Dimethyl sulfoxide decreases interleukin-8-mediated neutrophil recruitment in the airways

被引:21
作者
Massion, PP
Linden, A
Inoue, H
Mathy, M
Grattan, KM
Nadel, JA
机构
[1] UNIV CALIF SAN FRANCISCO, CARDIOVASC RES INST, DEPT MED, SAN FRANCISCO, CA 94143 USA
[2] UNIV LIEGE, CTR INTERDISCIPLINAIRE BIOCHIM NORMALE & PATHOL O, B-4000 LIEGE, BELGIUM
关键词
cytokine; airway epithelium; Pseudomonas aeruginosa; reactive oxygen species;
D O I
10.1152/ajplung.1996.271.5.L838
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
In this study, we investigated the role of dimethyl sulfoxide (DMSO) in inhibiting interleukin-8 (IL-8)-mediated neutrophil recruitment induced by Pseudomonas aeruginosa (PA) bacterial supernatant. First, we tested whether DMSO could inhibit IL-8 production induced by PA in human bronchial epithelial (16-HBE) cells in vitro. In these cells, exposure to PA or H2O2 induced IL-8 production dose dependently, an effect that was inhibited by 1% DMSO at both the protein and RNA level. Second, we tested whether DMSO could block the recruitment of neutrophils induced by PA in a bypassed segment of dog trachea in vivo. PA supernatant was placed in the tracheal segment for 6 h in four dogs, and neutrophil recruitment and IL-8 concentrations were measured in the superfusate. DMSO prevented the recruitment of neutrophils and IL-8 production induced by PA time dependently. The results suggest that DMSO may play an anti-inflammatory role in the airway by inhibiting IL-8 production in epithelial cells.
引用
收藏
页码:L838 / L843
页数:6
相关论文
共 30 条
[1]   OXIDATIVE STRESS INDUCES NF-KAPPA-B DNA-BINDING AND INDUCIBLE NOS MESSENGER-RNA IN HUMAN EPITHELIAL-CELLS [J].
ADCOCK, IM ;
BROWN, CR ;
KWON, O ;
BARNES, PJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 199 (03) :1518-1524
[2]   OXYGEN METABOLITES STIMULATE RELEASE OF HIGH-MOLECULAR-WEIGHT GLYCOCONJUGATES BY CELL AND ORGAN-CULTURES OF RODENT RESPIRATORY EPITHELIUM VIA AN ARACHIDONIC ACID-DEPENDENT MECHANISM [J].
ADLER, KB ;
HOLDENSTAUFFER, WJ ;
REPINE, JE .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (01) :75-85
[3]   DIMETHYLSULFOXIDE INHIBITS PHAGOCYTE INFLUX INTO INFECTED PLEURAL SPACES AND PHAGOCYTE LOCOMOTION INVITRO [J].
ANTONY, VB ;
SAHN, SA ;
REPINE, JE .
INFLAMMATION, 1983, 7 (04) :377-385
[4]   REACTIVE OXYGEN SPECIES AND AIRWAY INFLAMMATION [J].
BARNES, PJ .
FREE RADICAL BIOLOGY AND MEDICINE, 1990, 9 (03) :235-243
[5]   IMPROVED MICRO-FLUOROMETRIC DNA DETERMINATION IN BIOLOGICAL-MATERIAL USING 33258-HOECHST [J].
CESARONE, CF ;
BOLOGNESI, C ;
SANTI, L .
ANALYTICAL BIOCHEMISTRY, 1979, 100 (01) :188-197
[6]   CFTR EXPRESSION AND CHLORIDE SECRETION IN POLARIZED IMMORTAL HUMAN BRONCHIAL EPITHELIAL-CELLS [J].
COZENS, AL ;
YEZZI, MJ ;
KUNZELMANN, K ;
OHRUI, T ;
CHIN, L ;
ENG, K ;
FINKBEINER, WE ;
WIDDICOMBE, JH ;
GRUENERT, DC .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1994, 10 (01) :38-47
[7]   OXIDANTS AND RESPIRATORY-TRACT EPITHELIAL INJURY - PATHOGENESIS AND STRATEGIES FOR THERAPEUTIC INTERVENTION [J].
CRYSTAL, RG .
AMERICAN JOURNAL OF MEDICINE, 1991, 91 :S39-S44
[8]   OXYGEN RADICAL SCAVENGERS SELECTIVELY INHIBIT INTERLEUKIN-8 PRODUCTION IN HUMAN WHOLE-BLOOD [J].
DEFORGE, LE ;
FANTONE, JC ;
KENNEY, JS ;
REMICK, DG .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (05) :2123-2129
[9]  
DEFORGE LE, 1993, J BIOL CHEM, V268, P25568
[10]  
HOIBY N, 1975, ACTA PATH MICRO IM C, V83, P459