首页> 外文期刊>Journal of Ethnopharmacology: An Interdisciplinary Journal Devoted to Bioscientific Research on Indigenous Drugs >Evaluation of the anti-inflammatory and anti-proliferation tumoral cells activities of Antrodia camphorata, Cordyceps sinensis, and Cinnamomum osmophloeum bark extracts.
【24h】

Evaluation of the anti-inflammatory and anti-proliferation tumoral cells activities of Antrodia camphorata, Cordyceps sinensis, and Cinnamomum osmophloeum bark extracts.

机译:樟芝,冬虫夏草和肉桂皮提取物的抗炎和抗增殖肿瘤细胞活性评估。

获取原文
获取原文并翻译 | 示例
           

摘要

The extracts of chloroform (1) and methanol (2) from Antrodia camphorata (AC), and chloroform (3) and n-butanol (4) fractions of methanol extract from Cordyceps sinensis (CS), and hexane (5), ethyl acetate (6), and methanol (7) from Cinnamomum osmophloeum bark (CO) were evaluated for their anti-inflammatory as well as tumor-cell growth inhibitory activities in vitro. All the tested extracts dose dependently inhibited the enhanced production of inflammatory mediators such as nitric oxide (NO) through reducing inducible NO synthase expression, and cytokines (tumor necrosis factor (TNF)-alpha and interleukin (IL)-12 in LPS/IFN-gamma activated murine peritoneal macrophages. In addition, extracts 1 from AC, and 5 and 6 from CO significantly arrest the mitogen-stimulated spleen cells in G0/G1 stage. On the other hand, all these extracts were also evaluated for their tumor-cell proliferation activities in different type of cancer cell lines such as Jurkat, HepG2, PC 3, Colon 205, and MCF 7 as well as normal PBMCs. Compared to untreated controls, the extracts 1, 2, and 4-7 were most active and inhibited Jurkat cells with IC50 value of 22, 40, 18, 4, 5, and 45 microg/ml, respectively. In addition, the extracts 5, 6, and 7 from CO showed potent growth inhibition of HepG2 and PC 3 with IC50 values of 35, 80, 55 microg/ml; and 42, 125, and 50 microg/ml, respectively. Similarly, the extracts 1 and 5 inhibited the growth of Colon 205 and MCF 7 cells with IC50 values of 65, 33; and 95 and 30 microg/ml, respectively. Interestingly, none of the tested extract has shown cytotoxicity towards normal PBMCs up to the concentration range studies (0-150 microg/ml). Taken together, these data suggest that the anti-inflammatory and anti-cancer properties of AC, CS, and CO might result from the growth inhibition of NO, TNF-alpha and IL-12, and tumor cells proliferation, respectively.
机译:樟脑樟(AC)的氯仿(1)和甲醇(2)提取物,冬虫夏草(CS)的甲醇提取物的氯仿(3)和正丁醇(4)馏分以及己烷(5)和乙酸乙酯(6)和来自肉桂皮(CO)的甲醇(7)在体外具有抗炎和抑制肿瘤细胞生长的活性。所有测试的提取物均通过降低诱导型一氧化氮合酶的表达以及细胞因子(肿瘤坏死因子(TNF)-α和白介素(IL)-12在LPS /IFN-γ中的剂量依赖性)抑制炎症介质如一氧化氮(NO)的产生增加。 γ激活的小鼠腹膜巨噬细胞,此外,AC提取物1和CO提取物5和6可以显着阻滞G0 / G1期的促分裂原刺激的脾细胞,另一方面,还评估了所有这些提取物的肿瘤细胞在不同类型的癌细胞系(如Jurkat,HepG2,PC 3,Colon 205和MCF 7以及正常的PBMC)中,其增殖活性与未处理的对照组相比,提取物1、2和4-7最为活跃和抑制Jurkat细胞的IC50值分别为22、40、18、4、5和45微克/毫升,此外,CO提取物5、6和7表现出对HepG2和PC 3的有效生长抑制,IC50值为50。分别为35、80、55微克/毫升和42、125和50微克/毫升积极地。同样,提取物1和5抑制结肠205和MCF 7细胞的生长,IC50值为65、33;分别为95和30微克/毫升。有趣的是,直到浓度范围研究(0-150微克/毫升),测试的提取物都没有表现出对正常PBMC的细胞毒性。综上所述,这些数据表明AC,CS和CO的抗炎和抗癌特性可能分别来自NO,TNF-α和IL-12的生长抑制以及肿瘤细胞的增殖。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号