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阿奇霉素通过其 NF-κB 抑制活性测定的抗炎活性。

Anti-inflammatory activity of azithromycin as measured by its NF-kappaB, inhibitory activity.

机构信息

Preclinical Research, InSite Vision, Alameda, California 94501, USA.

出版信息

Ocul Immunol Inflamm. 2010 Jan;18(1):32-7. doi: 10.3109/09273940903359725.

Abstract

Growing data suggest that the antibiotic azithromycin mediates anti-inflammatory activity through the inhibition of the transcription factor NF-kappaB. The purpose of this study was to compare azithromycin's anti-inflammatory potency with that of hydrocortisone and dexamethasone as measured in an activated NF-kappaB assay. Dose-response curves and the corresponding inhibitory potencies (IC(50)) of azithromycin, hydrocortisone, and dexamethasone were evaluated in a fluorescence assay using A549 cells. All three compounds inhibited TNFalpha stimulated NF-kappaB activity in a dose-dependent manner. IC(50) values of azithromycin, hydrocortisone and dexamethasone were 56 microM, 2.6 nM, and 0.18 nM, respectively. Hydrocortisone was approximately 4 orders of magnitude more potent than azithromycin, while dexamethasone was approximately 14 times as potent as hydrocortisone. In relative terms the anti-inflammatory potency of azithromycin was about 4 orders of magnitude weaker than that of hydrocortisone.

摘要

越来越多的数据表明,抗生素阿奇霉素通过抑制转录因子 NF-κB 来发挥抗炎活性。本研究的目的是比较阿奇霉素、氢化可的松和地塞米松在激活的 NF-κB 测定中的抗炎效力。使用 A549 细胞在荧光测定中评估了阿奇霉素、氢化可的松和地塞米松的剂量反应曲线和相应的抑制效力(IC 50 )。这三种化合物均以剂量依赖性方式抑制 TNFα刺激的 NF-κB 活性。阿奇霉素、氢化可的松和地塞米松的 IC 50 值分别为 56μM、2.6nM 和 0.18nM。氢化可的松的效力大约比阿奇霉素高 4 个数量级,而地塞米松的效力大约是氢化可的松的 14 倍。相对而言,阿奇霉素的抗炎效力比氢化可的松弱大约 4 个数量级。

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