Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatography

Detalhes bibliográficos
Autor(a) principal: Costa, Ana Rita
Data de Publicação: 2023
Outros Autores: Gonçalves, Virgínia M. F., Castro, Bruno B., Carrola, João Soares, Langa, Ivan, Pereira, Ariana, Carvalho, Ana Rita, Tiritan, Maria Elizabeth, Ribeiro, Cláudia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/1822/85301
Resumo: MDMA (3,4-methylenedioxymethamphetamine) is a chiral psychoactive recreational drug sold in illicit markets as racemate. Studies on the impact of MDMA on aquatic organisms are scarce. While enantioselectivity in toxicity in animals and humans has been reported, none is reported on aquatic organisms. This study aimed to investigate the ecotoxicological effects of MDMA and its enantiomers in <i>Daphnia magna</i>. For that, enantiomers (enantiomeric purity > 97%) were separated by liquid chromatography using a homemade semipreparative chiral column. Daphnids were exposed to three concentrations of (<i>R</i>,<i>S</i>)-MDMA (0.1, 1.0 and 10.0 µg L<sup>−1</sup>) and two concentrations of (<i>R</i>)- and (<i>S</i>)-enantiomers (0.1 and 1.0 µg L<sup>−1</sup>) over the course of 8 days. Morphophysiological responses were dependent on the substance form and daphnia development stage, and they were overall not affected by the (<i>R</i>)-enantiomer. Changes in swimming behaviour were observed for both the racemate and its enantiomers, but enantioselective effects were not observed. Reproductive or biochemical changes were not observed for enantiomers whereas a significant decrease in acetylcholinesterase and catalase activity was noted at the highest concentration of (<i>R</i>,<i>S</i>)-MDMA (10 µg L<sup>−1</sup>). Overall, this study showed that sub-chronic exposure to MDMA racemate and its enantiomers can interfere with morphophysiological and swimming behaviour of <i>D. magna</i>. In general, the (<i>R</i>)-enantiomer demonstrated less toxicity than the (<i>S</i>)-enantiomer.
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spelling Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatographyAquatic organismsChiralityEcotoxicityEnantioselectivityPsychoactive drugsScience & TechnologyMDMA (3,4-methylenedioxymethamphetamine) is a chiral psychoactive recreational drug sold in illicit markets as racemate. Studies on the impact of MDMA on aquatic organisms are scarce. While enantioselectivity in toxicity in animals and humans has been reported, none is reported on aquatic organisms. This study aimed to investigate the ecotoxicological effects of MDMA and its enantiomers in <i>Daphnia magna</i>. For that, enantiomers (enantiomeric purity > 97%) were separated by liquid chromatography using a homemade semipreparative chiral column. Daphnids were exposed to three concentrations of (<i>R</i>,<i>S</i>)-MDMA (0.1, 1.0 and 10.0 µg L<sup>−1</sup>) and two concentrations of (<i>R</i>)- and (<i>S</i>)-enantiomers (0.1 and 1.0 µg L<sup>−1</sup>) over the course of 8 days. Morphophysiological responses were dependent on the substance form and daphnia development stage, and they were overall not affected by the (<i>R</i>)-enantiomer. Changes in swimming behaviour were observed for both the racemate and its enantiomers, but enantioselective effects were not observed. Reproductive or biochemical changes were not observed for enantiomers whereas a significant decrease in acetylcholinesterase and catalase activity was noted at the highest concentration of (<i>R</i>,<i>S</i>)-MDMA (10 µg L<sup>−1</sup>). Overall, this study showed that sub-chronic exposure to MDMA racemate and its enantiomers can interfere with morphophysiological and swimming behaviour of <i>D. magna</i>. In general, the (<i>R</i>)-enantiomer demonstrated less toxicity than the (<i>S</i>)-enantiomer.This work was financially supported by national funds through the FCT/MCTES (PIDDAC), under the project PTDC/CTA-AMB/6686/2020, and partially supported through the projects UIDB/04423/2020 and UIDP/04423/2020 (Group of Natural Products and Medicinal ChemistryCIIMAR).Multidisciplinary Digital Publishing Institute (MDPI)Universidade do MinhoCosta, Ana RitaGonçalves, Virgínia M. F.Castro, Bruno B.Carrola, João SoaresLanga, IvanPereira, ArianaCarvalho, Ana RitaTiritan, Maria ElizabethRibeiro, Cláudia2023-02-022023-02-02T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/85301engCosta, A.R.; Gonçalves, V.M.F.; Castro, B.B.; Carrola, J.S.; Langa, I.; Pereira, A.; Carvalho, A.R.; Tiritan, M.E.; Ribeiro, C. Toxicity of the 3,4-Methylenedioxymethamphetamine and Its Enantiomers to Daphnia magna after Isolation by Semipreparative Chromatography. Molecules 2023, 28, 1457. https://doi.org/10.3390/molecules280314571420-304910.3390/molecules28031457367711191457https://www.mdpi.com/1420-3049/28/3/1457info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:26:41Zoai:repositorium.sdum.uminho.pt:1822/85301Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:21:10.078871Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatography
title Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatography
spellingShingle Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatography
Costa, Ana Rita
Aquatic organisms
Chirality
Ecotoxicity
Enantioselectivity
Psychoactive drugs
Science & Technology
title_short Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatography
title_full Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatography
title_fullStr Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatography
title_full_unstemmed Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatography
title_sort Toxicity of the 3,4-methylenedioxymethamphetamine and its enantiomers to Daphnia magna after isolation by semipreparative chromatography
author Costa, Ana Rita
author_facet Costa, Ana Rita
Gonçalves, Virgínia M. F.
Castro, Bruno B.
Carrola, João Soares
Langa, Ivan
Pereira, Ariana
Carvalho, Ana Rita
Tiritan, Maria Elizabeth
Ribeiro, Cláudia
author_role author
author2 Gonçalves, Virgínia M. F.
Castro, Bruno B.
Carrola, João Soares
Langa, Ivan
Pereira, Ariana
Carvalho, Ana Rita
Tiritan, Maria Elizabeth
Ribeiro, Cláudia
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Costa, Ana Rita
Gonçalves, Virgínia M. F.
Castro, Bruno B.
Carrola, João Soares
Langa, Ivan
Pereira, Ariana
Carvalho, Ana Rita
Tiritan, Maria Elizabeth
Ribeiro, Cláudia
dc.subject.por.fl_str_mv Aquatic organisms
Chirality
Ecotoxicity
Enantioselectivity
Psychoactive drugs
Science & Technology
topic Aquatic organisms
Chirality
Ecotoxicity
Enantioselectivity
Psychoactive drugs
Science & Technology
description MDMA (3,4-methylenedioxymethamphetamine) is a chiral psychoactive recreational drug sold in illicit markets as racemate. Studies on the impact of MDMA on aquatic organisms are scarce. While enantioselectivity in toxicity in animals and humans has been reported, none is reported on aquatic organisms. This study aimed to investigate the ecotoxicological effects of MDMA and its enantiomers in <i>Daphnia magna</i>. For that, enantiomers (enantiomeric purity > 97%) were separated by liquid chromatography using a homemade semipreparative chiral column. Daphnids were exposed to three concentrations of (<i>R</i>,<i>S</i>)-MDMA (0.1, 1.0 and 10.0 µg L<sup>−1</sup>) and two concentrations of (<i>R</i>)- and (<i>S</i>)-enantiomers (0.1 and 1.0 µg L<sup>−1</sup>) over the course of 8 days. Morphophysiological responses were dependent on the substance form and daphnia development stage, and they were overall not affected by the (<i>R</i>)-enantiomer. Changes in swimming behaviour were observed for both the racemate and its enantiomers, but enantioselective effects were not observed. Reproductive or biochemical changes were not observed for enantiomers whereas a significant decrease in acetylcholinesterase and catalase activity was noted at the highest concentration of (<i>R</i>,<i>S</i>)-MDMA (10 µg L<sup>−1</sup>). Overall, this study showed that sub-chronic exposure to MDMA racemate and its enantiomers can interfere with morphophysiological and swimming behaviour of <i>D. magna</i>. In general, the (<i>R</i>)-enantiomer demonstrated less toxicity than the (<i>S</i>)-enantiomer.
publishDate 2023
dc.date.none.fl_str_mv 2023-02-02
2023-02-02T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/1822/85301
url https://hdl.handle.net/1822/85301
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Costa, A.R.; Gonçalves, V.M.F.; Castro, B.B.; Carrola, J.S.; Langa, I.; Pereira, A.; Carvalho, A.R.; Tiritan, M.E.; Ribeiro, C. Toxicity of the 3,4-Methylenedioxymethamphetamine and Its Enantiomers to Daphnia magna after Isolation by Semipreparative Chromatography. Molecules 2023, 28, 1457. https://doi.org/10.3390/molecules28031457
1420-3049
10.3390/molecules28031457
36771119
1457
https://www.mdpi.com/1420-3049/28/3/1457
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eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute (MDPI)
publisher.none.fl_str_mv Multidisciplinary Digital Publishing Institute (MDPI)
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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