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pubmed-article:1335883pubmed:abstractTextRecently, we demonstrated that an increased airway responsiveness in vitro can be measured 4, 8, and 16 days, but not 2 days, after intratracheal inoculation of parainfluenza-3 (PI-3) virus to guinea pigs. In the present study airway responsiveness was measured in vivo, and the number, types and activity of broncho-alveolar cells was determined. A significant increase in airflow resistance was measured in spontaneously breathing anesthetized guinea pigs in response to histamine and methacholine, 4 and 8 days after PI-3 virus inoculation. 2 days after inoculation with control solution or PI-3 virus, no difference in the total number of inflammatory cells was observed in the broncho-alveolar lavage fluid. In contrast, on days 4, 8, and 16 after infection a significant increase in the number of alveolar macrophages (102%, 76%, 68%, respectively), monocytes (552%, 374%, 360%, respectively), and lymphocytes (253%, 675%, 396%, respectively) was found. The number of eosinophils was increased as well, but faded with time (378%, 312%, 63%, respectively). PI-3 virus was found to be a very potent activator of broncho-alveolar cells as measured by chemiluminescence. The increase in chemiluminescence production in response to PI-3 virus was reduced in cells obtained from PI-3 virus pretreated animals (day 2, 42%; day 4, 65%; day 8, 22%; and day 16, 30%). In conclusion, PI-3 virus can stimulate broncho-alveolar cells and the virus-induced airway hyperresponsiveness is associated with an influx of inflammatory cells in the respiratory tract.lld:pubmed
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pubmed-article:1335883pubmed:dateRevised2011-11-17lld:pubmed
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pubmed-article:1335883pubmed:articleTitleVirus-induced airway hyperresponsiveness in guinea pigs in vivo: study of broncho-alveolar cell number and activity.lld:pubmed
pubmed-article:1335883pubmed:affiliationDepartment of Pharmacology, Faculty of Pharmacy, Utrecht University, Netherlands.lld:pubmed
pubmed-article:1335883pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1335883pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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