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Beta-adrenoceptor stimulation and neutrophil accumulation in mouse airways

Miyamoto, M. (author)
Tomaki, M. (author)
Lötvall, Jan, 1956 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för lungmedicin och allergologi,Institute of Internal Medicine, Dept of Respiratory Medicine/Allergology
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Lindén, Anders, 1961 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för lungmedicin och allergologi,Institute of Internal Medicine, Dept of Respiratory Medicine/Allergology
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 (creator_code:org_t)
2004-08-01
2004
English.
In: The European respiratory journal. - : European Respiratory Society (ERS). - 0903-1936 .- 1399-3003. ; 24:2, s. 231-7
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • This study characterised the effect of beta-adrenoceptor stimulation on endotoxin-induced accumulation of neutrophilic granulocytes in mouse airways, where the cytokines interleukin (IL)-6 and macrophage inflammatory protein (MIP)-2 are involed as mediators. The beta2-adrenoceptor agonist salbutamol (0.025-250 fMol) was administered intranasally in mice 24 h prior to administration of endotoxin (10 microg) intranasally. Bronchoalveolar lavage (BAL) fluid and venous blood, respectively, was harvested (6 or 24 h) after administration of endotoxin. Salbutamol substantially decreased the number of neutrophils in BAL fluid from endotoxin-exposed (6 and 24 h) mice and this effect was dose dependent (24 h). Pretreatment with the beta-adrenoceptor antagonist propranolol attenuated the inhibitory effect of salbutamol on BAL neutrophils (6 and 24 h), an attenuation that was not due to any unspecific effect of propranolol. Salbutamol also substantially decreased IL-6, but not MIP-2 in BAL fluid (6 h). In contrast to BAL fluid, salbutamol caused a moderate increase in blood neutrophils (24 h). In conclusion, as indicated in mouse airways in vivo, beta-adrenoceptor stimulation prior to endotoxin exposure inhibits the induced accumulation of neutrophils at a time point much later than that anticipated from its bronchodilatory effect. Even though the detailed molecular mechanisms behind this sustained "anti-inflammatory" effect remain unknown, it seems likely that this effect is in part due to a decrease in the local concentration of interleukin-6.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Dermatologi och venereologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Dermatology and Venereal Diseases (hsv//eng)

Keyword

Administration
Intranasal
Airway Resistance/drug effects
Albuterol/*pharmacology
Animals
Bronchoalveolar Lavage Fluid/chemistry/cytology
Chemotaxis
Leukocyte/drug effects
Cytokines/*metabolism
Drug Interactions
Endotoxins
Male
Mice
Mice
Inbred C57BL
Models
Animal
Monokines/*metabolism
Neutrophils/drug effects/*physiology
Probability
Receptors
Adrenergic
beta/*drug effects
Sensitivity and Specificity

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art (subject category)

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Miyamoto, M.
Tomaki, M.
Lötvall, Jan, 19 ...
Lindén, Anders, ...
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University of Gothenburg

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