Effects of dexamethasone on acute virus-induced airway dysfunction in adult rats

被引:8
作者
Mehta, H
Sorkness, R
Kaplan, MR
Castleman, WL
Lemanske, RF
机构
[1] UNIV WISCONSIN,CTR CLIN SCI,DEPT MED,DIV ALLERGY,MADISON,WI 53792
[2] UNIV WISCONSIN,DEPT PEDIAT,MADISON,WI 53792
[3] UNIV WISCONSIN,SCH PHARM,MADISON,WI 53792
[4] UNIV FLORIDA,DEPT PATHOBIOL,GAINESVILLE,FL 32610
关键词
D O I
10.1203/00006450-199706000-00012
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Respiratory viral infections have been associated with airway obstruction and hyperresponsiveness, and exacerbations of asthma. Although virus-induced asthma is thought to be precipitated by airway inflammation, the clinical efficacy and rationale for using antiinflammatory treatment during such exacerbations remains controversial. The purpose of this study was to use a well characterized animal model of respiratory viral illness to test the hypothesis that the inflammatory response to viral infection is responsible for the development of airway dysfunction. Adult rats were inoculated with either Sendai virus or sterile vehicle and treated with daily injections of dexamethasone or saline. At postinoculation d 4, 5, or 6, rats were evaluated for airway obstruction, hyperresponsiveness, inflammation, and lung viral titers. Saline-treated infected rats had significant airway obstruction (increased resistance, decreased dynamic compliance), hy perresponsiveness (i.v. methacholine), and inflammation (increased bronchoalveolar lavage leukocytes) compared with noninfected controls. In contrast, dexamethasone-treated infected rats had no increase in bronchoalveolar lavage leukocytes and significantly smaller changes in airway physiology, but had increased lung viral titers compared with saline-treated infected rats. We conclude that glucocorticoid suppression of the inflammatory response to respiratory viral infection largely prevents virus-associated airway dysfunction.
引用
收藏
页码:872 / 877
页数:6
相关论文
共 45 条
[1]   IMMUNOSUPPRESSION BY GLUCOCORTICOIDS - INHIBITION OF NF-KAPPA-B ACTIVITY THROUGH INDUCTION OF I-KAPPA-B SYNTHESIS [J].
AUPHAN, N ;
DIDONATO, JA ;
ROSETTE, C ;
HELMBERG, A ;
KARIN, M .
SCIENCE, 1995, 270 (5234) :286-290
[2]   VIRUSES AS PRECIPITANTS OF ASTHMA SYMPTOMS .2. PHYSIOLOGY AND MECHANISMS [J].
BARDIN, PG ;
JOHNSTON, SL ;
PATTEMORE, PK .
CLINICAL AND EXPERIMENTAL ALLERGY, 1992, 22 (09) :809-822
[3]  
BLAIR HT, 1976, AM REV RESPIR DIS, V114, P95
[4]  
BRATTSAND R, 1991, ASTHMA ITS PATHOLOGY, P667
[5]  
BRUNETTE MG, 1988, PEDIATRICS, V81, P624
[6]  
BUSSE WW, 1992, CHEST, V101, pS385, DOI 10.1378/chest.101.6.385S
[7]   A COMMON COLD VIRUS, RHINOVIRUS-16, POTENTIATES AIRWAY INFLAMMATION AFTER SEGMENTAL ANTIGEN BRONCHOPROVOCATION IN ALLERGIC SUBJECTS [J].
CALHOUN, WJ ;
DICK, EC ;
SCHWARTZ, LB ;
BUSSE, WW .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (06) :2200-2208
[8]   CYTO-TOXIC T-CELLS CLEAR VIRUS BUT AUGMENT LUNG PATHOLOGY IN MICE INFECTED WITH RESPIRATORY SYNCYTIAL VIRUS [J].
CANNON, MJ ;
OPENSHAW, PJM ;
ASKONAS, BA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (03) :1163-1168
[9]  
CASTLEMAN WL, 1990, AM J PATHOL, V137, P821
[10]   ACUTE AND PERSISTENT ALTERATIONS IN PULMONARY INFLAMMATORY CELLS AND AIRWAY MAST-CELLS INDUCED BY SENDAI VIRUS-INFECTION IN NEONATAL RATS [J].
CASTLEMAN, WL ;
OWENS, SB ;
BRUNDAGEANGUISH, LJ .
VETERINARY PATHOLOGY, 1989, 26 (01) :18-25