Deltamethrin induced alterations of hematological and biochemical parameters in fingerlings of Catla catla (Ham.) and their amelioration by dietary supplement of vitamin C

Pesticide Biochemistry and Physiology

Volumn 101, Issue 1, 2011, Pages 16-20

  Vani, T ^a   Saharan, N ^a   Mukherjee, S C ^a   Ranjan, Ritesh ^a   Kumar, Rajesh ^a   Brahmchari, R K ^a  

^a CENTRAL INSTITUTE OF FISHERIES EDUCATION   (India)

Author keywords

Catla catla; Enzyme activities; Hematology; Pyrethroid; Toxicity; Vitamin C

Indexed keywords

CATLA CATLA; PISCES;

EID: 80052260933     PISSN: 00483575     EISSN: 10959939     Source Type: Journal    
DOI: 10.1016/j.pestbp.2011.05.007     Document Type: Article

References (51)

1. Erstfeld K.M. Environmental fate of synthetic pyrethroids during spray drift and field runoff treatments in aquatic microcosms. Chemosphere 1999, 39:1737-1969.
2. Kale M., Rathore N., John S., Bhatnagar D. Lipid peroxidation damage on pyrethroid exposure and alterations in antioxidant status in rat erythrocyte: a possible involvement of reactive oxygen species. Toxicol. Lett. 1999, 105:197-205.
3. Fotoui H., Garou E., Makni-ayadi F., Zeghal N. Oxidative stress induced by Lambda-cyhalothrin (LTC) in rat erythrocytes and brain attenuation by vitamin C. Environ. Toxicol. Pharmacol. 2008, 26:225-231.
4. IARC, IARC Monographs on the evaluation of the carcinogenic risk of chemicals to humans. Occupational exposures in insecticide application, and some pesticides, vol. 53, International Agency for Research on Cancer, Lyon, 1991, pp. 1-612.
5. C.T. Pimpão, A.R. Zampronio, H.C.S. de Assis, Exposure of Ancistrus multispinis (Regan, 1912, Pisces, Teleostei) to deltamethrin: Effects on cellular immunity, Fish Shellfish Immunol. 25 (2008) 528-532.
6. Ural M.Ş., Saĝlam N. A study on the acute toxicity of pyrethroid deltamethrin on the fry rainbow trout (Oncorhynchus mykiss Walbaum, 1792). Pestic. Biochem. Physiol. 2005, 83:124-131.
7. de Assis H.C.S., Nicareta L., Salvo L.M., Klemz C., Truppel J.H., Calegari R. Biochemical biomarkers of exposure to Deltamethrin in freshwater fish Ancistrus multispinis. Braz. Arch. Biol. Technol. 2009, 52:1401-1407.
8. Crane M., Maltby L. The lethal and sublethal responses of Gammarus pulex to stress: sensitivity and sources of variation in an in situ bioassay. Environ. Toxicol. Chem. 1991, 10:1331-1339.
9. Miren P., Cajaraville M.J., Bebianno J.B., Cinta P., Carmen S., Aldo V. The use of biomarkers to assess the impact of pollution in coastal environments of the Iberian peninsula: a practical approach. Sci. Total Environ. 2000, 247:295-311.
10. Rendón-von Osten J., Ortíz-Arana A., Guilhermino L., Soares A.M.V.M. In vivo evaluation of three biomarkers in the mosquitofish (Gambusia yucatana) exposed to pesticides. Chemosphere 2005, 58:627-636.
11. Thrall M.A. Veterinary Hematology and Clinical Chemistry 2004, Williams & Wilkins, Philadelphia, pp. 277-289.
12. Chatterjee I.B., Majunmder A.K., Nandi B.K., Subramanian N. Synthesis and major functions of vitamin C in animals. Ann. NY Acad. Sci. 1975, 258:24-48.
13. Blom J., Dabrowski K. Vitamin C requirements of the angelfish, Pterophylum scalare. J. World Aquacult. Soc. 2000, 31:115-118.
14. Garcia F., Pilarski F., Onaka E.M., Moraes F.R., Martins M.L. Hematology of Piaractus mesopotamicus fed diets supplemented with vitamins C and E, challenged by Aeromonas hydrophila. Aquaculture 2007, 271:39-46.
15. Datta M., Kaviraj A. Ascorbic acid supplementation of diet for reduction of deltamethrin induced stress in freshwater catfish Clarias gariepinus. Chemosphere 2003, 53:883-888.
16. Ortuño J., Esteban M.A., Meseguer J. The effect of dietary intake of vitamins C and E on the stress response of gilthead seabream, Sparus aurata. Fish Shellfish Immunol. 2003, 14:145-156.
17. Zhou X., Niu C., Sun R. The effect of vitamin C on stress withstanding capability in the juvenile soft-shelled turtle, Pelodicus sinensis. Aquacult. Nutr. 2005, 11:169-174.
18. D.L. Reish, P.A. Oshida, Manual of methods in aquatic environment research, Part 10, Short-term static bioassay, FAO Fisheries Technical Paper, 247. FAO, Rome, 1987 pp. 1-62.
19. W. Schaperclaus, H. Kulow, K. Schreckenbach, Hematological and serological technique, in: V.S. Kothekar (Eds.), Fish Disease, vol. 1, 2nd ed., Gulab Primlani, Oxonian Press, New Delhi, India, 1991, pp. 71-108.
20. Wroblewski L., Ladue J.S. LDH activity in blood. Proc. Soc. Exp. Biol. Med. 1955, 90:210-213.
21. I.D.P. Wotton, Microanalysis, in: Medical Biochemistry, 4th ed. J. & A. Churchill, London, 1964, pp. 101-107.
22. Hestrin L. The reaction of Acetyl choline esters and other carboxylic acid derivatives with hydroxylamine and its analytical application. J. Biol. Chem. 1949, 180:249-261.
23. Augustinsson K.B. Assay methods for cholinesterases. Methods Biochem. Anal. 1957, 5:1-63.
24. Post R.L., Sen A.K. Sodium and potassium-stimulated ATPase. Methods in Enzymology 1967, vol. 10:762-768. Academic Press, New York.
25. Fiske C.H., Subbarow Y. The colorimetric determination of phosphorus. J. Biol. Chem. 1925, 66:375-400.
26. Jenkins F., Smith J., Rajanna B., Shameem U., Umadevi K., Sandhya V., Madhavi R. Effect of sub lethal concentration of endosulfan on hematological and serum biochemical parameters in the carp, Cyprinus carpio. Bull. Environ. Contam. Toxicol. 2003, 70:993-997.
27. Svobodova Z., Luskova V., Drastichova J., Svoboda M., Zlabek V. Effect of deltamethrin on haematological indices of commom carp (Cyprinus carpio L.). Acta. Vet. Brno. 2003, 72:79-85.
28. Shakoori A.R., Mughal A.L., Iqbal M.J. Effects of sublethal doses of Fenvalerate (a synthetic pyrethroid) administered continuously for four weeks on the blood, liver and muscles of a freshwater fish, Ctenopharyngodon idella. Bull. Environ. Contam. Toxicol. 1996, 57:487-494.
29. Sopinska A., Guz L. Influence of permethrin on phagocytic activity of carp. Med. Wet. 1998, 54:126-128.
30. Ortuńo J., Esteban M.A., Meseguer J. Effect of high dietary intake of vitamin C on non-specific immune response of gilt head sea bream (Sparus aurata L.). Fish Shellfish Immunol 1999, 9:429-443.
31. Thompson I., White A., Fletcher T.C., Houlihan D.F., Secombes C.J. The effect of stress on the immune response of Atlantic salmon (Salmo salar L.) fed diets containing different amount of vitamin C. Aquaculture 1993, 114:1-18.
32. Agrawal N.K., Juneja C.J., Mahajan C.L. Protective role of ascorbic acid in fishes exposed to organochlorine pollution. Toxicolology 1978, 11:369-375.
33. Velisek J., Svobodova Z., Machova J. Effects of bifenthrin on some haematological, biochemical and histopathological parameters of common carp (Cyprinus carpio L.). Fish Physiol. Biochem. 2009, 35:583-590.
34. Jee L.H., Masroor F., Kang J.C. Response of cypermethrin-induced stress in haematological parameters of Korean rock fish, Sebastes schlegeli (Hilgendorf.). Aquac. Res. 2005, 36:898-905.
35. Hussein S.Y., El-Nasser M.A., Ahmed S.M. Comparative studies on the effects of herbicide Atrazine on freshwater fish Oreochromis niloticus and Chrysichthyes auratus at Assiut. Egypt. Bull. Environ. Contam. Toxicol. 1996, 57:503-510.
36. D.P. Anderson, A.K. Siwicki, Basic haematology and serology for fish health programs, In: M. Shariff, J.R. Arthur, R.P. Subasinghe (Eds.), Diseases in Asian Aquaculture II, Fish Health Section, Asian Fisheries Society, Manila, Philippines, 1995, pp. 185-202.
37. H.M. Dutta, A composite approach for evaluation of the effects of pesticides on fish, In: J.S.D. Munshi, H.M. Dutta (Eds.) Fish Morphology: Horizon of New Research, Lebanon, New Hampshire Science Publishers Inc. and Oxford IBH, India, 1996, pp. 249-269.
38. Dutta H.M., Adhikari S., Singh N.K., Roy P.K., Munshi J.S. Histopathological changes induced by malathion in the liver of a freshwater catfish Heteropneustes fossilis (Bloch). Bull. Environ. Contam. Toxicol. 1993, 51:895-900.
39. Nayak A.K., Das B.K., Kohli M.P.S., Mukherjee S.C. The immunosuppressive effect of α-permethrin on Indian major carp, rohu (Labeo rohita Ham.). Fish Shellfish Immunol 2004, 16:41-50.
40. Sebert P., Simon B., Barthelemy L. Hydrostatic pressure induces a state resembling histotoxic hypoxia in Anguilla Anguilla. Comp. Biochem. Physiol. 1993, 105B:255-258.
41. Almeida-Val V.M.F., Farias I.P., Silva M.N.P., Duncan W.P., Val A.L. Biochemical adjustments to hypoxia by Amazon cichlids. Braz. J. Med. Biol. Res. 1995, 28:1257-1263.
42. Valarmathi S., Azariah J. Impact of chlorine on crab, Sesarma quadratum. J. Natcon 2002, 14:21-26.
43. Copper Z.L., Somero G.N. Temperature differences between the M41 lactate dehydrogenase of stenothermal and eurythermal sciaenid fishes. J. Exp. Zool. 1990, 254:127-133.
44. Sharma B., Gopal K. Change in lactic acid contents and activity of lactate dehydrogenase in C. batrachus exposed to carbaryl. Toxicol. Environ. Chem. 1995, 47:89-95.
45. Üner N., Oruç E.O., Sevgiler Y., Sahin N., Durmaz H., Usta D. Effects of diazinon on acetyl cholinesterase activity and lipid peroxidation in the brain of Oreochromis niloticus. Environ. Toxicol. Pharmacol 2006, 21:241-245.
46. Stagg R.M., Rusin J., Brown F. Na+, K+-ATPase activity in the gills of the flounder (Platichthys flesus) in a relation to mercury contamination in the Firth of Forth. Mar. Environ. Res. 1992, 33:255-266.
47. Parveza S., Sayeedb I., Raisuddinc S. Decreased gill ATPase activities in the freshwater fish Channa punctata (Bloch) exposed to a diluted paper mill effluent. Ecotoxicol. Environ. Safety 2006, 65:62-66.
48. Lionetto M.G., Giordano M.E., Vilella S., Schettino T. Inhibition of eel enzymatic activities by cadmium. Aquat. Toxicol. 2000, 48:561-571.
49. Waring C.P., Moore A. The effect of atrazine on Atlantic salmon (Salmo salar) smolts in fresh water and after sea water transfer. Aquat. Toxicol. 2004, 66:93-104.
50. Laughlin R.B., Guard H.E., Coleman W.M. Tributyltin in sea water: speciation and octanol-water partition coefficient. Environ. Sci. Technol. 1986, 20:201-204.
51. Morero R.D., Bloj B., Farias R.N., Trucco R.E. The allosteric transitions from membrane bound enzymes: Behaviour of erythrocyte acetyl cholinesterase from fat deficient rats. Biochem. Biophys. Acta 1972, 258:157-165.