Evidence map›Paper›PMID 32201650›Full record

ArticlePeerJ2020

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

Michael Ziegler, Sarah Knoll, Heinz-R Köhler, Selina Tisler, Carolin Huhn, Christian Zwiener, Rita Triebskorn

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 34 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Michael ZieglerAnimal Physiolgical Ecology, Eberhard-Karls-Universität Tübingen, Tübingen, Baden-Württemberg, Germany.
Sarah KnollEffect-based Environmental Analysis, Eberhard-Karls-Universität Tübingen, Tübingen, Baden-Württemberg, Germany.
Heinz-R KöhlerAnimal Physiolgical Ecology, Eberhard-Karls-Universität Tübingen, Tübingen, Baden-Württemberg, Germany.
Selina TislerEnvironmental Analytical Chemistry, Eberhard-Karls-Universität Tübingen, Tübingen, Baden-Württemberg, Germany.
Carolin HuhnEffect-based Environmental Analysis, Eberhard-Karls-Universität Tübingen, Tübingen, Baden-Württemberg, Germany.
Christian ZwienerEnvironmental Analytical Chemistry, Eberhard-Karls-Universität Tübingen, Tübingen, Baden-Württemberg, Germany.
Rita TriebskornAnimal Physiolgical Ecology, Eberhard-Karls-Universität Tübingen, Tübingen, Baden-Württemberg, Germany.
University of Tübingen · DESteinbeis Foundation · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOver 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.

methodsIn 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.

resultsDuring 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.

Indexed as

AntidepressantBehaviourBrown troutCitalopramCorisolFishPharmaceuticalStress hormone

Identifiers

PMID32201650
PMCPMC7073243
OpenAlexW3011447441

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.