Resveratrol potentiates the effect of dexamethasone in rat model of acute lung inflammation

被引:38
作者
Sadarani, Bhakti N. [1 ]
Majumdar, Anuradha S. [1 ]
机构
[1] Bombay Coll Pharm, Dept Pharmacol, Bombay 400068, Maharashtra, India
关键词
Cigarette smoke; Dexamethasone; Lipopolysaccharide; Matrix metalloproteinase-9; Resveratrol; OBSTRUCTIVE PULMONARY-DISEASE; CIGARETTE-SMOKE EXPOSURE; OXIDATIVE STRESS; MOUSE MODEL; COPD; INJURY; LIPOPOLYSACCHARIDE; ASTHMA; LPS; MYELOPEROXIDASE;
D O I
10.1016/j.intimp.2015.07.038
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Cigarette smoking is considered to be the main etiological factor in Chronic Obstructive Pulmonary Disease (COPD). In this study, we explored the potential of resveratrol, to reinstate the effectiveness of dexamethasone when administered as an adjunct in acute lung inflammation induced by cigarette smoke (CS) and lipopolysaccharide (LPS). CS and LPS instillation produced acute inflammatory response exhibited by increased leukocyte count, particularly neutrophils, total protein, MMP-9 activity, cytokines like TNF-alpha, IL-8 in bronchoalveolar lavage fluid (BALF) as well as elevated myeloperoxidase activity, and lipid peroxidation in lung. These alterations were not abated by dexamethasone (2.5 mg/kg & 10 mg/kg) and resveratrol (50 mg/kg) alone. Combination of resveratrol (50 mg/kg) and dexamethasone (2.5 mg/kg) significantly reduced all inflammatory parameters. The protective effect of the combination was abolished when co-administered with sirtinol, a SIRT1 inhibitor. The results indicate that the combination therapy may serve as a potential approach for treating lung inflammatory conditions like COPD. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:773 / 779
页数:7
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