脂肪生成
安普克
产热素
辅活化剂
产热
内科学
内分泌学
蛋白激酶A
3T3-L1
AMP活化蛋白激酶
化学
过氧化物酶体增殖物激活受体
脂肪组织
受体
生物
激酶
生物化学
医学
转录因子
基因
作者
Hara Lim,Jinbong Park,Hye‐Lin Kim,JongWook Kang,Mi‐Young Jeong,Dong‐Hyun Youn,Yunu Jung,Yong‐Il Kim,Hyunju Kim,Kwang Seok Ahn,Sujin Kim,Seong‐Kyu Choe,Seung‐Heon Hong,Jae‐Young Um
标识
DOI:10.3389/fphar.2016.00476
摘要
Chrysophanic acid (CA) is a member of the anthraquinone family abundant in rhubarb, a widely used herb for obesity treatment in Traditional Korean Medicine. Though several studies have indicated numerous features of CA, no study has yet reported the effect of CA on obesity. In this study, we tried to identify the anti-obesity effects of CA. By using 3T3-L1 adipocytes and primary cultured brown adipocytes as in vitro models, high-fat diet (HFD)-induced obese mice, and zebrafish as in vivo models, we determined the anti-obesity effects of CA. CA reduced weight gain in HFD-induced obese mice. They also decreased lipid accumulation and the expressions of adipogenesis factors including peroxisome proliferator-activated receptor gamma (PPARγ) and CCAAT/enhancer-binding protein alpha (C/EBPα) in 3T3-L1 adipocytes. In addition, uncoupling protein 1 (UCP1) and peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC1α), the brown fat specific thermogenic genes, were up-regulated in brown adipocytes by CA treatment. Furthermore, when co-treated with Compound C, the AMP-activated protein kinase (AMPK) inhibitor, the action of CA on AMPKα was nullified in both types of adipocytes, indicating the multi-controlling effect of CA was partially via the AMPKα pathway. Given all together, these results indicate that CA can ameliorate obesity by controlling the adipogenic and thermogenic pathway at the same time. On these bases, we suggest the new potential of CA as an anti-obese pharmacotherapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI