Targeting acetylcholine receptor M3 prevents the progression of airway hyperreactivity in a mouse model of childhood asthma
Autor: | Juliana Barrios, Kruti R. Patel, Yan Bai, Kenneth G. Trieu, Xingbin Ai |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Respiratory System Stimulation Biochemistry 03 medical and health sciences 0302 clinical medicine Neuroplasticity Muscarinic acetylcholine receptor Genetics medicine Animals Molecular Biology Asthma Acetylcholine receptor Mice Knockout Receptor Muscarinic M3 business.industry Research Muscle Smooth respiratory system medicine.disease Phenotype Acetylcholine Pathophysiology respiratory tract diseases Disease Models Animal 030104 developmental biology 030228 respiratory system Immunology Disease Progression Cholinergic Bronchial Hyperreactivity business Muscle Contraction Biotechnology |
Zdroj: | The FASEB Journal. 31:4335-4346 |
ISSN: | 1530-6860 0892-6638 |
DOI: | 10.1096/fj.201700186r |
Popis: | Asthma often progresses into adulthood from early-life episodes of adverse environmental exposures. However, how the injury to developing lungs contributes to the pathophysiology of persistent asthma remains poorly understood. In this study, we identified an age-related mechanism along the cholinergic nerve-airway smooth muscle (ASM) axis that underlies prolonged airway hyperreactivity (AHR) in mice. We showed that ASM continued to mature until ∼3 wk after birth. Coinciding with postnatal ASM maturation, there was a critical time window for the development of ASM hypercontractility after cholinergic stimulation. We found that allergen exposure in neonatal mice, but not in adult mice, elevated the level and activity of cholinergic nerves (termed neuroplasticity). We demonstrated that cholinergic neuroplasticity is necessary for the induction of persistent AHR after neonatal exposure during rescue assays in mice deficient in neuroplasticity. In addition, early intervention with cholinergic receptor muscarinic (ChRM)-3 blocker reversed the progression of AHR in the neonatal exposure model, whereas β2-adrenoceptor agonists had no such effect. Together, our findings demonstrate a functional relationship between cholinergic neuroplasticity and ASM contractile phenotypes that operates uniquely in early life to induce persistent AHR after allergen exposure. Targeting ChRM3 may have disease-modifying benefits in childhood asthma.-Patel, K. R., Bai, Y., Trieu, K. G., Barrios, J., Ai, X. Targeting acetylcholine receptor M3 prevents the progression of airway hyperreactivity in a mouse model of childhood asthma. |
Databáze: | OpenAIRE |
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