脂肪生成
安普克
产热
辅活化剂
内分泌学
内科学
蛋白激酶A
化学
脂肪组织
产热素
AMP活化蛋白激酶
过氧化物酶体增殖物激活受体
3T3-L1
受体
激酶
生物
医学
转录因子
生物化学
基因
作者
Jinbong Park,Hye‐Lin Kim,Yunu Jung,Kwang Seok Ahn,Hyun Jeong Kwak,Jae‐Young Um
出处
期刊:Nutrients
[MDPI AG]
日期:2019-08-22
卷期号:11 (9): 1988-1988
被引量:47
摘要
Obesity is a global health threat. Herein, we evaluated the underlying mechanism of anti-obese features of bitter orange (Citrus aurantium Linné, CA). Eight-week-administration of CA in high fat diet-induced obese C57BL/6 mice resulted in a significant decrease of body weight, adipose tissue weight and serum cholesterol. In further in vitro studies, we observed decreased lipid droplets in CA-treated 3T3-L1 adipocytes. Suppressed peroxisome proliferator-activated receptor gamma (PPARγ) and CCAAT/enhancer binding protein alpha indicated CA-inhibited adipogenesis. Moreover, CA-treated primary cultured brown adipocytes displayed increased differentiation associated with elevation of thermogenic factors including uncoupling protein 1 and PPARγ coactivator 1 alpha as well. The effects of CA in both adipocytes were abolished in AMP-activated protein kinase alpha (AMPKα)-suppressed environments, suggesting the anti-adipogenic and pro-thermogenic actions of CA were dependent on AMPKα pathway. In conclusion, our results suggest CA as a potential anti-obese agent which regulates adipogenesis and thermogenesis via AMPKα.
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