The impact of goldfish exposure for 96 h to herbicide Gesagard 500 FW at concentrations 0.2, 1, or 5 mg L−1(corresponding to 0.1, 0.5 or 2.5 mg L-1 of effective compound prometryn) on the hematological profile of blood andbiochemical parameters of plasma and liver was studied. Fish exposure to low concentration of the herbicide (0.2 mg L-1)slightly decreased liver glycogen and plasma lactate levels. Plasma glucose levels rose by 27% in goldfish exposed to 1 mg L-1 Gesagard. The activity of lactate dehydrogenase decreased by 63% and 36% in plasma of fish exposed to herbicide atconcentrations 1 and 5 mg L-1, respectively, but was not affected in liver.Goldfish exposure to the highest concentration of Gesagard (5 mg L-1) decreased hematocrit by 23% and increasedmonocyte count by 57%, and elevated triacylglycerol level by 91% in plasma. Overall, the results indicate that acute exposureto Gesagard induced minor changes in the hematological and biochemical parameters of goldfish, suggesting that disruptionsof these parameters may provide early warning signs that could be useful for assessing acute or sublethal toxic effects ofpesticides on aquatic species.
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Bakker, J., & de Lima, A.P. (2004). Increased blood lacate levels: an important warning signal in surgical practice. Critical care, 8(2), 96-98. http://dx.doi.org/ 10.1186/cc2841.
Banaee, M., Mirvagefei, A.R., Rafei, G.R., & Amiri B.M. (2008). Effect of sub-lethal diazinon concentrations on blood plasma biochemistry. International Journal of Environmental Research, 2(2), 189–198. Retrieved from http://www.bioline.org.br/pdf?er08025
Banaee, M., Sureda, A., Mirvaghefi, A.R., & Ahmadi, K. (2011). Effects of diazinon on biochemical parameters of blood in rainbow trout (Oncorhynchus mykiss). Pesticide Biochemistry and Physiology, 99(1), 1–6. http://dx.doi.org/10.1016/j.pestbp.2010.09.001
Bradford, M.M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analytical Biochemistry, 72(1-2), 248–254. http://dx.doi.org/10.1016/0003-2697(76)90527-3
Caquet, T., Roucaute, M., Mazzella, N., Delmas, F., Madigou, C., Farcy, E., & Gabellec, R. (2013). Risk assessment of herbicides and booster biocides along estuarine continuums in the Bay of Vilaine area (Brittany, France). Environmental Science and Pollution Research, 20(2), 651–666. http://dx.doi.org/ 10.1007/s11356-012-1171-y.
Chen, J., Cao, J., Wang, J., Jia, R., Xue, W., Li, Y., & Xie, L. (2013). Effects of fluoride on growth, body composition, and serum biochemical profile in a freshwater teleost, Cyprinus carpio. Environmental Toxicology and Chemistry, 32(10), 2315–2321. http://dx.doi.org/ 10.1002/etc.2305.
Cuddihee, R.W., & Fonda, M.L. (1982). Concentrations of lactate and pyruvate and temperature effects on lactate dehydrogenase activity in the tissues of the big brown bat (Eptesicus fuscus) during arousal from hibernation. Comparative Biochemistry and Physiology - Part B: Biochemistry & Molecular Biology, 73(4), 1001–1009. http://dx.doi.org/10.1016/0305-0491(82)90350-9
Das, P.C., McElroy, W.K., & Cooper, R.L. (2000). Differential modulation of catecholamines by chlorotriazine herbicides in pheochromocytoma (PC12) cells in vitro. Toxicological Sciences, 56(2), 324–331. Retrieved from https://academic.oup.com/toxsci/article/56/2/324/1653 373
DeLorenzo, M.E., Scott, G.I., & Ross, P.E. (2001). Toxicity of pesticides to aquatic microorganisms: a review. Environmental Toxicology and Chemistry, 20(1), 84– 98. http://dx.doi.org/10.1002/etc.5620200108
Dikić, D. (2014). Prometryn. In: P. Wexler (Ed). Encyclopedia of Toxicology (pp. 1077–1081). 3rd ed. Elsevier Inc., Academic Press. 5220 pp.
Dikić, D., Benković, V., Horvat-Knežević, A., Brozović, G., Oršolić, N., & Springer, O.P. (2009a). Subchronic oral exposure to prometryne changes relations of blood biochemistry indicators in mice. Acta Veterinaria Brno, 78(2), 243– 251. https://doi.org/10.2754/avb200978020243
Dikić, D., Zidovec-Lepej, S., Remenar, A., Bendelja, K., Benković, V., Horvat-Knežević, A., & Oršolić, N. (2009b). Effects of prometryne on apoptosis and necrosis in thymus, lymph node and spleen in mice. Environmental Toxicology and Pharmacology, 27(2), 182–186. http://dx.doi.org/10.1016/j.etap.2008.10.002.
Erickson,W., & Turner, L. (2002). Prometryn analysis of risks to endangered and threatened Salmon and Steelhead. Environmental Field Branch, Office of Pesticide Programs, 71 pp.
Fırat, Ö., Cogun, H.Y., Yüzereroğlu, T.A., Gök, G., Fırat, Ö., Kargin, F., & Kötemen, Y. (2011). A comparative study on the effects of a pesticide (cypermethrin) and two metals (copper, lead) to serum biochemistry of Nile tilapia, Oreochromis niloticus. Fish Physiology and Biochemistry, 37(3), 657–666. http://dx.doi.org/ 10.1007/s10695-011-9466-3
Fazio, F., Piccione, G., Tribulato, K., Ferrantelli, V., Giangrosso, G., Arfuso, F., & Faggio, C. (2014). Bioaccumulation of heavy metals in blood and tissue of striped mullet in two Italian lakes. Journal of Aquatic Animal Health, 26 (4), 278–284. http://afs.tandfonline.com/doi/abs/10.1080/08997659. 2014.938872#.WU063nJSDI
Hostovsky, M., Blahova, J., Plhalova, L., Kopriva, V., & Svobodova, Z. (2014). Effects of the exposure of fish to triazine herbicides. Neuroendocrinology Letters, 35(2:3), 3–25. Retrieved from http://www.nel.edu/archive_issues/o/35_s2/35_s2_Ho stovsky_3-25.pdf
Husak, V.V., Mosiichuk, N.M., Maksymiv, I.V., Sluchyk, I.Y., Storey, J.M., Storey, K.B., & Lushchak, V.I. (2014). Histopathological and biochemical changes in goldfish kidney due to exposure to the herbicide Sencor may be related to induction of oxidative stress. Aquatic Toxicology, 155, 181–189. http://dx.doi.org/10.1016/j.aquatox.2014.06.020
Ivanova, N.T. (1983). Atlas of Blood Cells in Fish. Comparative Morphology and Classification of Blood Corpuscles. Moscow, 80 pp.
Kumar, N., Sharma, R., Tripathi, G., Kumar, K., Dalvi, R.S., & Krishna, G. (2016). Cellular metabolic, stress, and histological response on exposure to acute toxicity of endosulfan in Tilapia (Oreochromis mossambicus). Environmental Toxicology, 31(1), 106–115. http://dx.doi.org/10.1002/tox.22026
Loteste, A., Scagnetti, J., Simoniello, M.F., Campana, M., & Parma, M.J. (2013). Hepatic enzymes activity in the fish Prochilodus lineatus (Valenciennes, 1836) after sublethal cypermethrin exposure. Bulletin of Environmental Contamination and Toxicology, 90(5), 601–604. http://dx.doi.org/10.1007/s00128-013-0961-3
Lushchak, V.I., Bagnyukova, T.V., Storey, J.M., & Storey, K.B. (2001). Influence of exercise on the activity and distribution between free and bound forms of glycolytic and associated enzymes of horse mackerel. Brazilian Journal of Medical and Biological Research, 34(8), 1055–1064. http://dx.doi.org/10.1590/S0100- 879X2001000800013
Lushchak, O.V., Kubrak, O.I., Storey, J.M., Storey, K.B., & Lushchak, V.I. (2009). Low toxic herbicide Roundup induces mild oxidative stress in goldfish tissues. Chemosphere, 76(7), 932–937. http://dx.doi.org/10.1016/j.chemosphere.2009.04.04
Maksymiv, I.V., Husak, V.V., Mosiichuk, N.M., Matviishyn, T.M., Sluchyk, I.Y., Storey, J.M., … Lushchak, V.I. (2015). Hepatotoxicity of herbicide Sencor in goldfish may result from induction of mild oxidative stress. Pesticide Biochemistry and Physiology, 122, 67–75.
http://dx.doi.org/10.1016/j.pestbp.2014.12.020
Martinez-Porchas, M., Martinez-Cordova, L.R., & Ramos- Enriquez, R. (2009). Cortisol and glucose: reliable indicators of fish stress. Pan-American Journal of Aquatic Sciences, 4(2), 158–178. Retrieved from http://www.panamjas.org/pdf_artigos/panamjas_4(2)_158-178.pdf
Mosiichuk, N.M., Husak, V.V., Maksymiv, I.V., Hlodan, O.Y., Storey, J.M., Storey, K.B., & Lushchak, V.I. (2015). Toxicity of environmental Gesagard to goldfish may be connected with induction of low intensity oxidative stress in concentration-and tissuerelated manners. Aquatic Toxicology, 165, 249–258. http://dx.doi.org/10.1016/j.aquatox.2015.06.007
Odo, G.E., Agwu, J.E., Ivoke, N., Ejere, V.C., Atama, C.I., & Anya, B.C. (2017). Effect of short term exposure to cyperdicot on behavioural and haematological responses in African catfish Clarias gariepinus. Turkish Journal of Fisheries and Aquatic Sciences, 17(1), 61–70. http://www.trjfas.org/uploads/pdf_973.pdf.
Oropesa, A.L., Garcia-Cambero, J.P., Gymez, L., Roncero, V., & Soler, F. (2009). Effect of long-term exposure to simazine on histopathology, hematological, and bio-chemical parameters in Cyprinus carpio. Environmental Toxicology, 24(2), 187–199. http://dx.doi.org/ 10.1002/tox.20412
Oruç, E.Ö., & Üner, N. (1999). Effects of 2,4-Diamin on some parameters of protein and carbohydrate metabolisms in the serum, muscle and liver of Cyprinus carpio. Environmental Pollution, 105(2), 267–272.
Parkinson, A., & Ogilvie, B. (2007). Biotransformation of Xenobiotics. In: L. Casarett, C. Klaassen & J. Doull (Eds.). Casarett and Doull's toxicology: the basic science of poisons (pp. 161–304). 7th ed. New York, McGraw-Hill Professional.
Phypers, B., & Pierce, J.T. (2006). Lactate physiology in health and disease. Continuing Education in Anaesthesia, Critical Care and Pain, 6(3), 128–132. https://doi.org/10.1093/bjaceaccp/mkl018
Ptashynski, M.D., Pedlar, R.M., Evans, R.E., Baron, C.L., & Klaverkamp, J.F. (2002). Toxicology of dietary nickel in lake whitefish (Coregonus clupeaformis). Aquatic Toxicology, 58, 229–247. http://dx.doi.org/10.1016/S0166-445X(01)00239-9
Reitman, S., & Frankel, S. (1957). A colorimetric method for the determination of oxaloacetic acid glutmic pyruvic transaminase. American Journal of Clinical Pathology, 28(1), 53–56.
Saravanan, M., Prabhu Kumar K., & Ramesh, M. (2011). Haematological and biochemical responses of freshwater teleost fish Cyprinus carpio (Actinopterygii: Cypriniformes) during acute and chronic sublethal exposure to lindane. Pesticide Biochemistry and Physiology, 100(3), 206–211. http://dx.doi.org/10.1016/j.pestbp.2011.04.002
Stará, A., Kristan, J., Zuskova, E., & Velisek, J. (2013). Effect of chronic exposure to prometryne on oxidative stress and antioxidant response in common carp (Cyprinus carpio L.). Pesticide Biochemistry and Physiology, 105(1), 18–23. http://dx.doi.org/10.1016/j.pestbp.2012.11.002
Stará, A., Kouba, A., & Velíšek, J. (2014). Effect of chronic exposure to prometryne on oxidative stress andantioxidant response in red swamp crayfish (Procambarus clarkii). BioMed Research International, 2014(2014), 6p. http://dx.doi.org/10.1155/2014/680131
Suneetha, K. (2012). Effects of endosulfan and fenvalerate on carbohydrate metabolism of the freshwater fish, Labeo rohita (Hamilton). International Journal of Pharmacy and Pharmaceutical Sciences, 4(1), 262– 268. Retrieved from http://www.ijppsjournal.com/Vol4Issue1/2977.pdf
Svobodova, Z., & Pecena, M. (1988). Changes in the red and white blood picture of carp after acute exposure to toxic substance. Bull RIFCH Vodnany 17, 116–128.
Vasylkiv, O.Y., Kubrak, O.I., Storey, K.B., & Lushchak, V.I. (2010). Cytotoxicity of chromium ions may be connected with induction of oxidative stress. Chemosphere, 80(9), 1044–1049. http://dx.doi.org/10.1016/j.chemosphere.2010.05.023
Velisek, J., Svobodova, Z., Piackova, V., & Sudova, E. (2009). Effects of acute exposure to metribuzin on some hematological, biochemical and histopathological parameters of common carp (Cyprinus carpio L.). Bulletin of Environmental Contamination and Toxicology, 82(4), 492–495. http://dx.doi.org/10.1007/s00128-009-9648-1
Velisek, J., Stará, A., Kolarova, J., & Svobodova, Z. (2011). Biochemical, physiological and morphological responses in common carp (Cyprinus carpio L.) after long-term exposure to terbutryn in real environmental concentration. Pesticide Biochemistry and Physiology, 100(3), 305–313. http://dx.doi.org/10.1016/j.pestbp.2011.05.004
Velisek, J., Stara, A., Machova, J., & Svobodova, Z. (2012). Effects of long-term exposure to simazine in real concentrations on common carp (Cyprinus carpio L.). Ecotoxicology and Environmental Safety, 76, 79–86. http://dx.doi.org/10.1016/j.ecoenv.2011.10.013
Velisek, J., Stara, A., Zuskova, E., & Svobodova, Z. (2013). Use of biometric, hematologic, and plasma biochemical variables, and histopathology to assess the chronic effects of the herbicide prometryn on common carp. Veterinary Clinical Pathology, 42(4), 508–515. http://dx.doi.org/10.1111/vcp.12081
Vryzas, Z., Alexoudis, C., Vassiliou, G., Galanis, K., & Papadopoulou-Mourkidou, E. (2011). Determination and aquatic risk assessment of pesticide residues in riparian drainage canals in northeastern Greece. Ecotoxicology and Environmental Safety, 74(2), 174– 181. http://dx.doi.org/10.1016/j.ecoenv.2010.04.011
Zhao, Q., & Zhu, L. (2016). Effect of humic acid on prometryn bioaccumulation and the induction of oxidative stress in zebrafish (Danio rerio). RSC Advances, 6, 16790–16797. http://dx.doi.org/10.1039/C5RA21488B
Ural, M.Ş. (2013). Chlorpyrifos-induced changes in oxidant/antioxidant status and haematological parameters of Cyprinus carpio carpio: Ameliorative effect of lycopene. Chemosphere, 90(7), 2059–2064. http://dx.doi.org/10.1016/j.chemosphere.2012.12.006