Modulation of hepatic glutathione transferases isoenzymes in three bivalve species exposed to purified microcystin-LR and Microcystis extracts. (October 2017)

• Record Type: Journal Article
• Authors: Carneiro, M.; Antas, P.; Reis, B.; Azevedo, J.; Osório, H.; Campos, A.; Vasconcelos, V.; Martins, J.C.
• Is Part Of: Toxicon. Volume 137(2017)
• Page Start: 150
• Page End: 157
• Publication Date: 2017-10
• Subjects: Microcystins -- Glutathione Transferases -- Biotransformation -- Mytilus galloprovincialis -- Ruditapes philippinarum -- Corbicula fluminea; Toxins -- Periodicals; Venom -- Periodicals; 615.9
• DOI: 10.1016/j.toxicon.2017.07.003
• Languages: English
• ISSNs: 0041-0101

Abstract

Abstract: This study compares the role of hepatic cytosolic glutathione transferases (cGST) isoforms of three different bivalve species to a Microcystis aeruginosa extract and purified MC-LR exposure (both at 150 μg MC-LR L −1 ) for 24 h. Characterization and alterations of the cytosolic GST activities in Mytilus galloprovincialis, Ruditapes philippinarum and Corbicula fluminea were measured using four class-specific substrates and changes in individual GST isoforms expression were achieved by a subsequent two-dimensional electrophoresis analysis. Evaluation of cGST activity basal levels using the four class-specific substrates denoted quantitative differences between the three bivalves. Purified MC-LR did not induce any significant response from bivalves. On the other hand, cell extracts caused significant alterations according to bivalves and substrates. Among the three bivalves, only R. philippinarum showed a significant induction of cGST activity using generic 1-chloro-2, 4-dinitrobenzene (CDNB) substrate. However, no significant alterations were detected in these clams by cell extracts using the other specific substrates. In contrast, C. fluminea revealed significant induction of cGST activity when using 3, 4-dichloronitrobenzene (DCNB) and ethacrynic acid (EA). In M. galloprovincialis, cell extracts promoted a significant decrease of cGST activity when using EA substrate. Altered protein expression was quantitatively detected upon exposure to cell extracts for one spot in R. philippinarum and another for C. fluminea, both upregulated (2.0 and 8.5-fold, respectively) and identified as a sigma1-class GST in the case of the first. The results showed that the three bivalves presented specific adaptive biotransformation responses to MCs and other cyanobacteria compounds supported by the modulation of distinct cGST classes. Highlights: Hepatic cGST activity basal levels denoted quantitative differences between bivalves. Purified MC-LR did not induce responses on bivalve's hepatic cGST system. M. extracts caused different induction of hepatic cGST in C. fluminea and R. philippinarum. M. galloprovincialis hepatic cGST system was less affected by the cell extracts.