Lipid peroxidation in type 2 normolipidemic diabetic patients

被引:28
作者
Freitas, JP
Filipe, PM
Rodrigo, FG
机构
[1] Clin. Dermatológica Univ., Faculdade de Medicina de Lisboa, Lisbon, Av. Prof. Egas Moniz
关键词
lipid peroxidation; free radicals; malondialdehyde; thiobarbituric acid reactive substances; type 2 diabetes mellitus; cholesterol; triglyceride; glycation;
D O I
10.1016/S0168-8227(97)00032-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular complications, as a consequence of atherosclerosis, are the main causes of morbidity and mortality in diabetes. Low density lipoprotein (LDL) oxidation is accepted as a relevant pathogenic mechanism in atherogenesis. The aim of this work was to study the relationship between lipid peroxidation (LPO) and metabolic control. LPO was evaluated in 40 type 2 normolipidemic diabetic patients by measuring thiobarbituric acid reactive substances (TEARS), in the plasma, using malondialdehyde (MDA), end product of the oxidation of polyunsaturated fatty acids, as a standard. Fast blood glucose (FBG), serum total cholesterol (TC) and serum triglycerides (TG) were evaluated by routine methods. Fructosamine (FR) was measured by the nitroblue tetrazolium (NET) colorimetric test. An elevated level of lipid peroxides (P < 0.001) was observed in the plasma of diabetic patients (4.51 +/- 1.29 nmol/ml) as compared to normal subjects (3.54 +/- 1.00 nmol/ml). Lipid peroxides did not correlate with the FR levels, nor with FBG, TC and TG. These results show an increase of LPO in type 2 normolipidemic diabetic patients. Probably the mechanism for higher lipid peroxide levels in diabetes is multifactorial. Our study supports the hypothesis of a role of oxidative stress in diabetes independently of the lipid serum content. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:71 / 75
页数:5
相关论文
共 45 条
[1]  
ALTOMARE E, 1992, DIABETES METAB, V18, P264
[2]   STIFFENING OF CONNECTIVE-TISSUE IN ELDERLY DIABETIC-PATIENTS - RELEVANCE TO DIABETIC NEPHROPATHY AND OXIDATIVE STRESS [J].
AOKI, Y ;
YAZAKI, K ;
SHIROTORI, K ;
YANAGISAWA, Y ;
OGUCHI, H ;
KIYOSAWA, K ;
FURUTA, S .
DIABETOLOGIA, 1993, 36 (01) :79-83
[3]  
Armstrong Donald, 1992, Journal of Diabetes and its Complications, V6, P116, DOI 10.1016/1056-8727(92)90022-D
[4]   SUPEROXIDE RADICAL GENERATION BY AMADORI COMPOUNDS [J].
AZEVEDO, M ;
FALCAO, J ;
RAPOSO, J ;
MANSO, C .
FREE RADICAL RESEARCH COMMUNICATIONS, 1988, 4 (05) :331-335
[5]   CLINICAL USEFULNESS OF ESTIMATION OF SERUM FRUCTOSAMINE CONCENTRATION AS A SCREENING-TEST FOR DIABETES-MELLITUS [J].
BAKER, JR ;
OCONNOR, JP ;
METCALF, PA ;
LAWSON, MR ;
JOHNSON, RN .
BRITISH MEDICAL JOURNAL, 1983, 287 (6396) :863-867
[6]   ROLE OF METAL-CATALYZED AUTOXIDATION IN MAILLARD REACTION DAMAGE TO PROTEINS IN-VIVO [J].
BAYNES, JW .
REDOX REPORT, 1994, 1 (01) :31-34
[7]   ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES [J].
BAYNES, JW .
DIABETES, 1991, 40 (04) :405-412
[8]   NONENZYMATIC GLYCOSYLATION AND THE PATHOGENESIS OF DIABETIC COMPLICATIONS [J].
BROWNLEE, M ;
VLASSARA, H ;
CERAMI, A .
ANNALS OF INTERNAL MEDICINE, 1984, 101 (04) :527-537
[9]   ADVANCED PRODUCTS OF NONENZYMATIC GLYCOSYLATION AND THE PATHOGENESIS OF DIABETIC VASCULAR-DISEASE [J].
BROWNLEE, M ;
CERAMI, A ;
VLASSARA, H .
DIABETES-METABOLISM REVIEWS, 1988, 4 (05) :437-451
[10]   LILLY LECTURE 1993 - GLYCATION AND DIABETIC COMPLICATIONS [J].
BROWNLEE, M .
DIABETES, 1994, 43 (06) :836-841