Indole-3-carbinol prevents diet-induced obesity through modulation of multiple genes related to adipogenesis, thermogenesis or inflammation in the visceral adipose tissue of mice

内分泌学 内科学 脂肪生成 脂肪组织 产热 脂肪细胞 炎症 生物 产热素 西妥因1 脂肪因子 过氧化物酶体增殖物激活受体 瘦素 医学 肥胖 受体 下调和上调 生物化学 基因
作者
Youngshim Choi,Yun Jung Kim,So‐Young Park,Ki Won Lee,Taesun Park
出处
期刊:Journal of Nutritional Biochemistry [Elsevier]
卷期号:23 (12): 1732-1739 被引量:71
标识
DOI:10.1016/j.jnutbio.2011.12.005
摘要

Indole-3-carbinol (I3C) is a compound found in high concentrations in Brassica family vegetables, including broccoli, cauliflower and cabbage, and is regarded as a promising chemopreventive agent against various cancers. This study assesses the protective effect of I3C against diet-induced obesity in mice. Mice were randomly grouped to receive either a normal diet, high-fat (40% energy as fat) diet (HFD) or I3C-supplemented diet (1 g/kg diet) for 10 weeks. I3C supplementation significantly ameliorated HFD-induced increases in body weight gain, visceral fat pad weights and plasma lipid levels. The visceral adipose tissue mRNA levels of uncoupling proteins 1 and 3, crucial factors of thermogenesis, and their regulators such as sirtuin 1, peroxisome proliferator-activated receptor (PPAR) α and PPARγ coactivator 1α, which were down-regulated by HFD, were normalized by supplementation with I3C. In contrast, I3C supplementation significantly decreased expression levels of a key adipogenic transcription factor, PPARγ2, and its target genes, such as leptin and adipocyte protein 2, in the visceral adipose tissue of mice maintained on the HFD. Furthermore, HFD-induced up-regulation in mRNA levels of inflammatory cytokines (tumor necrosis factor α, interferon β and interleukin 6) was significantly ameliorated by I3C. These findings suggest that I3C has a potential benefit in preventing obesity and metabolic disorders, and the action for I3C in vivo may involve multiple mechanisms including decreased adipogenesis and inflammation, along with activated thermogenesis.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
deer完成签到,获得积分10
2秒前
图图发布了新的文献求助10
2秒前
3秒前
GJK发布了新的文献求助10
3秒前
陈易关注了科研通微信公众号
3秒前
4秒前
4秒前
4秒前
聪明飞雪发布了新的文献求助10
5秒前
5秒前
善学以致用应助yimi采纳,获得10
5秒前
佳佳发布了新的文献求助10
5秒前
徐徐徐应助甜甜映菡采纳,获得10
5秒前
小不遛w完成签到,获得积分10
5秒前
Reese完成签到 ,获得积分10
6秒前
冰美式发布了新的文献求助10
6秒前
云瑾应助啊凡采纳,获得10
7秒前
7秒前
满意花生发布了新的文献求助10
8秒前
lin发布了新的文献求助10
10秒前
东山月发布了新的文献求助10
10秒前
11秒前
呼延访彤完成签到,获得积分20
11秒前
szy发布了新的文献求助10
13秒前
聪明飞雪完成签到,获得积分20
14秒前
15秒前
弄井发布了新的文献求助10
16秒前
19秒前
20秒前
完美世界应助佳佳采纳,获得10
21秒前
22秒前
upupup111发布了新的文献求助10
25秒前
华仔应助LIYY采纳,获得10
25秒前
冰美式完成签到,获得积分20
26秒前
26秒前
湘君发布了新的文献求助10
26秒前
情怀应助szy采纳,获得10
27秒前
nenoaowu发布了新的文献求助100
28秒前
30秒前
高分求助中
Evolution 10000
Sustainability in Tides Chemistry 2800
юрские динозавры восточного забайкалья 800
Diagnostic immunohistochemistry : theranostic and genomic applications 6th Edition 500
Chen Hansheng: China’s Last Romantic Revolutionary 500
China's Relations With Japan 1945-83: The Role of Liao Chengzhi 400
Classics in Total Synthesis IV 400
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3149493
求助须知:如何正确求助?哪些是违规求助? 2800565
关于积分的说明 7840531
捐赠科研通 2458065
什么是DOI,文献DOI怎么找? 1308242
科研通“疑难数据库(出版商)”最低求助积分说明 628460
版权声明 601706