Department of Pharmacology, College of Korean Medicine, Sangji University, 83 Sangjidae-gil, Wonju-si, Gangwon-do 26339, Republic of Korea.
Department of Prescription, College of Korean Medicine, Sangji University, 83 Sangjidae-gil, Wonju-si, Gangwon-do 26339, Republic of Korea.
Mol Immunol. 2020 Mar;119:123-131. doi: 10.1016/j.molimm.2020.01.010. Epub 2020 Jan 31.
We evaluated the anti-inflammatory activity of methanol extracts of Chinese medicinal plants from Beijing and determined which extract was the most effective. We found the methanol extract of Acalypha australis L. (AAL) to be the most effective. AAL has been used for clearing heat, toxic material, and hemostasia in Chinese medicine. Although these uses are closely related to inflammation, the anti-inflammatory effect of AAL has not yet been described and its underlying mechanism remains unclear. Therefore, we aimed to identify anti-inflammatory effect of AAL and its underlying mechanism in vitro and in vivo. In RAW 264.7 macrophages, cytotoxicity was evaluated by MTT assay and nitric oxide (NO) was measured with Griess reagent. To confirm the production of pro-inflammatory cytokines and its mRNA expression, enzyme immunoassay (EIA) and quantitative real-time PCR (qRT-PCR) were performed. Further, protein expression was analyzed by western blotting. Septic shock was induced by intraperitoneal injection of LPS (25 mg/kg) in mice. One hour before LPS injection, AAL (25 and 50 mg/kg) was administered orally. In LPS-stimulated macrophages, AAL inhibited NO production at concentrations without cytotoxicity. Additionally, AAL reduced not only inducible nitric oxide synthase (iNOS) expression but the production of tumor necrosis factor-α (TNF-α) and interleukin-6 (IL-6) by attenuating nuclear factor-kappa B (NF-κB)-related proteins (NF-κB p65, phosphorylation of inhibitor κB-α; p-IκB-α, phosphorylation of inhibitor κB kinase-α/β; p-Ikk-α/β). Moreover, AAL enhanced the survival rate of mice through the inhibition of iNOS expression and IL-6 and interleukin-1β (IL-1β) production in LPS-induced septic mice. Furthermore, AAL also reduced the expression of NF-κB-related proteins. These finding suggest that AAL is related to the modulation of inflammatory reactions by blocking NF-κB activation in LPS-stimulated RAW 264.7 macrophages and LPS-induced septic mice.
我们评估了来自北京的中草药甲醇提取物的抗炎活性,并确定了哪种提取物最有效。我们发现,山麻(Acalypha australis L.)的甲醇提取物(AAL)是最有效的。山麻在中医中用于清热、解毒和止血。虽然这些用途与炎症密切相关,但 AAL 的抗炎作用尚未被描述,其潜在机制也不清楚。因此,我们旨在确定 AAL 在体外和体内的抗炎作用及其潜在机制。在 RAW 264.7 巨噬细胞中,通过 MTT 测定评估细胞毒性,并用 Griess 试剂测量一氧化氮(NO)。为了证实促炎细胞因子的产生及其 mRNA 表达,进行了酶免疫测定(EIA)和定量实时 PCR(qRT-PCR)。此外,通过蛋白质印迹分析蛋白质表达。通过腹腔内注射 LPS(25mg/kg)在小鼠中诱导脓毒性休克。在 LPS 注射前 1 小时,口服给予 AAL(25 和 50mg/kg)。在 LPS 刺激的巨噬细胞中,AAL 在无细胞毒性的浓度下抑制 NO 的产生。此外,AAL 通过减弱核因子-κB(NF-κB)相关蛋白(NF-κB p65、抑制κB-α的磷酸化;p-IκB-α、抑制κB 激酶-α/β的磷酸化;p-Ikk-α/β)来减少诱导型一氧化氮合酶(iNOS)表达以及肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)的产生。此外,AAL 通过抑制 iNOS 表达以及 LPS 诱导的脓毒症小鼠中 IL-6 和白细胞介素-1β(IL-1β)的产生来提高小鼠的存活率。此外,AAL 还降低了 NF-κB 相关蛋白的表达。这些发现表明,AAL 通过阻断 LPS 刺激的 RAW 264.7 巨噬细胞和 LPS 诱导的脓毒症小鼠中 NF-κB 的激活来调节炎症反应。