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Effects of Gwaruhaengryeon-hwan on COPD and Particulate Matter Induced Lung Injury on a Mouse Model

만성폐쇄성폐질환 및 미세먼지 유발 폐손상 동물모델에서 과루행련환의 효과

  • Lee, Chul-wha (Dept. of Internal Medicine, College of Korean Medicine, Dae-Jeon University) ;
  • Yang, Won-kyung (Dept. of Internal Medicine, College of Korean Medicine, Dae-Jeon University) ;
  • Lyu, Yee-ran (Dept. of Internal Medicine, College of Korean Medicine, Dae-Jeon University) ;
  • Kim, Seung-hyeong (Institute of Traditional Medicine and Bioscience, Dae-Jeon University) ;
  • Park, Yang-chun (Dept. of Internal Medicine, College of Korean Medicine, Dae-Jeon University)
  • 이철화 (대전대학교 한의과대학 내과학교실) ;
  • 양원경 (대전대학교 한의과대학 내과학교실) ;
  • 유이란 (대전대학교 한의과대학 내과학교실) ;
  • 김승형 (대전대학교 동서생명과학연구원) ;
  • 박양춘 (대전대학교 한의과대학 내과학교실)
  • Received : 2017.05.31
  • Accepted : 2017.06.29
  • Published : 2017.06.30

Abstract

Objective: This study aimed to use a mouse model to evaluate the effects of Gwaruhaengryeon-hwan (GHH) on chronic obstructive pulmonary disease (COPD) and particulate matter induced lung injury. Materials and Methods: The study was carried out in two ways (in vitro, in vivo). In vitro RAW 264.7 cells (mouse macrophage) were used and analyzed by flow cytometry, ELISA. In vivo lipopolysaccharide (LPS) and cigarette smoke solution (CSS), or coal, fly ash, diesel exhaust particle (CFD) challenged mice were used and its BALF was analyzed by ELISA, lung tissue by real-time PCR. Results: In vitro, GHH maintained an 80-100% rate of viability. So cytotoxicity was not shown. In the ELISA analysis with RAW 264.7 cells, GHH significantly decreased NO over $30{\mu}g/ml$. In the ELISA analysis, GHH significantly decreased $TNF-{\alpha}$, IL-6 over $300{\mu}g/ml$. In the COPD model, the GHH 200 mg/kg dosage group, the application of GHH significantly decreased the increasing of neutrophils, $TNF-{\alpha}$, IL-17A, MIP2, CXCL-1 in BALF, $TNF-{\alpha}$, $IL-1{\beta}$ mRNA expression in lung tissue and histological lung injury. In the CFD induced lung injury model, the GHH 200 mg/kg dosage group, the application of GHH significantly decreased the increase of neutrophils, $TNF-{\alpha}$, IL-17A, MIP2, CXCL-1 in BALF, MUC5AC, $TGF-{\beta}$ mRNA expression in lung tissue and histological lung injury. Conclusion: This study suggests the usability of GHH for COPD patients by controlling lung tissue injury.

Keywords

References

  1. Global Initiative for Chronic Obstructive Lung Disease. Global Strategy for Diagnosis, Management, and Prevention of Chronic Obstructive Pulmonary Disease 2017 Report. Available from: http://www.goldcopd.org. Accessed Nov 11, 2016.
  2. Yoo CG. Pathogenesis and pathophysiology of COPD. Korean J Intern Med 2009;77(4):383-400.
  3. Pelkonen M. Smoking: relationship to chronic bronchitis, chronic obstructive pulmonary disease and mortality. CurrOpinPulm Med 2008;14(2):105-9.
  4. Rodriguez-Roisin R. Toward a consensus definition for COPD exacerbations. Chest 2000;117:398S-401S. https://doi.org/10.1378/chest.117.5_suppl_2.398S
  5. Sint T, Donohue JF, Ghio AJ. Ambient air pollution particles and the acute exacerbation of chronic obstructive pulmonary disease. InhalToxicol 2008;20(1):25-9.
  6. Ling SH, van Eeden SF. Particulate matter air pollution exposure: role in the development and exacerbation of chronic obstructive pulmonary disease. Int J Chron Obstruct Pulmon Dis 2009;4:233-43.
  7. World Health Organization. Air pollution including WHO's 1999 guidelines for air pollution control. Geneva: World Health Organization; 2000.
  8. Pope CA, Ezzati M, Dockery DW. Fine-particulate air pollution and life expectancy in the United States. N Engl J Med 2009;360:376-86. https://doi.org/10.1056/NEJMsa0805646
  9. Lee BJ, Jung HJ, Choi JY, Kang W, Jung SK. Preliminary study to develop a Korean oriental medicine assessment tool for syndrome differentiation of chronic obstructive pulmonary disease. J Korean Oriental Med 2012;33(3):82-94.
  10. Lee ES, Han JM, Kim MH, Namgung U, Yeo Y, Park YC. Effects of inhalable microparticles of Socheongryong-tang on chronic obstructive pulmonary disease in a mouse model. J Korean Med 2013;34(3):54-68. https://doi.org/10.13048/jkm.13012
  11. Lee JG, Yang SY, Kim MH, Namgung U, Park YC. Protective effects of Socheongryong-tang on elastase-induced lung injury. J Korean Oriental Med 2011;32(4):83-99.
  12. Kim HW, Yang SY, Kim MH, Namgung U, Park YC. Protective effects of Maekmundong-tang on elastase-induced lung injury. J Korean Oriental Med 2011;32(2):63-78.
  13. Kim Y, Yang SY, Kim MH, Namgung U, Park YC. Effects of Saengmaekcheongpye-eum on LPS-induced COPD model. Korean J Oriental Int Med 2011;32(2):217-31.
  14. Lee H, Kim Y, Kim HJ, Park S, Jang YP, Jung S, et al. Herbal Formula, PM014, Attenuates Lung Inflammation in a Murine Model of Chronic Obstructive Pulmonary Disease. Evid Based Complement Alternat Med 2012;2012:769830.
  15. Han JM, Yang WK, Kim SH, Park YC. Effects of Sagan-tang and individual herbs on COPD mice model. J Korean Med Soc Herb Formula Study 2015;23(2):171-87.
  16. Hur J. Dong-Eui-Bo-Gam. Seoul: Namsandang; 1986, p. 473.
  17. Food and Drug Administration. Revision of the Guidelines for Measures for Hazard component of inhibitor of smoking desire. Available at: http://www.mfds.go.kr. Accessed Nov 1, 2014.
  18. Kim SH, Park YC, Lee JE, Yang WK, Choi JJ, Oh JG. Method for preparing mouse model induced ambient particulate matter. Korea Patent 10-2016-0156279, Nov. 23, 2016.
  19. Jung YM, Lee HY. Chronic Obstructive Pulmonary Disease in Korea: Prevalence, Risk Factors, and Quality of Life. J Korean Acad Nurs 2011;41(2):149-56. https://doi.org/10.4040/jkan.2011.41.2.149
  20. Barnes PJ. The cytokine network in asthma and chronic obstructive pulmonary disease. J Clin Invest 2008;118(11):3546-56. https://doi.org/10.1172/JCI36130
  21. Lambrecht BN, Prins JB, Hoogsteden HC. Lung dendritic cells and host immunity to infection. Eur Respir J 2001;18(4):692-704.
  22. Wang G, Xu Z, Wang R, Al-Hijji M, Salit J, Strulovici-Barel Y, et al. Genes associated with MUC5AC expression in small airway epithelium of human smokers and nonsmokers. BMC Med Genomics 2012;5:21. https://doi.org/10.1186/1755-8794-5-21
  23. Chen L, Yang W, Jennison BL, Omaye ST. Air particulate pollution and hospital admissions for chronic obstructive pul-monary disease in Reno, Nevada. Inhal Toxicol 2000;12(4):281-98. https://doi.org/10.1080/713856633
  24. Sunyer J, Basagana X. Particles, and not gases, are associated with the risk of death in patients with chronic obstructive pulmonary disease. Int J Epidemiol 2001;30(5):1138-40. https://doi.org/10.1093/ije/30.5.1138
  25. McCreanor J, Cullinan P, Nieuwenhuijsen MJ, Stewart-Evans J, Malliarou E, Jarup L, et al. Respiratory effects of exposure to diesel traffic in persons with asthma. N Engl J Med 2007;357(23):2348-58. https://doi.org/10.1056/NEJMoa071535
  26. Gang BS, Kim IR, Kim HC, Guk YB, Park YG, Seo BI, et al. Bonchohak. Seoul: Younglimsa; 2006, p. 180-1, 461-2, 478-9.
  27. Schaberg T, Haller H, Rau M, Kaiser D, Fassbender M, Lode H. Superoxide anion release induced by platelet-activating factor is increased in human alveolar macrophages from smokers. Eur Respir J 1992;5(4):387-93.
  28. Keatings VM, Collins PD, Scott DM, Barnes PJ. Differences in interleukin-8 and tumor necrosis factor-alpha in induced sputum from patients with chronic obstructive pulmonary disease or asthma. Am J Respir Crit Care Med 1996;153(2):530-4. https://doi.org/10.1164/ajrccm.153.2.8564092
  29. Aaron SD, Angel JB, Lunau M, Wright K, Fex C, Le Saux N, et al. Granulocyte inflammatory markers and airway infection during acute exacerbation of chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2001;163(2):349-55. https://doi.org/10.1164/ajrccm.163.2.2003122
  30. Deveci Y, Deveci F, Ilhan N, Karaca I, Turgut T, Muz MH. Serum ghrelin, IL-6 and $TNF-{\alpha}$ levels in patients with chronic obstructive pulmonary disease. Tuberk Toraks 2010;58(2):162-72.
  31. Levanen B, Glader P, Dahlen B, Billing B, Qvarfordt I, Palmberg L, et al. Impact of tobacco smoking on cytokine signaling via interleukin-17A in the peripheral airways. Int J Chron Obstruct Pulmon Dis 2016;11:2109-16. https://doi.org/10.2147/COPD.S99900
  32. Lukacs NW, Hogaboam CM, Kunkel SL. Chemokines and their receptors in chronic pulmonary disease. Curr Drug Targets Inflamm Allergy 2005;4(3):313-7. https://doi.org/10.2174/1568010054022088
  33. Traves SL, Culpitt SV, Russell RE, Barnes PJ, Donnelly LE. Increased levels of the chemokines $GRO{\alpha}$ and MCP-1 in sputum samples from patients with COPD. Thorax 2002;57(7):590-5. https://doi.org/10.1136/thorax.57.7.590
  34. Guzman K, Gray TE, Yoon JH, Nettesheim P. Quantitation of mucin RNA by PCR reveals induction of both MUC2 and MUC5AC mRNA levels by retinoids. Am J Physiol 1996;271(6 Pt 1):1023-8.
  35. Borchers MT, Carty MP, Leikauf GD. Regulation of human airway mucins by acrolein and inflammatory mediators. Am J Physiol 1999;276(4 Pt 1):549-55.

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