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Activation of cannabinoid receptors prevents antigen-induced asthma-like reaction in guinea pigs

In this study we evaluated the effects of the CB(1)/CB(2) cannabinoid receptor agonist CP55, 940 (CP) on antigen-induced asthma-like reaction in sensitized guinea pigs and we tested the ability of the specific CB2 receptor antagonist SR144528 (SR) and CB1 receptor antagonist AM251 (AM) to interfere...

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Autores principales: Giannini, L, Nistri, S, Mastroianni, R, Cinci, L, Vannacci, A, Mariottini, C, Passani, M B, Mannaioni, P F, Bani, D, Masini, E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514116/
https://www.ncbi.nlm.nih.gov/pubmed/18266975
http://dx.doi.org/10.1111/j.1582-4934.2008.00258.x
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author Giannini, L
Nistri, S
Mastroianni, R
Cinci, L
Vannacci, A
Mariottini, C
Passani, M B
Mannaioni, P F
Bani, D
Masini, E
author_facet Giannini, L
Nistri, S
Mastroianni, R
Cinci, L
Vannacci, A
Mariottini, C
Passani, M B
Mannaioni, P F
Bani, D
Masini, E
author_sort Giannini, L
collection PubMed
description In this study we evaluated the effects of the CB(1)/CB(2) cannabinoid receptor agonist CP55, 940 (CP) on antigen-induced asthma-like reaction in sensitized guinea pigs and we tested the ability of the specific CB2 receptor antagonist SR144528 (SR) and CB1 receptor antagonist AM251 (AM) to interfere with the effects of CP. Ovalbumin-sensitized guinea pigs placed in a respiratory chamber were challenged with the antigen given by aerosol. CP (0.4 mg/kg b.wt.) was given i.p. 3 hrs before ovalbumin challenge. Sixty minutes before CP administration, some animals were treated i.p. with either AM, or SR, or both (0.1 mg/kg b.wt.). Respiratory parameters were recorded and quantified. Lung tissue specimens were then taken for histopathological and morphometric analyses and for eosinophilic major basic protein immunohistochemistry. Moreover, myeloperoxidase activity, 8-hydroxy-2-deoxyguanosine, cyclic adenosine monophosphate (cAMP) and guanosine monophosphate (cGMP) levels, and CB(1) and CB(2) receptor protein expression by Western blotting were evaluated in lung tissue extracts. In the bronchoalveolar lavage fluid, the levels of prostaglandin D(2) and tumour necrosis factor-α TNF-α were measured. Ovalbumin challenge caused marked abnormalities in the respiratory, morphological and biochemical parameters assayed. Treatment with CP significantly reduced these abnormalities. Pre-treatment with SR, AM or both reverted the protective effects of CP, indicating that both CB(1) and CB(2) receptors are involved in lung protection. The noted treatments did not change the expression of cannabinoid receptor proteins, as shown by Western blotting. These findings suggest that targeting cannabinoid receptors could be a novel preventative therapeutic strategy in asthmatic patients.
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spelling pubmed-45141162015-07-27 Activation of cannabinoid receptors prevents antigen-induced asthma-like reaction in guinea pigs Giannini, L Nistri, S Mastroianni, R Cinci, L Vannacci, A Mariottini, C Passani, M B Mannaioni, P F Bani, D Masini, E J Cell Mol Med Articles In this study we evaluated the effects of the CB(1)/CB(2) cannabinoid receptor agonist CP55, 940 (CP) on antigen-induced asthma-like reaction in sensitized guinea pigs and we tested the ability of the specific CB2 receptor antagonist SR144528 (SR) and CB1 receptor antagonist AM251 (AM) to interfere with the effects of CP. Ovalbumin-sensitized guinea pigs placed in a respiratory chamber were challenged with the antigen given by aerosol. CP (0.4 mg/kg b.wt.) was given i.p. 3 hrs before ovalbumin challenge. Sixty minutes before CP administration, some animals were treated i.p. with either AM, or SR, or both (0.1 mg/kg b.wt.). Respiratory parameters were recorded and quantified. Lung tissue specimens were then taken for histopathological and morphometric analyses and for eosinophilic major basic protein immunohistochemistry. Moreover, myeloperoxidase activity, 8-hydroxy-2-deoxyguanosine, cyclic adenosine monophosphate (cAMP) and guanosine monophosphate (cGMP) levels, and CB(1) and CB(2) receptor protein expression by Western blotting were evaluated in lung tissue extracts. In the bronchoalveolar lavage fluid, the levels of prostaglandin D(2) and tumour necrosis factor-α TNF-α were measured. Ovalbumin challenge caused marked abnormalities in the respiratory, morphological and biochemical parameters assayed. Treatment with CP significantly reduced these abnormalities. Pre-treatment with SR, AM or both reverted the protective effects of CP, indicating that both CB(1) and CB(2) receptors are involved in lung protection. The noted treatments did not change the expression of cannabinoid receptor proteins, as shown by Western blotting. These findings suggest that targeting cannabinoid receptors could be a novel preventative therapeutic strategy in asthmatic patients. John Wiley & Sons, Ltd 2008-12 2008-02-06 /pmc/articles/PMC4514116/ /pubmed/18266975 http://dx.doi.org/10.1111/j.1582-4934.2008.00258.x Text en © 2008 The Authors Journal compilation © 2008 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Articles
Giannini, L
Nistri, S
Mastroianni, R
Cinci, L
Vannacci, A
Mariottini, C
Passani, M B
Mannaioni, P F
Bani, D
Masini, E
Activation of cannabinoid receptors prevents antigen-induced asthma-like reaction in guinea pigs
title Activation of cannabinoid receptors prevents antigen-induced asthma-like reaction in guinea pigs
title_full Activation of cannabinoid receptors prevents antigen-induced asthma-like reaction in guinea pigs
title_fullStr Activation of cannabinoid receptors prevents antigen-induced asthma-like reaction in guinea pigs
title_full_unstemmed Activation of cannabinoid receptors prevents antigen-induced asthma-like reaction in guinea pigs
title_short Activation of cannabinoid receptors prevents antigen-induced asthma-like reaction in guinea pigs
title_sort activation of cannabinoid receptors prevents antigen-induced asthma-like reaction in guinea pigs
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514116/
https://www.ncbi.nlm.nih.gov/pubmed/18266975
http://dx.doi.org/10.1111/j.1582-4934.2008.00258.x
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