DOI QR코드

DOI QR Code

소자도담강기탕(蘇子導痰降氣湯)의 호흡기 염증 완화효과

Relieving effect for respiratory inflammation of Sojadodamgangki-tang

  • 한윤지 (상지대학교 한의과대학 병리학교실 ) ;
  • 선창우 (상지대학교 한의과대학 침구의학교실 ) ;
  • 우연주 (상지대학교 한의과대학 생리학교실 ) ;
  • 이동혁 (상지대학교 한의학연구소) ;
  • 서진우 (상지대학교 한의과대학 한방신경정신의학교실 ) ;
  • 유준상 (상지대학교 한의학연구소) ;
  • 김주희 (상지대학교 한의학연구소) ;
  • 권보인 (상지대학교 한의학연구소)
  • Younji Han (Department of Pathology, College of Korean Medicine, Sangji University) ;
  • Changwoo Seon (Department of Acupuncture & Moxibustion, College of Korean Medicine, Sangji University) ;
  • Yeonju Woo (Department of Physiology, College of Korean Medicine, Sangji University) ;
  • Dong Hyuk Lee (Research Institute of Korean Medicine, Sangji University) ;
  • Jin-woo Suh (Department of Korean neuropsychiatry, College of Korean Medicine, Sangji University) ;
  • Jun-Sang Yu (Department of Sasang Constitutional Medicine, College of Korean Medicine, Sangji University) ;
  • Joo-Hee Kim (Department of Acupuncture & Moxibustion, College of Korean Medicine, Sangji University) ;
  • Bo-In Kwon (Department of Pathology, College of Korean Medicine, Sangji University)
  • 투고 : 2023.07.25
  • 심사 : 2023.08.20
  • 발행 : 2023.08.31

초록

Objectives : Sojadodamgangki-tang and its main components are traditional korean medicinal methods for treatment of cough, sputum and dyspnea. Using a respiratory inflammatory model, we intend to reveal the anti-inflammatory effect and its immune mechanism of Sojadodamgangki-tang. Methods : We used a papain-induced respiratory inflammatory mouse model. 8-week-old female BALB/C mice were divided into 3 groups as follows: the following groups: saline control group, papain treated group (vehicle), papain and Sojadodamgangki-tang(200 mg/kg) treated group (n=4). To evaluate the anti-inflammatory effect of Sojadodamgangki-tang extracts, inflammatory cell infiltration was measured in bronchoalveolar lavage fluid (BALF) and nasal lavage fluid (NALF). In addition, the effects of Sojadodamgangki-tang extracts on Th2 cell population in lung were determined by using flow cytometry. Results : Sojadodamgangki-tang extracts administration reduced inflammatory cell infiltration in BALF and NALF, especially of eosinophils. Furthermore, total immunogloblin (Ig)-E levels was reduced in BALF and serum by drug administration. Interestingly, Sojadodamgangki-tang extracts treatment also decreased the Th2 cell (CD4+GATA3+) population in lung. Conclusions : Our findings indicate Sojadodamgangki-tang extracts have anti-inflammatory effects by mediating Th2 cell and B cell activation.

키워드

과제정보

본 결과물은 2023년도 교육부의 재원으로 한국연구재단의 지원을 받아 수행된 지자체-대학 협력 기반 지역혁신 사업의 결과입니다(2022RIS-005).

참고문헌

  1. Wang, I.J., Tung, T.H., Tang, C.S., Zhao, Z.H. Allergens, air pollutants, and childhood allergic disease. International Journal of Hygiene and Environmental Health. 2016;219:66-71.  https://doi.org/10.1016/j.ijheh.2015.09.001
  2. Kang, D., Kim, J.E. Fine, ultrafine, and yellow dust: emerging health problems in Korea. Journal of Korean Medical Science. 2014;29(5):621-622.  https://doi.org/10.3346/jkms.2014.29.5.621
  3. Gilies, G., Morrison, S., Thompson, B., Thomas, P.S., Hui, J., Perret, J.L., Abramson, M.J., Walters, H., Matheson, M.C., Dharmage, S.C. Traffic-related air pollution exposure is associated with allergic sensitization, asthma, and poor lung function in middle age. Journal of Allergy and Clinical Immunology. 2017;139:122-129.  https://doi.org/10.1016/j.jaci.2016.05.008
  4. Lee, M.-Y., Seo, C.-S., Lee, J.-A., Lee, N.-H., Kim, J.-H., Ha, H.K., Zheng, M.-S., Son, J.-K., Shin, H.-K. Anti-asthmatic effects of Angelica dahurica against ovalbumin-induced airway inflammation via upregulation of heme oxygenase-1. Food and chemical toxicology. 2011;49:829-837.  https://doi.org/10.1016/j.fct.2010.12.004
  5. Seo, Y.-S., Kim, H.S., Lee, A.Y., Chun, J.M., Kim S.B., Moon, B.C., Kwon, B.-I. Codonopsis lanceolata attenuates allergic lung inflammation by inhibiting Th2 cell activation and augmenting mitochondrial ROS dismutase (SOD2) expression. Scientific Reports. 2019;9:2312. 
  6. Walford, H.H., Doherty, T.A. Diagnosis and management of eosinophilic asthma: a US perspective. Journal of Asthma Allergy. 2014;7:53-65.  https://doi.org/10.2147/JAA.S39119
  7. Richard, L., Russ, E., Jennifer, N.W., Jeremy A.H., Klaus, I.M., Paul, S.F., Paul, M.O'B., Mark D.I. Type 2 cytokines in the pathogenesis of sustained airway dysfunction and airway remodeling in mice. American Journal of Respiratory and Critical Care Medicine. 2004;169(7):860-867.  https://doi.org/10.1164/rccm.200305-706OC
  8. Rose JR, C.E., Lannigan, J.A., Kim, P., Lee, J.J., Fu, S.M., Sung, S.-S.J. Murine lung eosinophil activation and chemokine production in allergic airway inflammation. Cellular & Molecular immunolgy. 2010;7:361-374.  https://doi.org/10.1038/cmi.2010.31
  9. Kay, A.B. Allergy and allergic diseases. First of two parts. New England of Journal of Medicine. 2001;344(1):30-37  https://doi.org/10.1056/NEJM200101043440106
  10. Kay, A.B. Allergy and allergic diseases. Second of two parts. New England of Journal of Medicine. 2001;344(2):109-113  https://doi.org/10.1056/NEJM200101113440206
  11. Chu, D.K., Jimenez-Saiz, R., Verschoor, C.P., Walker, T.D., Goncharova, S., Llop-Guevara, A., Shen, P., Gordon, M.E., Barra, N.G., Bassett, J.D., Kong, J., Fattouhm R., McCoy, K.M., Bowdish, D.M., Erjefalt, J.S., Pabst, O., Humbles, A.A., Kolbeck, R., Waserman, S., Jordana, M. Indigenous enteric eosinophils control DCs to initiate a primary Th2 immune response in vivo. Journal of Experimental Medicine. 2014;211(8):1657-1672.  https://doi.org/10.1084/jem.20131800
  12. George, L., Brightling, C.E. Eosinophilic airway inflammation: role of in asthma and chronic obstructive pulmonary disease. Therapeutic Advances in Chronic Disease. 2016;7(1):34-51.  https://doi.org/10.1177/2040622315609251
  13. Busse, W., Chupp, G., Nagase, H., Albers, F.C., Doyle, S., Shen, Q., Bratton, D.J., Gunsoy, N.B. Anti-IL-5 treatments in patients with severe asthma by blood eosinophil thresholds: Indirect treatment comparison. Journal of Allergy and Clinical Immunology. 2019;143(1):190-200.  https://doi.org/10.1016/j.jaci.2018.08.031
  14. Zheng, W., Wu, J. Effect of Suzi Jiangqi decoction combined with Western medicine on aucte exacerbation of chronic obstructive pulmonary disease. Chinese Medicine Modern Distance Education of China 9. 2011;15:48-49. 
  15. Liu, c., Tseng, A., Yang, S. Chinese Herbal Medicine: Mordern Applications of Traditional Formulas, first ed. CRC press, Florida. 
  16. Liu, Z. Essentials of Chinese Medicine. Springer, New York. 
  17. Coyle, M., Shergis, J.L., Liu, S., Wu, L., Zhang, A.L., Guo, X., Lu, C., Xue, C.C. Safety of chinese herbal medicine for chronic obstructive pulmonary disease. Evidence Based Complementary Alternative Medicine. 2015;Article ID 380678. 
  18. Ok, I.-S., Kim, S.-H., Kim, B.-K., Lee, J.-C., Lee, Y.-C. Pinellia ternata, Citrus reticulata, and their Combinational Prescription Inhibit Eosinophil Infiltration and Airway Hyperresponsiveness by Suppressing CCR3+ and Th2 Cytokines Production in the Ovalbumin-Induced Asthma Model. 2009;Article ID 413270. 
  19. Yim, Y.-K., Lee, H., Hong, K.-E., Kim, Y.-I., Ko, S.-K., Kim, J.-E., Lee, S.-Y., Park, K.-S. Anti-Inflammatory and Immune-Regulatory Effects of Subcutaneous Perillae fructus Extract Injections on OVA-Induced Asthma in Mice. Evidence-Based Complementary and Alternative Medicine. 2010;7(1):79-86.  https://doi.org/10.1093/ecam/nem118
  20. Fukuda, K., Matsuzaki, H., Mikami, Y., Makita, K., Miyakawa, K., Miyashita, N., Hosoki, K., Ishii, T., Noguchi, S., Urushiyama, H., Horie, M., Mitani, A., Yamauchi, Y., Shimura, E., Nakae, S., Saito, A., Nagase, T., Hiraishi, Y. A mouse model of asthma-chronic obstructive pulmonary disease overlap induced by intratracheal papain. Allergy. 2021;76(1):390-394.  https://doi.org/10.1111/all.14528
  21. Cai, T., Qiu, J., Ji, Y., Li, W., Ding, Z., Suo, C., Chang, J., Wang, J.J., He, R., Qian, Y., Guo, X., Zhou, L., Sheng, H., Shen, L., Qiu, J. IL-17 producing ST2+ group 2 innate lymphoid cells play a pathogenic role in lung inflammation. Journal of Allergy and Clinical Immunology. 2019;143(1):229-244.  https://doi.org/10.1016/j.jaci.2018.03.007
  22. Kwon, B.-I., Hong, S,C., Shin, K., Choi, E.-H., Hwang, J.-J., Lee, S.-H. Innate type2 Immuntiy is Associated with Eosinophilic Pleural Effusion in Primary Spontaneous Pneumothorax. American Journal of Respiratory and Critical Care Medicine. 2013;188:577-585.  https://doi.org/10.1164/rccm.201302-0295OC
  23. Han SR, Park G, Kwon OY. National University of Dept. of Internal Medicine Pulmonary system. Internal Medicine Pulmonary system. Seoul: Na Do publisher; 2007;332-45. 
  24. Heo, J. Donguibogam. Seoul: Nansandang Publishing; 1989;474-5. 
  25. Shin, HJ, Jeong SH, Jeong, HS, Lee, KG. Effect of Sojagangqi-tang on the Immunomodulatory Action. Korean J Oriental Physiology & Pathology. 2003;17(5):1182-7. 
  26. Kang, RW, Park, DI. The Effects of GamiSojagangki-tang on the Respiratory Pattern-sand Tracheal Tissues in Allergic Asthma. Journal of Dong-Eui Oriental Medicine 2000;4(0):5-17. 
  27. Kim, B.-I., Park, D.-I. The effect of Sojadodamgangkitang on the pulmonary injury caused by SO2 in rats. K.O.M.S. Vol. 18. No. 1.1997. 
  28. Jung, S.Y., Park, J.K., Park, J.W., Jo, H., Seo, C.-S., Jeon, W.-Y., Lee, M.-Y., Kwon, B.-I. Sojadodamgangki-tang attenuates allergic lung inflammation by inhibiting T helper 2 cells and Augmenting alveolar macrophages. Journal of Ethnopharmacology. 2020;263(5):113152 
  29. Kim, M.-K., Yoon, T.Y., Choi, B.K. Asthma diagnosis and treatment - 1006. Perillae semen abolished allergic asthmatic response in murine model. World Allergy Organization Journal. 2013;6(Supple 1):p6 
  30. Hu, M., Liu, Y., Wang, L., Wang, J., Li, J.L., Li, L., Wu, C.J. Purification, Characterization of Two Polysaccharides form Pinelliae Rhizoma Praeparatum Cum Alumine and Their AntiInflammatory Effects on Mucus Secretion of Airway Epithelium. International Journal of Molecular Science. 2019;20(14):3553. 
  31. Lee, M-Y., Shin, I.-S., Jeon, W.-Y., Lim, H.-S., Kim, J.-H., Ha, H.K. Pinellia ternata Breitenbach attenuates ovalbumin-induced allergic airway inflammation and mucus secretion in a murine model of asthma. Immunopharmacol Immunotoxicol. 2013;35(3):410-8  https://doi.org/10.3109/08923973.2013.770522
  32. Tao, X., Liu, H., Xia, J., Zeng, P., Wang, H., Xie, Y., Wang, C., Cheng, Y., Li, J., Zhang, X., Zhang, P., Chen, S., Yu, H., Wu, H. Processed product (Pinelliae Rhizoma Praeparatum) of Pinellia ternata (Thunb.) Breit. Alleviates the allergic airway inflammation of clod phlegm via regulation of PKC/EGFR/MAPK/PI3K-AKT signaling pathway. Journal of Ethnopharmacology. 2022;295:115449. 
  33. Walsh, E.R., Sahu, N., Kearley, J., Benjamin, E., Kang, B.H., Humbles, A. Strain-specific requirement for eosinophils in the recruitment of T cells to the lung during the development of allergic asthma. Journal of Experimental Medicine. 2008;205(6):1285-1292. https://doi.org/10.1084/jem.20071836