Toxicity of sodium arsenite in the gill of an economically important mollusc of India

Fish and Shellfish Immunology

Volumn 29, Issue 1, 2010, Pages 136-148

  Chakraborty, Sudipta ^a   Ray, Mitali ^b   Ray, Sajal ^b  

^a DARJEELING GOVERNMENT COLLEGE   (India)

^b UNIVERSITY OF CALCUTTA   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMALIA; LAMELLIDENS MARGINALIS; MOLLUSCA;

EID: 77955054048     PISSN: 10504648     EISSN: 10959947     Source Type: Journal    
DOI: 10.1016/j.fsi.2010.02.025     Document Type: Article

References (71)

1. Chakraborty S., Ray M., Ray S. Sodium arsenite induced alteration of hemocyte density of Lamellidens marginalis - an edible mollusk from India. Clean - Soil Air Water 2008, 36(2):195-200.
2. Acharyya S.K., Chakraborty P., Lahiri S., Raymahashay B.C., Guha S., Bhowmik A. Arsenic poisoning in the Ganges delta. Nature 1999, 401(6753):545-550.
3. Neumann R.B., Ashfaque K.N., Badruzzaman A.B.M., Ali M.A., Shoemaker J.K., Harvey C.F. Anthropogenic influences on groundwater arsenic concentrations in Bangladesh. Nat Geosci 2010, 3:46-52.
4. Roberts L.C., Hug S.J., Dittmar J., Voegelin A., Kretzschmar R., Wehrli B., et al. Arsenic release from paddy soils during monsoon flooding. Nat Geosci 2010, 3:53-59.
5. Islam M.R., Lahermo P., Salminen R., Rojstaczer S., Peuraniemi V. Lake and reservoir water quality affected by metals leaching from tropical soils. Bangladesh Environ Geol 2000, 39(10):1083-1089.
6. Aggett J., O'brien G.A. Detailed model for mobility of arsenic in Lacustrine sediments based on measurements in Lake Ohakuri. Environ Sci Technol 1985, 19(3):231-238.
7. Aggett J., Kriegman M.R. The extent of formation of arsenic (III) in sediment interstitial waters and its release to hypolimnetic waters in Lake Ohakuri. Water Res 1988, 22(4):407-411.
8. Chakraborty S., Ray S. Nuclear morphology and lysosomal stability of molluskan hemocyte as possible biomarkers of arsenic toxicity. Clean - Soil Air Water 2009, 37(10):669-675.
9. Vaughn C.C., Hakenkamp C.C. The functional role of burrowing bivalves in freshwater ecosystems. Freshwater Biol 2001, 46:1431-1446.
10. Gregory M.A., Marshall D.J., George R.C., Anandraj A., McClurg T.P. Correlations between metal uptake in the soft tissue of Perna perna and gill filament pathology after exposure to mercury. Mar Pollut Bull 2002, 45:114-125.
11. Sunila I. Acute histological responses of the gill of the mussel, Mytilus edulis, to exposure by environmental pollutants. J Invertebr Pathol 1988, 52:137-141.
12. Cheng T.C., Sullivan J.T. Effects of heavy metals on phagocytosis by mollusca hemocytes. Mar Environ Res 1984, 14:305-315.
13. Cheng T.C. In vivo effects of heavy metals on cellular defence mechanisms of Crassostrea virginica: phagocytic and endocytotic indices. J Invertebr Pathol 1988, 51:215-220.
14. Pipe R.K., Coles J.A., Carissan F.M.M., Ramanathan K. Copper induced immunomodulation in the marine mussel Mytilus edulis. Aquat Toxicol 1999, 46:43-54.
15. Fries C.R., Tripp M.R. Depression of phagocytosis in Mercenaria following chemical stress. Dev Comp Immunol 1980, 4:233-244.
16. Alvarez M.R., Friedl F.E. Effects of a fungicide on in vitro hemocyte viability, phagocytosis and attachment in the American oyster, Crassostrea virginica. Aquaculture 1992, 107:135-140.
17. Beckmann N., Morse M.P., Moore C.M. Comparative study of phagocytosis in normal and diseased hemocytes of the bivalve mollusc Mya arenaria. J Invertebr Pathol 1992, 59:124-132.
18. Coles J.A., Farley S.R., Pipe R.K. Effects of fluoranthene on the immunocompetence of the common marine mussel, Mytilus edulis. Aquat Toxicol 1994, 30:367-379.
19. Cima F., Marin M.G., Matozzo V., Da Ros L., Ballarin L. Immunotoxic effects of organotin compounds in Tapes philippinarum. Chemosphere 1998, 37:3035-3045.
20. Das S., Jana B.B. In situ cadmium reclamation by freshwater bivalve Lamellidens marginalis from an industrial pollutant-fed river canal. Chemosphere 2003, 52(1):161-173.
21. Das S., Jana B.B. Distribution pattern of ambient cadmium in wetland ponds distributed along an industrial complex. Chemosphere 2004, 55(2):175-185.
22. Pipe R.K. Hydrolytic enzymes associated with the granular haemocytes of the marine mussel Mytilus edulis. Histochem J 1990, 22:595-603.
23. Cheng T.C., Dougherty W.J. Ultrastructural evidence for the destruction of Schistosoma mansoni sporocysts associated with elevated lysosomal enzyme levels in Biomphalaria glabrata. J Parasitol 1989, 75:928-941.
24. Pfeifer S., Doris S., Dippner J.W. Effect of temperature and salinity on acetylcholinesterase activity, a common pollution biomarker, in Mytilus sp. from the south-western Baltic Sea. J Exp Mar Biol Ecol 2005, 320(1):93-103.
25. Cajaraville M.P., Bebianno M.J., Blasco J., Porte C., Sarasquete C., Viarengo A. The use of biomarkers to assess the impact of pollution in coastal environment of the Iberian Peninsula: a practical approach. Sci Total Environ 2000, 247:295-311.
26. Escartin E., Porte C. The use of cholinesterase and carboxylesterase activities from Mytilus galloprovincialis in pollution monitoring. Environ Toxicol Chem 1997, 16:2090-2095.
27. Lionetto M.G., Caricato R., Giordano M.E., Pascariello M.F., Marinosci L., Schettino T. Integrated use of biomarkers (acetylcholinesterase and antioxidant enzymes activities) in Mytilus galloprovincialis and Mullus barbatus in an Italian coastal marine area. Mar Pollut Bull 2003, 46(3):324-330.
28. Galgani F., Bocquené G., Cadiou Y. Evidence of variation in cholinesterase activity in fish along a pollution gradient in the North Sea. Mar Ecol Prog Ser 1992, 91:77-82.
29. SenGupta R., Sarkar A., Kureishy T.W. Bio-degradation and anticholinesterase activity of methyl isocyanate in the aquatic environment of Bhopal. Water Res 1991, 25(2):179-183.
30. Bocquené G., Roig A., Fournier D. Cholinesterases from the common oyster (Crassostrea gigas): evidence for the presence of a soluble acetylcholinesterase insensitive to organophosphate and carbamate inhibitors. FEBS Lett 1997, 407(3):261-266.
31. Binelli A., Ricciardi F., Riva C., Provini A. Screening of POP pollution by AChE and EROD activities in Zebra mussels from the Italian Great Lakes. Chemosphere 2005, 61(8):1074-1082.
32. Conte A., Ottaviani E. Nitric oxide synthase activity in molluscan hemocytes. FEBS Lett 1995, 365:120-124.
33. Bogdan C. Nitric oxide and the immune response. Nat Immunol 2001, 2(10):907-916.
34. Arumugam M., Romestand B., Torreilles J. Nitrite released in hemocytes from Mytilus galloprovincialis, Cassostrea gigas and Ruditapes decussates upon stimulation with phorbol myristate acetate. Aquat Living Resour 2000, 13:173-177.
35. Asokan R., Arumugam M., Mullainadhan P. Activation of prophenoloxidase in the plasma and haemocytes of the marine mussel Perna viridis Linnaeus. Dev Comp Immunol 1997, 21(1):1-12.
36. Perendija B.R., Borković S.S., Kovačević T.B., Pavlović S.Z., Stojanović B.D., Paunović M.M., et al. Glutathione dependent enzyme activities in the foot of three freshwater mussel species in the Sava river. Serbia Arch Biol Sci 2007, 59(3):169-175.
37. Mannervik B., Danielson U.H. Glutathione transferase - structure and catalytic activity. CRC Crit Rev Biochem 1988, 23:283-337.
38. Saint-Denis M., Labrot F., Narbonne J.F., Ribera D. Glutathione, glutathione-related enzymes, and catalase activities in the earthworm Eisenia fetida andrei. Arch Environ Contam Toxicol 1998, 35:602-614.
39. Chakraborty S., Ray M., Ray S. Evaluation of phagocytic activity and nitric oxide generation by molluscan haemocytes as biomarkers of inorganic arsenic exposure. Biomarkers 2009, 14(8):539-546.
40. Raut S.K. Laboratory rearing of medically and economically important molluscs. Snails, flukes and man 1991, 79-83. Zoological Survey of India Publication. M.S. Jairajpuri (Ed.).
41. Das S., Roy Chowdhury A. Arsenic-A global monster. Sci Cult 2006, 72:230-237.
42. Gomez-Caminero A., Howe P., Hughes M., Kenyon E., Lewis D.R., Moor M., et al. Summary. Environmental health criteria 224, arsenic and arsenic compounds 2001, 1-8. World Health Organization, Geneva. 2nd ed.
43. Adema C.M., Van Deutekom-Mulder E.C., van der Knapp W.P.W., Meuleman E.A., Sminia T. Generation of oxygen radicals in hemocytes of the Lymnaea stagnalis in relation to the rate of phagocytosis. Dev Comp Immunol 1991, 15:17-26.
44. Lowry O.H., Rosebrough N.J., Farr A.L., Randall R.J. Protein measurement with the folin phenol reagent. J Biol Chem 1951, 193:265-275.
45. Michell R.H., Karnovsky M.J., Karnovsky M.L. The distributions of some granule-associated enzymes in guinea-pig polymorphonuclear leucocytes. Biochem J 1970, 116:207-216.
46. Bergmeyer H.U., Bernt E. Glutamate-oxaloacetate trans-aminase. Methods of enzymatic analysis 1965, 837-845. Academic Press, New York. H.U. Bergmeyer (Ed.).
47. Bergmeyer H.U., Bernt E. Glutamate-pyruvate transaminase. Methods of enzymatic analysis 1965, 846-851. Academic Press, New York. H.U. Bergmeyer (Ed.).
48. Hestrin S. The reaction of acetylcholine and other carboxylic acid derivatives with hydroxylamine, and its analytical application. J Biol Chem 1949, 180:249-261.
49. 15) nitrate in biological fluids. Anal Biochem 1982, 126:131-138.
50. Habig W.H., Pabst M.J., Jakoby W.B. Glutathione S-transferase: the first enzymatic step in mercapturic acid formation. J Biol Chem 1974, 249(22):7130-7139.
51. Sung H.H., Chang H.J., Her C.H., Chang J.C., Song Y.L. Phenoloxidase activity of haemocytes derived from Penaeus monodon and Macrobrachium rosenbergii. J Invertebr Pathol 1998, 71:26-33.
52. Aebi H. Catalase in vitro. Methods Enzymol 1984, 105:121-126.
53. Sokal R.B., Rohlf F.J. Introduction to biostatistics 1973, Freeman WH, New York.
54. Glew R.H., Shah A.K., Das S., Remaley A.T. Biochemistry of the Leishmania species. Microbiol Rev 1988, 52:412-432.
55. Zheng Y.Z., Lan W.S., Qiao C.L., Mulchandani A., Chen W. Decontamination of vegetables sprayed with organophosphate pesticides by organophosphorus hydrolase and carboxylesterase (BI). Appl Biochem Biotechnol 2007, 136(3):233-242.
56. Monin M.A., Rangneker P.V. Histochemical localization of acid and alkaline phosphatases and glucose-6-phosphate of the hepatopancreas of the crab Scylla serrata. Exp Mar Biol Ecol 1974, 14(1):1-16.
57. Sarkar A. Evaluation of the toxicity of organic matter in marine sediments. Water Sci Technol 1992, 25(3):255-257.
58. Mmartinez Tabche L., Ramirez Mora B., German Faz C., Galar Castelan I., Madrigal Ortiz M., Ulloa Gonzalez V., et al. Toxic effect of sodium dodecylbenzenesulfonate, lead, petroleum, and their mixtures on the activity of acetylcholinesterase of Moina macropa in vitro. Environ Toxicol Water Qual 1997, 12:211-215.
59. Sturm A., da Silva de Assis H.C., Hansen P.D. Cholinesterases of marine teleost fish: enzymological characterization and potential use in the monitoring of neurotoxic contamination. Mar Environ Res 1999, 47(4):389-398.
60. Wells P.G., Depledge M.H., Butler J.N., Manock J.J., Knap A.H. Rapid toxicity assessment and biomonitoring of marine contaminants-exploiting the potential of rapid biomarker assays and microscale toxicity tests. Mar Pollut Bull 2001, 42(10):799-804.
61. Matozzo V., Ballarin L., Pampanin D.M., Marin M.G. Effects of copper and cadmium exposure on functional responses of hemocytes in the clam, Tapes philippinarum. Arch Environ Contam Toxicol 2001, 41:163-170.
62. Ischiropoulos H., Zhu L., Beckman J.S. Peroxynitrite formation from macrophage-derived nitric oxide. Arch Biochem Biophys 1992, 298:446-451.
63. Balabaskaran S., Chen S., Segaran M. Studies on glutathione S-transferase in molluscs. Comp Biochem Physiol 1986, 85B:183-192.
64. LeBlanc G.A., Cochrane B.J. Modulation of substrate-specific glutathione S-transferase activity in Daphnia magna with concomitant effects on toxicity tolerance. Comp Biochem Physiol 1985, 82C:37-42.
65. Sugumaran M. Comparative biochemistry of eumelanogenesis and the protective roles of phenoloxidase and melanin in insects. Pigment Cell Res 2002, 15:2-9.
66. Akyol Ö, Arslanoglu R., Durak I. Activities of free radical and DNA turn-over enzymes in cancerous and non-cancerous human brain tissues. Redox Rep 1995, 1:255-259.
67. Papagiannis I., Kagalou I., Leonardos J., Petridis D., Kalfakakou V. Copper and zinc in four freshwater fish species from Lake Pamvotis (Greece). Environ Int 2004, 30:357-362.
68. Box A., Sureda A., Deudero S. Antioxidant response of the bivalve Pinna nobilis colonised by invasive red macroalgae Lophocladia lallemandii. Comp Biochem Physiol Part C: Toxicol Pharmacol 2009, 149(4):456-460.
69. 2+ exposed oysters (Crassostrea gigas): an immunohistochemical approach. Comp Biochem Physiol Part C: Toxicol Pharmacol 2005, 141(2):151-156.
70. Söderhäll K., Cerenius L. Role of prophenoloxidase-activating system in invertebrate immunity. Curr Opin Immunol 1998, 10:23-28.
71. Jordan P.J., Deaton L.E. Characterization of phenoloxidase from Crassostrea virginica hemocytes and the effect of Perkinsus marinus on phenoloxidase activity in the hemolymph of Crassostrea virginica and Geukensia demissa. J Shellfish Res 2005, 24(2):477-482.