Kamikubo Ryosuke, Kai Kenji, Tsuji-Naito Kentaro, Akagawa Mitsugu
Department of Biological Chemistry, Division of Applied Life Sciences, Graduate School of Life and Environmental Sciences, Osaka Prefecture University, Sakai, Japan.
Division 2, DHC Corporation Laboratories, Hamada, Mihama-ku, Chiba, Japan.
Mol Nutr Food Res. 2016 Oct;60(10):2228-2242. doi: 10.1002/mnfr.201600197. Epub 2016 Jun 16.
Nonalcoholic fatty liver disease is currently the most common chronic liver disease worldwide, characterized by excessive hepatic lipid accumulation without significant ethanol consumption. We have performed a screening for medicinal foods that inhibit hepatocytic lipid accumulation through activation of AMP-activated protein kinase (AMPK), which is a critical regulator of the hepatic lipid metabolism.
We found that clove (Syzygium aromaticum), which is commonly used as a spice, markedly inhibits palmitate-inducible lipid accumulation in human HepG2 hepatocytes. Analyses of the clove extracts found that β-caryophyllene, an orally-active cannabinoid, is the principal suppressor of the lipid accumulation, and stimulates the phosphorylation of AMPK and acetyl-CoA carboxylase 1 (ACC1). Our data also showed that β-caryophyllene prevents the translocation of sterol regulatory element-binding protein-1c (SREBP-1c) into the nucleus and forkhead box protein O1 (FoxO1) into the cytoplasm through AMPK signaling, and consequently, induces a significant downregulation of fatty acid synthase (FAS) and upregulation of adipose triglyceride lipase, respectively. Moreover, we demonstrated that the β-caryophyllene-induced activation of AMPK could be mediated by the cannabinoid type 2 receptor-dependent Ca signaling pathway.
Our results suggest that β-caryophyllene has the potential efficacy in preventing and ameliorating nonalcoholic fatty liver disease and its associated metabolic disorders.
非酒精性脂肪性肝病是目前全球最常见的慢性肝病,其特征是在无大量乙醇摄入的情况下肝脏脂质过度蓄积。我们进行了一项筛选,以寻找通过激活AMP活化蛋白激酶(AMPK)来抑制肝细胞脂质蓄积的药用食品,AMPK是肝脏脂质代谢的关键调节因子。
我们发现,常用作香料的丁香(丁香属)能显著抑制棕榈酸诱导的人HepG2肝细胞脂质蓄积。对丁香提取物的分析发现,具有口服活性的大麻素β-石竹烯是脂质蓄积的主要抑制因子,并能刺激AMPK和乙酰辅酶A羧化酶1(ACC1)的磷酸化。我们的数据还表明,β-石竹烯通过AMPK信号通路阻止固醇调节元件结合蛋白-1c(SREBP-1c)易位至细胞核以及叉头框蛋白O1(FoxO1)易位至细胞质,因此,分别诱导脂肪酸合酶(FAS)显著下调和脂肪甘油三酯脂肪酶上调。此外,我们证明β-石竹烯诱导的AMPK激活可能由2型大麻素受体依赖性钙信号通路介导。
我们的结果表明,β-石竹烯在预防和改善非酒精性脂肪性肝病及其相关代谢紊乱方面具有潜在疗效。