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天然产物对培养的小鼠巨噬细胞中诱导型环氧化酶(COX-2)和一氧化氮合酶(iNOS)抑制作用的评估。

Evaluation of natural products on inhibition of inducible cyclooxygenase (COX-2) and nitric oxide synthase (iNOS) in cultured mouse macrophage cells.

作者信息

Hong Chae Hee, Hur Sun Kyung, Oh O-Jin, Kim Sun Sook, Nam Kyung Ae, Lee Sang Kook

机构信息

Department of Pharmacy, College of Pharmacy, Ewha Womans University, 11-1 Daehyun-dong, Seodaemun-ku, 120-750, Seoul, South Korea.

出版信息

J Ethnopharmacol. 2002 Nov;83(1-2):153-9. doi: 10.1016/s0378-8741(02)00205-2.

Abstract

The inhibitors of prostaglandin biosynthesis and nitric oxide production have been considered as potential anti-inflammatory and cancer chemopreventive agents. In this study, we evaluated approximately 170 methanol extracts of natural products including Korean herbal medicines for the inhibition of prostaglandin E(2) production (for COX-2 inhibitors) and nitric oxide formation (for iNOS inhibitors) in lipopolysaccharide (LPS)-induced mouse macrophages RAW264.7 cells. As a result, several extracts such as Aristolochia debilis, Cinnamomum cassia, Cinnamomum loureirii, Curcuma zedoaria, Eugenia caryophyllata, Pterocarpus santalius, Rehmania glutinosa and Tribulus terrestris showed potent inhibition of COX-2 activity (>80% inhibition at the test concentration of 10 micro g/ml). In addition, the extracts of A. debilis, Caesalpinia sappan, Curcuma longa, C. zedoaria, Daphne genkwa and Morus alba were also considered as potential inhibitors of iNOS activity (>70% inhibition at the test concentration of 10 micro g/ml). These active extracts mediating COX-2 and iNOS inhibitory activities are warranted for further elucidation of active principles for development of new cancer chemopreventive and/or anti-inflammatory agents.

摘要

前列腺素生物合成抑制剂和一氧化氮生成抑制剂已被视为潜在的抗炎和癌症化学预防剂。在本研究中,我们评估了约170种天然产物的甲醇提取物,包括韩国草药,以检测其对脂多糖(LPS)诱导的小鼠巨噬细胞RAW264.7中前列腺素E(2)生成(用于COX - 2抑制剂)和一氧化氮形成(用于iNOS抑制剂)的抑制作用。结果,几种提取物,如马兜铃、肉桂、阴香、莪术、丁香、降香、地黄和刺蒺藜,在10μg/ml的测试浓度下显示出对COX - 2活性的强效抑制(>80%抑制)。此外,马兜铃、苏木、姜黄、莪术、芫花和桑白皮的提取物也被认为是iNOS活性的潜在抑制剂(在10μg/ml的测试浓度下>70%抑制)。这些介导COX - 2和iNOS抑制活性的活性提取物有必要进一步阐明其活性成分,以开发新的癌症化学预防剂和/或抗炎剂。

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