Bioaccumulation of PCB-153 and effects on molecular biomarkers acetylcholinesterase, glutathione-S-transferase and glutathione peroxidase in Mytilus galloprovincialis mussels

In this study, PCB-153 bioaccumulation kinetics and concentration-response experiments were performed employing wild Mytilus galloprovincialis mussels. In addition, the activity of three enzymatic biomarkers: glutathione S-transferase (GST), glutathione peroxidase (GPx) and acetylcholinesterase (ACh...

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Detalles Bibliográficos
Autores: Vidal-Liñán, Leticia, Bellas, Juan, Soriano-Sanz, José Antonio, Concha-Graña, Estefanía, Muniategui-Lorenzo, Soledad, Beiras, Ricardo
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2016
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:dnet:digitalcsic_::83497cb626f44837929e733780dfe26b
Acceso en línea:http://hdl.handle.net/10261/324028
Access Level:acceso abierto
Palabra clave:Centro Oceanográfico de Vigo
Mytilus galloprovincialis
Medio Marino
Biomarkers
PCB-153
bioaccumulation
acetylcholinesterase
antioxidant enzymes
Descripción
Sumario:In this study, PCB-153 bioaccumulation kinetics and concentration-response experiments were performed employing wild Mytilus galloprovincialis mussels. In addition, the activity of three enzymatic biomarkers: glutathione S-transferase (GST), glutathione peroxidase (GPx) and acetylcholinesterase (AChE), were measured in the mussel gills. The experimental data fitted well to an asymptotic accumulation model with a high bioconcentration factor (BCF) of 9324 L Kg-1 and a very limited depuration capacity, described by a low excretion rate coefficient (Kd = 0.083 d-1). This study reports by first time in mussels significant inhibition of GST activity and significant induction of GPx activity as a result of exposure to dissolved PCB-153. In contrast, AChE activity was unaffected at all concentrations and exposure times tested. The effects on both enzymes are time-dependent, which stresses the difficulties inherent to the use of these biomarkers in chemical pollution monitoring programs.