Characterisation of ChE in Solea solea and exposure of isoflavones in juveniles of commercial flatfish (Solea solea and Solea senegalensis)

Author:

Albendín María Gemma1,Aranda Vanessa1,Corrales Alejandro1,Ortiz‐Delgado Juan Bosco2,Sarasquete Carmen2,Arellano Juana María1ORCID

Affiliation:

1. Toxicology Laboratory, University Institute of Marine Research (INMAR), International Campus of Excellence of the Sea (CEI MAR), Faculty of Marine and Environmental Sciences University of Cádiz Cádiz Spain

2. Institute of Marine Sciences of Andalucía, ICMAN‐CSIC Cádiz Spain

Abstract

AbstractThe isoflavones genistein and daidzein are flavonoid compounds mainly found in legumes, especially in soybeans and their derived products. These flavonoids can be present in agricultural, domestic and industrial wastewater effluents as a result of anthropogenic activities and may be discharged in the environment. Due to the large growth of the aquaculture sector in recent decades, new and cost‐effective fish feeds are being sought, but there is also a particular need to determine the effects of exposed flavonoids on fish in the aquatic environment, as this is the main route of exposure of organisms to endocrine disruptors. This study evaluated the possible effects of these isoflavones on juveniles of Solea senegalensis and Solea solea. After 48–96 h of exposure, the acetylcholinesterase activity in the sole head tissues was measured, and the cholinesterase activity in juveniles of common sole (S. solea) was determined. Experiments were carried out to determine the optimal pH, investigate the specificity of three substrates (acetylthiocholine, butyrylthiocholine, propionylthiocholine) on cholinesterase activity and determine the kinetic parameters (Vmax and Km). The results obtained showed that neither genistein nor daidzein exposure to S. senegalensis and S. solea inhibited the activity of acetylcholinesterase at the tested concentrations (genistein: 1.25, 2.5, 5, 10 and 20 mg/L; daidzein: 0.625, 1.25, 2.5, 5 and 10 mg/L).

Publisher

Wiley

Subject

Toxicology

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