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Xiao-Qing-Long-Tang attenuates allergic airway inflammation and remodeling in repetitive Dermatogoides pteronyssinus challenged chronic asthmatic mice model.

AbstractETHNOPHARMACOLOGICAL RELEVANCE:
Xiao-Qing-Long-Tang (XQLT) has been used for centuries in Asia to effectively treat patients with bronchial asthma.
AIM OF THE STUDY:
We previously found that single and multiple doses of XQLT administered to sensitized mice before allergen challenge resulted in suppressed airway hyper-responsiveness and airway inflammation. In this study we aimed to investigate whether XQLT has the potential to attenuate the severity of asthma symptoms, and immunomodulatory mechanism of XQLT in a repetitive Dermatogoides pteronyssinus (D. pteronyssinus)-challenged chronic asthmatic mice model.
MATERIALS AND METHODS:
BALB/c mice were intratracheally (i.t.) inoculated with five doses of D. pteronyssinus (50 μl, 1mg/ml) and orally administered of XQLT (1 g/kg) at 1-week intervals. At three days after the last challenge, mice were sacrificed to evaluate airway remodeling, inflammation, lung histological features, and the expression profiles of cytokines and various genes.
RESULTS:
XQLT significantly reduced bronchial inflammatory cell infiltration and airway remodeling. It inhibited D. pteronyssinus-induced total IgE and D. pteronyssinus-specific IgG1 in serum, and changed the "T(H)2-bios" in BALF by inhibiting the activation of NF-κB. Collagen assay and Histopathology indicated that XQLT reduced airway remodeling in the lung. Simultaneously, the RT-PCR analysis showed that XQLT downregulated IL-10, IL-13, RANTES, Eotaxin, and MCP-1 mRNA expression in the lung. Moreover, EMSA and immunohistochemistry staining demonstrated that XQLT inhibited NF-κB expression in the nucleus of bronchial epithelial cells.
CONCLUSIONS:
These results suggest that XQLT exhibits anti-airway inflammatory, anti-airway remodeling, and specific immunoregulatory effects in a chronic asthmatic mice model.
AuthorsShulhn-Der Wang, Li-Jen Lin, Chih-Lung Chen, Shih-Chang Lee, Chin-Che Lin, Jiu-Yao Wang, Shung-Te Kao
JournalJournal of ethnopharmacology (J Ethnopharmacol) Vol. 142 Issue 2 Pg. 531-8 (Jul 13 2012) ISSN: 1872-7573 [Electronic] Ireland
PMID22658987 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2012 Elsevier Ireland Ltd. All rights reserved.
Chemical References
  • Anti-Asthmatic Agents
  • Chemokine CCL5
  • Chemokines, CC
  • Drugs, Chinese Herbal
  • Immunoglobulin G
  • Interleukin-13
  • NF-kappa B
  • sho-seiryu-to
  • Interleukin-10
  • Immunoglobulin E
Topics
  • Airway Remodeling (drug effects)
  • Animals
  • Anti-Asthmatic Agents (pharmacology, therapeutic use)
  • Asthma (drug therapy, immunology, metabolism, pathology)
  • Bronchial Hyperreactivity (drug therapy, immunology, metabolism)
  • Cell Nucleus (metabolism)
  • Chemokine CCL5 (metabolism)
  • Chemokines, CC (metabolism)
  • Chronic Disease
  • Disease Models, Animal
  • Down-Regulation
  • Drugs, Chinese Herbal (pharmacology, therapeutic use)
  • Epithelial Cells (metabolism)
  • Immunoglobulin E (blood)
  • Immunoglobulin G (blood)
  • Inflammation (drug therapy, metabolism)
  • Interleukin-10 (metabolism)
  • Interleukin-13 (metabolism)
  • Lung (drug effects, immunology, metabolism, pathology)
  • Male
  • Mice
  • Mice, Inbred BALB C
  • NF-kappa B (metabolism)
  • Phytotherapy
  • Pyroglyphidae

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