Abstract

To gain a better understanding of which pharmaceuticals could pose a risk to fish, 94 pharmaceuticals representing 23 classes were analyzed in blood plasma from wild bream, chub, and roach captured at 18 sites in Germany, the Czech Republic and the UK, respectively. Based on read across from humans, we evaluated the risks of pharmacological effects occurring in the fish for each measured pharmaceutical. Twenty-three compounds were found in fish plasma, with the highest levels measured in chub from the Czech Republic. None of the German bream had detectable levels of pharmaceuticals, whereas roach from the Thames had mostly low concentrations. For two pharmaceuticals, four individual Czech fish had plasma concentrations higher than the concentrations reached in the blood of human patients taking the corresponding medication. For nine additional compounds, determined concentrations exceeded 10% of the corresponding human therapeutic plasma concentration in 12 fish. The majority of the pharmaceuticals where a clear risk for pharmacological effects was identified targets the central nervous system. These include e.g. flupentixol, haloperidol, and risperidone, all of which have the potential to affect fish behavior. In addition to identifying pharmaceuticals of environmental concern, the results emphasize the value of environmental monitoring of internal drug levels in aquatic wildlife, as well as the need for more research to establish concentration-response relationships.

Highlights

  • It is accepted that most pharmaceuticals are not completely metab­ olized in the body and many are incompletely removed in wastewater treatment plants (WWTP)

  • Abso­ lute recoveries in fish plasma are shown in Table S1, Supporting Information

  • When trying to identify pharmaceuticals with increased risks to affect wild fish, we show that a strategy that takes advantage of the drugs inherent biological potency combined with actual levels found in wild fish represents a promising approach

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Summary

Introduction

It is accepted that most pharmaceuticals are not completely metab­ olized in the body and many are incompletely removed in wastewater treatment plants (WWTP). They can be found in receiving waters around the world. Verte­ brates, often have conserved drug targets with humans, including many receptors and enzymes. Such conservation provides a potential for pharmacological effects via high-affinity interactions with target mole­ cules in non-target species (Gunnarsson et al, 2008; Brown et al, 2014)

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