Immune responses in the aquatic gastropod Lymnaea stagnalis under short-term exposure to pharmaceuticals of concern for immune systems: Diclofenac, cyclophosphamide and cyclosporine A

This is a pioneering study in the ecotoxicological assessment of immunotoxic effects of the three selected drugs of concern to a freshwater gastropod species. Lymnaea stagnalis was exposed in the laboratory for 3 days to three drugs used for immune systems: diclofenac (nonsteroidal anti-inflammatory...

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Veröffentlicht in:Ecotoxicology and environmental safety 2017-05, Vol.139, p.358-366
Hauptverfasser: Boisseaux, P., Noury, P., Thomas, H., Garric, J.
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Noury, P.
Thomas, H.
Garric, J.
description This is a pioneering study in the ecotoxicological assessment of immunotoxic effects of the three selected drugs of concern to a freshwater gastropod species. Lymnaea stagnalis was exposed in the laboratory for 3 days to three drugs used for immune systems: diclofenac (nonsteroidal anti-inflammatory drug), cyclophosphamide (anti-cancer immunosuppressive drug) or cyclosporine A (anti-xenograft immunosuppressive drug). Exposure ranges included environmental realistic (1–10μgL−1) and therapeutic concentrations (100–1000μgL−1). At the end of exposure times, the immune parameters of individual snails were measured: hemocyte density and viability, hemocyte phagocytosis capacity and hemocyte-related oxidative activities (basal and NADPH-oxidase stimulated with zymosan particles). Diclofenac and cyclosporine A induced immune responses, although the effects were not strong. No immunosuppression was observed. Such subtle immunomodulations bring further interrogations regarding their long-term immunotoxicity and possible resulting tradeoffs with life-history traits. On the other hand, the prodrug cyclophosphamide did not induce significant immune responses. Since metabolism pathways differ greatly between vertebrates and invertebrates, this study also suggests that relevant vertebrate metabolites should be included in the immunotoxicity assessment of pharmaceuticals in non-target invertebrate species. Finally, the possible interactive effects of these pharmaceuticals sharing similar modes of action or effects features should also be explored. •Weak immune responses were observed following short-term exposure to diclofenac and cyclosporine A.•Pharmaceuticals of concern for immune system of mammals do not systematically induce immunotoxicity in L. stagnalis.•It is recommended to use relevant metabolites to properly assess the immunotoxicity of pharmaceuticals to L. stagnalis.
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Lymnaea stagnalis was exposed in the laboratory for 3 days to three drugs used for immune systems: diclofenac (nonsteroidal anti-inflammatory drug), cyclophosphamide (anti-cancer immunosuppressive drug) or cyclosporine A (anti-xenograft immunosuppressive drug). Exposure ranges included environmental realistic (1–10μgL−1) and therapeutic concentrations (100–1000μgL−1). At the end of exposure times, the immune parameters of individual snails were measured: hemocyte density and viability, hemocyte phagocytosis capacity and hemocyte-related oxidative activities (basal and NADPH-oxidase stimulated with zymosan particles). Diclofenac and cyclosporine A induced immune responses, although the effects were not strong. No immunosuppression was observed. Such subtle immunomodulations bring further interrogations regarding their long-term immunotoxicity and possible resulting tradeoffs with life-history traits. On the other hand, the prodrug cyclophosphamide did not induce significant immune responses. Since metabolism pathways differ greatly between vertebrates and invertebrates, this study also suggests that relevant vertebrate metabolites should be included in the immunotoxicity assessment of pharmaceuticals in non-target invertebrate species. 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On the other hand, the prodrug cyclophosphamide did not induce significant immune responses. Since metabolism pathways differ greatly between vertebrates and invertebrates, this study also suggests that relevant vertebrate metabolites should be included in the immunotoxicity assessment of pharmaceuticals in non-target invertebrate species. 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subjects Animals
Anti-Inflammatory Agents, Non-Steroidal - toxicity
Biodiversity and Ecology
Blood Cell Count
Cell Survival - drug effects
Cellular Biology
Cyclophosphamide
Cyclophosphamide - toxicity
Cyclosporine - toxicity
Cyclosporine A
Diclofenac
Diclofenac - toxicity
Ecotoxicity
Environmental Sciences
Gastropod
Global Changes
Hemocytes - drug effects
Hemocytes - immunology
Immunology
Immunosuppressive Agents - toxicity
Immunotoxicity
Life Sciences
Lymnaea - drug effects
Lymnaea - immunology
Phagocytosis - drug effects
Pharmaceuticals
Water Pollutants, Chemical - toxicity
title Immune responses in the aquatic gastropod Lymnaea stagnalis under short-term exposure to pharmaceuticals of concern for immune systems: Diclofenac, cyclophosphamide and cyclosporine A
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