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没食子酸甲酯对实验性关节炎的抗炎作用:抑制中性粒细胞募集、炎症介质产生和巨噬细胞活化。

Anti-inflammatory Effect of Methyl Gallate on Experimental Arthritis: Inhibition of Neutrophil Recruitment, Production of Inflammatory Mediators, and Activation of Macrophages.

机构信息

Laboratory of Applied Pharmacology, Farmanguinhos, and ‡National Institute for Science and Technology on Innovation on Neglected Diseases (INCT/IDN), Center for Technological Development in Health (CDTS), Oswaldo Cruz Foundation (Fiocruz) , Rio de Janeiro, RJ, Brazil.

出版信息

J Nat Prod. 2016 Jun 24;79(6):1554-66. doi: 10.1021/acs.jnatprod.5b01115. Epub 2016 May 26.

Abstract

Methyl gallate (MG) is a prevalent phenolic acid in the plant kingdom, and its presence in herbal medicines might be related to its remarkable biological effects, such as its antioxidant, antitumor, and antimicrobial activities. Although some indirect evidence suggests anti-inflammatory activity for MG, there are no studies demonstrating this effect in animal models. Herein, we demonstrated that MG (0.7-70 mg/kg) inhibited zymosan-induced experimental arthritis in a dose-dependent manner. The oral administration of MG (7 mg/kg) attenuates arthritis induced by zymosan, affecting edema formation, leukocyte migration, and the production of inflammatory mediators (IL-1β, IL-6, TNF-α, CXCL-1, LTB4, and PGE2). Pretreatment with MG inhibited in vitro neutrophil chemotaxis elicited by CXCL-1, as well as the adhesion of these cells to TNF-α-primed endothelial cells. MG also impaired zymosan-stimulated macrophages by inhibiting IL-6 and NO production, COX-2 and iNOS expression, and intracellular calcium mobilization. Thus, MG is likely to present an anti-inflammatory effect by targeting multiple cellular events such as the production of various inflammatory mediators, as well as leukocyte activation and migration.

摘要

没食子酸甲酯(MG)是植物界中一种常见的酚酸,其在草药中的存在可能与其显著的生物学效应有关,如抗氧化、抗肿瘤和抗菌活性。尽管有一些间接证据表明 MG 具有抗炎活性,但在动物模型中尚未证明这种作用。在此,我们证明了 MG(0.7-70mg/kg)以剂量依赖性方式抑制酵母聚糖诱导的实验性关节炎。MG(7mg/kg)的口服给药可减轻酵母聚糖诱导的关节炎,影响水肿形成、白细胞迁移和炎症介质(IL-1β、IL-6、TNF-α、CXCL-1、LTB4 和 PGE2)的产生。MG 预处理可抑制 CXCL-1 诱导的中性粒细胞趋化作用,以及这些细胞与 TNF-α 预处理的内皮细胞的黏附。MG 还通过抑制 IL-6 和 NO 产生、COX-2 和 iNOS 表达以及细胞内钙动员来抑制酵母聚糖刺激的巨噬细胞。因此,MG 可能通过针对各种炎症介质的产生以及白细胞激活和迁移等多种细胞事件发挥抗炎作用。

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