Toxic effects of microcystins in the hepatopancreas of the estuarine crab Chasmagnathus granulatus (Decapoda, Grapsidae)

Microcystins are toxins produced by cyanobacteria, being toxic to aquatic fauna. It was evaluated alternative mechanisms of microcystins toxicity, including oxidative stress and histopathology in the hepatopancreas of the estuarine crab Chasmagnathus granulatus (Decapoda, Grapsidae). Microcystins wa...

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Autor principal: Pinho, G.L.L
Otros Autores: Moura Da Rosa, C., Yunes, J.S, Luquet, C.M, Bianchini, A., Monserrat, J.M
Formato: Capítulo de libro
Lenguaje:Inglés
Publicado: 2003
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Acceso en línea:Registro en Scopus
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LEADER 16575caa a22016217a 4500
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024 7 |2 scopus  |a 2-s2.0-1642352609 
024 7 |2 cas  |a catalase, 9001-05-2; glutathione transferase, 50812-37-8; superoxide dismutase, 37294-21-6, 9016-01-7, 9054-89-1; Bacterial Toxins; Catalase, EC 1.11.1.6; Glutathione Transferase, EC 2.5.1.18; Lipid Peroxides; Melanins; microcystin, 77238-39-2; Microcystins; Peptides, Cyclic; Superoxide Dismutase, EC 1.15.1.1 
040 |a Scopus  |b spa  |c AR-BaUEN  |d AR-BaUEN 
030 |a CBPPF 
100 1 |a Pinho, G.L.L. 
245 1 0 |a Toxic effects of microcystins in the hepatopancreas of the estuarine crab Chasmagnathus granulatus (Decapoda, Grapsidae) 
260 |c 2003 
270 1 0 |m Monserrat, J.M.; Depto. de Cie. Fisiológicas, Fund. Univ. Federal Do Rio Grande, R. Eng Alfredo Huch 475, Rio Grande 96201-900, Brazil; email: jose@octopus.furg.br 
506 |2 openaire  |e Política editorial 
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520 3 |a Microcystins are toxins produced by cyanobacteria, being toxic to aquatic fauna. It was evaluated alternative mechanisms of microcystins toxicity, including oxidative stress and histopathology in the hepatopancreas of the estuarine crab Chasmagnathus granulatus (Decapoda, Grapsidae). Microcystins was administered to crabs (MIC group) over 1 week, whereas the control (CTR group) received the saline from cyanobacteria culture medium. At day 7, catalase activity was higher in the MIC than in the CTR group, although a decrease of activity was verified in both groups with respect to time 0. Glutathione-S-transferase activity augmented in MIC with respect to CTR, suggesting a higher conjugation rate of the toxins with glutathione. No differences were detected in the superoxide dismutase activity. Lipid peroxidation remained stable in both groups. Histopathological analyses showed that the number of B cells decreased significantly in the CTR as a possible effect of starvation, while no significant change was observed in the MIC group. The hepatopancreas from the MIC group exhibited some necrotic tubules and melanin-like deposits. Overall, results showed that some enzymes of the antioxidant defense system were activated after microcystins exposure, this response being able to maintain lipid peroxidation levels, but insufficient to completely prevent histological damage. © 2003 Elsevier Inc. All rights reserved.  |l eng 
536 |a Detalles de la financiación: Universidad de Buenos Aires, X 222 
536 |a Detalles de la financiación: Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul 
536 |a Detalles de la financiación: This research was supported by a grant from FAPERGS (Proc. No. 0021350) to J.M. Monserrat. Cristiane Moura da Rosa is an undergraduate fellow from FAPERGS and Grasiela Lopes Leães Pinho is a graduate fellow from CAPES. A. Bianchini and J.S. Yunes are research fellows of the Brazilian CNPq. C.M. Luquet was supported by the University of Buenos Aires (Grant X 222). 
593 |a Depto. de Cie. Fisiológicas, Fund. Univ. Federal Do Rio Grande, R. Eng Alfredo Huch 475, Rio Grande 96201-900, Brazil 
593 |a Programa de Pós, Graduacao Em Cie. Fisologicas, Fisiologia Animal Comparada, Brazil 
593 |a Unidade Pesquisa Em Cianobacterias, Fund. Univ. Federal Do Rio Grande, Rio Grande 96201-900, Brazil 
593 |a Laboratório de Histologia, Fac. de Ciencias Exactas Y Naturales, Universidad de Buenos Aires (UBA), Buenos Aires, Argentina 
690 1 0 |a B CELLS 
690 1 0 |a CATALASE 
690 1 0 |a CHASMAGNATHUS GRANULATUS 
690 1 0 |a ESTUARINE CRAB 
690 1 0 |a GLUTATHIONE-S-TRANSFERASE 
690 1 0 |a HISTOPATHOLOGY 
690 1 0 |a MICROCYSTINS 
690 1 0 |a OXIDATIVE STRESS 
690 1 0 |a CATALASE 
690 1 0 |a CYANOGINOSIN 
690 1 0 |a GLUTATHIONE TRANSFERASE 
690 1 0 |a SUPEROXIDE DISMUTASE 
690 1 0 |a ANIMAL EXPERIMENT 
690 1 0 |a ANIMAL MODEL 
690 1 0 |a ANIMAL TISSUE 
690 1 0 |a ARTICLE 
690 1 0 |a B LYMPHOCYTE 
690 1 0 |a CONTROLLED STUDY 
690 1 0 |a CRAB 
690 1 0 |a ENZYME ACTIVITY 
690 1 0 |a HEPATOPANCREAS 
690 1 0 |a HISTOPATHOLOGY 
690 1 0 |a LIPID PEROXIDATION 
690 1 0 |a LIVER TOXICITY 
690 1 0 |a LYMPHOCYTE COUNT 
690 1 0 |a MALE 
690 1 0 |a MINIMUM INHIBITORY CONCENTRATION 
690 1 0 |a NONHUMAN 
690 1 0 |a OXIDATIVE STRESS 
690 1 0 |a PRIORITY JOURNAL 
690 1 0 |a ANIMALS 
690 1 0 |a BACTERIAL TOXINS 
690 1 0 |a CATALASE 
690 1 0 |a CYANOBACTERIA 
690 1 0 |a DECAPODA (CRUSTACEA) 
690 1 0 |a GLUTATHIONE TRANSFERASE 
690 1 0 |a HEPATOPANCREAS 
690 1 0 |a HISTOCYTOCHEMISTRY 
690 1 0 |a LIPID PEROXIDES 
690 1 0 |a MALE 
690 1 0 |a MELANINS 
690 1 0 |a MICROCYSTINS 
690 1 0 |a OXIDATIVE STRESS 
690 1 0 |a PEPTIDES, CYCLIC 
690 1 0 |a SUPEROXIDE DISMUTASE 
690 1 0 |a CHASMAGNATHUS GRANULATA 
690 1 0 |a CYANOBACTERIA 
690 1 0 |a DECAPODA (CRUSTACEA) 
690 1 0 |a GRAPSIDAE 
650 1 7 |2 spines  |a NECROSIS 
700 1 |a Moura Da Rosa, C. 
700 1 |a Yunes, J.S. 
700 1 |a Luquet, C.M. 
700 1 |a Bianchini, A. 
700 1 |a Monserrat, J.M. 
773 0 |d 2003  |g v. 135  |h pp. 459-468  |k n. 4  |p Comp. Biochem. Physiol. C Toxicol. Pharmacol.  |x 15320456  |w (AR-BaUEN)CENRE-4256  |t Comparative Biochemistry and Physiology - C Toxicology and Pharmacology 
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