The effects of resveratrol on hepatic oxidative stress in metabolic syndrome model induced by high fructose diet

被引:22
作者
Demirtas, Yilmaz C. [1 ]
Bircan, F. S. [1 ,2 ]
Pasaoglu, O. T. [1 ,3 ]
Turkozkan, N. [1 ]
机构
[1] Gazi Univ, Dept Biochem, Fac Med, Ankara, Turkey
[2] Gazi Univ, Dept Biol, Fac Sci, TR-06500 Ankara, Turkey
[3] Gazi Univ, Fac Hlth Sci, Ankara, Turkey
来源
BRATISLAVA MEDICAL JOURNAL-BRATISLAVSKE LEKARSKE LISTY | 2018年 / 119卷 / 01期
关键词
resveratrol; metabolic syndrome; fructose; oxidative stress; liver; CARDIOVASCULAR-DISEASES; POTENTIAL ROLE; POLYPHENOLS; LIVER; EXPRESSION; OXIDANT; OBESITY; KIDNEY; RATS;
D O I
10.4149/BLL_2018_008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: The purpose of this study was to evaluate probable protective effects of resveratrol treatment on hepatic oxidative events in a rat model of metabolic syndrome (MetS). METHODS: Thirty-two male adult rats were randomly divided into 4 groups: control, fructose, resveratrol, and fructose plus resveratrol. To induce MetS, fructose solution (20 % in drinking water) was used. Resveratrol (10 mg/kg/day) was given by oral gavage. All treatments were given for 8 weeks. Serum lipid profile, glucose and insulin levels, liver total oxidant status (TOS) levels and paraoxonase (PON), glutathione peroxidase (GPx), superoxide dismutase (SOD) and catalase (CAT) activities were analyzed. RESULTS: Fructose-fed rats displayed statistically significant increases in TOS levels, and decreases in PON activity compared to the control group. Resveratrol treatment moderately prevented the decrease in liver PON activity caused by fructose. On the other hand, resveratrol, alone or in combination with fructose, did not change the TOS levels when compared to the fructose group. The SOD and CAT activities in all groups did not change. CONCLUSION: In this experimental design, high-fructose consumption led to elevated TOS levels and low PON activities. The resveratrol therapy shown beneficial effects on PON activity. However, it was found to behave like a prooxidant when administered together with fructose and alone in some parameters. Our results can inspire the development of new clinical therapy in patients with MetS (Tab. 2, Ref. 34).
引用
收藏
页码:36 / 40
页数:5
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