In situ studies on physiological and biochemical responses of four fishes with different trophic levels to toxic cyanobacterial blooms in a large Chinese lake

Toxicon

Volumn 50, Issue 3, 2007, Pages 365-376

  Qiu, Tong ^a   Xie, Ping ^a   Ke, Zhixin ^a   Li, Li ^b   Guo, Longgen ^a  

^a INSTITUTE OF HYDROBIOLOGY   (China)

^b HUAZHONG AGRICULTURAL UNIVERSITY   (China)

Author keywords

Antioxidants system; Cyanobacterial blooms; Fish; Liver; Ultrastructure

Indexed keywords

ANTIOXIDANT; BACTERIAL TOXIN; CHLORAMPHENICOL ACETYLTRANSFERASE; CYANOGINOSIN; GLUTATHIONE; GLUTATHIONE PEROXIDASE; GLUTATHIONE TRANSFERASE; SUPEROXIDE DISMUTASE;

ANIMAL CELL; ANIMAL TISSUE; ANTIOXIDANT ACTIVITY; ARISTICHTHYS NOBILIS; ARTICLE; CELL NUCLEUS; CELL STRUCTURE; CHEMICAL ANALYSIS; CHINESE; CONCENTRATION RESPONSE; CONTROLLED STUDY; CORRELATION ANALYSIS; CULTER ILISHAEFORMIS; CYANOBACTERIUM; FISH; GOLDFISH; HYPOPHTHALMICHTHYS MOLITRIX; LIVER; LIVER CELL; LIVER STRUCTURE; MEMBRANE; NONHUMAN; PHYTOPLANKTON; PRIORITY JOURNAL; TROPHIC LEVEL;

ANIMALS; BACTERIAL TOXINS; CHINA; CYANOBACTERIA; ECOSYSTEM; ENVIRONMENTAL MONITORING; FEEDING BEHAVIOR; FISHES; FOOD CHAIN; FRESH WATER; SEASONS; TIME FACTORS;

CARASSIUS AURATUS; CULTER; CYANOBACTERIA; HYPOPHTHALMICHTHYS MOLITRIX; HYPOPHTHALMICHTHYS NOBILIS; PISCES;

EID: 34547109365     PISSN: 00410101     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.toxicon.2007.04.006     Document Type: Article

References (49)

1. Andersen R.J., Luu H.A., Chen D.Z.X., Holmes C.F.B., Kent M.L., Le Blanc M., Taylor F.J.R., and Williams D.E. Chemical and biological evidence links microcystins to salmon netpen liver disease. Toxicon 31 (1993) 1315-1323
2. Bayer W.F., and Fridovich J.L. Assaying for superoxide dismutase activity: some large consequences of minor changes in conditions. Anal. Biochem. 161 (1987) 559-566
3. Best J.H., Pflugmacher S., Wiegand C., Eddy F.B., Metcalf J.S., and Codd G.A. Effects of enteric bacterial and cyanobacterial lipopolysaccharides, and of microcystin-LR, on glutathione-S-transferase activities in zebra fish (Danio rerio). Aquat. Toxicol. 60 (2002) 223-231
4. Blaha L., Kopp R., Simkova K., and Mares J. Oxidative stress biomarkers are modulated in silver carp (Hypophthalmichthys molitrix Val) exposed to microcystin-producing cyanobacterial water bloom. Acta Vet. Brno. 73 (2004) 477-482
5. Bradford M.M. A rapid and sensitive method for the quantification of microgram quantities of proteins utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976) 248-254
6. Bury N.R., McGeer J.C., Eddy F.B., and Codd G.A. Liver damage in brown trout, Salmo trutta L., and rainbow trout, Oncorhynchus mykiss (Walbaum), following administration of cyanobacteria hepatotoxin microcystin-LR via the dorsal aorta. J. Fish Dis. 20 (1997) 209-215
7. Carbis C.R., Rawlin G.T., Grant P., Mitchell G.F., Anderson J.W., and McCauley I. A study of feral carp, Cyprinus carpio L., exposed to Microcystis aeruginosa at Lake Mokoan, Australia, and possible implication for fish health. J. Fish Dis. 20 (1997) 81-91
8. Carmichael W.W. Cyanobacteria secondary metabolites-the cyanotoxins. J. Appl. Bacteriol. 72 (1992) 455-459
9. Carmichael W.W., and Falconer I.R. Diseases related to freshwater blue-green algal toxins, and control measures. In: Falconer I.R. (Ed). Algal Toxins in Seafood and Drinking Water (1993), Academic Press, London 187-209
10. Cazenave J., Bistoni M.A., Pesce S.F., and Wunderlin D.A. Differential detoxification and antioxidant response in diverse organs of Corydoras paleatus exposed to microcystin-RR. Aquat. Toxicol. 76 (2006) 1-12
11. Cazenave J., Bistoni M.A., Zwirnmann E., Wunderlin D.A., and Wiegand C. Attenuating effects of natural organic matter on microcystin toxicity on zebra fish (Danio rerio) embryos-benefits and costs of microcystin detoxification. Environ. Toxicol. 21 (2006) 22-32
12. Claiborne A. Catalase activity. In: Greenwald R.A. (Ed). CRC Handbook of Methods in Oxygen Radical Research (1985), CRC Press, Boca Raton, FL 283-284
13. Dokulil M., Chen W., and Cai Q. Anthropogenic impacts to large lakes in China: the TaiHu example. Aquat. Ecosyst. Health Manage. 3 (2000) 81-94
14. Drotar A., Phelps P., and Fall R. Evidence for glutathione peroxidase activities in cultured plant cells. Plant Sci. 42 (1985) 35-40
15. Dröge W. Free radicals in the physiological control of cell function. Phys. Rev. 82 (2002) 47-95
16. English W.R., Schwedler T.E., and Dyck L.A. Aphanizomenon flos-aquae, a toxic blue-green alga in commercial catfish, Ictalurus punctatus, ponds: a case history. J. Appl. Aquaculture 3 (1994) 195-209
17. Eriksson J.E., Toivola D., Meriluoto J.A.O., Karaki H., Han Y., and Hartshorne D. Hepatocyte deformation induced by cyanobacterial toxin reflects inhibition of protein phosphatases. Biochem. Biophys. Res. Commun. 173 (1990) 1347-1353
18. Falconer I.R., and Yeung D.S.K. Cytoskeletal changes in hepatocytes induced by Microcystis toxins and their relation to hyperphosphorylation of cell proteins. Chem. Biol. Interact. 81 (1992) 181-196
19. Griffith O. Determination of glutathione and glutathione disulfide using glutathione reductase and 2-vinylpyridine. Anal. Biochem. 106 (1980) 207-212
20. Habig W.H., and Jakoby W.B. Assays for differentiation of glutathione S-transferases. Methods Enzymol. 77 (1981) 398-405
21. Habig W.H., Pabst M.J., and Jakoby W.B. Glutathine-S-transferases: the first enzymatic step in mercapturic acid formation. Biol. Chem. 249 (1974) 7130-7139
22. Halliwell B., and Gutteridge J.M.C. Free Radicals in Biology and Medicine. third ed (1999), Clarendon Press, Oxford
23. Hermansky S.J., Stohs S.J., Eldeen Z.M., Roche U.F., and Mereish K.A. Evaluation of potential chemoprotectants against microcystin-LR hepatotoxicity in mice. J. Appl. Toxicol. 11 (1991) 65-74
24. Ito F., Kondo F., and Harada K.I. Hepatic necrosis in aged mice by oral administration of microcystin-LR. Toxicon 35 (1997) 231-239
25. Ito F., Kondo F., and Harada K.I. First report on the distribution of orally administered microcystin-LR in mouse tissue using an immunostaining method. Toxicon 38 (2000) 37-48
26. Jewel M.A., Affan M.A., and Khan S. Fish mortality due to cyanobacterial blooms in an aquaculture pond in Bangladesh. Pakistan J. Biol. Sci. 6 (2003) 1046-1050
27. Kondo F., Ikai Y., Oka H., Masanao O., Ishikawa N., Harada K.I., Matsuura K., Murata H., and Suzuki M. Formation characterization and toxicity of the glutathione and cysteine conjugates of toxic heptapeptide microcystins. Chem. Res. Toxicol. 5 (1992) 591-596
28. Li X.Y., Liu Y.D., Song L.R., and Liu J.T. Responses of antioxidant systems in the hepatocytes of common carp (Cyprinus carpio L.) to the toxicity of microcystin-LR. Toxicon 42 (2003) 85-89
29. Li X.Y., Chung I., Kim J., and Lee J. Oral exposure to Microcystis increases activity-augmented antioxidant enzymes in the liver of loach (Misgurnus mizolepis) and has no effect on lipid peroxidation. Comp. Biochem. Physiol. C 141 (2005) 292-296
30. Li L., Xie P., and Chen J. In vivo studies on toxin accumulation in liver and ultrastructural changes of hepatocytes of the phytoplanktivorous bighead carp ip-injected with extracted microcystins. Toxicon 46 (2005) 533-545
31. Malbrouck C., Trausch G., Devos P., and Kestemont P. Hepatic accumulation and effects of microcystin-LR on juvenile goldfish Carassius auratus L. Comp. Biochem. Phys. C 135 (2003) 39-48
32. Malbrouck C., Trausch G., Devos P., and Kestemont P. Effect of microcystin-LR on protein phosphatase activity and glycogen content in isolated hepatocytes of fed and fasted juvenile goldfish Carassius auratus L. Toxicon 44 (2004) 927-932
33. Opuszynski K., and Shireman J.V. Merbivorous Fishes-Culture and Use for Weed Management (1995), CRC Press, Boca Raton, FL, USA
34. Park H.D., and Lwami C. Temperal variabilities of the concentrations of intra- and extracellular microcystin and toxic microcystis species in a hypertrophic lake, Lake Suwa, Japan (1991-1994). Environ. Toxicol. Water Qual. 13 (1998) 61-72
35. Pinho G.L., Moura da R.C., Yunes J.S., Yunes J.S., Bianchini A., and Monserrat J.M. Toxic effects of microcystins in the hepatopancreas of the estuarine crab Chasmagnathus granulatus (Decapoda, Grapsidae). Comp. Biochem. Phys. C 135 (2003) 459-468
36. Pflugmacher S., Wiegand C., Oberemm A., Beattie K.A., Krause E., Codd G.A., and Steinberg C.E.W. Identification of an enzymatically formed glutathione conjugate of the cyanobacterial hepatotoxin microcystin-LR: the first step of detoxication. Biochim. Biophys. Acta 1425 (1998) 527-533
37. Pu P.M., Hu W.P., Wang G.X., Zhang S.Z., Hu C.G., and Yan J.S. The new strategy for improving the aqua-ecological environmental in Taihu Lake Basin, China. How can we solve the problem of lakc of qualified water and deterioration of environment and natural resources in Taihu Lake basin. J. Lake Sci. 10 (1998) 47-58
38. Pu P.M., Hu W.P., Yan J.S., Wang G.X., and Hu C.G. A physico-ecological engineering experiment for water treatment in a hypertrophic lake in China. Ecol. Eng. 10 (1998) 79-90
39. Qin B.Q., Hu W.P., and Chen W.M. Processes and Mechanisms of the Changes in Aquatic Environments in Lake Taihu (2004), Science Press, Beijing (in Chinese)
40. Siegers C.P. Glutathione and glutathione dependent enzymes. Progr. Pharmacol. Clin. Pharmacol. 7 (1989) 171-180
41. Snyder G.S., Goodwin A.E., and Freeman D.W. Evidence that channel catfish, Ictalurus punctatus (Rafinesque) mortality is not linked to ingestion of the hepatotoxin MC-LR. J. Fish Dis. 25 (2002) 275-285
42. Takenaka S., and Otsu R. Effects of l-cysteine and reduced glutathione on the toxicities of microcystin-LR: the effect for acute liver failure and inhibition of protein phosphatase activity. Aquat. Toxicol. 48 (1999) 65-68
43. Takenaka S. Covalent glutathione to cyanobacterial hepatotoxin microcystin-LR by F344 rat cytosolic and microsomal glutathione-S-transferases. Environ. Toxicol. Pharm. 9 (2001) 135-139
44. World Health Organization, 2003. Algae and cyanobacteria in freshwater. In: Guidelines for Safe Recreational Water Environments, vol. 1: Coastal and Fresh Waters. Geneva, Switzerland, pp. 136-158.
45. Xie P., and Liu J.K. Practical success of biomanipulation using filter-feeding fish to control cyanobacteria blooms: synthesis of decades of research and application in a subtropical hypereutrophic lake. Sci. World J. 1 (2001) 337-356
46. Xie L.Q., Xie P., Ozawa K., Honma T., Yokoyama A., and Park H.D. Dynamics of microcystins-LR and -RR in the phytoplanktivorous silver carp in a sub-chronic toxicity experiment. Environ. Pollut. 127 (2004) 431-439
47. Xie L.Q., Xie P., Guo L., Li L., Miyabara Y., and Park H.-D. Organ distribution and bioaccumulation of microcystins in freshwater fish at different trophic levels from the eutrophic Lake Chaohu, China. Environ. Toxicol. 20 (2005) 293-300
48. Zimba P.V., Khoo L., Gaunt P.S., Brittain S., and Carmichael W.W. Confirmation of catfish, Ictalurus punctatus (Rafinesque), mortality from Microcystis toxins. J. Fish Dis. 24 (2001) 41-47
49. Zhang Y.Y., Xu L.H., Zhou B.S., and Xu Y. Preiliminary studies on the role of GSH in detoxification of microcystin-LR in fish. Acta Hydrobiol. Sinica 20 (1996) 284-286