Pro-oxidant–antioxidant balance in Iranian veterans with sulfur mustard toxicity and different levels of pulmonary disorders

References

• Alamdari DH, Ghayour-Mobarhan M, Tavallaie S, et al. (2008). Prooxidant–antioxidant balance as a new risk factor in patients with angiographically defined coronary artery disease. Clin Biochem 41:375–380
   PubMed Web of Science ®Google Scholar
• Alamdari DH, Ordoudi SA, Nenadis N, et al. (2009). Comparison of prooxidant–antioxidant balance method with crocin method for determination of total prooxidant–antioxidant capacity. Iran J Basic Med Sci 12:93–99
   Web of Science ®Google Scholar
• Alamdari DH, Paletas K, Pegiou T, et al. (2007). A novel assay for the evaluation of the prooxidant–antioxidant balance, before and after antioxidant vitamin administration in type II diabetes patients. Clin Biochem 40:248–254
   PubMed Web of Science ®Google Scholar
• Anand T, Vijayaraghavan R, Bansal I, Bhattacharya B. (2009). Role of inflammatory cytokines and DNA damage repair proteins in sulfur mustard exposed mice liver. Toxicol Mech Methods 19:356–362
   PubMed Web of Science ®Google Scholar
• Anderson MT, Staal F, Gitler C, Herzenberg LA. (1994). Separation of oxidant-initiated and redox-regulated steps in the NF-kappa B signal transduction pathway. Proc Natl Acad Sci 91:11527–11531
   PubMed Web of Science ®Google Scholar
• Arroyo CM, Broomfield CA, Hackley BE. (2001). The role of interleukin-6 (IL-6) in human sulfur mustard (HD) toxicology. Int J Toxicol 20:281–296
   PubMed Web of Science ®Google Scholar
• Arroyo CM, Kan RK, Burman DL, et al. (2003). Regulation of 1‐α, 25‐dihydroxyvitamin D3 on interleukin‐6 and interleukin‐8 induced by sulfur mustard (HD) on human skin cells. Pharmacol Toxicol 92:204–213
   PubMedGoogle Scholar
• Arroyo C, Schafer R, Kurt E, et al. (1999). Response of normal human keratinocytes to sulfur mustard (HD): cytokine release using a non-enzymatic detachment procedure. Hum Exp Toxicol 18:1–11
   PubMed Web of Science ®Google Scholar
• Arroyo CM, Schafer RJ, Kurt EM, et al. (2000). Response of normal human keratinocytes to sulfur mustards: cytokine release. J Appl Toxicol 20:S63–S72
   PubMed Web of Science ®Google Scholar
• Attaran D, Lari SM, Towhidi M, et al. (2010). Interleukin-6 and airflow limitation in chemical warfare patients with chronic obstructive pulmonary disease. Int J Chron Obstruct Pulmon Dis 5:335–340
   PubMedGoogle Scholar
• Balali-Mood M, Hefazi M. (2005). The pharmacology, toxicology, and medical treatment of sulphur mustard poisoning. Fundam Clin Pharmacol 19:297–315
   PubMed Web of Science ®Google Scholar
• Behr J, Maier K, Braun B, et al. (2000). Evidence for oxidative stress in bronchiolitis obliterans syndrome after lung and heart–lung transplantation. Transplantation 69:1856–1860
   PubMed Web of Science ®Google Scholar
• Benzie IF, Strain J. (1996). The ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal Biochem 239:70–76
   PubMed Web of Science ®Google Scholar
• Black AT, Joseph LB, Casillas RP, et al. (2010). Role of MAP kinases in regulating expression of antioxidants and inflammatory mediators in mouse keratinocytes following exposure to the half mustard, 2-chloroethyl ethyl sulfide. Toxicol Appl Pharmacol 245:352–360
   PubMed Web of Science ®Google Scholar
• Cao G, Alessio HM, Cutler RG. (1993). Oxygen-radical absorbance capacity assay for antioxidants. Free Radic Biol Med 14:303–311
   PubMed Web of Science ®Google Scholar
• Comhair SA, Bhathena PR, Dweik RA, et al. (2000). Rapid loss of superoxide dismutase activity during antigen-induced asthmatic response. The Lancet 355:624
   PubMed Web of Science ®Google Scholar
• Dong R, Wang Q, He XL, et al. (2007). Role of nuclear factor kappa B and reactive oxygen species in the tumor necrosis factor-alpha-induced epithelial-mesenchymal transition of MCF-7 cells. Braz J Med Biol Res 40:1071–1078
   PubMed Web of Science ®Google Scholar
• Elsayed NM, Omaye ST, Klain GJ, Korte JRDW. (1992). Free radical-mediated lung response to the monofunctional sulfur mustard butyl 2-chloroethyl sulfide after subcutaneous injection. Toxicology 72:153–165
   PubMed Web of Science ®Google Scholar
• Emad A, Rezaian GR. (1997). The diversity of the effects of sulfur mustard gas inhalation on respiratory system 10 years after a single, heavy exposure: analysis of 197 cases. Chest J 112:734–738
   PubMed Web of Science ®Google Scholar
• Erel O. (2005). A new automated colorimetric method for measuring total oxidant status. Clin Biochem 38:1103–1111
   PubMed Web of Science ®Google Scholar
• Ham HY, Hong CW, Lee SN, et al. (2012). Sulfur mustard primes human neutrophils for increased degranulation and stimulates cytokine release via TRPM2/p38 MAPK signaling. Toxicol Appl Pharmacol 258:82–88
   PubMed Web of Science ®Google Scholar
• Husain K, Dube S, Sugendran K, et al. (1996). Effect of topically applied sulphur mustard on antioxidant enzymes in blood cells and body tissues of rats. J Appl Toxicol 16:245–248
   PubMed Web of Science ®Google Scholar
• Janssen Y, Marsh J, Absher M, et al. (1992). Expression of antioxidant enzymes in rat lungs after inhalation of asbestos or silica. J Biol Chem 267:10625–10630
   PubMed Web of Science ®Google Scholar
• Johnson JL, Moore EE, Patrick DA, et al. (1999). Extracellular signal-related kinase 1/2 and p38 mitogen-activated protein kinase pathways serve opposite roles in neutrophil cytotoxicity. Arch Surg 134:1074–1078
   PubMedGoogle Scholar
• Kirkham P, Rahman I. (2006). Oxidative stress in asthma and COPD: antioxidants as a therapeutic strategy. Pharmacol Ther 111:476–494
   PubMed Web of Science ®Google Scholar
• Kotani K, Taniguchi N. (2012). Correlation between high-sensitivity C-reactive protein and reactive oxygen metabolites during a one-year period among asymptomatic subjects. J Clin Med Res 4:52–55
   PubMedGoogle Scholar
• Lardot C, Dubois V, Lison D. (1999). Sulfur mustard upregulates the expression of interleukin-8 in cultured human keratinocytes. Toxicol Lett 110:29–33
   PubMed Web of Science ®Google Scholar
• Li X, Moody MR, Engel D, et al. (2000). Cardiac-specific overexpression of tumor necrosis factor – causes oxidative stress and contractile dysfunction in mouse diaphragm. Circulation 102:1690–1696
   PubMed Web of Science ®Google Scholar
• Nourani MR, Yazdani S, Habibi Roudkenar M, et al. (2010). HO1 mRNA and protein do not change in parallel in bronchial biopsies of patients after long term exposure to sulfur mustard. Gene Regul Syst Bio 4:83–90
   Google Scholar
• Papirmeister B, Feister AJ, Robinson SI, Ford RD. (1991). Medical defense against mustard gas: toxic mechanisms and pharmacological implications. Boca Raton: CRC Press
   Google Scholar
• Park S, Kim M, Paik JK, et al. (2013). Oxidative stress is associated with C‐reactive protein in nondiabetic postmenopausal women, independent of obesity and insulin resistance. Clin Endocrinol 79:65–70
   PubMed Web of Science ®Google Scholar
• Paromov V, Suntres Z, Smith M, Stone WL. (2007). Sulfur mustard toxicity following dermal exposure: role of oxidative stress, and antioxidant therapy. J Burns Wounds 7:60–85
   Google Scholar
• Pohanka M, Sobotka J, Jilkova M, Stetina R. (2011). Oxidative stress after sulfur mustard intoxication and its reduction by melatonin: efficacy of antioxidant therapy during serious intoxication. Drug Chem Toxicol 34:85–91
   PubMed Web of Science ®Google Scholar
• Rebholz B, Kehe K, Ruzicka T, Rupec RA. (2008). Role of NF-kappaB/RelA and MAPK pathways in keratinocytes in response to sulfur mustard. J Invest Dermatol 128:1626–1632
   PubMed Web of Science ®Google Scholar
• Renshaw B. (1946). Mechanisms in production of cutaneous injuries by sulfur and nitrogen mustards. Chem Warfare Agents Relat Chem Probl 1:479–520
   Google Scholar
• Repine JE, Bast A, Lankhorst I. (1997). Oxidative stress in chronic obstructive pulmonary disease. Am J Respir Crit Care Med 156:341–357
   PubMed Web of Science ®Google Scholar
• Rowell M, Kehe K, Balszuweit F, Thiermann H. (2009). The chronic effects of sulfur mustard exposure. Toxicology 263:9–11
   PubMed Web of Science ®Google Scholar
• Seagrave J, Weber WM, Grotendorst GR. (2010). Sulfur mustard vapor effects on differentiated human lung cells. Inhal Toxicol 22:896–902
   PubMed Web of Science ®Google Scholar
• Shohrati M, Ghanei M, Shamspour N, et al. (2010). Glutathione and malondialdehyde levels in late pulmonary complications of sulfur mustard intoxication. Lung 188:77–83
   PubMed Web of Science ®Google Scholar
• Stentz FB, Umpierrez GE, Cuervo R, Kitabchi AE. (2004). Proinflammatory cytokines, markers of cardiovascular risks, oxidative stress, and lipid peroxidation in patients with hyperglycemic crises. Diabetes 53:2079–2086
   PubMed Web of Science ®Google Scholar
• United Nations Security Council. (1987). Report of the mission dispatched by the Secretary General to investigate allegations of the use of chemical weapons in the conflict between the Islamic Republic of Iran and Iraq. S/18852 and S/18852/Addedum 1
   Google Scholar
• Vestbo J, Hurd SS, Agusti AG, et al. (2013). Global strategy for the diagnosis, management, and prevention of chronic obstructive pulmonary disease: GOLD executive summary. Am J Respir Crit Care Med 187:347–365
   PubMed Web of Science ®Google Scholar
• Wassmann S, Stumpf M, Strehlow K, et al. (2004). Interleukin-6 induces oxidative stress and endothelial dysfunction by overexpression of the angiotensin II type 1 receptor. Circul Res 94:534–541
   PubMed Web of Science ®Google Scholar
• Wheeler GP. (1962). Studies related to the mechanisms of action of cytotoxic alkylating agents: a review. Cancer Res 22:651–688
   PubMed Web of Science ®Google Scholar
• Won SY, Kim SR, Maeng S, Jin BK. (2013). Interleukin-13/Interleukin-4-induced oxidative stress contributes to death of prothrombinkringle-2 (pKr-2)-activated microglia. J Neuroimmunol 265:36–42
   PubMed Web of Science ®Google Scholar