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盐肤木化学成分对巨噬细胞系炎性细胞因子分泌的调控作用

The regulation of inflammatory cytokine secretion in macrophage cell line by the chemical constituents of Rhus sylvestris.

作者信息

Ding Yan, Nguyen Huu Tung, Kim Sung In, Kim Ha Won, Kim Young Ho

机构信息

College of Pharmacy, Chungnam National University, Daejeon 305-764, Republic of Korea.

出版信息

Bioorg Med Chem Lett. 2009 Jul 1;19(13):3607-10. doi: 10.1016/j.bmcl.2009.04.129. Epub 2009 May 3.

Abstract

In our preliminary screening study on the anti-inflammatory activity, eight triterpenes, one sterol, and one chalcone were isolated from the CH(2)Cl(2)-soluble extract of the stems and leaves of Rhus sylvestris Siebold and Zucc (Anacardiaceae). On the basis of their spectroscopic data, these compounds were identified as 10alpha-cucurbitadienol (1), glut-5-en-3-ol (2), beta-amyrin acetate (3), beta-amyrin (4) and lupeol (5), cycloart-24-en-3-one (6), cycloart-25-en-3,24-dione (7), 24-hydroxycycloart-25-en-3-one (8), beta-sitosterol (9), and 2'-hydroxy-4,4'-dimethoxychalcone (10). All of them were isolated from this plant for the first. Furthermore, the compounds in non-cytotoxic concentrations (0-1.0microM) were tested for their ability to block inflammatory cytokine secretion in the presence of LPS in the murine RAW264.7 macrophage cell line. Among the compounds that were tested, compounds 8 and 9 reduced the LPS-induced secretion of IL-6, as well as TNF-alpha, in a mouse RAW264.7 macrophage cell line. Moreover, compounds 2, 3, 7, and 10 specifically diminished only the secretion of TNF-alpha even in 0.01microM concentrations. It is thus suggested that they are potential therapeutics of TNF-alpha-related diseases and conditions, such as transplant rejection, type II diabetes, and atherosclerosis.

摘要

在我们关于抗炎活性的初步筛选研究中,从野漆树(漆树科)茎叶的二氯甲烷可溶提取物中分离出了8种三萜、1种甾醇和1种查尔酮。根据它们的光谱数据,这些化合物被鉴定为10α-葫芦二烯醇(1)、羽扇-5-烯-3-醇(2)、β-香树脂醇乙酸酯(3)、β-香树脂醇(4)和羽扇豆醇(5)、环阿尔廷-24-烯-3-酮(6)、环阿尔廷-25-烯-3,24-二酮(7)、24-羟基环阿尔廷-25-烯-3-酮(8)、β-谷甾醇(9)以及2'-羟基-4,4'-二甲氧基查尔酮(10)。所有这些化合物均首次从该植物中分离得到。此外,对非细胞毒性浓度(0 - 1.0微摩尔)的化合物进行了测试,以检测它们在小鼠RAW264.7巨噬细胞系中存在脂多糖(LPS)的情况下阻断炎性细胞因子分泌的能力。在测试的化合物中,化合物8和9在小鼠RAW264.7巨噬细胞系中降低了LPS诱导的白细胞介素-6(IL-6)以及肿瘤坏死因子-α(TNF-α)的分泌。此外,化合物2、3、7和10即使在0.01微摩尔浓度下也仅特异性地减少了TNF-α的分泌。因此,提示它们是TNF-α相关疾病和病症(如移植排斥、II型糖尿病和动脉粥样硬化)的潜在治疗药物。

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