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山苍子氯仿提取物抑制肿瘤坏死因子α并表现出多效生物活性:对人肿瘤细胞的抑制作用。

Chloroform Fraction of Centratherum anthelminticum (L.) Seed Inhibits Tumor Necrosis Factor Alpha and Exhibits Pleotropic Bioactivities: Inhibitory Role in Human Tumor Cells.

机构信息

Department of Pharmacology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.

出版信息

Evid Based Complement Alternat Med. 2012;2012:627256. doi: 10.1155/2012/627256. Epub 2012 Feb 28.

DOI:10.1155/2012/627256
PMID:22474512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3303680/
Abstract

We investigated the antioxidant potential, cytotoxic effect, and TNF-α inhibition activity with NF-κB activation response in a chloroform fraction of Centratherum anthelminticum seeds (CACF). The antioxidant property of CACF was evaluated with DPPH, ORAC, and FRAP assays, which demonstrated significant antioxidant activity. The cytotoxicity of CACF was tested using the MTT assay; CACF effective inhibitory concentrations (IC(50)) for A549, PC-3, MCF-7, and WRL-68 cells were 31.42 ± 5.4, 22.61 ± 1.7, 8.1 ± 0.9, and 54.93 ± 8.3 μg/mL, respectively. CACF effectively and dose-dependently inhibited TNF-α release, in vitro and in vivo. CACF inhibited TNF-α secretion in stimulated RAW264.7 macrophage supernatants with an IC(50) of 0.012 μg/mL, without affecting their viability; the highest dose tested reduced serum TNF-α by 61%. Acute toxicity testing in rats revealed that CACF was non-toxic at all doses tested. Matching the cytotoxic activity towards a mechanistic approach, CACF dose-dependently exhibited in vitro inhibitory effects against the activation of NF-κB translocation in MCF-7 cells. Preliminary phytochemical screening with GC/MS analysis detected 22 compounds in CACF, of which morpholinoethyl isothiocyanate was the most abundant (29.04%). The study reveals the potential of CACF in the treatment of breast cancer and in oxidative stress conditions with associated inflammatory responses.

摘要

我们研究了 Centratherum anthelminticum 种子的氯仿部分 (CACF) 的抗氧化潜力、细胞毒性作用以及对 TNF-α 的抑制活性和 NF-κB 激活反应。通过 DPPH、ORAC 和 FRAP 测定法评估 CACF 的抗氧化特性,结果表明其具有显著的抗氧化活性。通过 MTT 测定法测试 CACF 的细胞毒性;CACF 对 A549、PC-3、MCF-7 和 WRL-68 细胞的有效抑制浓度 (IC50) 分别为 31.42 ± 5.4、22.61 ± 1.7、8.1 ± 0.9 和 54.93 ± 8.3μg/mL。CACF 有效且呈剂量依赖性地抑制 TNF-α 的释放,无论是在体外还是体内。CACF 以 0.012μg/mL 的 IC50 抑制刺激 RAW264.7 巨噬细胞上清液中 TNF-α 的分泌,而不影响其活力;测试的最高剂量可使血清 TNF-α降低 61%。在大鼠中的急性毒性测试表明,CACF 在所有测试剂量下均无毒。与细胞毒性活性相匹配的是,CACF 以剂量依赖的方式在 MCF-7 细胞中表现出对 NF-κB 易位激活的体外抑制作用。用 GC/MS 分析进行的初步植物化学筛选在 CACF 中检测到 22 种化合物,其中亚氨基乙基异硫氰酸酯含量最丰富(29.04%)。该研究揭示了 CACF 在治疗乳腺癌和氧化应激条件下伴随炎症反应方面的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/290b/3303680/51e355f4d30b/ECAM2012-627256.008.jpg
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