Institute for Combinatorial Advanced Research and Education (KDU-CARE), General Sir John Kotelawala Defence University, Ratmalana 10390, Sri Lanka.
Department of Marine Life Sciences, Jeju National University, Jeju 690-756, Republic of Korea.
Mar Drugs. 2023 Apr 3;21(4):231. doi: 10.3390/md21040231.
In the present investigation, 24-methylcholesta-5(6), 22-diene-3β-ol (MCDO), a major phytosterol was isolated from the cultured marine diatom, Bohlin, and in vitro and in vivo anti-inflammatory effects were determined. MCDO demonstrated very potent dose-dependent inhibitory effects on the production of nitric oxide (NO) and prostaglandin E (PGE) against lipopolysaccharide (LPS)-induced RAW 264.7 cells with minimal cytotoxic effects. MCDO also demonstrated a strong and significant suppression of pro-inflammatory cytokines of interleukin-1β (IL-1β) production, but no substantial inhibitory effects were observed on the production of cytokines, including tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) at the tested concentrations against LPS treatment on RAW macrophages. Western blot assay confirmed the suppression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) protein expressions against LPS-stimulated RAW 264.7 cells. In addition, MCDO was assessed for in vivo anti-inflammatory effects using the zebrafish model. MCDO acted as a potent inhibitor for reactive oxygen species (ROS) and NO levels with a protective effect against the oxidative stress induced by LPS in inflammatory zebrafish embryos. Collectively, MCDO isolated from the cultured marine diatom exhibited profound anti-inflammatory effects both in vitro and in vivo, suggesting that this major sterol might be a potential treatment for inflammatory diseases.
在本研究中,我们从培养的海洋硅藻 Bohlin 中分离出 24-甲基胆甾-5(6),22-二烯-3β-醇(MCDO),这是一种主要的植物甾醇,并测定了其体外和体内抗炎作用。MCDO 对脂多糖(LPS)诱导的 RAW 264.7 细胞产生的一氧化氮(NO)和前列腺素 E(PGE)表现出非常有效的剂量依赖性抑制作用,且细胞毒性最小。MCDO 还表现出对白细胞介素-1β(IL-1β)产生的促炎细胞因子的强烈和显著抑制作用,但在测试浓度下,对 RAW 巨噬细胞中 LPS 处理的细胞因子(包括肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6))的产生没有实质性的抑制作用。Western blot 分析证实,MCDO 抑制了 LPS 刺激的 RAW 264.7 细胞中诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)蛋白的表达。此外,我们还使用斑马鱼模型评估了 MCDO 的体内抗炎作用。MCDO 作为一种有效的活性氧(ROS)和 NO 水平抑制剂,对 LPS 诱导的炎症斑马鱼胚胎中的氧化应激具有保护作用。总之,从培养的海洋硅藻中分离出的 MCDO 表现出显著的体外和体内抗炎作用,表明这种主要甾醇可能是治疗炎症性疾病的潜在药物。