Key Laboratory of Chemistry of Plant Resources in Arid Regions, State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, 830011, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Key Laboratory of Chemistry of Plant Resources in Arid Regions, State Key Laboratory Basis of Xinjiang Indigenous Medicinal Plants Resource Utilization, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, 830011, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
J Ethnopharmacol. 2022 Mar 25;286:114899. doi: 10.1016/j.jep.2021.114899. Epub 2021 Dec 6.
ETHNOPHARMACOLOGICAL RELEVANCE: Anchusa italica Retz. (Boraginaceae) is an important medicinal plant for the treatment of meningitis and pneumonia in traditional Uygur medicines. AIM OF THE STUDY: To clarify the anti-inflammatory activity of A. italica, to reveal its molecular mechanisms, and to discover the anti-inflammatory active ingredients. MATERIALS AND METHODS: Dried and crushed aerial parts of A. italica were extracted with 75% ethanol to yield crude extract (AICE) and AICE was fractionated to obtain petroleum ether extract (AIPE), dichloromethane extract (AIDE), ethyl acetate extract (AIEE), n-butanol extract (AIBE) and residues (AIW). By measuring the effects of AIPE, AIDE, AIEE, AIBE and AIW on cell viability and nitric oxide (NO) in Lipopolysaccharide (LPS) stimulated RAW264.7 cell lines, AIDE with the lowest cytotoxicity and NO contents was finally selected for further chemical and anti-inflammatory investigations. LC-MS/MS experiment was applied to analyze the chemical composition of AIDE. MTT and Griess methods were used to detect the cell viability and to quantify the nitrite levels in culture supernatants, respectively. Prostaglandin E (PGE), interleukin-6 (IL-6), interleukin-1β (IL-1β) and tumor necrosis factor α (TNF-α) production was examined by ELISA assays. Real-time quantitative PCR was used to detect the expression of hemeoxygenase-1 (HO-1), Nrf2-mediated quinone oxidoreductase 1 (NQO-1), glutathione S-transferase A 1 (GSTA1) and glutathione S-transferase M 1 (GSTM1) mRNA. Western blot analysis was employed to examine the protein expression and enzymatic activities. RESULTS: In preliminary anti-inflammatory screening, AIDE showed the lowest cytotoxicity and the most significant inhibitory effect on the production of NO (the inhibitory is 89%) induced by LPS among the tested five extracts. Thirty-three compounds including twenty-five triterpenoids were identified by LC-MS/MS analysis. AIDE could inhibit LPS-induced the over-expression of NO, IL-6, PGE, IL-1β and TNF-α and down-regulate the levels of extracellular signal-regulated protein kinase (ERK), c-Jun N-terminal kinase (JNK), P38-MAPK (P38) and nuclear transcription factors κB-P65 (P65) phosphorylation. It promoted the mRNA expression level of HO-1, NQO-1, GSTA1 and GSTM1 and the protein expression level of nuclear factor erythroid 2-related factor 2 (Nrf2) and HO-1. After the treatment of AIDE, P65 nuclear translocation was inhibited and Nrf2 nuclear translocation was increased. In addition, the protein expression of pyrolytic relevant protein nod-like receptor family pyrin domain-containing 3 (NLRP3) and IL-1β were decreased after the AIDE treatment. CONCLUSIONS: Anchusa italica Retz. exerted its anti-inflammatory activity by inhibiting the mitogen-activated protein kinase (MAPK), nuclear transcription factors κB (NF-κB) and pyrolytic relevant proteins, down-regulating inflammatory factor levels, and activating the Nrf2/HO-1 pathway. Triterpenoids might be its major active anti-inflammatory ingredients.
民族药理学相关性: Anchusa italica Retz.(紫草科)是维吾尔传统医学治疗脑膜炎和肺炎的重要药用植物。
研究目的:阐明 A. italica 的抗炎活性,揭示其分子机制,并发现抗炎活性成分。
材料和方法:用 75%乙醇提取 Anchusa italica 的干燥粉碎的地上部分,得到粗提取物(AICE),并对 AICE 进行分段,得到石油醚提取物(AIPE)、二氯甲烷提取物(AIDE)、乙酸乙酯提取物(AIEE)、正丁醇提取物(AIBE)和残渣(AIW)。通过测量 AIPE、AIDE、AIEE、AIBE 和 AIW 对脂多糖(LPS)刺激的 RAW264.7 细胞系细胞活力和一氧化氮(NO)的影响,选择具有最低细胞毒性和最低 NO 含量的 AIDE 进行进一步的化学和抗炎研究。LC-MS/MS 实验用于分析 AIDE 的化学成分。MTT 和格里斯方法分别用于检测细胞活力和定量培养上清液中的亚硝酸盐水平。酶联免疫吸附试验(ELISA)用于检测前列腺素 E(PGE)、白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)和肿瘤坏死因子 α(TNF-α)的产生。实时定量 PCR 用于检测血红素加氧酶-1(HO-1)、Nrf2 介导的醌氧化还原酶 1(NQO-1)、谷胱甘肽 S-转移酶 A1(GSTA1)和谷胱甘肽 S-转移酶 M1(GSTM1)mRNA 的表达。Western blot 分析用于检测蛋白质表达和酶活性。
结果:在初步抗炎筛选中,AIDE 在测试的五种提取物中显示出最低的细胞毒性和对 LPS 诱导的 NO 产生的最显著抑制作用(抑制率为 89%)。通过 LC-MS/MS 分析鉴定出 33 种化合物,包括 25 种三萜类化合物。AIDE 可抑制 LPS 诱导的 NO、IL-6、PGE、IL-1β和 TNF-α过度表达,并下调细胞外信号调节蛋白激酶(ERK)、c-Jun N-末端激酶(JNK)、P38-MAPK(P38)和核转录因子κB-P65(P65)磷酸化。它促进 HO-1、NQO-1、GSTA1 和 GSTM1 的 mRNA 表达水平,并促进核因子红细胞 2 相关因子 2(Nrf2)和 HO-1 的蛋白表达水平。AIDE 处理后,P65 核易位受到抑制,Nrf2 核易位增加。此外,AIDE 处理后,pyrolytic 相关蛋白 nod-like 受体家族 pyrin 域包含 3(NLRP3)和 IL-1β的蛋白表达减少。
结论:Anchusa italica Retz. 通过抑制丝裂原活化蛋白激酶(MAPK)、核转录因子 κB(NF-κB)和 pyrolytic 相关蛋白、下调炎症因子水平以及激活 Nrf2/HO-1 通路来发挥抗炎作用。三萜类化合物可能是其主要的抗炎活性成分。
Inflammopharmacology. 2025-6-23
Parasit Vectors. 2025-4-3
J Tradit Complement Med. 2024-3-6