4.7 Article

Effect of protein-bound uraemic toxins on the thermodynamic characteristics of human albumin

Journal

BIOCHEMICAL PHARMACOLOGY
Volume 63, Issue 7, Pages 1287-1296

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0006-2952(02)00869-9

Keywords

albumin; uraemic toxin; hippuric acid; indoxyl sulphate; 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid; binding thermodynamics

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The ability of albumin to bind drugs and other lipophilic organic acids is decreased in chronic renal failure by the accumulation of albumin-bound uraemic toxins such as hippuric acid, indoxyl sulphate and 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid (CMPF). This furan acid is the most highly bound and is not removed by haemodialysis. The inhibitory effects of these three uraemic toxins on the interaction of three marker ligands sodium octanoate (for medium chain fatty acids), salicylic acid and phenol red (bilirubin site/site I) with albumin have been investigated by differential scanning microcalorimetry and flow microcalorimetry. CMPF was the most potent inhibitor and its binding site coincided with that of bilirubin (site I). Indoxyl sulphate binds to the site for medium-chain fatty acids and tryptophan (site II) and hippuric acid, the weakest inhibitor, inhibited binding to the salicylic acid site. (C) 2002 Elsevier Science Inc. All rights reserved.

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