Kurşuna Maruz Bırakılan Gammarus pulex’de Antioksidan Enzim Yanıtları

Bu çalışmada, kurşuna maruz bırakılan G. pulex'de süperoksit dismutaz, katalaz ve glutatyon peroksidaz antioksidan enzimlerinin aktivite yanıtlarının araştırılması amaçlanmaktadır.  G. pulex, 96 saat boyunca 10, 30, 50 µg/L kurşun içeren sentetik çözeltilere maruz bırakılmıştır.  Süperoksit dismutaz, katalaz ve glutatyon peroksidaz aktiviteleri ELISA kiti kullanılarak belirlenmiştir.  Süperoksit dismutaz aktivitelerindeki değişimler istatistiksel olarak anlamlı bulunmamıştır (P>0.05). Kurşuna maruz bırakıldıktan sonra tüm uygulama gruplarında katalaz aktiviteleri azalmıştır (P<0.05).  Glutatyon peroksidaz aktiviteleri kurşun maruziyetine bağlı olarak azalmıştır (P>0.05).  Bulgularımız, reaktif oksijen türleri üreterek ve sülfhidril bağımlı antioksidan enzim aktivitelerini inhibe ederek kurşunun oksidatif strese neden olabileceğini göstermektedir.  Sonuç olarak, antioksidan enzimlerdeki değişiklikler, kurşunun çevresel risk değerlendirmesi için potansiyel olarak hassas biyobelirteçler olarak kullanılabilir ve deşarj standartlarının oluşturulmasına katkıda bulunabilir.

Antioxidant Enzyme Responses to Lead Exposure of Gammarus pulex

It is aimed to investigate the activity response of the antioxidant enzymes superoxide dismutase, catalase and glutathione peroxidase of G. pulex exposed to lead.  The G. pulex were exposed synthetic solutions containing 10, 30, 50 µg/L lead for 96 h.  Superoxide dismutase, catalase, glutathione peroxidase activities were determined by using ELISA kit.  The differences in superoxide dismutase activities were statistically insignificant (P>0.05).  Catalase decreased in all treatment groups after lead exposure (P<0.05).  The glutathione peroxidase activities were decreased depending on lead exposure (P>0.05).  Our findings suggest that lead can induce oxidative stress by generating reactive oxygen species and inhibiting sulfhydryl dependent antioxidant enzymes activities.  In conclusion, alterations in antioxidant enzymes may potentially be used as sensitive biomarkers for risk assessment of lead in the environment and may contribute to the establishment of discharge regulations.

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  • Adonaylo, V.N. & Oteiza, P.I. (1999). Lead intoxication: antioxidant defenses and oxidative damage in rat brain. Toxicology, 135, 77-85.
  • Ahmad, I., Hamid, T., Fatima, M., Chand, H.S., Jain, S.K., Athar, M. & Raisudd, S. (2000). Induction of hepatic antioxidants in freshwater catfish (Channa punctatus bloch) is a biomarker of paper mill effluent exposure. Biochimica et Biophysica Acta, 1523, 37-48.
  • Blokhina, O., Virolainen, E. & Fagerstedt, K.V. (2003). Antioxidants, oxidative damage and oxygen deprivation stress: a review. Annals of Botany, 91, 179–194. Carocci A., Catalano A., Lauria G., Sinicropi M.S. & Genchi G. (2016). Lead toxicity, antioxidant defense and environment, P. de Voogt (ed.). Reviews of Environmental Contamination and Toxicology, 238, XVI, 123p.
  • Chaurasia S.S. & Kar A. (1997a). Protective effects of vitamin E against lead induced deterioration of membrane associated type-1 iodothyronine 5’ monodeiodinase (5’D-I) activity in male mice. Toxicology, 124, 203-209.
  • Chaurasia S.S. & Kar A. (1997b). Influence of lead on type I iodothyromne 5’ monadeoidinase activity in male Mouse. Hormone and Metabolic Research, 29, 532-533. Chiba M., Shinohara A.K., Matsushita Watanabe H. & Inaba Y. (1996). Indices of lead exposure in blood and urine of lead-exposed workers and concentrations of major and trace elements and activities of SOD, GSH-Px and catalase in their blood. The Tohoku Journal of Experimental Medicine, 178, 49-62.
  • Courtois E., Marques M. & Barrientos A. (2003). Lead-induced downregulation of soluble guanylate cyclase in isolated rat aortic segments mediated by reactive oxygen species and cyclooxygenase- 2. Journals of the American Society of Nephrology, 14, 1464–1470.
  • Ercal N., Gürer-Orhan H. & Aykin-Burns N. (2001). Toxic metals and oxidative stress part I: mechanisms involved in metal-induced oxidative damage. Current Topics in Medicinal Chemistry, 6, 529-539.
  • Farmand F., Ehdaie A., Roberts C.K. & Sindhu R.K. (2005). Lead-induced dysregulation of superoxide dismutases, catalase, glutathione peroxidase, and guanylate cyclase. Environmental Research, 98, 33–39.
  • Feldman R.G. & White R.F. (1992). Lead Neurotoxicity and Disorders of Learning. Journal of Child Neurology, 7, 354-359.
  • Flora S.J.S. (2009). Structural, chemical and biological aspects of antioxidants for strategies against metal and metalloid exposure. Oxidative Medicine and Cellular Longevity, 2, 191–206.
  • Flora S.J.S., Pachauri V. & Saxena G. (2011). Arsenic, cadmium and lead. Reproductive and Developmental Toxicology, 33, 415–438.
  • Gaetani G.F., Kirkman H.N., Mangerini R. & Ferraris A.M. (1994). Importance of catalase in the disposal of hydrogen peroxide within human erythrocytes. Blood, 84, 325-330.
  • Gidlow D.A. (2015). Lead toxicity. Occupational Medicine, 65, 348-356.
  • Gürer H. & Ercal N. (2000). Can antioxidant be beneficial in the treatment of lead poisoning?. Free Radical Biology & Medicine, 29, 927-945.
  • Güven K., Özbay C., Ünlü E. & Satar A. (1999). Acute lethal toxicity and accumulation of copper in Gammarus pulex (L.) (amphipoda). Turkish Journal of Biology, 23(4): 513-521.
  • Hsu P.C. & Guo Y.L. (2002). Antioxidant Nutrients and Lead Toxicity. Toxicology, 180, 33-44. Kasperczyk S., Birkner E., Kasperczyk A. & Zalejska-Fiolka J. (2004). Activity of superoxide dismutase and catalase in people protractedly exposed to lead compounds. Annals of Agricultural and Environmental Medicine, 11, 291-296.
  • Koller L.D. (1990). The immunotoxic effects of lead in lead exposed laboratory animals. Annals of the New York Academy of Sciences, 587, 160-167.
  • Latha M. & Pari L. (2004). Effect of an aqueous extract of scoparia dulcis on blood glucose, plasma insulin and some polyol pathway enzymes in experimental rat diabetes. Brazilian Journal of Medical and Biological Research, 37, 577-586.
  • Liebler D.C. & Reed D.J. (1997). Free-radical defense and repair mechanisms. Free Radicals in Toxicology, 141-171.
  • Michiels C., Raes M., Toussaint O. & Remacle J. (1994). Importance of Se–glutathione peroxidase, catalase and Cu/Zn SOD for cell survival against oxidative stress. Free Radical Biology & Medicine, 17, 235–248.
  • Monteiro D.A., Rantin F.T. & Kalinin A.L. (2010). Inorganic mercury exposure: toxicological effects, oxidative stress biomarkers and bioaccumulation in the tropical freshwater fish matrinxã, Brycon amazonicus (Spix and Agassiz, 1829). Ecotoxicology, 19, 105-123.
  • Padmini E. & Rani M.U. (2009). Evaluation of oxidative stress biomarkers in hepatocytes of grey mullet inhabiting natural and polluted estuaries. Science of the Total Environment, 407, 4533-4541.
  • Patra R., Amiya C., Rautray K. & Swarup D. (2011). Oxidative stress in lead and cadmium toxicity and its amelioration. Veterinary Medicine International, 9 p., doi:10.4061/2011/457327.
  • Ruas C.B.G., Carvalho C.S., Araújo H.S.S., Espíndola E.L.G. & Fernandes M.N. (2008). Oxidative stress biomarkers of exposure in the blood of three cichlid species from a polluted river. Ecotoxicology and Environmental Safety, 71, 86-93.
  • Schlenk D., Davis K.B. & Griffin B.R. (1999). Relationship between expression of hepatic metallothionein and sublethal stress in channel catfish following acute exposure to copper sulphate. Aquaculture, 177, 367-379.
  • Sharma S., Sharma V. & Pracheta P.R. (2011). Lead toxicity, oxidative damage and health implications. a review. International Journal of Biotechnology and Molecular Biology Research, 2(13): 215-221.
  • Soltanianejad K., Kebriaeezadeh A. & Minaiee B. (2003). Biochemical and ultrastructural evidences for toxicity of lead through free radicals in rat brain. Human & Experimental Toxicology, 22, 417-433.
  • Tagliari K.C., Vargas V.M.F., Zimiani K. & Cecchini R. (2004). Oxidative stress damage in the liver of fish and rats receiving an intraperitoneal injection of hexavalent chromium as evaluated by chemiluminescence. Environmental Toxicology and Pharmacology, 17, 149-157.
  • Vaziri N.D., Lin C.Y., Farmand F. & Sindhu R.K. (2003). Superoxide dismutase, catalase, glutathione peroxidase and nadph oxidase in lead induced hypertension. Kidney International, 63, 186-194.
  • Wang H.P., Qian S.Y., Schafer F.Q., Domann F.E., Oberley L.W. & Buettner G.R. (2001). Phospholipid hydroperoxide glutathione peroxidase protects against singlet oxygen-induced cell damage of photodynamic therapy. Free Radical Biology & Medicine, 30, 825-835.
  • Weeks J.M. & Rainbow P.S. (1992). The effect of salinity on copper and zinc concentrations in three species of talitrid amphopods (crustacea). Comparative Biochemistry and Physiology, 101C, 399–405.
  • Williams P.L. & Dusenbery D.B. (1990). Aquatic toxicity testing using the nematode Caenorhabditis elegans. Environmental Toxicology and Chemistry, 9, 1285–1290. Yokoyama K., Araki S., Muraka M., Morita Y., Katsuno N., Tanigawa T., Mori N., Yokota J., Ito A. & Sakata E. (1997). Subclinical vestibulo-cerebellar, anterior cerebellar lobe and spinocerebellar effects in lead workers in relation to current and past exposure. Neurotoxicology, 18(2): 371-380.
  • Yung L.M., Leung F.P., Yao X., Chen Z.Y. & Huang Y. (2006). Reactive oxygen species in vascular Wall. Cardiovascular & Haematological Disorders - Drug Targets, 6(1): 1–19.
Journal of Anatolian Environmental and Animal Sciences-Cover
  • Yayın Aralığı: Yılda 4 Sayı
  • Başlangıç: 2016
  • Yayıncı: Bülent VEREP
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