Inhibition of protein glycation and advanced glycation end products by ascorbic acid and other vitamins and nutrients

被引:199
作者
Vinson, JA
Howard, TB
机构
[1] Department of Chemistry, University of Scranton, Scranton, PA
[2] Department of Chemistry, University of Scranton, Scranton
关键词
glycation; advanced glycation end products; vitamins; nutrients; ascorbic acid;
D O I
10.1016/S0955-2863(96)00128-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nonenzymatic glycation, the reaction of glucose and other reducing sugars with protein, reversibly produces Amadori products and over a long period irreversible advanced glycation end products. In diabetes, these reactions are greatly accelerated and are important in the pathogenesis of diabetic complications. In vitro glycation was studied with bovine albumin as the model protein. A mixture of 25 mM glucose/fructose was used as the glycating agent. The Amadori product was quantitated by thiobarbituric acid colorimetry after hydrolysis. Advanced glycation endproducts were measured by their intrinsic fluorescence. A number of vitamins and nutrients were found to be potent inhibitors of both the glycation reaction and the subsequent end products. The nutrients were effective at physiological concentrations and exhibited dose-response relationships. The inhibitors included ascorbic acid, tocopherol, pyridoxal, niacinamide, sodium selenite, selenium yeast, and carnosine. A significant correlation was found between the inhibition of glycation and the inhibition of AGE formation (P <0.001). One of the nutrients, ascorbic acid, was used in a pilot study. Eighteen normal subjects, 7 college age and 10 middle age, were supplemented with 1,000 mg of ascorbic acid in the form of Re-Natured Vitamin C(R) for a period of 4 weeks. Serum protein glycation was decreased an average of 46.8% (P <0.01). These results underline the importance of nutrition in diabetes and indicate the possibility of therapeutic use of these nutrients for the prevention of diabetic complications. (C) Elsevier Science Inc. 1996
引用
收藏
页码:659 / 663
页数:5
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