Effect of sulfur dioxide on inflammatory and immune regulation in asthmatic rats

Chemosphere

Volumn 112, Issue , 2014, Pages 296-304

  Li, Ruijin ^a   Kou, Xiaojing ^a   Tian, Jingjing ^a   Meng, Ziqiang ^a   Cai, Zongwei ^b   Cheng, Fangqin ^a   Dong, Chuan ^a  

^a SHANXI UNIVERSITY   (China)

^b HONG KONG BAPTIST UNIVERSITY   (Hong Kong)

Author keywords

Asthma; Immune regulation; Inflammatory regulation; Rats; Sulfur dioxide

Indexed keywords

BIOINFORMATICS; IMMUNE SYSTEM; PROTEINS; RATING; RATS; SULFUR DIOXIDE; T-CELLS;

ASTHMA; IMMUNE REGULATION; INFLAMMATORY REGULATION; INFLAMMATORY RESPONSE; MOLECULAR MECHANISM; NUCLEAR TRANSLOCATIONS; PATHOLOGICAL CHANGES; PROTEIN EXPRESSIONS;

DISEASES;

GAMMA INTERFERON; I KAPPA B; I KAPPA B KINASE BETA; IMMUNOGLOBULIN E; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; INTERLEUKIN 4; INTERLEUKIN 6; MESSENGER RNA; OVALBUMIN; SULFUR DIOXIDE; TRANSCRIPTION FACTOR FOXP3; TUMOR NECROSIS FACTOR ALPHA;

ASTHMA; DISEASE INCIDENCE; GENE EXPRESSION; GENETIC MARKER; HEALTH RISK; HISTOPATHOLOGY; IMMUNE RESPONSE; RODENT; SULFUR DIOXIDE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ASTHMA; BINDING AFFINITY; CELL COUNT; CONTROLLED STUDY; DOWN REGULATION; ENZYME LINKED IMMUNOSORBENT ASSAY; HISTOPATHOLOGY; IMMUNE RESPONSE; IMMUNOGLOBULIN BLOOD LEVEL; IMMUNOREGULATION; INFLAMMATION; INFLAMMATORY CELL; LUNG LAVAGE; MALE; NONHUMAN; NUCLEOTIDE SEQUENCE; PROTEIN BLOOD LEVEL; PROTEIN EXPRESSION; RAT; REGULATORY T LYMPHOCYTE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TH1 TH2 BALANCE; UPREGULATION; WESTERN BLOTTING;

ASTHMA; IMMUNE REGULATION; INFLAMMATORY REGULATION; RATS; SULFUR DIOXIDE;

ANIMALS; ASTHMA; CYTOKINES; DRUG INTERACTIONS; ENVIRONMENTAL POLLUTANTS; GENE EXPRESSION REGULATION; IMMUNOGLOBULIN E; INFLAMMATION; LUNG; MALE; OVALBUMIN; RATS; RATS, WISTAR; RNA, MESSENGER; SULFUR DIOXIDE;

EID: 84904410740     PISSN: 00456535     EISSN: 18791298     Source Type: Journal    
DOI: 10.1016/j.chemosphere.2014.04.065     Document Type: Article

References (48)

1. Andersson E., Knutsson A., Hagberg S., Nilsson T., Karlsson B., Alfredsson L., Torén K. Incidence of asthma among workers exposed to sulphur dioxide and other irritant gases. Eur. Respir. J. 2006, 27:720-725.
2. Barnes P.J. The cytokine network in asthma and chronic obstructive pulmonary disease. J. Clin. Invest. 2008, 118:3546-3556.
3. Bethel R.A., Epstein J., Sheppard D., Nadel J.A., Boushey H.A. Exercise increases sulfur dioxide-induced bronchoconstriction in asthmatic subjects. Am. Rev. Respir. Dis. 1983, 128:987-990.
4. 2 exposure promotes airway inflammation and subepithelial fibrosis following repeated ovalbumin challenge. Clin. Exp. Allergy 2008, 38:1680-1687.
5. Chang Y.K., Wu C.C., Lee L.T., Lin R.S., Yu Y.H., Chen Y.C. The short-term effects of air pollution on adolescent lung function in Taiwan. Chemosphere 2012, 87:26-30.
6. Deger L., Plante C., Jacques L., Goudreau S., Perron S., Hicks J., Kosatsky T., Smargiassi A. Active and uncontrolled asthma among children exposed to air stack emissions of sulphur dioxide from petroleum refineries in Montreal, Quebec: a cross-sectional study. Can. Respir. J. 2012, 19:97-102.
7. Deo S.S., Mistry K.J., Kakade A.M., Niphadkar P.V. Role played by Th2 type cytokines in IgE mediated allergy and asthma. Lung India 2010, 7:66-71.
8. Dröge W. Free radicals in the physiological control of cell function. Physiol. Rev. 2002, 82:47-95.
9. Fang S.P., Tanaka T., Tago F., Okamoto T., Kojima S. Immunomodulatory effects of gyokuheifusan on INF-gamma/IL-4 (Th1/Th2) balance in ovalbumin (OVA)-induced asthma model mice. Biol. Pharm. Bull. 2005, 28:829-833.
10. Hansson S.O., Rudén C. Evaluating the risk decision process. Toxicology 2006, 218:100-111.
11. Hunt T.B., Holman C.J.D. Asthma hospitalisation in relation to sulphur dioxide atmospheric contamination in the Kwinana industrial area of Western Australia. Commun. Health Stud. 1987, 11:197-201.
12. Ivanenkov Y.A., Balakin K.V., Lavrovsky Y. Small molecule inhibitors of NF-kB and JAK/STAT signal transduction pathways as promising anti-inflammatory therapeutics. Mini. Rev. Med. Chem. 2011, 11:55-78.
13. Jaeger M.J., Tribble D., Wittig H.J. Effect of 0.5ppm sulfur dioxide on the respiratory function of normal and asthmatic subjects. Lung 1979, 156:119-127.
14. Kara E., Özdilek H.G., Kara E.E. Ambient air quality and asthma cases in Niǧde, Turkey. Environ. Sci. Pollut. Res. Int. 2013, 20:4225-4234.
15. Kips J.C., Tavernier J.H., Joos G.F., Peleman R.A., Pauwels R.A. The potential role of tumor necrosis factor α in asthma. Clin. Exp. Allergy 1993, 23:247-250.
16. Li M., Shang Y.X. Inhaled corticosteroids inhibit substance P receptor expression in asthmatic rat airway smooth muscle cells. BMC Pulm Med. 2012, 12:79.
17. 2 derivatives on expressions of MUC5AC and IL-13 in human bronchial epithelial cells. Arch. Toxicol. 2007, 81:867-874.
18. Li R., Meng Z., Xie J. Effects of sulfur dioxide on the expressions of MUC5AC and ICAM-1 in airway of asthmatic rats. Regul. Toxicol. Pharmacol. 2007, 48:284-291.
19. Li R., Meng Z., Xie J. Effects of sulfur dioxide derivatives on four asthma-related gene expressions in human bronchial epithelial cells. Toxicol. Lett. 2007, 175:71-81.
20. Li R., Meng Z., Xie J. Effects of sulfur dioxide on the expressions of EGF, EGFR, and COX-2 in airway of asthmatic rats. Arch. Environ. Contam. Toxicol. 2008, 54:748-757.
21. Lin H.J., Qi H.W., Fang L.P., Li S.J., Li Z.C., Xie B.M. To explore the mechanisms of neurogenic inflammation and airway hyperresponsiveness of rat by inhaled sulfur. Chin. J. Appl. Physiol. 2009, 25:113-116.
22. + regulatory T-cells suppression of allergen driven T-cell activation to atopic status and expression of allergic disease. Lancet 2004, 363:608-615.
23. Mazzarella G., Bianco A., Catena E.R., Palma De., Abbate G.F. Th1/Th2 lymphocyte polarization in asthma. Allergy 2000, 55:6-9.
24. Manni M.L., Trudeau J.B., Scheller E.V., Mandalapu S., Elloso M.M., Kolls J.K., Wenzel S.E., Alcorn J.F. The complex relationship between inflammation and lung function in severe asthma. Mucosal Immunol. 2014, 10.1038/mi.2014.8.
25. Meng Z., Qin G., Zhang B., Geng H., Bai J., Bai W., Liu C. Oxidative damage of sulfur dioxide inhalation on lungs and hearts of mice. Environ. Res. 2003, 93:285-292.
26. Meng Z., Liu Y., Wu D. Effect of sulfur dioxide inhalation on cytokine levels in lungs and serum of mice. Inhal. Toxicol. 2005, 17:303-307.
27. 2) on asthmatic patients. Nihon Naika Gakkai Zasshi 1969, 58:719-730.
28. Napetschnig J., Wu H. Molecular basis of NF-κB signaling. Annu. Rev. Biophys. 2013, 42:443-468.
29. Ngoc P.L., Gold D.R., Tzianabos A.O., Weiss S.T., Celedón J.C. Cytokines, allergy, and asthma. Curr. Opin. Allergy Clin. Immunol. 2005, 5:161-166.
30. Ochs H.D., Ziegler S.F., Torgerson T.R. FOXP3 acts as a rheostat of the immune response. Immunol. Rev. 2005, 203:156-164.
31. 2) enhances the development of ovalbumin-induced asthmatic reactions in guinea pigs. Ann. Allergy Asthma Immunol. 2001, 86:62-67.
32. Provoost S., Maes T., van Durme Y.M., Gevaert P., Bachert C., Schmidt-Weber C.B., Brusselle G.G., Joos G.F., Tournoy K.G. Decreased FOXP3 protein expression in patients with asthma. Allergy 2009, 64:1539-1546.
33. Pruitt B., Lawson R. Assessing and managing asthma: a global initiative for asthma update. Nursing 2011, 41:46-52.
34. Qureshi A.A., Tan X., Reis J.C., Badr M.Z., Papasian C.J., Morrison D.C., Qureshi N. Suppression of nitric oxide induction and pro-inflammatory cytokines by novel proteasome inhibitors in various experimental models. Lipids Health Dis. 2011, 12:177.
35. 2 exposure on allergic sensitization in the guinea pig. J. Allergy Clin. Immunol. 1988, 82:527-534.
36. Shao J.X., Wang H.Y. Progress of studies on mechanism of eosinophils activation in airways. Int. J. Resp. 2011, 31:360-364.
37. 2- toxicity. J. Inorg. Biochem. 1994, 56:155-165.
38. Shi Y., Shi G., Wan H., Jiang L., Ai X., Zhu H., Tang W., Ma J., Jin X., Zhang B. Coexistence of Th1/Th2 and Th17/Treg imbalances in patients with allergic asthma. Chin. Med. J. 2011, 124:1951-1956.
39. Smargiassi A., Kosatsky T., Hicks J., Plante C., Armstrong B., Villeneuve P.J., Goudreau S. Risk of asthmatic episodes in children exposed to sulfur dioxide stack emissions from a refinery point source in Montreal, Canada. Environ. Health Perspect. 2009, 117:653-659.
40. Su L., Chi Y., Yuan X., Zhang Y., Zheng R. Effects of sulfur dioxide on the immediate asthma reaction in rats. Chin. Occup. Med. 2010, 37:376-378.
41. Tak P.P., Firestein G.S. NF-kappaB: a key role in inflammatory diseases. J. Clin. Invest. 2001, 107:7-11.
42. + immune regulatory cells are required for induction of tolerance to alloantigen via costimulatory blockade. J. Exp. Med. 2001, 193:1311-1318.
43. Tseng C.Y., Huang Y.C., Su S.Y., Huang J.Y., Lai C.H., Lung C.C., Ho C.C., Liaw Y.P. Cell type specificity of female lung cancer associated with sulfur dioxide from air pollutants in Taiwan: an ecological study. BMC Public Health 2012, 12:4.
44. Teramoto S., Hida N., Ishikawa H., Hizawa N. Inverse U shape of the trachea during an asthma attack. Intern. Med. 2013, 52:2289-2290.
45. Tomasiak-Łozowska M.M., Bodzenta-Łukaszyk A., Tomasiak M., Skiepko R., Zietkowski Z. The role of interleukin 13 and interleukin 5 in asthma. Postepy. Hig. Med. Dosw. 2010, 64:146-155.
46. Wagner U., Fehmann H.C., Bredenbröker D., Yu F., Barth P.J., von Wichert P. Galanin and somatostatin inhibition of substance P-induced airway mucus secretion in the rat. Neuropeptides 1995, 28:59-64.
47. Walters S., Griffiths R.K., Ayres J.G. Temporal association between hospital admissions for asthma in Birmingham and ambient levels of sulphur dioxide and smoke. Thorax 1994, 49:133-140.
48. Yanagisawa N., Shimada K., Miyazaki T., Kume A., Kitamura Y., Sumiyoshi K., Kiyanagi T., Iesaki T., Inoue N., Daida H. Enhanced production of nitric oxide, reactive oxygen species, and pro-inflammatory cytokines in very long chain saturated fatty acid-accumulated macrophages. Lipids Health Dis. 2008, 7:48.