Assessing neurological and cardiovascular effects caused by pharmaceuticals in river water: Insights from Daphnia magna and Danio rerio embryos

dc.contributor
Universitat Ramon Llull. IQS
dc.contributor.author
Romero Alfano, Irene
dc.contributor.author
Prats, Eva
dc.contributor.author
Raldua, Demetrio
dc.contributor.author
Blazquez, Mercedes
dc.contributor.author
Tauler, Roma
dc.contributor.author
Piña, Benjamí
dc.contributor.author
Gómez-Canela, Cristian
dc.contributor.author
Barata, Carlos
dc.date.accessioned
2025-07-11T06:42:27Z
dc.date.available
2025-07-11T06:42:27Z
dc.date.issued
2025-09
dc.identifier.issn
1879-1298
dc.identifier.uri
http://hdl.handle.net/20.500.14342/5390
dc.description.abstract
Pharmaceutical residues in surface waters are an emerging environmental and public health issue, yet their biological impacts on aquatic life remain poorly understood. This study presents a cost-effective bioanalytical framework using Daphnia magna juveniles and zebrafish (Danio rerio) embryos to evaluate neurotoxic and cardiotoxic effects of pharmaceutical mixtures in rivers downstream of wastewater treatment plant (WWTP) effluents. Water samples from three rivers in north-eastern Spain (Besòs, Llobregat, and Onyar) were concentrated up to 5- and 20-fold using solid-phase extraction. Bioassays were conducted over 24 h for D. magna and five days for zebrafish embryos. Eighty pharmaceutical compounds were quantified via HPLC-MS and linked with phenotypic endpoints including locomotion, feeding, heart rate, neurotransmitter profiles, and metabolomic alterations. Of the 28 concentrated extracts, four were acutely toxic to zebrafish embryos. Altered behavioral and cardiovascular responses were observed in 22.2 % (D. magna) and 35.1 % (D. rerio) of extracts, primarily at higher enrichment. Concentrations of 31 pharmaceuticals were statistically associated with observed effects. Neuroactive drugs such as topiramate, rasagiline, citalopram, and fluvoxamine showed strong correlations with altered neurotransmitter levels in zebrafish, consistent with their known mechanisms. Seven additional compounds with secondary neuroactive properties were linked to similar neurological disruptions. Seventeen pharmaceuticals were associated with disturbances in amino acid metabolism and urea cycle pathways, indicating broader metabolic dysregulation. Overall, nearly 75 % of river extracts showed no observable effect, but several samples were acutely toxic or induced sublethal neurobehavioral and metabolic responses. These findings support the utility of D. magna and zebrafish (D. rerio) embryos as sensitive and complementary biosentinels for monitoring pharmaceutical pollution and highlight zebrafish as a relevant model for studying environmentally driven neurotoxicity with potential human health implications.
dc.format.extent
p.13
dc.language.iso
eng
dc.publisher
Elsevier
dc.relation.ispartof
Chemosphere 2025, 385
dc.rights
© L'autor/a
dc.rights
Attribution 4.0 International
dc.rights.uri
http://creativecommons.org/licenses/by/4.0/
dc.subject
Pharmaceuticals
dc.subject
Neurotoxic
dc.subject
Daphnia magna
dc.subject
Zebrafish
dc.subject
Wastewater
dc.subject
Environmental risk assessment
dc.subject
Indústria farmacèutica
dc.subject
Neurotoxines
dc.subject
Clàdocers
dc.subject
Peix zebra
dc.subject
Aigua--Contaminació
dc.subject
Medi ambient--Avaluació del risc
dc.title
Assessing neurological and cardiovascular effects caused by pharmaceuticals in river water: Insights from Daphnia magna and Danio rerio embryos
dc.type
info:eu-repo/semantics/article
dc.subject.udc
502
dc.subject.udc
615
dc.description.version
info:eu-repo/semantics/publishedVersion
dc.embargo.terms
cap
dc.relation.projectID
info:eu-repo/grantAgreement/AEI-MCIN/PN I+D/TED2021-130845A-C32
dc.relation.projectID
info:eu-repo/grantAgreement/AEI-MCIN/PN I+D/TED2021-130845B–C31
dc.relation.projectID
info:eu-repo/grantAgreement/MCIU/PN I+D/PID2023–148502OB-C21
dc.relation.projectID
info:eu-repo/grantAgreement/MCIU/PN I+D/PID2023–148502OB-C22
dc.relation.projectID
info:eu-repo/grantAgreement/SUR del DEC/SGR/236SGR21
dc.identifier.doi
https://doi.org/10.1016/j.chemosphere.2025.144541
dc.rights.accessLevel
info:eu-repo/semantics/openAccess


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