SERUM PARAOXONASE ACTIVITY, CONCENTRATION, AND PHENOTYPE DISTRIBUTION IN DIABETES-MELLITUS AND ITS RELATIONSHIP TO SERUM-LIPIDS AND LIPOPROTEINS

被引:333
作者
ABBOTT, CA [1 ]
MACKNESS, MI [1 ]
KUMAR, S [1 ]
BOULTON, AJ [1 ]
DURRINGTON, PN [1 ]
机构
[1] UNIV MANCHESTER, MANCHESTER ROYAL INFIRM, DEPT MED, MANCHESTER M13 9WL, LANCS, ENGLAND
关键词
PARAOXONASE; HIGH-DENSITY LIPOPROTEIN; APOLIPOPROTEIN A-1; NEUROPATHY; DIABETES MELLITUS;
D O I
10.1161/01.ATV.15.11.1812
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Human serum paraoxonase is physically associated with HDL and has been implicated in the detoxification of organophosphates and possibly in the prevention of LDL lipid peroxidation. We investigated the serum activity and concentration of paraoxonase in 78 patients with type 1 diabetes mellitus, 92 with type 2 diabetes, and 82 nondiabetic control subjects. Paraoxonase activity was generally lower in diabetics than in control subjects. This decrease was unrelated to differences in paraoxonase phenotype distribution or its serum concentration. Rather, the difference in paraoxonase activity was explained by its specific activity, which was lower in diabetics, indicating either the presence of a circulating inhibitor or disturbance of the interaction of paraoxonase with HDL affecting its activity. Paraoxonase specific activity was lowest in patients with peripheral neuropathy, suggesting an association of paraoxonase with neuropathy. In control subjects but not patients with diabetes, paraoxonase correlated with HDL cholesterol and apolipoprotein A-1. Our results indicate that the low paraoxonase activity in diabetes is due to decreased specific activity. In other studies low serum paraoxonase activity has been associated with increased susceptibility to atherosclerosis, and the present results also suggest an association with peripheral neuropathy, which could be due to reduced capacity to detoxify lipid peroxides in diabetes.
引用
收藏
页码:1812 / 1818
页数:7
相关论文
共 34 条
[1]  
ADKINS S, 1993, AM J HUM GENET, V52, P598
[3]   IDENTIFICATION OF A DISTINCT HUMAN HIGH-DENSITY-LIPOPROTEIN SUBSPECIES DEFINED BY A LIPOPROTEIN-ASSOCIATED PROTEIN, K-45 - IDENTITY OF K-45 WITH PARAOXONASE [J].
BLATTER, MC ;
JAMES, RW ;
MESSMER, S ;
BARJA, F ;
POMETTA, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1993, 211 (03) :871-879
[4]  
DURRINGTON PN, 1989, HYPERLIPIDAEMIA DIAG
[5]  
Eto M, 1974, ORGANOPHOSPHORUS PES
[6]   HUMAN AND RABBIT PARAOXONASES - PURIFICATION, CLONING, SEQUENCING, MAPPING AND ROLE OF POLYMORPHISM IN ORGANOPHOSPHATE DETOXIFICATION [J].
FURLONG, CE ;
COSTA, LG ;
HASSETT, C ;
RICHTER, RJ ;
SUNDSTROM, JA ;
ADLER, DA ;
DISTECHE, CM ;
OMIECINSKI, CJ ;
CHAPLINE, C ;
CRABB, JW ;
HUMBERT, R .
CHEMICO-BIOLOGICAL INTERACTIONS, 1993, 87 (1-3) :35-48
[7]   QUANTIFICATION OF HUMAN SERUM PARAOXONASE BY ENZYME-LINKED IMMUNOASSAY - POPULATION DIFFERENCES IN PROTEIN CONCENTRATIONS [J].
GARIN, MCB ;
ABBOTT, C ;
MESSMER, S ;
MACKNESS, M ;
DURRINGTON, P ;
POMETTA, D ;
JAMES, RW .
BIOCHEMICAL JOURNAL, 1994, 304 :549-554
[8]   A POLYMORPHISM OF THE PARAOXONASE GENE ASSOCIATED WITH VARIATION IN PLASMA-LIPOPROTEINS IN A GENETIC ISOLATE [J].
HEGELE, RA ;
BRUNT, JH ;
CONNELLY, PW .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1995, 15 (01) :89-95
[9]   THE MOLECULAR-BASIS OF THE HUMAN SERUM PARAOXONASE ACTIVITY POLYMORPHISM [J].
HUMBERT, R ;
ADLER, DA ;
DISTECHE, CM ;
HASSETT, C ;
OMIECINSKI, CJ ;
FURLONG, CE .
NATURE GENETICS, 1993, 3 (01) :73-76
[10]   OXIDATIVE DAMAGE IN NEURODEGENERATIVE DISEASE [J].
JENNER, P .
LANCET, 1994, 344 (8925) :796-798