Evidence that pioglitazone, metformin and pentoxifylline are inhibitors of glycation

被引:125
作者
Rahbar, S
Natarajan, R
Yerneni, KK
Scott, S
Gonzales, N
Nadler, JL
机构
[1] City Hope Natl Med Ctr, Dept Diabet Endocrinol & Metab, Duarte, CA 91010 USA
[2] Univ Virginia, Ctr Hlth, Div Endocrinol & Metab, Charlottesville, VA 22908 USA
关键词
glycation inhibitors; glycation; AGEs; pioglitazone; pentoxifylline; metformin;
D O I
10.1016/S0009-8981(00)00327-2
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Enhanced formation and accumulation of advanced glycation end products (AGEs) have been proposed to play a major. role in the pathogenesis of diabetic complications, and atherosclerosis, leading to the development of a range of diabetic complications including nephropathy, retinopathy and neuropathy. Several potential drug candidates as AGE inhibitors have been reported recently. Aminoguanidine is the first drug extensively studied. However, there are no currently available medications known to block AGE formation. We have previously reported a number of novel and structurally diverse compounds as potent inhibitors of glycation and ACE formation. We have now studied several of the existing drugs, which are in therapeutic practice for lowering blood sugar ol the treatment of peripheral vascular disease in diabetic patients, for possible inhibitory effects on glycation. We show that that three compounds; pioglitazone, metformin and pentoxifylline are also inhibitors of glycation. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:65 / 77
页数:13
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