Natural Medicine Center, KIST Gangneung Institute, Gangneung 210-340, Republic of Korea.
Biochem Biophys Res Commun. 2013 Mar 1;432(1):73-9. doi: 10.1016/j.bbrc.2013.01.083. Epub 2013 Jan 29.
Peroxisome proliferator-activated receptors (PPARs) have been considered as desirable targets for metabolic syndrome treatments, even though their specific agonists have several side effects, including body weight gain, edema, and tissue failure. The effects of amorphastilbol (APH) on glucose- and lipid metabolism were investigated with in vitro 3T3-L1 adipocyte systems and in vivo db/db mice model. APH selectively stimulates the transcriptional activities of both PPARα and PPARγ, which are able to enhance fatty acid oxidation and glucose utilization. Furthermore, APH improves glucose and lipid impairment in db/db mice. More importantly, there are no significant side effects, such as weight gain or hepatomegaly, in APH-treated animals, implying that APH do not adversely affect liver or lipid metabolism. All our data suggest that APH can be used as potential therapeutic agents against type 2 diabetes and related metabolic disorders, including obesity, by enhancing glucose and lipid metabolism.
过氧化物酶体增殖物激活受体 (PPARs) 已被认为是治疗代谢综合征的理想靶点,尽管它们的特定激动剂有多种副作用,包括体重增加、水肿和组织衰竭。本文采用体外 3T3-L1 脂肪细胞系统和体内 db/db 小鼠模型研究了变形醇(APH)对葡萄糖和脂质代谢的影响。APH 选择性地刺激 PPARα 和 PPARγ 的转录活性,从而增强脂肪酸氧化和葡萄糖利用。此外,APH 改善了 db/db 小鼠的葡萄糖和脂质损伤。更重要的是,在 APH 处理的动物中没有明显的副作用,如体重增加或肝肿大,这意味着 APH 不会对肝脏或脂质代谢产生不利影响。所有这些数据表明,APH 可通过增强葡萄糖和脂质代谢,用于治疗 2 型糖尿病和相关代谢紊乱,包括肥胖症。