disease (CKD) afflicts more than 500 million people worldwide and is one of the fastest growing global causes of mortality. When glomerular filtration rate begins to fall, uremic toxins accumulate in the serum and significantly increase the risk of death from cardiovascular disease and other causes. Several of the most harmful uremic toxins are produced by the gut microbiota. Furthermore, many such toxins are protein-bound and are therefore recalcitrant to removal by dialysis. We review the derivation and pathological mechanisms of gut-derived, protein-bound uremic toxins (PBUTs). We further outline the emerging relationship between kidney disease and gut dysbiosis, including the bacterial taxa altered, the regulation of microbial uremic toxin-producing genes, and their downstream physiological and neurological consequences. Finally, we discuss gut-targeted therapeutic strategies employed to reduce PBUTs. We conclude that targeting the gut microbiota is a promising approach for the treatment of CKD by blocking the serum accumulation of PBUTs that cannot be eliminated by dialysis.https://www.mdpi.com/2072-6651/12/9/590protein-bound uremic toxinsintestinal microbiotagut-kidney axis
collection DOAJ
language English
format Article
sources DOAJ
author Amanda L. Graboski
Matthew R. Redinbo
spellingShingle Amanda L. Graboski
Matthew R. Redinbo
Gut-Derived Protein-Bound Uremic Toxins
Toxins
protein-bound uremic toxins
intestinal microbiota
gut-kidney axis
author_facet Amanda L. Graboski
Matthew R. Redinbo
author_sort Amanda L. Graboski
title Gut-Derived Protein-Bound Uremic Toxins
title_short Gut-Derived Protein-Bound Uremic Toxins
title_full Gut-Derived Protein-Bound Uremic Toxins
title_fullStr Gut-Derived Protein-Bound Uremic Toxins
title_full_unstemmed Gut-Derived Protein-Bound Uremic Toxins
title_sort gut-derived protein-bound uremic toxins
publisher MDPI AG
series Toxins
issn 2072-6651
publishDate 2020-09-01
description Chronic kidney disease (CKD) afflicts more than 500 million people worldwide and is one of the fastest growing global causes of mortality. When glomerular filtration rate begins to fall, uremic toxins accumulate in the serum and significantly increase the risk of death from cardiovascular disease and other causes. Several of the most harmful uremic toxins are produced by the gut microbiota. Furthermore, many such toxins are protein-bound and are therefore recalcitrant to removal by dialysis. We review the derivation and pathological mechanisms of gut-derived, protein-bound uremic toxins (PBUTs). We further outline the emerging relationship between kidney disease and gut dysbiosis, including the bacterial taxa altered, the regulation of microbial uremic toxin-producing genes, and their downstream physiological and neurological consequences. Finally, we discuss gut-targeted therapeutic strategies employed to reduce PBUTs. We conclude that targeting the gut microbiota is a promising approach for the treatment of CKD by blocking the serum accumulation of PBUTs that cannot be eliminated by dialysis.
topic protein-bound uremic toxins
intestinal microbiota
gut-kidney axis
url https://www.mdpi.com/2072-6651/12/9/590
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