The potential interaction of MARCKS-related peptide and diltiazem on acrolin-induced airway mucus hypersecretion in rats

Airway mucus hypersecretion is recognized as a pathophysiological feature of airway inflammation. Ca2+ entry and myristoylated alanine-rich C kinase substrate translocation are considered as important factors in such process. To investigate the potential interaction of myristoylated alanine-rich C k...

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Veröffentlicht in:International immunopharmacology 2013-11, Vol.17 (3), p.625-632
Hauptverfasser: Chen, Peng, Deng, Zhiping, Wang, Tao, Chen, Lei, Li, Jiqiong, Feng, Yulin, Zhang, Shangfu, Nin, Yunyie, Liu, Daishun, Chen, Yajuan, Ou, Xuemei, Wen, Fuqiang
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Sprache:eng
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Zusammenfassung:Airway mucus hypersecretion is recognized as a pathophysiological feature of airway inflammation. Ca2+ entry and myristoylated alanine-rich C kinase substrate translocation are considered as important factors in such process. To investigate the potential interaction of myristoylated alanine-rich C kinase substrate (MARCKS)-related peptide and diltiazem on acrolein-induced airway mucus hypersecretion in rats, rat model of airway mucus hypersecretion was established by inhalation of acrolein on 12 consecutive days. MARCKS-related peptide, diltiazem, saline or the combination (MARCKS-related peptide+diltiazem) was intratracheally administered respectively. The rats were received pilocarpine to stimulate mucus release before sacrifices. The expression of Mucin5ac in bronchoalveolar lavage fluid (BALF) was measured by ELISA. Intracellular Muc5ac level was detected by immunohistochemical staining and western-blot. Muc5ac mRNA in lung was analyzed by RT-PCR. Results: Instillation of MARCKS-related peptide attenuated the release of Muc5ac in BALF induced by acrolein(p
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2013.08.001