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Dexmedetomidine represses TGF-beta1-induced extracellular matrix production and proliferation of airway smooth muscle cells by inhibiting MAPK signaling pathway
Rong, Zhou; Xiaoyan, Chen.
Affiliation
  • Rong, Zhou; Hospital of Traditional Chinese Medicine. Department of Anesthesiology. Nantong. China
  • Xiaoyan, Chen; Hospital of Traditional Chinese Medicine. Department of Anesthesiology. Nantong. China
Allergol. immunopatol ; 50(2): 16-22, mar. 03, 2022. graf, ilus
Article in English | IBECS | ID: ibc-203098
Responsible library: ES1.1
Localization: ES15.1 - BNCS
ABSTRACT
Background Airway remodeling is implicated in the pathogenesis of asthma, and abnormal proliferation of airway smooth muscle cells (ASMCs) contribute to airway remodeling. Inflammatory mediator, transforming growth factor-β1 (TGF-β1), stimulates the proliferation of ASMCs, and is associated with airway remodeling in asthma. Dexmedetomidine (DEX) has been widely used in the adjuvant therapy of acute asthma.Objective The potential effects of DEX on extracellular matrix (ECM) production and proliferation of ASMCs were investigated in this study.Material and Methods Human ASMCs were incubated with TGF-β1 for 48 hours, and then treated with different concentrations of DEX for another 24 hours. Cell proliferation was detected by MTT and BrdU (5’-bromo-2’-deoxyuridine) staining. Flow cytometry was used to assess cell apoptosis, and western blot was applied to identify the underlying mechanism.Results TGF-β1 induced increase in cell viability and bromodeoxyuridine (BrdU) positive cells in ASMCs while repressed cell apoptosis. Second, TGF-β1-induced ASMCs were then treated with different concentrations of DEX. Cell viability of TGF-β1-induced ASMCs was decreased by incubation of DEX. The number of BrdU positive cells in TGF-β1-induced ASMCs was reduced by incubation of DEX. Moreover, incubation of DEX promoted cell apoptosis of TGF-β1-induced ASMCs. Third, incubation of DEX attenuated TGF-β1-induced increase in fibronectin, collagen I, MMP9, and versican in ASMCs. Lastly, the up-regulation of phosphorylated extracellular receptor kinase (p-ERK), phosphorylated Jun N-terminal Kinase (p-JNK), and p-p38 in TGF-β1-induced ASMCs was reversed by incubation of DEX.Conclusion DEX suppressed TGF-β1-induced ECM production and proliferation of ASMCs through inactivation of p38 mitogen-activated protein kinase (MAPK) pathway, providing a potential strategy for prevention of asthma (AU)
Subject(s)

Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Dexmedetomidine Limits: Humans Language: English Journal: Allergol. immunopatol Year: 2022 Document type: Article Institution/Affiliation country: Hospital of Traditional Chinese Medicine/China
Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Dexmedetomidine Limits: Humans Language: English Journal: Allergol. immunopatol Year: 2022 Document type: Article Institution/Affiliation country: Hospital of Traditional Chinese Medicine/China
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