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Research articles

Characterisation of the multixenobiotic resistance (MXR) mechanism in the freshwater snail Physa acuta from Patagonia (Argentina)

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Pages 86-96 | Received 22 Feb 2013, Accepted 16 Sep 2013, Published online: 13 Nov 2013
 

Abstract

P-glycoprotein (P-gp) mediated multixenobiotic resistance (MXR) is a mechanism analogous to multidrug resistance (MDR), which has been extensively characterised in mammalian tumours. The expression and function of the MXR mechanism has been demonstrated in numerous aquatic organisms and has been proposed as a biomarker for pollution assessment. The purpose of this study was to evaluate the activity and expression of the MXR mechanism in freshwater snails (Physa acuta) of the Andean–Patagonian region. The accumulation and efflux rates of the model P-gp substrate Rhodamine B in snails previously exposed to pollution were measured. Results confirmed that MXR activity decreased after maintenance in clean water, and that a depuration period of 7 d was long enough to observe a significant deinduction of this system. The results demonstrate the presence of a P-gp-like transport system in the freshwater snail P. acuta from Patagonia, and suggest its function as a defence system. The results of this study could be used to provide information on the possible use of these snails as bioindicators in toxicological testing.

Acknowledgements

We would like to thank Dr Basilio A. Kotsias who kindly revised the manuscript, Dr Diego Gutierrez Gregoric from the Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata, Argentina for taxonomic determination and Dr Maria Laura Miserendino from the Universidad Nacional de la Patagonia San Juan Bosco, Argentina for her assistance in the site characterisation. Thanks also to the editor and anonymous reviewers for constructive suggestions which greatly improved the manuscript. This work has been supported in part by the National Research Council of Argentina (CONICET; Project Res No 1735/11). Yanina Assef is a member of CONICET.

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