Muscarinic receptors, leukotriene B4 production and neutrophilic inflammation in COPD patients
Background: Acetylcholine (ACh) plays an important role in smooth muscle contraction and in the development of airway narrowing; preliminary evidences led us to hypothesize that ACh might also play a role in the development of airways inflammation in chronic obstructive pulmonary disease (COPD). Me...
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Published in | Allergy (Copenhagen) Vol. 60; no. 11; pp. 1361 - 1369 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Munksgaard International Publishers
01.11.2005
Blackwell |
Subjects | |
Online Access | Get full text |
ISSN | 0105-4538 1398-9995 |
DOI | 10.1111/j.1398-9995.2005.00892.x |
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Abstract | Background: Acetylcholine (ACh) plays an important role in smooth muscle contraction and in the development of airway narrowing; preliminary evidences led us to hypothesize that ACh might also play a role in the development of airways inflammation in chronic obstructive pulmonary disease (COPD).
Methods: We evaluated the concentrations of leukotriene B4 (LTB4) in induced sputum, and the expression of Ach M1, M2, and M3 receptors in sputum cells (SC) obtained from 16 patients with COPD, 11 smokers, and 14 control subjects. The SC were also treated with ACh and the production of LTB4 assessed in the presence or absence of a muscarinic antagonist (oxitropium). In blood monocytes, we evaluated LTB4 release and activation of the extracellular signal‐regulated kinases (ERK) pathway after treatment with Ach.
Results: The LTB4 concentrations were higher in COPD than in controls (P < 0.01) and correlated with the number of neutrophil (P < 0.01). The M3 receptors expression was increased in COPD subjects when compared to smokers and control (P < 0.05 and 0.0001, respectively), while M2 expression resulted decreased (P < 0.05 and 0.01). The ACh‐induced LTB4 production was observed in peripheral blood monocytes, and was sensitive to ERK inhibition. Similarly, ACh significantly increased neutrophil chemotactic activity and LTB4 released from SC of COPD patients only, and these effects were blocked by pretreatment with the inhibitor of ERK pathway PD98059.
Conclusions: The results obtained show that muscarinic receptors may be involved in airway inflammation in COPD subjects through ACh‐induced, ERK1/2‐dependent LTB4 release. Muscarinic antagonism may contribute to reduce neutrophil infiltration and activation in COPD. |
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AbstractList | Acetylcholine (ACh) plays an important role in smooth muscle contraction and in the development of airway narrowing; preliminary evidences led us to hypothesize that ACh might also play a role in the development of airways inflammation in chronic obstructive pulmonary disease (COPD).BACKGROUNDAcetylcholine (ACh) plays an important role in smooth muscle contraction and in the development of airway narrowing; preliminary evidences led us to hypothesize that ACh might also play a role in the development of airways inflammation in chronic obstructive pulmonary disease (COPD).We evaluated the concentrations of leukotriene B4 (LTB4) in induced sputum, and the expression of Ach M1, M2, and M3 receptors in sputum cells (SC) obtained from 16 patients with COPD, 11 smokers, and 14 control subjects. The SC were also treated with ACh and the production of LTB4 assessed in the presence or absence of a muscarinic antagonist (oxitropium). In blood monocytes, we evaluated LTB4 release and activation of the extracellular signal-regulated kinases (ERK) pathway after treatment with Ach.METHODSWe evaluated the concentrations of leukotriene B4 (LTB4) in induced sputum, and the expression of Ach M1, M2, and M3 receptors in sputum cells (SC) obtained from 16 patients with COPD, 11 smokers, and 14 control subjects. The SC were also treated with ACh and the production of LTB4 assessed in the presence or absence of a muscarinic antagonist (oxitropium). In blood monocytes, we evaluated LTB4 release and activation of the extracellular signal-regulated kinases (ERK) pathway after treatment with Ach.The LTB4 concentrations were higher in COPD than in controls (P < 0.01) and correlated with the number of neutrophil (P < 0.01). The M3 receptors expression was increased in COPD subjects when compared to smokers and control (P < 0.05 and 0.0001, respectively), while M2 expression resulted decreased (P < 0.05 and 0.01). The ACh-induced LTB(4) production was observed in peripheral blood monocytes, and was sensitive to ERK inhibition. Similarly, ACh significantly increased neutrophil chemotactic activity and LTB4 released from SC of COPD patients only, and these effects were blocked by pretreatment with the inhibitor of ERK pathway PD98059.RESULTSThe LTB4 concentrations were higher in COPD than in controls (P < 0.01) and correlated with the number of neutrophil (P < 0.01). The M3 receptors expression was increased in COPD subjects when compared to smokers and control (P < 0.05 and 0.0001, respectively), while M2 expression resulted decreased (P < 0.05 and 0.01). The ACh-induced LTB(4) production was observed in peripheral blood monocytes, and was sensitive to ERK inhibition. Similarly, ACh significantly increased neutrophil chemotactic activity and LTB4 released from SC of COPD patients only, and these effects were blocked by pretreatment with the inhibitor of ERK pathway PD98059.The results obtained show that muscarinic receptors may be involved in airway inflammation in COPD subjects through ACh-induced, ERK1/2-dependent LTB4 release. Muscarinic antagonism may contribute to reduce neutrophil infiltration and activation in COPD.CONCLUSIONSThe results obtained show that muscarinic receptors may be involved in airway inflammation in COPD subjects through ACh-induced, ERK1/2-dependent LTB4 release. Muscarinic antagonism may contribute to reduce neutrophil infiltration and activation in COPD. Background: Acetylcholine (ACh) plays an important role in smooth muscle contraction and in the development of airway narrowing; preliminary evidences led us to hypothesize that ACh might also play a role in the development of airways inflammation in chronic obstructive pulmonary disease (COPD). Methods: We evaluated the concentrations of leukotriene B4 (LTB4) in induced sputum, and the expression of Ach M1, M2, and M3 receptors in sputum cells (SC) obtained from 16 patients with COPD, 11 smokers, and 14 control subjects. The SC were also treated with ACh and the production of LTB4 assessed in the presence or absence of a muscarinic antagonist (oxitropium). In blood monocytes, we evaluated LTB4 release and activation of the extracellular signal‐regulated kinases (ERK) pathway after treatment with Ach. Results: The LTB4 concentrations were higher in COPD than in controls (P < 0.01) and correlated with the number of neutrophil (P < 0.01). The M3 receptors expression was increased in COPD subjects when compared to smokers and control (P < 0.05 and 0.0001, respectively), while M2 expression resulted decreased (P < 0.05 and 0.01). The ACh‐induced LTB4 production was observed in peripheral blood monocytes, and was sensitive to ERK inhibition. Similarly, ACh significantly increased neutrophil chemotactic activity and LTB4 released from SC of COPD patients only, and these effects were blocked by pretreatment with the inhibitor of ERK pathway PD98059. Conclusions: The results obtained show that muscarinic receptors may be involved in airway inflammation in COPD subjects through ACh‐induced, ERK1/2‐dependent LTB4 release. Muscarinic antagonism may contribute to reduce neutrophil infiltration and activation in COPD. Acetylcholine (ACh) plays an important role in smooth muscle contraction and in the development of airway narrowing; preliminary evidences led us to hypothesize that ACh might also play a role in the development of airways inflammation in chronic obstructive pulmonary disease (COPD). We evaluated the concentrations of leukotriene B4 (LTB4) in induced sputum, and the expression of Ach M1, M2, and M3 receptors in sputum cells (SC) obtained from 16 patients with COPD, 11 smokers, and 14 control subjects. The SC were also treated with ACh and the production of LTB4 assessed in the presence or absence of a muscarinic antagonist (oxitropium). In blood monocytes, we evaluated LTB4 release and activation of the extracellular signal-regulated kinases (ERK) pathway after treatment with Ach. The LTB4 concentrations were higher in COPD than in controls (P < 0.01) and correlated with the number of neutrophil (P < 0.01). The M3 receptors expression was increased in COPD subjects when compared to smokers and control (P < 0.05 and 0.0001, respectively), while M2 expression resulted decreased (P < 0.05 and 0.01). The ACh-induced LTB(4) production was observed in peripheral blood monocytes, and was sensitive to ERK inhibition. Similarly, ACh significantly increased neutrophil chemotactic activity and LTB4 released from SC of COPD patients only, and these effects were blocked by pretreatment with the inhibitor of ERK pathway PD98059. The results obtained show that muscarinic receptors may be involved in airway inflammation in COPD subjects through ACh-induced, ERK1/2-dependent LTB4 release. Muscarinic antagonism may contribute to reduce neutrophil infiltration and activation in COPD. |
Author | Sala, A. Gjomarkaj, M. Giorgi, R. Di Bousquet, J. Bonsignore, G. Riccobono, L. Bonanno, A. Vignola, A. M. Mirabella, F. Profita, M. |
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Keywords | Human Immunopathology Lung disease Allergy Respiratory disease Enzyme Chronic disease Arachidonic acid derivatives Mitogen-activated protein kinase Inflammation muscarinic receptors Cholinergic receptor ERK1/2 Immunology Leukotriene B4 Extracellular signal-regulated protein kinase 1 Eicosanoid Bronchus disease Muscarinic receptor Obstructive pulmonary disease Induced sputum chronic obstructive pulmonary disease |
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Notes | During the course of this study Prof. Maurizio Vignola untimely died after suffering a malignant leukemia. We wish to dedicate this work to his memory. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
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References | 1993; 48 2002; 16 2001; 167 1987; 32 2001; 163 2000; 279 1996; 92 1999; 266 2003; 72 1998; 84 2003; 112 1989; 28 1998; 274 1993; 6 2001; 234 2000; 15 1999; 160 2002; 300 2000; 75 1988; 334 1996; 271 2003; 3 1999; 97 2001; 1 1998; 53 |
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Snippet | Background: Acetylcholine (ACh) plays an important role in smooth muscle contraction and in the development of airway narrowing; preliminary evidences led us... Acetylcholine (ACh) plays an important role in smooth muscle contraction and in the development of airway narrowing; preliminary evidences led us to... |
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SubjectTerms | Acetylcholine - pharmacology Aged Allergic diseases Biological and medical sciences Calcium-Binding Proteins - antagonists & inhibitors Calcium-Binding Proteins - pharmacology Cells, Cultured Chemotaxis, Leukocyte chronic obstructive pulmonary disease ERK1/2 Female Flavonoids - pharmacology Fundamental and applied biological sciences. Psychology Fundamental immunology Humans Immunohistochemistry Immunopathology induced sputum Leukocytes, Mononuclear - drug effects Leukocytes, Mononuclear - metabolism leukotriene B4 Leukotriene B4 - analysis Leukotriene B4 - metabolism Male Medical sciences Middle Aged Mitogen-Activated Protein Kinase 3 - drug effects Mitogen-Activated Protein Kinase 3 - metabolism muscarinic receptors Neutrophils - metabolism Protozoan Proteins - antagonists & inhibitors Protozoan Proteins - pharmacology Pulmonary Disease, Chronic Obstructive - immunology Pulmonary Disease, Chronic Obstructive - metabolism Receptors, Muscarinic - metabolism Sputum - cytology Sputum - metabolism |
Title | Muscarinic receptors, leukotriene B4 production and neutrophilic inflammation in COPD patients |
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