EFFECTS OF TEBUCONAZOLE ON LIVER AND INTESTINE OF FRESHWATER FISH Cyprinus carpio (Linnaeus, 1758)
DOI:
https://doi.org/10.48165/abr.2024.26.01.37Keywords:
Aquatic ecosystem, Cyprinuscarpio,, histopathology, tebuconazoleAbstract
The wide application of fungicides in agriculture and human medicines have raised environmental concerns and potential impact on aquatic ecosystem. Tebuconazole is a broad-spectrum fungicide used as curative and protective against several fungal pathogens. However, owing to its environmental persistence, it can have long term adverse effects. The present study was aimed to assess the toxic effects of tebuconazole on the digestive system of fish carp Cyprinus carpio. The fish were exposed to 6.47 and 8.09 µL L-1 concentrations of tebuconazole for 30 days. Biochemical parameters viz., lipid peroxidation, protein content, glutathione-s-transferase and phosphatases were determined in the liver and intestine of carp on exposure to tebuconazole. Histopathological analysis was also performed. Reduction in protein and glutathione-s-transferase was observed in time- and dose-dependent manner which may cause rise in lipid peroxides and oxidative stress. Acid and alkaline phosphatase showed elevated activity during the entire exposure time. Significant alterations in the histology of hepatic and intestinal tissues were observed including nuclear alteration, vacuolation and cytoplasmic degeneration in hepatocytes and mucosal alterations in intestine. The result revealed that tebuconazole not only altered the enzymatic activity but also caused oxidative stress and cellular damage. The results confirm the severe damage to fish organs due to tebuconazole, thereby revealing potential impact on aquatic environment.
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Atli, G. and Canli, M. 2007. Enzymatic responses to metal exposures in a freshwater fish Oreochromis niloticus. Comparative Biochemistry and Physiology Part C: Toxicology and Pharmacology, 145: 282-287.
Banerjee, S. and Bhattacharya, S. 1995. Histopathological changes induced by chronic nonlethal levels of elsan, mercury, and ammonia in the small intestine of Channa punctatus (Bloch). Ecotoxicology and Environmental Safety, 31: 62-68.
Bertahas, I., Dimitriou, E., Karaouzas, I., Laschou, S. and Zacharias, I. 2006. Climate change and agricultural pollution effects on the trophic status of a Mediterranean lake. Acta Hydrochimica et Hydrobiologica, 34: 349-359.
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: 248-254.
Clasen, B., Loro, V.L., Murussi, C.R., Tiecher, T.L., Moraes, B. and Zanella, R. 2018. Bio- accumulation and oxidative stress caused by pesticides in Cyprinus carpio reared in a rice-fish system. Science of the Total Environment, 626: 737-743.
Das, S.K. and Chakrabarty, D. 2007. The use of fish community structure as a measure of ecological degradation: A case study in two tropical rivers of India. Biosystems, 90: 188-196.
Dey, S., Samanta, P., Pal, S., Mukherjee, A.K., Kole, D. and Ghosh, A.R. 2016. Integrative assessment of biomarker responses in teleostean fishes exposed to glyphosate-based herbicide (Excel Mera 71). Emerging Contaminants, 2: 191-203.
Dhindsa, R. S., Plumb-Dhindsa, P. A. M. E. L. A. and Thorpe, T. A. 1981. Leaf senescence: correlated with increased levels of membrane permeability and lipid peroxidation, and decreased levels of superoxide dismutase and catalase. Journal of Experimental Botany, 32: 93-101.
Dinu, D., Marinescu, D., Munteanu, M.C., Staicu, A.C., Costache, M. and Dinischiotu, A. 2010. Modulatory effects of deltamethrin on antioxidant defense mechanisms and lipid peroxidation in Carassius auratus gibelio liver and intestine. Archives of Environmental Contamination and Toxicology, 58: 757-764.
George, S.G. and Buchanan, G. 1990. Isolation, properties and induction of plaice liver cytosolic glutathione-s-transferases. Fish Physiology and Biochemistry, 8: 437-449.
Habig, W. H., Pabst, M. J. and Jakoby, W. B. 1974. Glutathione S-transferases: the first enzymatic step in mercapturic acid formation. Journal of Biological Chemistry, 249: 7130-7139.
Hadi, A.A. and Alwan, S.F. 2012. Histopathological changes in gills, liver and kidney of fresh water fish, Tilapia zillii, exposed to aluminum. International Journal of Pharmacy and Life Sciences, 3: 2071-2081.
Helfrich, L.A., Weigmann, D.L., Hipkins, P.A. and Stinson, E.R. 2009. Pesticides and aquatic animals: A guide to reducing impacts on aquatic systems. Virginia Cooperation Extension, 420: 1-24.
Jiang, H., Yang, H., Kong, X., Wang, S., Liu, D. and Shi, S. 2012. Response of acid and alkaline phosphatase activities to copper exposure and recovery in freshwater fish Carassius auratus gibelio var. Life Science Journal, 9: 233-245.
Jos, A., Pichardo, S., Prieto, A.I., Repetto, G., Vazquez, C.M., Moreno, I. and Camean, A.M. 2005. Toxic cyanobacterial cells containing microcystins induce oxidative stress in exposed tilapia fish (Oreochromis sp.) under laboratory conditions. Aquatic Toxicology, 72: 261-271.
Karan, V., Vitorovic, S., Tutundzic, V. and Poleksic, V. 1998. Functional enzymes activity and gill histology of carp after copper sulfate exposure and recovery. Ecotoxicology and Environmental Safety, 40: 49-55.
Kruatrachue, M., Rangsayatorn, N., Pokethitiyook, P., Upatham, E.S. and Singhakaew, S. 2003. Histopathological changes in the gastrointestinal tract of fish, Puntius gonionotus, fed on dietary cadmium. Bulletin of Environmental Contamination and Toxicology, 71: 561-569.
Kumar, N., Awoyemi, O., Willis, A., Schmitt, C., Ramalingam, L., Moustaid‐Moussa, N. and Crago,
J. 2019. Comparative lipid peroxidation and apoptosis in embryo‐larval zebrafish exposed to 3 azole fungicides, tebuconazole, propiconazole, and myclobutanil, at environmentally relevant concentrations. Environmental Toxicology and Chemistry, 38: 1455-1466.
Lanjewar, K.H., Zade, S.B., Bhaisare, L.Y. and Chaudhary, D.D. 2023. Impact of hexaconazole on histo-architecture of liver and intestine of freshwater African catfish, Clarias gariepinus (Burchell, 1822). Biochemical and Cellular Archives, 23: 639-646.
Latif, A., Ali, M., Sayyed, A.H., Iqbal, F., Usman, K., Rauf, M. and Kaoser, R. 2013. Effect of copper sulphate and lead nitrate, administered alone or in combination, on the histology of liver and kidney of Labeo rohita. Pakistan Journal of Zoology, 45: 913-920.
Li, S., Jiang, Y., Sun, Q., Coffin, S., Chen, L., Qiao, K. and Zhu, G. 2020. Tebuconazole induced oxidative stress related hepatotoxicity in adult and larval zebrafish (Danio rerio). Chemosphere, 241: 125-129.
Li, S., Sun, Q., Wu, Q., Gui, W., Zhu, G. and Schlenk, D. 2019. Endocrine disrupting effects of tebuconazole on different life stages of zebrafish (Danio rerio). Environmental Pollution, 249: 1049-1059.
Lushchak, V.I. 2011. Environmentally induced oxidative stress in aquatic animals. Aquatic Toxicology, 101: 13-30.
Macirella, R., Curcio, V., Ahmed, A.I.M., Pellegrino, D. and Brunelli, E. 2022. Effect of short-term exposure to low concentration of tebuconazole: Morphological, histometric and functional modifications in Danio rerio liver. The European Zoological Journal, 89: 331-345.
Mateos, R. and Bravo, L. 2007. Chromatographic and electrophoretic methods for the analysis of biomarkers of oxidative damage to macromolecules (DNA, lipids, and proteins). Journal of Separation Science, 30: 175-191.
Mela, M., Randi, M.A.F., Ventura, D.F., Carvalho, C.E.V., Pelletier, E. and Ribeiro, C.O. 2007. Effects of dietary methylmercury on liver and kidney histology in the neotropical fish Hoplias malabaricus. Ecotoxicology and Environmental Safety, 68: 426-435.
Narra, M.R. 2016. Single and cartel effect of pesticides on biochemical and haematological status of
Clarias batrachus: A long-term monitoring. Chemosphere, 144: 966-974.
Oguz, E.K., Ergoz, B. and Oguz, A.R. 2022. Histopathological alterations in Van fish (Alburnus tarichi Guldenstadt, 1814) exposed to tebuconazole. Chemistry and Ecology, 38: 17-26.
Oruc, E. 2012. Oxidative stress responses and recovery patterns in the liver of Oreochromis niloticus exposed to chlorpyrifos-ethyl. Bulletin of Environmental Contamination and Toxicology, 88: 678-684.
Pacheco, M. and Santos, M.A. 2002. Biotransformation, genotoxic, and histopathological effects of environmental contaminants in European eel (Anguilla anguilla L.). Ecotoxicology and Environmental Safety, 53: 331-347.
Patil, V.K. and David, M. 2013. Oxidative stress in freshwater fish, Labeo rohita as a biomarker of malathion exposure. Environmental Monitoring and Assessment, 18: 10191-10199.
Ram, R.N. and Sathyanesan, A.G. 1987. Histopathological and biochemical changes in the liver of a teleost fish, Channa punctatus (Bloch) induced by a mercurial fungicide. Environmental Pollution, 47: 135-145.
Sancho, E., Villarroel, M.J., Fernández, C., Andreu, E. and Ferrando, M.D. 2010. Short-term exposure to sublethal tebuconazole induces physiological impairment in male zebrafish (Danio rerio). Ecotoxicology and Environmental Safety, 73: 370-376.
Sastry, K.V. and Gupta, P.K. 1978. Histopathological and enzymological studies on the effects of chronic lead nitrate intoxication in the digestive system of a freshwater teleost, Channa punctatus. Environmental Research, 17: 472-479.
Shaheen, T. and Akhtar, T. 2012. Assessment of chromium toxicity in Cyprinus carpio through hematological and biochemical blood markers. Turkish Journal of Zoology, 36: 682-690.
Subbiah, S., Ramesh, M., Ashokan, A.P. and Narayanasamy, A. 2020. Acute and sublethal toxicity of an azole fungicide tebuconazole on ionic regulation and Na+/K+-ATPase activity in a freshwater fish Cirrhinus mrigala. International Journal of Fisheries and Aquatic Studies, 8: 361-371.
Tabassum, H., Dawood, A. Q., Sharma, P., Khan, J., Raisuddin, S. and Parvez, S. 2016. Multi-organ toxicological impact of fungicide propiconazole on biochemical and histological profile of freshwater fish Channa punctata Bloch. Ecological Indicators, 63: 359-365.
Toni, C., Ferreira, D., Kreutz, L.C., Loro, V.L. and Barcellos, L.J.G. 2011. Assessment of oxidative stress and metabolic changes in common carp (Cyprinus carpio) acutely exposed to different concentrations of the fungicide tebuconazole. Chemosphere, 83: 579-584.
Troncoso, I.C., Cazenave, J., Bacchetta, C. and Bistoni, M.D.L.A. 2012. Histopathological changes in the gills and liver of Prochilodus lineatus from the Salado river basin (Santa Fe, Argentina). Fish Physiology and Biochemistry, 38: 693-702.
Velmurugan, B., Selvanayagam, M., Cengiz, E.I. and Unlu, E. 2007. Histopathology of lambda- cyhalothrin on tissues (gill, kidney, liver and intestine) of Cirrhinus mrigala. Environmental Toxicology and Pharmacology, 24: 286-291. [10.1016/j.etap.2007.07.001].
Wang, G., Xiong, D., Wu, M., Wang, L. and Yang, J. 2020. Induction of time-and dose-dependent oxidative stress of triazophos to brain and liver in zebrafish (Danio rerio). Comparative Biochemistry and Physiology Part C: Toxicology and Pharmacology, 228: 108640. [https://doi.org/10.1016/j.cbpc.2019.108640].
Weil, L. and Russel, M.A. 1940. Studies on plasma phosphate activity in relation to fat metabolism in rats. Journal of Biological Chemistry, 136: 9-16.
Yadav, S., Haldar, S. and Mohapatra, A.K. 2019. Monocrotophos induced histopathological and biochemical changes in gills, stomach and intestine of Anabas testudineus (Cuvier). Journal of Applied and Natural Science, 11: 534-544.
Yang, C., Lim, W. and Song, G. 2020. Mediation of oxidative stress toxicity induced by pyrethroid pesticides in fish. Comparative Biochemistry and Physiology Part C: Toxicology and Pharmacology, 234: 108758. [https://doi.org/10.1016/j.cbpc.2020.108758].
Yu, L., Chen, M., Liu, Y., Gui, W. and Zhu, G. 2013. Thyroid endocrine disruption in zebrafish larvae following exposure to hexaconazole and tebuconazole. Aquatic Toxicology, 138: 35-42.
Zahran, E., Risha, E., Awadin, W. and Palic, D. 2018. Acute exposure to chlorpyrifos induces reversible changes in health parameters of Nile tilapia (Oreochromis niloticus). Aquatic Toxicology, 197: 47-59.