Impact of the antidepressant citalopram on the behaviour of two different life stages of brown trout

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Impact of the antidepressant citalopram on the behaviour of two different life stages of brown trout. / Ziegler, Michael; Knoll, Sarah; Köhler, Heinz R.; Tisler, Selina; Huhn, Carolin; Zwiener, Christian; Triebskorn, Rita.

In: PeerJ, Vol. 2020, No. 3, e8765, 2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ziegler, M, Knoll, S, Köhler, HR, Tisler, S, Huhn, C, Zwiener, C & Triebskorn, R 2020, 'Impact of the antidepressant citalopram on the behaviour of two different life stages of brown trout', PeerJ, vol. 2020, no. 3, e8765. https://doi.org/10.7717/peerj.8765

APA

Ziegler, M., Knoll, S., Köhler, H. R., Tisler, S., Huhn, C., Zwiener, C., & Triebskorn, R. (2020). Impact of the antidepressant citalopram on the behaviour of two different life stages of brown trout. PeerJ, 2020(3), [e8765]. https://doi.org/10.7717/peerj.8765

Vancouver

Ziegler M, Knoll S, Köhler HR, Tisler S, Huhn C, Zwiener C et al. Impact of the antidepressant citalopram on the behaviour of two different life stages of brown trout. PeerJ. 2020;2020(3). e8765. https://doi.org/10.7717/peerj.8765

Author

Ziegler, Michael ; Knoll, Sarah ; Köhler, Heinz R. ; Tisler, Selina ; Huhn, Carolin ; Zwiener, Christian ; Triebskorn, Rita. / Impact of the antidepressant citalopram on the behaviour of two different life stages of brown trout. In: PeerJ. 2020 ; Vol. 2020, No. 3.

Bibtex

@article{5b2ddb2749154d36a97cfa460854efdc,
title = "Impact of the antidepressant citalopram on the behaviour of two different life stages of brown trout",
abstract = "Background. Over the last two decades, there has been a constant increase in prescription rates of antidepressants. In parallel, neuroactive pharmaceuticals are making their way into aquatic environments at increasing concentrations. Among the antidepressants detected in the environment citalopram, a selective serotonin reuptake inhibitor, is one of the most commonly found. Given citalopram is specifically designed to alter mood and behaviour in humans, there is growing concern it can adversely affect the behaviour on non-target wildlife Methods. In our study, brown trout were exposed to citalopram (nominal concentrations: 1, 10, 100, 1000 μg/L) in two different life stages. Larvae were exposed at 7 and 11 °C from the eyed ova stage until 8 weeks post yolk sac consumption, and juvenile brown trout were exposed for 4 weeks at 7 °C. At both stages we measured mortality, weight, length, tissue citalopram concentration, behaviour during exposure and behaviour in a stressfull environment. For brown trout larvae additionally hatching rate and heart rate, and for juvenile brown trout the tissue cortisol concentration were assessed. Results. During the exposure, both larvae and juvenile fish exposed to the highest test concentration of citalopram (1 mg/L) had higher swimming activity and spent longer in the upper part of the aquaria compared to control fish, which is an indicator for decreased anxiety. Most probably due to the higher swimming activity during the exposure, the juveniles and larvae exposed to 1 mg/L citalopram showed decreased weight and length. Additionally, in a stressful artificial swimming measurement device, brown trout larvae displayed the anxiolytic effect of the antidepressant by reduced swimming activity during this stress situation, already at concentrations of 100 μg/L citalopram. Chemical analysis of the tissue revealed rising citalopram tissue concentrations with rising exposure concentrations. Tissue concentrations were 10 times higher in juvenile fish compared to brown trout larvae. Fish plasma concentrations were calculated, which exceeded human therapeutic levels for the highest exposure concentration, matching the behavioural results. Developmental parameters like hatching rate and heart rate, as well as mortality and tissue cortisol content were unaffected by the antidepressant. Overall, we could trace the pharmacological mode of action of the antidepressant citalopram in the non-target organism brown trout in two different life stages.",
keywords = "Antidepressant, Behaviour, Brown trout, Citalopram, Corisol, Fish, Pharmaceutical, Stress hormone",
author = "Michael Ziegler and Sarah Knoll and K{\"o}hler, {Heinz R.} and Selina Tisler and Carolin Huhn and Christian Zwiener and Rita Triebskorn",
year = "2020",
doi = "10.7717/peerj.8765",
language = "English",
volume = "2020",
journal = "PeerJ",
issn = "2167-8359",
publisher = "PeerJ",
number = "3",

}

RIS

TY - JOUR

T1 - Impact of the antidepressant citalopram on the behaviour of two different life stages of brown trout

AU - Ziegler, Michael

AU - Knoll, Sarah

AU - Köhler, Heinz R.

AU - Tisler, Selina

AU - Huhn, Carolin

AU - Zwiener, Christian

AU - Triebskorn, Rita

PY - 2020

Y1 - 2020

N2 - Background. Over the last two decades, there has been a constant increase in prescription rates of antidepressants. In parallel, neuroactive pharmaceuticals are making their way into aquatic environments at increasing concentrations. Among the antidepressants detected in the environment citalopram, a selective serotonin reuptake inhibitor, is one of the most commonly found. Given citalopram is specifically designed to alter mood and behaviour in humans, there is growing concern it can adversely affect the behaviour on non-target wildlife Methods. In our study, brown trout were exposed to citalopram (nominal concentrations: 1, 10, 100, 1000 μg/L) in two different life stages. Larvae were exposed at 7 and 11 °C from the eyed ova stage until 8 weeks post yolk sac consumption, and juvenile brown trout were exposed for 4 weeks at 7 °C. At both stages we measured mortality, weight, length, tissue citalopram concentration, behaviour during exposure and behaviour in a stressfull environment. For brown trout larvae additionally hatching rate and heart rate, and for juvenile brown trout the tissue cortisol concentration were assessed. Results. During the exposure, both larvae and juvenile fish exposed to the highest test concentration of citalopram (1 mg/L) had higher swimming activity and spent longer in the upper part of the aquaria compared to control fish, which is an indicator for decreased anxiety. Most probably due to the higher swimming activity during the exposure, the juveniles and larvae exposed to 1 mg/L citalopram showed decreased weight and length. Additionally, in a stressful artificial swimming measurement device, brown trout larvae displayed the anxiolytic effect of the antidepressant by reduced swimming activity during this stress situation, already at concentrations of 100 μg/L citalopram. Chemical analysis of the tissue revealed rising citalopram tissue concentrations with rising exposure concentrations. Tissue concentrations were 10 times higher in juvenile fish compared to brown trout larvae. Fish plasma concentrations were calculated, which exceeded human therapeutic levels for the highest exposure concentration, matching the behavioural results. Developmental parameters like hatching rate and heart rate, as well as mortality and tissue cortisol content were unaffected by the antidepressant. Overall, we could trace the pharmacological mode of action of the antidepressant citalopram in the non-target organism brown trout in two different life stages.

AB - Background. Over the last two decades, there has been a constant increase in prescription rates of antidepressants. In parallel, neuroactive pharmaceuticals are making their way into aquatic environments at increasing concentrations. Among the antidepressants detected in the environment citalopram, a selective serotonin reuptake inhibitor, is one of the most commonly found. Given citalopram is specifically designed to alter mood and behaviour in humans, there is growing concern it can adversely affect the behaviour on non-target wildlife Methods. In our study, brown trout were exposed to citalopram (nominal concentrations: 1, 10, 100, 1000 μg/L) in two different life stages. Larvae were exposed at 7 and 11 °C from the eyed ova stage until 8 weeks post yolk sac consumption, and juvenile brown trout were exposed for 4 weeks at 7 °C. At both stages we measured mortality, weight, length, tissue citalopram concentration, behaviour during exposure and behaviour in a stressfull environment. For brown trout larvae additionally hatching rate and heart rate, and for juvenile brown trout the tissue cortisol concentration were assessed. Results. During the exposure, both larvae and juvenile fish exposed to the highest test concentration of citalopram (1 mg/L) had higher swimming activity and spent longer in the upper part of the aquaria compared to control fish, which is an indicator for decreased anxiety. Most probably due to the higher swimming activity during the exposure, the juveniles and larvae exposed to 1 mg/L citalopram showed decreased weight and length. Additionally, in a stressful artificial swimming measurement device, brown trout larvae displayed the anxiolytic effect of the antidepressant by reduced swimming activity during this stress situation, already at concentrations of 100 μg/L citalopram. Chemical analysis of the tissue revealed rising citalopram tissue concentrations with rising exposure concentrations. Tissue concentrations were 10 times higher in juvenile fish compared to brown trout larvae. Fish plasma concentrations were calculated, which exceeded human therapeutic levels for the highest exposure concentration, matching the behavioural results. Developmental parameters like hatching rate and heart rate, as well as mortality and tissue cortisol content were unaffected by the antidepressant. Overall, we could trace the pharmacological mode of action of the antidepressant citalopram in the non-target organism brown trout in two different life stages.

KW - Antidepressant

KW - Behaviour

KW - Brown trout

KW - Citalopram

KW - Corisol

KW - Fish

KW - Pharmaceutical

KW - Stress hormone

U2 - 10.7717/peerj.8765

DO - 10.7717/peerj.8765

M3 - Journal article

C2 - 32201650

AN - SCOPUS:85083497153

VL - 2020

JO - PeerJ

JF - PeerJ

SN - 2167-8359

IS - 3

M1 - e8765

ER -

ID: 256507542