VIRUS-INDUCED AIRWAY INFLAMMATION AND HYPERRESPONSIVENESS IN THE GUINEA-PIG IS INHIBITED BY LEVODROPROPIZINE

被引:3
作者
FOLKERTS, G [1 ]
VANDERLINDE, HJ [1 ]
OMINI, C [1 ]
NIJKAMP, FP [1 ]
机构
[1] DOMPE FARMACEUT SPA, RES & DEV LABS, MILAN, ITALY
关键词
VIRAL RESPIRATORY INFECTIONS; AIRWAY RESPONSIVENESS; INFLAMMATORY CELL COUNTS; GUINEA-PIG; LEVODROPROPIZINE;
D O I
10.1007/BF00164801
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Intratracheal Parainfluenza type 3 (PI-3) virus inoculation of guinea pigs leads to a non-specific airway hyperresponsiveness in vivo and in vitro which coincides with a significant increase in the number of inflammatory cells in the broncho-alveolar lavage fluid (90% increase, 4 days after inoculation). The activity of the bronchoalveolar cells, as measured by the chemiluminescence production of infected animals is significantly diminished (34.2%, 4 days after inoculation) after renewed stimulation with PI-3 virus in vitro as compared to the chemiluminescence production by bronchoalveolar cells obtained from control guinea pigs. Pretreatment of the guinea-pigs with the antitussive agent levodropropizine, administered intra-peritoneally twice a day for five successive days at a dose of 10 mg/kg, prevents the virus-induced airway hyperresponsiveness in vivo and in vitro, and inhibits the influx of broncho-alveolar cells. Levodropropizine at a dose of 1 mg/kg did not modulate these responses. Further, the decrease in chemiluminescence production of broncho-alveolar cells obtained from virus-infected animals after PI-3 virus stimulation in vitro was inhibited by levodropropizine (10 mg/kg). These data demonstrate the ability of levodropropizine to counteract the hyperresponsiveness phenomenon and the associated inflammatory event induced by PI-3 virus, an effect which may be due to its capacity to act on the peptidergic system or may be due to the anti-allergic/bronchoconstrictor property of this compound.
引用
收藏
页码:213 / 219
页数:7
相关论文
共 38 条
[1]  
BARNES PJ, 1988, PHARMACOL REV, V40, P49
[2]   MODULATION OF NEUROGENIC INFLAMMATION - NOVEL APPROACHES TO INFLAMMATORY DISEASE [J].
BARNES, PJ ;
BELVISI, MG ;
ROGERS, DF .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1990, 11 (05) :185-189
[3]   ELEVATED BRONCHOALVEOLAR LAVAGE FLUID HISTAMINE LEVELS IN ALLERGIC ASTHMATICS ARE ASSOCIATED WITH METHACHOLINE BRONCHIAL HYPERRESPONSIVENESS [J].
CASALE, TB ;
WOOD, D ;
RICHERSON, HB ;
TRAPP, S ;
METZGER, WJ ;
ZAVALA, D ;
HUNNINGHAKE, GW .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (04) :1197-1203
[4]  
CASTLEMAN WL, 1990, AM J PATHOL, V137, P821
[5]  
DAFFONCHIO L, 1991, American Review of Respiratory Disease, V143, pA703
[6]  
DAFFONCHIO L, 1992, EUR J PHARM ENV TOXI, V228, P257
[7]   MUCOSAL INFLAMMATION IN ASTHMA [J].
DJUKANOVIC, R ;
ROCHE, WR ;
WILSON, JW ;
BEASLEY, CRW ;
TWENTYMAN, OP ;
HOWARTH, PH ;
HOLGATE, ST .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1990, 142 (02) :434-457
[8]   CIGARETTE-SMOKE INDUCES BRONCHOCONSTRICTOR HYPERRESPONSIVENESS TO SUBSTANCE-P AND INACTIVATES AIRWAY NEUTRAL ENDOPEPTIDASE IN THE GUINEA-PIG - POSSIBLE ROLE OF FREE-RADICALS [J].
DUSSER, DJ ;
DJOKIC, TD ;
BORSON, DB ;
NADEL, JA .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (03) :900-906
[9]   BRONCHOALVEOLAR MAST-CELLS IN EXTRINSIC-ASTHMA - A MECHANISM FOR THE INITIATION OF ANTIGEN SPECIFIC BRONCHOCONSTRICTION [J].
FLINT, KC ;
LEUNG, KBP ;
HUDSPITH, BN ;
BROSTOFF, J ;
PEARCE, FL ;
JOHNSON, NM .
BRITISH MEDICAL JOURNAL, 1985, 291 (6500) :923-926
[10]   VIRUS-INDUCED AIRWAY HYPERRESPONSIVENESS IN THE GUINEA-PIG - POSSIBLE INVOLVEMENT OF HISTAMINE AND INFLAMMATORY CELLS [J].
FOLKERTS, G ;
DECLERCK, F ;
REIJNART, I ;
SPAN, P ;
NIJKAMP, FP .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (04) :1083-1093