IS OBESITY ASSOCIATED WITH INCREASED PLASMA LIPID PEROXIDATION AND OXIDATIVE STRESS IN WOMEN?

被引:0
作者
Amirkhizi, Farshad [1 ]
Siassi, Fereydoun [1 ]
Minaie, Sara [1 ]
Djalali, Mahmoud [1 ]
Rahimi, Abbas [2 ]
Chamari, Maryam [1 ]
机构
[1] Tehran Univ Med Sci, Sch Publ Hlth, Nutr & Biochem Dept, Tehran, Iran
[2] Tehran Univ Med Sci, Sch Publ Hlth, Epidemiol & Biostat Dept, Tehran, Iran
关键词
Obesity; Lipid peroxidation; Cytoprotective enzymes; Oxidative stress; Women;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
INTRODUCTION: The role of obesity in diabetes mellitus, hyperlipidemia, colon cancer, sudden death and other cardiovascular diseases has been confirmed by many studies. In this study, it was hypothesized that obesity is an independent risk factor for lipid peroxidation and decreased activity of cytoprotective enzymes in humans. methods: To test the study hypothesis, we assessed lipid peroxidation by measuring the concentrations of plasma malondialdehyde (MDA) and the activity of erythrocyte copper-zinc superoxide dismutase (CuZn-SOD), glutathione peroxidase (GPX) and catalase (CAT) in 25 obese women (BMI=30-40 Kg/m2) and 25 women with healthy BMI (19-25Kg/m2). results: The concentration of plasma MDA was significantly higher (P<0.001) in obese women (3.4 +/- 0.7 mu mol/L) compared to women with healthy BMI (1.4 +/- 0.3 mu mol/L). Furthermore, there was a significantly positive correlation (r =0.75, P<0.0001) between BMI and plasma MDA. On the other hand, women with healthy BMI had significantly higher (P<0.001) erythrocyte CuZn-SOD (873 +/- 52 U/g Hb) and GPX (64.7 +/- 14.2 U/g Hb) activity than obese women (660 +/- 39 U/g Hb) and (48.5 +/- 13.1 U/g Hb), respectively. Furthermore, erythrocyte CuZn-SOD and GPX activity were negatively correlated with BMI (r =-0.52, P<0.0001 and r =-0.42, P<0.001), respectively. No significant difference was observed between two groups in erythrocyte CAT activity. CONCLUSIONS: From these observations, it is concluded that obesity even in the absence of smoking, diabetes, renal or liver disease can decrease the activities of bodys protective antioxidants, and can enhance the systemic oxidative stress.
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页码:189 / 192
页数:4
相关论文
共 20 条
[11]   Developmental changes of erythrocyte catalase activity in rats exposed to acute hypoxia [J].
Rauchová, H ;
Vokurková, M ;
Koudelová, J .
PHYSIOLOGICAL RESEARCH, 2005, 54 (05) :527-532
[12]   Anti-oxidant status and lipid peroxidation in patients with essential hypertension [J].
Russo, C ;
Olivieri, O ;
Girelli, D ;
Faccini, G ;
Zenari, ML ;
Lombardi, S ;
Corrocher, R .
JOURNAL OF HYPERTENSION, 1998, 16 (09) :1267-1271
[13]  
SATOH K, 1978, CLIN CHIM ACTA, V90, P37
[14]  
Shattock MJ, 1995, METHODS ENZYMOL
[15]   A critical look at the evidence for the oxidation of LDL in atherogenesis [J].
Steinberg, D .
ATHEROSCLEROSIS, 1997, 131 :S5-S7
[16]   Superoxide production by the mitochondrial respiratory chain [J].
Turrens, JF .
BIOSCIENCE REPORTS, 1997, 17 (01) :3-8
[17]  
VANGAAL LF, 1995, INT J OBESITY, V19, pS21
[18]   Obesity is associated with increased myocardial oxidative stress [J].
Vincent, HK ;
Powers, SK ;
Stewart, DJ ;
Shanely, RA ;
Demirel, H ;
Naito, H .
INTERNATIONAL JOURNAL OF OBESITY, 1999, 23 (01) :67-74
[19]   ROLE OF OXIDIZED LOW-DENSITY-LIPOPROTEIN IN ATHEROGENESIS [J].
WITZTUM, JL ;
STEINBERG, D .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 88 (06) :1785-1792
[20]   CELLULAR DEFENSES AGAINST DAMAGE FROM REACTIVE OXYGEN SPECIES [J].
YU, BP .
PHYSIOLOGICAL REVIEWS, 1994, 74 (01) :139-162