Fang Yangyi, Kang Yanhua, Zou Han, Cheng Xiaxuan, Xie Tian, Shi Liyun, Zhang Hang
Key Laboratory of Immunology and Molecular Medicine, Division of Basical Medicine, School of Medicine, Hangzhou Normal University, Hangzhou, Zhejiang, China.
Key Laboratory of Immunology and Molecular Medicine, Division of Basical Medicine, School of Medicine, Hangzhou Normal University, Hangzhou, Zhejiang, China; Department of Immunology, School of Basic Medical Science, Nanjing University of Chinese Medicine, Nanjing, China.
Fitoterapia. 2018 Jan;124:92-102. doi: 10.1016/j.fitote.2017.10.015. Epub 2017 Oct 21.
β-elemene, extracted from Rhizoma zedoariae, has been widely used as a traditional medicine for its antitumor activity against a broad range of cancers. However, the effect of β-elemene in inflammation disorders has yet to be determined. The present study was designed to investigate the anti-inflammatory effects and potential molecular mechanisms of β-elemene in lipopolysaccharide (LPS)-induced murine macrophage cells RAW264.7. We found that the production of pro-inflammatory mediators, including interleukin-6(IL-6), tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β), induced by LPS was significantly suppressed by β-elemene in a dose-dependent manner in RAW264.7 macrophage cell line. Also, β-elemene inhibited LPS-induced nitric oxide synthase (iNOS) and interleukin-10 (IL-10) expression by RAW264.7, which was related to the down-regulation of Wnt/β-catenin signaling pathway. Importantly, this study demonstrates that β-catenin was significantly inhibited by β-elemene, which appeared to be largely responsible for the down-regulation of Wnt/β-catenin signaling pathway. Accordingly, the deletion of β-catenin in primary macrophages reversed β-catenin-elicited inhibition of immune response. Furthermore, β-catenin expression and Wnt/β-catenin signaling pathway induced by LPS in RAW264.7 was also significantly inhibited by α-humulene, one isomeric sesquiterpene of β-elemene. α-humulene was also found to significantly inhibit LPS-induced production of proinflammatory cytokines. However, α-humulene showed more cytotoxic ability than β-elemene. Collectively, our data illustrated that β-elemene exerted a potent inhibitory effect on pro-inflammatory meditator and cytokines production via the inactivation of β-catenin, and also demonstrated the protective functions of β-elemene in endotoxin-induced inflammation. β-elemene may serve as potential nontoxic modulatory agents for the prevention and treatment of inflammatory diseases.
莪术烯是从莪术中提取的,因其对多种癌症具有抗肿瘤活性而被广泛用作传统药物。然而,莪术烯在炎症性疾病中的作用尚未确定。本研究旨在探讨莪术烯在脂多糖(LPS)诱导的小鼠巨噬细胞RAW264.7中的抗炎作用及潜在分子机制。我们发现,在RAW264.7巨噬细胞系中,莪术烯以剂量依赖的方式显著抑制LPS诱导的促炎介质的产生,包括白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)。此外,莪术烯抑制RAW264.7细胞中LPS诱导的一氧化氮合酶(iNOS)和白细胞介素-10(IL-10)的表达,这与Wnt/β-连环蛋白信号通路的下调有关。重要的是,本研究表明莪术烯显著抑制β-连环蛋白,这似乎是Wnt/β-连环蛋白信号通路下调的主要原因。因此,原代巨噬细胞中β-连环蛋白的缺失逆转了β-连环蛋白引起的免疫反应抑制。此外,莪术烯的同分异构体α-葎草烯也显著抑制RAW264.7细胞中LPS诱导的β-连环蛋白表达和Wnt/β-连环蛋白信号通路。还发现α-葎草烯显著抑制LPS诱导的促炎细胞因子的产生。然而,α-葎草烯比莪术烯表现出更强的细胞毒性。总的来说,我们的数据表明,莪术烯通过使β-连环蛋白失活,对促炎介质和细胞因子的产生发挥了强大的抑制作用,也证明了莪术烯在内毒素诱导的炎症中的保护作用。莪术烯可能作为预防和治疗炎症性疾病的潜在无毒调节剂。