A protective effect of adiponectin against oxidative stress in Japanese Americans: the association between adiponectin or leptin and urinary isoprostane

被引:96
作者
Nakanishi, S [1 ]
Yamane, K [1 ]
Kamei, N [1 ]
Nojima, H [1 ]
Okubo, M [1 ]
Kohno, N [1 ]
机构
[1] Hiroshima Univ, Dept Mol & Internal Med, Grad Sch Biomed Sci, Hiroshima 7348551, Japan
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2005年 / 54卷 / 02期
关键词
D O I
10.1016/j.metabol.2004.08.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adiponectin, which is produced by adipose tissue, is thought to play an important role in inflammation. On the other hand, adiposity, or the hypertrophy of adipose tissue, has been reported to increase oxidative stress. Accordingly, the possibility exists that adiponectin, as well as leptin, influences oxidative stress, resulting in a proinflammatory state. However, the relationship between adiponectin and oxidative stress is unclear. We examined 259 Japanese Americans living in Hawaii who were diagnosed as having normal glucose tolerance (NGT), impaired glucose tolerance, or diabetes by a 75-g oral glucose tolerance test. First, we measured their serum adiponectin, leptin, and high-sensitivity C-reactive protein levels as markers of inflammation, and urinary 8-iso-protaglandin F-2alpha (isoprostane) as a relevant marker of oxidative stress. We investigated the relationship between adiponectin or leptin and isoprostane among these subjects. In the diabetic subjects, the adiponectin and leptin levels were significantly lower and higher, respectively, than among the NGT subjects. Urinary isoprostane levels tended to decrease significantly after a rise in adiponectin levels (P = .014) among the NGT subjects. Next, we investigated the association between the 2 adipocytokines and isoprostane by regression models. Adiponectin was negatively but significantly associated with urinary isoprostane levels adjusted for age, gender, and smoking status, whereas leptin was positively and significantly correlated with urinary isoprostane levels (P = .014 and .004, respectively). With respect to adiponectin, this association was attenuated but still significant when further adjustments were made for waist-to-hip ratio, body mass index, percent body fat, C-reactive protein levels, glucose tolerance status, or homeostasis model assessment. In conclusion, this study suggests that adiponectin and leptin might be associated with oxidative stress levels. These results also suggest the possibility that adiponectin might modulate oxidative stress, leading to antidiabetic and anti-arteriosclerotic effects. (C) 2005 Elsevier Inc. All rights reserved.
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收藏
页码:194 / 199
页数:6
相关论文
共 28 条
[1]   Leptin decreases plasma paraoxonase 1 (PON1) activity and induces oxidative stress: the possible novel mechanism for proatherogenic effect of chronic hyperleptinemia [J].
Beltowski, J ;
Wojcicka, G ;
Jamroz, A .
ATHEROSCLEROSIS, 2003, 170 (01) :21-29
[2]   Leptin induces oxidative stress in human endothelial cells [J].
Bouloumié, A ;
Marumo, T ;
Lafontan, M ;
Busse, R .
FASEB JOURNAL, 1999, 13 (10) :1231-1238
[3]   Isoprostanes as a biomarker of lipid peroxidation in humans: physiology, pharmacology and clinical implications [J].
Cracowski, JL ;
Durand, T ;
Bessard, G .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2002, 23 (08) :360-366
[4]   Decreased serum levels of adiponectin are a risk factor for the progression to type 2 diabetes in the Japanese population - The Funagata study [J].
Daimon, M ;
Oizumi, T ;
Saitoh, T ;
Kameda, W ;
Hirata, A ;
Yamaguchi, H ;
Ohnuma, H ;
Igarashi, M ;
Tominaga, M ;
Kato, T .
DIABETES CARE, 2003, 26 (07) :2015-2020
[5]   WESTERNIZED FOOD-HABITS AND CONCENTRATIONS OF SERUM-LIPIDS IN THE JAPANESE [J].
EGUSA, G ;
MURAKAMI, F ;
ITO, C ;
MATSUMOTO, Y ;
KADO, S ;
OKAMURA, M ;
MORI, H ;
YAMANE, K ;
HARA, H ;
YAMAKIDO, M .
ATHEROSCLEROSIS, 1993, 100 (02) :249-255
[6]   Body mass index, diabetes, and C-reactive protein among US adults [J].
Ford, ES .
DIABETES CARE, 1999, 22 (12) :1971-1977
[7]   Leptin and the regulation of body weight in mammals [J].
Friedman, JM ;
Halaas, JL .
NATURE, 1998, 395 (6704) :763-770
[8]  
Gavin JR, 1997, DIABETES CARE, V20, P1183
[9]   RATE OF WEIGHT-GAIN, WEIGHT FLUCTUATION, AND INCIDENCE OF NIDDM [J].
HANSON, RL ;
NARAYAN, KMV ;
MCCANCE, DR ;
PETTITT, DJ ;
JACOBSSON, LTH ;
BENNETT, PH ;
KNOWLER, WC .
DIABETES, 1995, 44 (03) :261-266
[10]   OBESITY AS AN INDEPENDENT RISK FACTOR FOR CARDIOVASCULAR-DISEASE - A 26-YEAR FOLLOW-UP OF PARTICIPANTS IN THE FRAMINGHAM HEART-STUDY [J].
HUBERT, HB ;
FEINLEIB, M ;
MCNAMARA, PM ;
CASTELLI, WP .
CIRCULATION, 1983, 67 (05) :968-977