Free Radical Research Communications · 1992 · 53 citations · 20 references
Life SciencesBiochemistryDiabetologyGlycobiologyProtein BiochemistryDiabetes MellitusDiabetes Mellitus BiochemistryProtein GlycosylationAdvanced Glycation End ProductsBovine Serum AlbuminDiabetes-related ComplicationsExtrinsic FluorescenceGlycosylation In DiseaseProtein Glycosylation AnalysisProtein GlycoxidationSubsequent Modification
Nonenzymatic glycation has been found to increase in a variety of proteins in diabetic patients. The present study examined a possibility of preventing glycation and subsequent structural modifications of proteins by alpha-lipoic acid (thioctic acid) as lipoate, a substance which has gained attention as a potential therapeutic agent for diabetes-induced complications. Incubation of bovine serum albumin (BSA) at 2 mg/ml with glucose (500 mM) in a sterile condition at 37 degrees C for seven days caused glycation and structural modifications of BSA observed by SDS-PAGE, near UV absorption, tryptophan and nontryptophan fluorescence, and fluorescence of an extrinsic probe, TNS (6-(p-toluidinyl)naphthalene-2-sulfonate). When BSA and glucose were incubated in the presence of lipoate (20 mM), glycation and structural modifications of BSA were significantly prevented. Glycation and inactivation of lysozyme were also prevented by lipoate. These results suggest a potential for the therapeutic use of lipoic acid against diabetes-induced complications.
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The Metabolic Basis of Inherited Diseases
R.K. Winkelmann · Archives of Dermatology · 1972 · 1.8K citations
In vitro synthesis of hemoglobin A<sub>Ic</sub>
Rudolf Flückiger, Kaspar H. Winterhalter · FEBS Letters · 1976 · 460 citations · Full text