The “time-response” effect of Wenyang Pingchuan Formula on miR-19a in asthmatic mice experiment
Main Article Content
Keywords
asthma, miR-19a, Wenyang Pingchuan Formula, JAK/STAT, NF-κB
Abstract
Background: Wenyang Pingchuan Formula (WPCF) is an empirical formula for the treatment of acute childhood asthma. However, the “time-effect” relationship of this prescription is not clear. This paper explores the relationship between Janus activated kinase signal transducer and activator of transcriptions (JAK/STAT), nuclear factor-κB (NF-κB), and microRNA (miR-19a), and also preliminarily determines the best time-effect relationship of WPCF in reducing the airway inflammation in asthmatic mice.
Method: 80 BALB/c mice were randomly divided into four groups: control (CON) group, model (MDL) group, dexamethasone (DEX) group, and WPCF group. MDL group was established through intraperitoneal injection of 10% ovalbumin (OVA) and Al(OH)3 solution and the inhalation of aerosolized 5% OVA solution. Enzyme-linked immunosorbent assay (ELISA), real-time PCR and Western blot were conducted to determine the levels of interleukin (IL)-4, IL-13, interferon-γ (IFN-γ) in bronchoalveolar lavage fluid (BALF), contents of miR-19a mRNA and STAT6, phosphorylated signal transducers and activators of transcription 6 (p-STAT6), p65, phosphorylated p65 (p-p65), suppressors of cytokine signaling 1 (SOCS1), and tumor necrosis factor α-induced protein-3 (Tnfaip3) proteins after 7 and 28 days of intervention respectively.
Results: Significant down-regulation of IL-4 and IL-13 expression (P<0.05) and up-regulation of IFN-γ expression (P<0.05) in BALF have been observed for WPCF group compared with the MDL group. The significant down-regulation of miR-19a mRNA and STAT6, p-STAT6, p65, p-p65 proteins (P<0.05) and up-regulation of SOCS1 and Tnfaip3 proteins (P<0.05) in BALF was also observed for WPCF group compared to the MDL group. During the experiment, the weight of the mice in DEX group significantly decreased (P<0.05) compared with the other groups.
Conclusions: WPCF could restore Th1/Th2 balance. The longer the intervention time, the more effective the treatment. The down-regulation of miR-19a mRNA by activating JAK/STAT and NF-κB signal pathways may be a possible mechanism by which WPCF alleviates airway inflammation.
References
2. Gergen PJ, Arbes SJ, Calatroni A, Mitchell HE, Zeldin DC. Total IgE levels and asthma prevalence in the US population: results from the National Health and Nutrition Examination Survey 2005–2006. Allergy Clin Immunol. 2009;124(3):447–453. 10.1016/j.jaci.2009.06.011
3. Moore WC, Bleecker ER, Curran-Everett D, Erzurum SC, Ameredes BT, Bacharier L, et al. Characterization of the severe asthma phenotype by the National Heart, Lung, and Blood Institute’s Severe Asthma Research Program. Allergy Clin Immunol. 2007;119(2):405–413. 10.1016/j.jaci.2006.11.639
4. National Cooperative Group on Childhood Asthma, Institute of Environmental Health and Related Product Safety, Chinese Center for Disease Control and Prevention, Chinese Center for Disease Control and Prevention. Third nationwide survey of childhood asthma in urban areas of China. Chinese Journal of Pediatrics. 2013;51(10):729–735. 10.3760/cma.j.issn.0578-1310.2013.10.003
5. Liu CH, Hong JG, Shang YX, Sun J, Shan MN, Gao Y, et al. Comparison of asthma prevalence in children from 16 cities of China in 20 years. Chinese Journal of Practical Pediatrics. 2015;30(8):596–600. 10.7504/ek2015080609
6. Singh PB, Pua HH, Happ HC, Schneider C, Moltke JV, Locksley RM, et al. MicroRNA regulation of type 2 innate lymphoid cell homeostasis and function in all alergic inflammation. Journal of Experimental Medicine. 2017;214(12):3627–3643. 10.1084/jem.20170545
7. Simpson LJ, Patel S, Bhakta NR, Choy DF, Brightbill HD, Ren X, et al. A miRNA upregulated in asthma airway T cells promotes TH2 cytokine production. Nature Immunology. 2014;15(12):1162–1170. 10.1038/ni.3026
8. Liu F, Yu J, Bai L, Xue Z, Zhang X. Pingchuan formula improves asthma via restoration of the Th17/Treg balance in a mouse mode. BMC Complementary and Alternative Medicine. 2015;15(1):1-11. 10.1186/s12906-015-0755-8
9. Li YK. Experimental methodology of pharmacology of traditional Chinese medicine. 2nd Edition, Shanghai Science and Technology Press. 2006 119–120. https://max.book118.com/html/2019/0119/6005204234002002.shtm
10. Zhao YT, Zhang XG, Bai L, Li LQ, Yu JE. Effects of Chinese herbal medicine Pingchuan Formula on airway inflammation, interferon-γ and interleukin-4 in mice with asthma. Journal of Chinese Integrative Medicine. 2012;10(7):807. 10.3736/jcim20120712
11. The Respiratory Allergy Group of Chinese Society of Allergy, The Asthma Group of Chinese Thoracic Society, Chinese Medical Association. Chinese guidelines for the diagnosis and treatment of allergic asthma (2019, the first edition). Chin J Intern Med. 2019;58(9):636–655. 10.3760/cma.j.issn.0578-1426.2019.09.004
12. Zhao FD, Dong JC, Xie JY, Fei ZY, Cui Y, Gong ZH, et al. Effects of Chinese Herbs for Replenishing Shen and Strengthening Qi on Some Indexes of Neuro-endocrino-immune Network in Asthmatic Rats. Chinese Journal of integrated traditional and Western medicine. 2007;27(8):715–719. 10.3321/j.ISSN:1003-5370.2007.08.014
13. Yao L, Deng KY, Luo JB. Comparative study on antitussive and antiasthmatic effects of total alkaloids of Ephedra and ephedrine. Pharmacology and Clinics of Chinese Materia Medica. 2008;24(2):18–19. 10.3969/j.issn.1001-859X.2008.02.009
14. Zhang SQ, Chen XL. Influence of Icariin on Adrenal Cortex Function in Rats with Asthma. Journal of Anhui University of Chinese Medicine. 2017;36(4):67–70. 10.3969/j.issn.2095-7246.2017.04.020
15. Holgate ST. Innate and adaptive immune responses in asthma. Nature Medicine. 2012;18(5):673–683. 10.1038/nm.2731
16. Li JF, Wang CY, Xu C, Li L, Wang GZ, Li CL, et al. Cryptotanshinone Alleviates Asthmatic Airway Inflammation by Inhibiting p38 MAPK/NF-κB Pathway. Traditional Chinese Drug Research and Clinical Pharmacology. 2020;31(1):15–20. 10.19378/j.issn.1003-9783.2020.01.003
17. Wang JQ, Ma FC, Tian WB, Wang SC, Zhao HP. Effects of zanthoxylum seed oilA2 on NF-кB signaling pathway and inflammatory factor in lung tissue of asthmatic mice. Chinese Journal of Pathophysiology. 2010;26(6):1120–1126. 10.3969/j.issn.1000-4718.2010.06.015
