Changes on swimming behavior induced by 3,4-methylenedioxypyrovalerone (MDPV) enantiomers on Daphnia magna
DOI:
https://doi.org/10.48797/sl.2023.36Keywords:
PosterAbstract
Background: Synthetic cathinones (SC) are a group of novel illicit psychotropic substances that have been found in the aquatic environment at low concentrations [1] and nonetheless they can impact aquatic invertebrates [2]. SC can pose unwanted diverse adverse effects such as behavioral toxicity to non-target organisms [3]. The 3,4-methylenedioxypyrovalerone (MDPV) is a chiral SC with psychotropic properties similar to methamphetamine and is traded as “bath salts” [4]. MDPV may be found in distinct forms, racemate or its enantiomers, that may exhibit different biological activities [2, 5]. Nevertheless, MDPV enantiotoxicity continued to be ignored as well as its impact on freshwater aquatic organisms, including invertebrates. Objective: This work aimed to assess the potential adverse effects of (R)-MDPV and (S)-MDPV on the swimming behavior of Daphnia magna. Methods: For that, neonates (< 24 hours) were exposed to 0.1 and 1.0 µg L-1 of both MDPV enantiomers for 5 days (5 replicates with 20 organisms each). After the end of exposure, 6 organisms of each replicate were randomly collected, placed into a 6-well plate (with ≈ 5 mL of the respective exposure medium) and video recorded for 1 minute. Parameters such as swimming speed, total distance travelled, and active time were evaluated using TheRealFishTracker program. Results: A significant increase in swimming speed was observed for the organisms exposed only to (S)-MDPV. On the contrary, an increase in active time was found in the organisms exposed to (R)-MDPV. No changes were detected for the total distance travelled for both enantiomers. Conclusions: This study showed that MDPV can interfere with the swimming behavior pattern of daphnia and that effects are enantioselective. However, for a better understanding of the enantioselective toxicity of MDPV on the fitness of daphnia, other parameters should be included (i.e., morphophysiological, reproductive and biochemical).
References
1. Castiglioni S.; Salgueiro-González N.; Bijlsma L.; Celma A.; Gracia-Lor E.; Beldean-Galea M.; Mackuľak T.; Emke E.; Heath E.; Kasprzyk-Hordern B.; Petkovic A.; Poretti F.; Rangelov J.; Santos M.; Sremaˇcki M.; Styszko K.; Hernández F.; Zuccato E. New psychoactive substances in several European populations as-sessed by wastewater-based epidemiology. Water Res 2021, 195, 116983.
2. Ribeiro A.; Maia A.; Ribeiro C.; Tiritan M. Analysis of chiral drugs in environmental matrices: Current knowledge and trends in environmental, biodegradation and forensic fields. TrAC Trend Anal Chem 2020, 124, 115783.
3. Kuropka P.; Zawadzki M.; Szpot P. A review of synthetic cathinones emerging in recent years (2019–2022). Forensic Toxicol 2022, 41(1), 25-46.
4. Soares J.; Costa V.; Bastos M.; Carvalho F.; Capela J. An updated review on synthetic cathinones. Arch Toxicol 2021, 95(9), 2895-2940.
5. Pérez-Pereira A.; Ribeiro C.; Teles F.; Gonçalves R.; Goncalves V.; Pereira J.; Carrola J.; Pires C.; Tiritan M. Ketamine and norketamine: enantioresolution and enantioselective aquatic ecotoxicity studies. Environ Toxicol Chem 2021, 41(3), 569-579.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2023 A. Pérez-Pereira, A. Carvalho, B. Castro, J. S. Carrola, C. Fernandes, M. Tiritan, C. Ribeiro
This work is licensed under a Creative Commons Attribution 4.0 International License.
In Scientific Letters, articles are published under a CC-BY license (Creative Commons Attribution 4.0 International License), the most open license available. The users can share (copy and redistribute the material in any medium or format) and adapt (remix, transform, and build upon the material for any purpose, even commercially), as long as they give appropriate credit, provide a link to the license, and indicate if changes were made (read the full text of the license terms and conditions of use).
The author is the owner of the copyright.