Beneficial effects of cannabinoids (CB) in a murine model of allergen-induced airway inflammation: role of CB1/CB2 receptors |
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Authors: | Braun Andrea Engel Tabea Aguilar-Pimentel Juan Antonio Zimmer Andreas Jakob Thilo Behrendt Heidrun Mempel Martin |
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Affiliation: | a ZAUM - Center for Allergy and Environment, Division of Environmental Dermatology and Allergy, Helmholtz Zentrum München/Technische Universität München (TUM), Ingolstädter Landstraße 1, 85764 Neuherberg, Germany b Institute for Molecular Psychiatry, University of Bonn, Sigmund Freud Str. 25, 53127 Bonn, Germany c Allergy Research Group, Department of Dermatology, University Medical Center Freiburg, Hauptstraße 7, 79104 Freiburg, Germany d Department of Dermatology and Allergy Biederstein, TUM, Biedersteiner Str. 29, 80802 München, Germany e Department of Dermatology and Allergy, Georg-August-Universität, Göttingen, von Siebold Str. 3, 37075 Göttingen, Germany |
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Abstract: | The endocannabinoid system (ECS) consists of two cannabinoid (CB) receptors, namely CB1 and CB2 receptor, and their endogenous (endocannabinoids) and exogenous (cannabinoids, e.g. delta-9-tetrahydrocannabinol (THC)) ligands which bind to these receptors. Based on studies suggesting a role of THC and the ECS in inflammation, the objective of this study was to examine their involvement in type I hypersensitivity using a murine model of allergic airway inflammation. THC treatment of C57BL/6 wildtype mice dramatically reduced airway inflammation as determined by significantly reduced total cell counts in bronchoalveolar lavage (BAL). These effects were greatest when mice were treated during both, the sensitization and the challenge phase. Furthermore, systemic immune responses were significantly suppressed in mice which received THC during sensitization phase. To investigate a role of CB1/2 receptors in this setting, we used pharmacological blockade of CB1 and/or CB2 receptors by the selective antagonists and moreover CB1/CB2 receptor double-knockout mice (CB1−/−/CB2−/−) and found neither significant changes in the cell patterns in BAL nor in immunoglobulin levels as compared to wildtype mice. Our results indicate that the activation of the ECS by applying the agonist THC is involved in the development of type I allergies. However, CB1/CB2 receptor-independent signalling seems likely in the observed results. |
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Keywords: | ANOVA, analysis of variance BAL, bronchoalveolar lavage c, challenge phase CB, cannabinoid DMSO, dimethyl solfoxide ELISA, enzyme-linked immunosorbent assay FACS, fluorescence activated cell scanning Ig, immunoglobulin IL, interleukin IFNγ, interferon-gamma i.p., intraperitoneal Ova, ovalbumin PBS, phosphate-buffered saline s, sensitization phase SR1, SR141716A, N-(piperidine-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide hydrochloride SR2, SR144528, N-[(1S)-endo-1,3,3-trimethyl bicyclo [2.2.1]-heptan-2-yl]-5-(4-chloro-3-methylphenyl)-1-(4-ethylbenzyl)-pyrazole-3-carboxamide Th, T helper cell THC, delta-9-tetrahydrocannabinol WT, wildtype |
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