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Redox balance and DNA fragmentation in arsenic-exposed occupational workers from different industries of Pakistan

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Abstract

Occupational exposure accounts for a contact between workers and different toxicants. Present study was designed to measure the arsenic-induced DNA fragmentation and oxidative stress in exposed workers. Blood, hair, and nail samples were collected from welding, brick kiln, furniture, pesticide, and paint industries (n = 50/industry) of Pakistan along with 200 controls. DNA damage was calculated using DNA fragmentation assay. Antioxidant enzymes (CAT, SOD, GPx) were measured using ELISA. Results revealed that arsenic exposure induced DNA fragmentation in brick kiln, furniture, and welding industries. Enzyme activity was reduced in five industries compared to control. In exposed group, significant depletion of enzymes was observed in furniture, welding, and brick kiln workers. Based on age and time of exposure, significant difference was observed in welding and brick kiln group. Smokers of exposed group showed significantly reduced levels of enzymes compared to controls. Arsenic deposition was observed higher in the hair, nail, and blood samples of exposed group (P < 0.001) compared to control. Likewise, lead and cadmium contents were higher in the blood samples of industrial workers compared to control. This study suggests increased trend of cellular damage and oxidative stress in occupational workers profoundly in welding, furniture, and brick kiln industries. Moreover, this study recognizes the contribution of age, exposure time, and smoking status toward arsenic-induced oxidative stress and DNA fragmentation.

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References

  • Abernathy CO, Liu YP, Longfellow D, Aposhian HV, Beck B, Fowler B, Goyer R, Menzer R, Rossman T, Thompson C, Waalkes M (1999) Arsenic: health effects, mechanisms of actions, and research issues. Environ Health Perspect 107:593–597

    Article  CAS  Google Scholar 

  • Ahmed YF, Eldebaky HAA, Mahmoud KM, Nawito M (2012) Effects of lead exposure on DNA damage and apoptosis in reproductive and vital organs in female rabbit. Global Vet 9:401–408

    Google Scholar 

  • ATSDR (2007) Toxicological profile for arsenic. Agency for Toxic Substances and Disease Registry, U.S. Department of Health and Human Services, Public Health Service, Atlanta, G.A

    Google Scholar 

  • Barata C, Varo I, Navarro JC, Arun S, Porte C (2005) Antioxidant enzyme activities and lipid peroxidation in the freshwater cladoceran Daphnia magna exposed to redox cycling compounds. Comp Biochem Physiol C Toxicol Pharmacol 140:175–186

    Article  Google Scholar 

  • Bau DT, Wang TS, Chung CH, Wang AS, Wang AS, Jan KY (2002) Oxidative DNA adducts and DNA-protein cross-links are the major DNA lesions induced by arsenite. Environ. Health Perspect 110:S753–S756

    Article  Google Scholar 

  • Bertini I, Cavallaro G (2008) Metals in the “omics” world: copper homeostasis and cytochrome c oxidase assembly in a new light. J Biol Inorg Chem 13:3–14

    Article  CAS  Google Scholar 

  • Bibi M, Hashmi MZ, Malik RN (2015) Human exposure to arsenic in groundwater from Lahore district, Pakistan. Environ Toxicol Pharmacol 39:42–52

    Article  CAS  Google Scholar 

  • Birben E, Sahiner UM, Sackesen C, Erzurum S, Kalayci O (2012) Oxidative stress and antioxidant defense. World Allergy Organ J 5:9–19

    Article  CAS  Google Scholar 

  • Bulat P, Potkonjak B, Dujic I (2008) Lipid peroxidation and antioxidative enzyme activity in erythrocytes of workers occupationally exposed to aluminium. Arch Ind Hygiene Toxicol 59:81–87

    CAS  Google Scholar 

  • Cassini C, Calloni C, Bortolini G, Garcia SC, Dornelles MA, Henriques JAP, Salvador M (2011) Occupational risk assessment of oxidative stress and genotoxicity in workers exposed to paints during a working week. Int J Occup Med Environ Health 24:308–318

    Article  Google Scholar 

  • Chamba P, Nunes E (2016) Work-related asthma among workers in the wood-processing industry: a review: allergies in the workplace. Curr Allergy Clin Immunol 29:110–117

    Google Scholar 

  • Choi S, Krishnan J, Ruckmani K (2017) Cigarette smoke and related risk factors in neurological disorders: an update. Biomed Pharmacother 85:79–86

    Article  Google Scholar 

  • Dasheng L, Morimoto K, Takeshita T, Yuquan LU (2001) Arsenic induces DNA damage via reactive oxygen species in human cells. Environ Health Prev Med 6:27–32

    Article  Google Scholar 

  • DeLuca M, Lardy H, Cross RL (eds) (2014) Enzyme catalysis and control (Vol. 24). Elsevier, New York

    Google Scholar 

  • EPA (1998) Arsenic, inorganic (CASRN 7440-38-2): Carcinogenicity assessment for lifetime exposure. Integrated Risk Information System (IRIS), U.S. Environmental Protection Agency, Washington, DC

    Google Scholar 

  • Farahat SA, Ibrahim YH, Abdel-Latif MN (2010) Genotoxicity and oxidative stress due to exposure to wood dust among carpenters. Egyptian J Occup Med 34:83–95

    Article  Google Scholar 

  • Flora SJA (2011) Arsenic-induced oxidative stress and its reversibility. Free Radic Biol Med 51:257–281

    Article  CAS  Google Scholar 

  • Florea AM, Busselberg D (2006) Occurrence, use and potential toxic effects of metals and metal compounds. Biometals 19:419–427

    Article  CAS  Google Scholar 

  • Gobba NAEK, Hussien AMA, Sharawy DEE, Hussein MA (2017) The potential hazardous effect of exposure to iron dust in Egyptian smoking and non-smoking welders. Arch Environ and Occup Health 4:1–14

    Google Scholar 

  • Halatek T, Sinczuk-Walczak H, Rabieh S, Wasowicz W (2009) Association between occupational exposure to arsenic and neurological, respiratory and renal effects. Toxicol App Pharmacol 239:193–199

    Article  CAS  Google Scholar 

  • Hall MN, Niedzwiecki M, Liu X, Harper KN, Alam S, Slavkovich V, Ilievski V, Levy D, Siddique AB, Parvez F, Mey JL, van Geen A, Graziano J, Gamble MV (2014) Chronic arsenic exposure and blood glutathione and glutathione disulfide concentrations in Bangladeshi adults. Environ. Health Perspect 121:1068–1074

    Article  Google Scholar 

  • Hanlon DP, Ferm VH (1977) Placental permeability of arsenate ion during early embryogenesis in the hamster. Association of arsenic levels in soil and water with urinary arsenic concentration of residents in the vicinity of closed metal mines. Experientia 33:1221–1222

    Article  CAS  Google Scholar 

  • Hemnani T, Parihar MS (1998) Reactive oxygen species and oxidative DNA damage. Indian J Physiol Pharmacol 42:440–452

    CAS  Google Scholar 

  • Hempel S (2013) The inheritor’s powder: a tale of arsenic, murder, and the new forensic science. WW Norton & Company, New York City

    Google Scholar 

  • Henle ES, Linn S (1997) Formation, prevention and repair of DNA damage by ion/hydrogen peroxide. J Biol Chem 272:19095–19103

    Article  CAS  Google Scholar 

  • Hong YS, Song KH, Chung JY (2014) Health effect of chronic arsenic exposure. J Prev Med Public Health 47:245–252

    Article  Google Scholar 

  • Hughes MF (2002) Arsenic toxicity and potential mechanisms of action. Toxicol Lett 133:1–16

    Article  CAS  Google Scholar 

  • IARC (2012) Monograph on the evaluation of carcinogenic risks to human; arsenic and arsenic compounds. Monograph 100C:41–85

    Google Scholar 

  • Ishaq M, Khan MA, Jan FA, Ahmad I (2010) Heavy metals in brick kiln located area using atomic absorption spectrophotometer: a case study from the city of Peshawar, Pakistan. Environ Monit Assess 166:409–420

    Article  CAS  Google Scholar 

  • Ismail M, Muhammad D, Khan FU, Munsif F, Ahmad T, Ali S, Ahmad M (2012) Effect of brick kilns emissions on heavy metal (Cd and Cr) content of contiguous soil and plants. Sarhad J Agri 28:403–409

    Google Scholar 

  • Jahan S, Falah S, Ullah H, Ullah A, Rauf N (2016) Antioxidant enzymes status and reproductive health of adult male workers exposed to brick kiln pollutants in Pakistan. Environ Sci Pollution Res 23:12932–12940

    Article  CAS  Google Scholar 

  • Jarup L, Pershagen G, Wal S (1989) Cumulative arsenic exposure and lung cancer in smelter workers: a dose–response study. Am J Ind Med 15:31–41

    Article  CAS  Google Scholar 

  • Jomova K, Jenisova Z, Feszterova M, Baros S, Liska J, Hudecova D, Valko M (2011) Arsenic: toxicity, oxidative stress and human disease. J App Toxicol 31(2):95–107

    CAS  Google Scholar 

  • Kitchin KT, Conolly R (2010) Arsenic-induced carcinogenesis oxidative stress as a possible mode of action and future research needs for more biologically based risk assessment. Chem Res Toxicol 23:327–335

    Article  CAS  Google Scholar 

  • Ko JL, Cheng YJ, Liu GC, Hsin IL, Chen HL (2017) The association of occupational metals exposure and oxidative damage, telomere shortening in fitness equipments manufacturing workers. Ind Health 8:345–353

    Article  Google Scholar 

  • Liu SX, Athar M, Lippai I, Waldren C, Hei TK (2001) Induction of oxyradicals by arsenic: implication for mechanism of genotoxicity. Proc Natl Acad Sci USA 98:1643–1648

    Article  CAS  Google Scholar 

  • Liu HH, Lin MH, Liu PC, Chan CI, Chen HL (2009) Health risk assessment by measuring plasma malondialdehyde (MDA), urinary 8-hydroxydeoxyguanosine (8-OH-dG) and DNA strand breakage following metal exposure in foundry workers. J Hazard Mater 170:699–704

    Article  CAS  Google Scholar 

  • Manafa PO, Okafor CC, Okeke CO, Chukwuma GO, Ibeh NC, Ogenyi SI, Aneke JC (2017) Assessment of superoxide dismutase activity and total antioxidant capacity in adult male cigarette smokers in Nnewi metropolis, Nigeria. JMR 3:23–26

    Google Scholar 

  • Manna P, Sinha M, Sil PC (2008) Arsenic-induced oxidative myocardial injury: protective role of arjunolic acid. Arch. Toxicol 82:137–149

    Article  CAS  Google Scholar 

  • Moro AM, Charao M, Brucker N, Bulcao R, Freitas F, Guerreiro G, Linden R (2010) Effects of low-level exposure to xenobiotics present in paints on oxidative stress in workers. Sci Total Environ 408:4461–4467

    Article  CAS  Google Scholar 

  • Muenyi CS, Ljungman M, States JC (2016) Arsenic disruption of DNA damage responses potential role in carcinogenesis and chemotherapy. Biomolecules 5:2184–2193

    Article  Google Scholar 

  • Muniz JF, McCauley L, Scherer J, Lasarev M, Koshy M, Kow YW, Kisby GE (2008) Biomarkers of oxidative stress and DNA damage in agricultural workers: a pilot study. Toxicol App Pharmacol 227:97–107

    Article  CAS  Google Scholar 

  • Navarro-Yepes J, Zavala-Flores L, Anandhan A, Wang F, Skotak M, Chandra N, Quintanilla-Vega B (2014) Antioxidant gene therapy against neuronal cell death. Pharmacol Ther 142:206–230

    Article  CAS  Google Scholar 

  • O’Brien T, Mandel HG, Pritchard DE, Patierno SR (2002) Critical role of chromium (Cr)-DNA interactions in the formation of Cr-induced polymerase arresting lesions. Biochem 41:12529–12537

    Article  Google Scholar 

  • Parvez M, Akram M (2016) Suffering water of Pakistan: arsenic-a major threat. Bulg Chem Commun 48:203–208

    Google Scholar 

  • Petrick JS, Ayala-Fierro F, Cullen WR, Carter DE, Aposhian HV (2000) Monomethylarsonous acid (MMA(III)) is more toxic than arsenite in Chang human hepatocytes. Toxicol Appl Pharmacol 163:203–207

    Article  CAS  Google Scholar 

  • Rekhadevi PV, Mahboob M, Rahman MF, Grover P (2009) Genetic damage in wood dust-exposed workers. Mutagenesis 24:59–65

    Article  CAS  Google Scholar 

  • Rossman T (2003) Mechanism of arsenic carcinogenesis: an integrated approach. Mutat Res 533:37–65

    Article  CAS  Google Scholar 

  • Rubino FM (2015) Toxicity of glutathione-binding metals: a review of targets and mechanisms. Toxics 3:20–62

    Article  CAS  Google Scholar 

  • Safty AE, Rashed L, Samir A, Teleb H (2014) Oxidative stress and arsenic exposure among copper smelters. British J Med Med Res 4:2955–2968

    Article  Google Scholar 

  • Schuhmacher-Wolz U, Dieter HH, Klein D (2009) Oral exposure to inorganic arsenic: evaluation of its carcinogenic and non-carcinogenic effects. Crit Rev Toxicol 39:271–298

    Article  CAS  Google Scholar 

  • Schulte PA, Chun H (2009) Climate change and occupational safety and health: establishing a preliminary framework. J Occup Environ Hyg 6(9):542–554

    Article  CAS  Google Scholar 

  • Shi H, Shi X, Liu KJ (2004) Oxidative mechanism of arsenic toxicity and carcinogenesis. Mol Cell Biochem 255:67–78

    Article  CAS  Google Scholar 

  • Soleimani E, Moghadam RH, Ranjbar A (2015) Occupational exposure to chemicals and oxidative toxic stress. Toxicol Environ Health Sci 7:1–24

    Article  Google Scholar 

  • Soltaninejad K, Abdollahi M (2009) Current opinion on the science of organophosphate pesticides and toxic stress: a systematic review. Med Sci Monitor 15:RA75–RA90

    CAS  Google Scholar 

  • Sood A, Petersen H, Blanchette C, Meek P, Belinsky S, Picchi M, Tesfaigzi Y (2009) Wood smoke-associated chronic obstructive pulmonary disease (COPD)–underappreciated in the United States? Am J Respir Crit Care Med 179:4742

    Google Scholar 

  • Styblo M, Del Razo LM, Vega L, Germolec DR, LeCluvse EL, Hamilton GA, Reed W, Wang C, Cullen WR, Thomas DJ (2000) Comparative toxicity of trivalent and pentavalent inorganic and methylated arsenicals in rat and human cells. Arch Toxicol 74:289–299

    Article  CAS  Google Scholar 

  • Surdu S, Fitzgerald E, Bloom MS, Boscoe FP, Carpenter DO, Hasse RF, Gurzau E (2013) Occupational exposure to arsenic and risk of nonmelanoma skin cancer in a multinational European study. Int J Cancer 133:2182–2191

    Article  CAS  Google Scholar 

  • Tchounwou PB, Patlolla AK, Centeno JA (2003) Invited reviews: carcinogenic and systemic health effects associated with arsenic exposure. A critical review. Toxicol Pathol 31:575–588

    CAS  Google Scholar 

  • Vahter M, Concha G (2010) Role of metabolism in arsenic toxicity. Pharmacol Toxicol 89:1–5

    Article  Google Scholar 

  • Valko M, Morris H, Cronin MT (2005) Metals, toxicity and oxidative stress. Curr Med Chem 12:1161–1208

    Article  CAS  Google Scholar 

  • Vejahati F, Xu Z, Gupta R (2010) Trace elements in coal: associations with coal and minerals and their behavior during coal utilization–a review. Fuel 89:904–911

    Article  CAS  Google Scholar 

  • Vuyyuri SB, Ishaq M, Kuppala D, Grover P, Ahuja YR (2006) Evaluation of micronucleus frequencies and DNA damage in glass workers exposed to arsenic. Environ. Mol Mutagen 47:562–570

    Article  CAS  Google Scholar 

  • Wang TS, Huang H (1994) Active oxygen species are involved in the induction of micronuclei in XRS-5 cells. Mutagenesis 9:253–257

    Article  CAS  Google Scholar 

  • WHO (2001) Arsenic and arsenic compounds, 2nd edn. Environmental Health Criteria 224, International Program on Chemical Safety, World Health Organization, Geneva, Switzerland

    Google Scholar 

  • Yamanaka K, Ohba H, Hasegawa A, Sawamura R, Okada S (1989) Mutagenicity of dimethylated metabolites of inorganic arsenics. Chem Pharm Bull 37:2753–2756

    Article  CAS  Google Scholar 

  • Yamanaka K, Hoshino M, Okamoto M, Sawamura R, Hasegawa A, Okada S (1990) Induction of DNA damage by dimethylarsine, a metabolite of inorganic arsenics, is for the major part likely due to its peroxyl radical. Biochem Biophys Res Commun 168:58–64

    Article  CAS  Google Scholar 

  • Zeneli L, Sekovanic A, Ajvazi M, Kurti L, Daci N (2016) Alterations in antioxidant defense system of workers chronically exposed to arsenic, cadmium and mercury from coal flying ash. Environ Geochem Health 38:65–72

    Article  CAS  Google Scholar 

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This part of work was supported by the Higher Education Commission Pakistan (HEC).

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Correspondence to Zertashia Akram.

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Raza, M., Mahjabeen, I., Fahim, M. et al. Redox balance and DNA fragmentation in arsenic-exposed occupational workers from different industries of Pakistan. Environ Sci Pollut Res 25, 33381–33390 (2018). https://doi.org/10.1007/s11356-018-3274-6

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  • DOI: https://doi.org/10.1007/s11356-018-3274-6

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