Garcinia Cambogia attenuates diet-induced adiposity but exacerbates hepatic collagen accumulation and inflammation

被引:63
作者
Kim, Young-Je [1 ]
Choi, Myung-Sook [1 ,2 ]
Park, Yong Bok [3 ]
Kim, Sang Ryong [3 ,4 ]
Lee, Mi-Kyung [5 ]
Jung, Un Ju [2 ]
机构
[1] Kyungpook Natl Univ, Dept Food Sci & Nutr, Taegu 702701, South Korea
[2] Kyungpook Natl Univ, Ctr Food & Nutr Genom Res, Taegu 702701, South Korea
[3] Kyungpook Natl Univ, Sch Life Sci & Biotechnol, Taegu 702701, South Korea
[4] Kyungpook Natl Univ, Brain Sci & Engn Inst, Taegu 702701, South Korea
[5] Sunchon Natl Univ, Dept Food & Nutr, Jeonnam 540742, South Korea
基金
新加坡国家研究基金会;
关键词
Garcinia Cambogia; Anti-adiposity; Metabolic changes; Hepatic collagen accumulation; Hepatic inflammation; Hepatic oxidative stress; FATTY LIVER-DISEASE; BODY-WEIGHT REDUCTION; INSULIN-RESISTANCE; OXIDATIVE STRESS; HYDROXYCITRIC ACID; MANAGEMENT; STEATOSIS; GLUCOSE; OBESITY; MODEL;
D O I
10.3748/wjg.v19.i29.4689
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To investigate long-term effects of Garcinia Cambogia (GC), weight-loss supplement, on adiposity and non-alcoholic fatty liver disease in obese mice. METHODS: Obesity-prone C57BL/6J mice were fed a high-fat diet (HFD, 45 kcal% fat) with or without GC (1%, w/w) for 16 wk. The HFD contained 45 kcal% fat, 20 kcal% protein and 35 kcal% carbohydrate. They were given free access to food and distilled water, and food consumption and body weight were measured daily and weekly, respectively. Data were expressed as the mean +/- SE. Statistical analyses were performed using the statistical package for the social science software program. Student's t test was used to assess the differences between the groups. Statistical significance was considered at P < 0.05. RESULTS: There were no significant changes in body weight and food intake between the groups. However, the supplementation of GC significantly lowered visceral fat accumulation and adipocyte size via inhibition of fatty acid synthase activity and its mRNA expression in visceral adipose tissue, along with enhanced enzymatic activity and gene expression involved in adipose fatty acid beta-oxidation. Moreover, GC supplementation resulted in significant reductions in glucose intolerance and the plasma resistin level in the HFD-fed mice. However, we first demonstrated that it increased hepatic collagen accumulation, lipid peroxidation and mRNA levels of genes related to oxidative stress (superoxide dismutase and glutathione peroxidase) and inflammatory responses (tumor necrosis factor-a and monocyte chemoattractant protein-1) as well as plasma alanine transaminase and aspartate transaminase levels, although HFD-induced hepatic steatosis was not altered. CONCLUSION: GC protects against HFD-induced obesity by modulating adipose fatty acid synthesis and beta-oxidation but induces hepatic fibrosis, inflammation and oxidative stress. (C) 2013 Baishideng. All rights reserved.
引用
收藏
页码:4689 / 4701
页数:13
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