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Environmental Contamination of Chrysotile Asbestos and Its Toxic Effects on Antioxidative System of Lemna gibba

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Abstract

Asbestos was monitored in various plant samples around an asbestos cement factory. Asbestos residue was found on the surface of all plant samples monitored. Based on asbestos concentration found in different plant samples during monitoring and on the property of asbestos to cause reactive oxygen species-mediated oxidative stress in animal models, laboratory experiments were conducted to assess the toxicity of chrysotile asbestos on an aquatic macrophyte, duckweed (Lemna gibba.). L. gibba plants were exposed to four concentrations (0.5, 1.0, 2.0, and 5.0 μg/mL) of chrysotile asbestos under laboratory conditions, and alterations in the glutathione and ascorbate antioxidative system were estimated at postexposure days 7, 14, 21, and 28 in order to assess changes in their level as suitable biomarkers of chrysotile contamination. Chrysotile exposure caused a decrease in total and reduced glutathione and an enhancement in the oxidized glutathione as well as the reduced/oxidized glutathione ratio. An increase in ascorbate pool size, and reduced as well as oxidized ascorbate was found to be accompanied by a decrease in the ratio of reduced/oxidized ascorbate. Alteration in the glutathione and ascorbate level might be considered as a biomarker of exposure to an unsafe environment because these are essential compounds of the general antioxidative strategy to overcome oxidative stress due to environmental constraints. Because an increase in the oxidation rate of antioxidants weakens cellular defenses and indicates a precarious state, they could constitute indicators of toxicity.

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References

  • American Public Health Association, American Water Works Association, Water Environment Federation (1998) Standard methods for the examination of water and wastewater, 20th ed. APHA, Washington, DC

    Google Scholar 

  • Badiani M, Schenone G, Paolacci AR, Fumagalli I (1993) Daily fluctuations of antioxidants in bean (Phaseolus vulgaris L.) leaves as affected by the presence of ambient air pollutants. Plant Cell Physiol 34:271–279

    CAS  Google Scholar 

  • Burger J, Gochfeld M (2001) On developing bioindicators for human and ecological health. Environ Monit Assess 66:23–46

    Article  CAS  Google Scholar 

  • Cakmak I, Marschner H (1992) Magnesium deficiency and high light intensity enhance activities of superoxide dismutase, ascorbate peroxidase and glutathione reductase in bean leaves. Plant Physiol 98:1222–1227

    CAS  Google Scholar 

  • Danilov RA, Ekelund NGA (2001) Applicability of growth rate, cell shape and motility of Euglena gracilis as physiological parameters for bioassessment at lower concentrations of toxic substances: An experimental approach. Environ Tox 16:78–83

    Article  CAS  Google Scholar 

  • Dhindsa RS, Matowe W (1981) Drought tolerance in two mosses: Correlated with enzymatic defense against lipid peroxidation. J Exp Bot 32:79–91

    Article  CAS  Google Scholar 

  • Di Giulio RT, Monosson E (1996) Interconnections between human and ecosystem health. Chapman & Hall, London, UK

    Google Scholar 

  • Donahue JL, Okpodu CM, Cramer CL, Grabau EA, Alscher RG (1997) Responses of antioxidants to paraquat in pea leaves, relationship to resistance. Plant Physiol 113:249–257

    CAS  Google Scholar 

  • Ebenhardt MK, Roman-Franco AA, Quiles MR (1985) Asbestos induced decomposition of hydrogen peroxide. Environ Res 37:287–292

    Article  Google Scholar 

  • Fadzilla NM, Finch RP, Burdon RH (1997) Salinity, oxidative stress and antioxidant responses in shoot cultures of rice. J Exp Bot 48:325–331

    Article  CAS  Google Scholar 

  • Foyer CH, Lopez-Delgado H, Dat JF, Scott IM (1997) Hydrogen peroxide and glutathione associated mechanisms of acclimatory stress tolerance and signaling. Physiol Plant 100:241–254

    Article  CAS  Google Scholar 

  • Gossett DR, Banks SW, Millhollon EP, Lucas C (1996) Antioxidant responses to NaCl stress in a control and an NaCl-tolerant cotton cell line grown in the presence of paraquat, butathione sulfoximine and exogenous glutathione. Plant Physiol 112:803–809

    Google Scholar 

  • Gossett DR, Millhollon EP, Lucas C (1994a) Antioxidant response to NaCl stress in salt-tolerant and salt-sensitive cultivars of cotton. Crop Sci 34:706–714

    Article  CAS  Google Scholar 

  • Gossett DR, Millhollon EP, Lucas C, Banks SW, Marney MM (1994b) The effects of NaCl on antioxidant enzyme activities in callus tissue of salt-tolerant and salt-sensitive cultivars of cotton. Plant Cell Rep 13:498–503

    Article  CAS  Google Scholar 

  • Griffith OW (1980) Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine. Analyt Biochem 106:207–212

    Article  CAS  Google Scholar 

  • Harington JS, Allison AC, Badami DV (1975) Mineral fibers: Chemical, physico-chemical and biological properties. Adv Pharmacol Chemother 12:291–402

    Article  CAS  Google Scholar 

  • Harvey T, Mahaffrey KR, Vasquez S, Dourson M (1995) Holistic risk assessment: An emerging process for environmental decisions. Regul Toxicol Pharmacol 22:110–117

    Article  CAS  Google Scholar 

  • Hauptmann M, Pohlabeln H, Lubin JH, Jockel KH, Ahrens W, Bruske-Hohlfeld I, Wichman HE (2002) The exposure-time-response relationship between occupational asbestos exposure and lung cancer in two German case-control studies. Am J Ind Med 41:89–97

    Article  CAS  Google Scholar 

  • Indian Standards (IS) (1986) Method for determination of airborne asbestos fibre concentration in work environment by light microscopy (membrane filter method). Indian Standards Institution, New Delhi. IS-11450

  • IPCS (1998) Environmental Health Criteria 203, Chrysotile Asbestos, Geneva, World Health Organization, International Programme on Chemical Safety, p 29

  • Iturbe-Ormaetxe I, Moran JF, Arrese-Igor C, Gogorcena Y, Klucas RV, Becana M (1995) Activated oxygen and antioxidant defences in iron-deficient pea plants. Plant Cell Environ 18:421–429

    Article  CAS  Google Scholar 

  • Jagtap V, Bhargava S (1995) Variation in the antioxidant metabolism of drought tolerant and drought susceptible varieties of Sorghum bicolor (L) Moench expressed to high light, low water and high temperature stress. J Plant Physiol 145:195–197

    CAS  Google Scholar 

  • Kamp DW, Graceffa P, Pryor WA, Weitzman SA (1992) The role of free radicals in asbestos-induced diseases. Free Rad Biol Med 12:293–315

    Article  CAS  Google Scholar 

  • Knorzer OC, Durner J, Boger P (1996) Alterations in the antioxidative system of suspension-cultured soybean cells (Glycine max) induced by oxidative stress. Physiol Plant 97:388–396

    Article  Google Scholar 

  • Kumari A, Sinha RK, Gopal K, Prasad K (2001) Dietary intake of persistent organic chlorine residue through gangetic fishes in India. Int J Eco Environ Sci 27:117–120

    Google Scholar 

  • Lehman PW, Silk WK, Knight AW (1981) Protein and nitrate content of Lemna sp. as a function of developmental stage and incubation temperature. Plant Physiol 68:127–132

    CAS  Google Scholar 

  • Lichtenthaler HK (1996) Vegetation stress: An introduction to the stress concept in plants. J Plant Physiol 148:4–14

    CAS  Google Scholar 

  • Light WG, Wei ET (1977) Surface charge and asbestos toxicity. Nature 265:537–539

    Article  CAS  Google Scholar 

  • Mabagwu IG, Adeniji HA (1988) The nutritional content of duckweed (Lemna pausicostata Hogelm) in the Kainji Lake area. Nigeria Aquat Bot 29:357–366

    Article  Google Scholar 

  • Mahan JR (1994) Thermal dependence of glutathione reductase: Thermal limitations on antioxidant protection in plants. Crop Sci 34:1550–1556

    Article  CAS  Google Scholar 

  • Majid FZ, Khatun R, Akhtar N, Rehman A (1984) Aquatic weeds as source of protein in Bangladesh. In: Singh N (ed), Progress in leaf protein research. Today and Tomorrow Printers and Publishers, New Delhi, pp 91–94

    Google Scholar 

  • Marrs KA (1996) The function and regulation of glutathione S-transferase in plants. Ann Rev Plant Physiol Plant Mol Biol 47:127–158

    Article  CAS  Google Scholar 

  • Mossman BT, Marsh JP, Shatos MA (1986) Alteration of superoxide dismutase activity in tracheal epithelial cells by asbestos and inhibition of cytotoxicity by antioxidants. Lab Invest 54:204–212

    CAS  Google Scholar 

  • Nasu Y, Kugimoto M (1981) Lemna (duckweed) as an indicator of water pollution. I. The sensitivity of Lemna paucicostata to heavy metals. Arch Environ Contam Toxicol 19:159–169

    Article  Google Scholar 

  • NIPHEP (1989) National Institute for Public Health and Environmental Protection, The Netherlands, Report No. 758473013

  • Okamura M (1980) An improved method for determination of L-ascorbic acid and L-dehydroascorbic acid in blood plasma. Clin Chim Acta 103:259–268

    Article  CAS  Google Scholar 

  • Oron G, Wildschut LR, Porath D (1985) Waste water recycling by duckweed for protein production and effluent renovation. Water Sci Technol 17:803–817

    CAS  Google Scholar 

  • Paranhos A, Fernandez-Tarrago J, Corchete P (1999) Relationship between active oxygen species and cardenolide production in cell cultures of Digitalis thapsi: Effect of calcium restriction. Phytol 141:51–60

    Article  CAS  Google Scholar 

  • Pinhero RG, Rao MV, Paliyath G, Murr DP, Fletcher RA (1997) Changes in activities of antioxidant enzymes and their relationship to genetic and paclobutrazol-induced chilling tolerance of maize seedlings. Plant Physiol 114:695–704

    CAS  Google Scholar 

  • Prasad TK, Anderson MD, Martin BA, Stewart CR (1994) Evidence for chilling-induced oxidative stress in maize seedlings and a regulatory role for hydrogen peroxide. Plant Cell 6:65–74

    Article  CAS  Google Scholar 

  • Prescott DM (1982) Cancer, the misguided cell. Charles Scribner’s Sons, New York

    Google Scholar 

  • Price A, Lucas PW, Lea PJ (1990) Age dependent damage and glutathione metabolism in ozone fumigated barley: A leaf section approach. J Exp Bot 41:1309–1317

    Article  CAS  Google Scholar 

  • Rahman Q, Ahmad I, Rastogi SK, Trivedi AK, Musthapa MS, Shankar P (2001) Environmental monitoring and ecological impact assessment of asbestos (report: I). Submitted to Ministry of Environment and Forests (Govt of India), New Delhi

  • Ramnathan AL, Subramanian V (2001) Present status of asbestos mining and related health problems in India—A survey. Ind Health 39:309–315

    Google Scholar 

  • Rauser WE (1995) Phytochelatin and related peptides. Plant Physiol 109:1141–1149

    Article  CAS  Google Scholar 

  • Shalata A, Tal M (1998) The effect of salt stress on lipid peroxidation and antioxidants in the leaf of the cultivated tomato and its wild salt tolerant relative Lycopersicon pennelli. Physiol Plant 104:169–174

    Article  CAS  Google Scholar 

  • Sharma YK, Davis KR (1995) Ozone induced expression of stress related genes in Arabidopsis thaliana. Plant Physiol 105:1089–1096

    Google Scholar 

  • Speil S, Leinweber JP (1969) Asbestos minerals in modern technology. Environ Res 2:166–208

    Article  CAS  Google Scholar 

  • Spychalla JP, Desborough SL (1990) Superoxide dismutase, catalase, and α-tocopherol content of stored potato tubers. Plant Physiol 94:1214–1218

    Article  CAS  Google Scholar 

  • Teisseire H, Vernet G (2000) Ascorbate and glutathione contents in duckweed, Lemna minor, as biomarkers of stress generated by copper, folpet and diuron. Biomarkers 5:263–273

    Article  CAS  Google Scholar 

  • Torsethaugen G, Pitcher LH, Zhanska BA, Pell EJ (1997) Overproduction of ascorbate peroxidase in the tobacco chloroplast does not provide protection against ozone. Plant Physiol 114:529–537

    CAS  Google Scholar 

  • TRI 99 (2001) Toxic chemical release inventory. National Library of Medicine, National Toxicology Information Program, Bethesda, Maryland

  • Trivedi AK, Ahmad I, Musthapa MS, Ansari FA, Rahman Q (2004) Environmental contamination of chrysotile asbestos and its toxic effects on growth and physiological and Biochemical Parameters of Lemna gibba. Arch Environ Contam Toxicol 47:281–289

    Article  CAS  Google Scholar 

  • U.S. EPA (1975) U.S. Environmental Protection Agency, Test methods for assessing the effects of chemicals on plants. Report no. EPA 560/5-75-008 Environment Protection Agency, Washington, DC

  • U.S. EPA (1985) U.S. Environmental Protection Agency, Lemna acute toxicity test, Fed. Regist. 50:39331–39333

  • U.S. EPA (1993) U.S. Environmental Protection Agency, Test method for the determination of asbestos in bulk building materials. U.S. Environmental Protection Agency, Washington, DC, EPA 600/R-93/116

  • Willekens H, Langebartels C, Tire D, Van Montagu M, Inze D, Van Camp W (1994a) Differential expression of catalase genes in Nicotiana plumbaginifolia (L.). Proc Natl Acad Sci USA 91:10450–10454

    Article  CAS  Google Scholar 

  • Willekens H, Van Camp W, Van Montagu M, Inze D, Langebartels C, Sandermann H (1994b) Ozone, sulphur dioxide and ultraviolet B have similar effects on mRNA accumulation of antioxidant gene in Nicotiana plumbaginifolia (L.). Plant Physiol 106:1007–1014

    CAS  Google Scholar 

  • Williamson JD, Scandalios JG (1992) Differential responses of maize catalase and superoxide dismutases to the photoactivated fungal toxin cercosporin. Plant J 2:351–358

    CAS  Google Scholar 

  • Zhang J, Kirkham MB (1996) Lipid peroxidation in sorghum and sunflower seedlings as affected by ascorbic acid, benzoic acid, and propyl gallate. J Plant Physiol 149:489–493

    CAS  Google Scholar 

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Acknowledgments

Authors are thankful to Dr. P. K. Seth, Director, Industrial Toxicology Research Centre, Lucknow for his keen interest in the study and Mohd. M. Ashquin for his skillful technical assistance. Financial assistance from Ministry of Environment and Forests (Govt. of India), New Delhi is also gratefully acknowledged.

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Trivedi, A.K., Ahmad, I., Musthapa, M.S. et al. Environmental Contamination of Chrysotile Asbestos and Its Toxic Effects on Antioxidative System of Lemna gibba . Arch Environ Contam Toxicol 52, 355–362 (2007). https://doi.org/10.1007/s00244-006-0056-9

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