Gut-Derived Protein-Bound Uremic Toxins

被引:100
作者
Graboski, Amanda L. [1 ]
Redinbo, Matthew R. [2 ,3 ,4 ,5 ]
机构
[1] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Biochem, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Microbiol, Chapel Hill, NC 27599 USA
[5] Univ N Carolina, Dept Genom, Chapel Hill, NC 27599 USA
关键词
protein-bound uremic toxins; intestinal microbiota; gut-kidney axis; CHRONIC KIDNEY-DISEASE; GLYCATION END-PRODUCTS; P-CRESYL SULFATE; FURAN FATTY-ACID; INDOXYL SULFATE; HEMODIALYSIS-PATIENTS; RENAL-FAILURE; HIPPURIC-ACID; MEDITERRANEAN DIET; PHENYLACETIC ACID;
D O I
10.3390/toxins12090590
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
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.
引用
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页数:20
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