Cellular mechanisms of 1,3-DMAA-induced neurotoxicity in SH-SY5Y cells
DOI:
https://doi.org/10.48797/sl.2026.481Keywords:
Poster CommunicationAbstract
Background: 1,3-Dimethylamylamine (1,3-DMAA) is a chiral sympathomimetic amine commonly added to dietary supplements marketed for weight loss, performance enhancement, and recreational purposes [2]. Despite regulatory bans, 1,3-DMAA continues to be detected in doping controls and dietary supplements, raising toxicological concerns. However, the cellular mechanisms underlying its neurotoxic potential remain incompletely characterized [3]. Objective: This study aimed to investigate the cytotoxic mechanisms induced by 1,3-DMAA in a human neuronal cell model (SH-SY5Y), contributing to a better understanding of its toxicodynamics. Methods: SH-SY5Y cells were exposed for 48 h to 1,3-DMAA (1.3×10⁻⁴ to 1.5×10¹ mM; n=5); mitochondrial metabolic activity was assessed using the MTT assay and the lysosomal integrity through the neutral red uptake (NR) assay. Based on the MTT results, cells were subsequently exposed to the EC20 (4.21 mM), EC40 (4.91 mM), and EC60 (5.59 mM), and changes in intracellular reactive oxygen species (ROS) production and mitochondrial membrane potential (ΔΨm) were assessed using fluorometric probes. Autophagic features were evaluated using acridine orange (AO) staining to detect acidic vesicular organelles. Results: 1,3-DMAA induced concentration-dependent cytotoxicity, with a greater impact on mitochondrial function than lysosomal integrity, as evidenced by lower EC50 values in the MTT assay compared to the NR assay (5.24 mM versus 6.36 mM, respectively). 1,3-DMAA induced a concentration-dependent increase in intracellular ROS levels from EC20 (236.67%; p<0.001) and EC40 (211.87%; p<0.01) and peaking at EC60 (272.05%; p<0.0001). In contrast, ΔΨm remained unchanged at lower concentrations, with a significant increase observed at EC60 (317.32%; p<0.0001). AO staining showed increased acidic vesicular organelles at higher concentrations. Conclusions: The concomitant increase in ROS and mitochondrial hyperpolarization of ΔΨm indicates a pro-oxidant state. The increase in acidic vesicular organelles suggests activation of autophagic processes and/or progression to apoptosis. These findings provide mechanistic insight into 1,3-DMAA-induced neurotoxicity and establish a foundation for further toxicological investigations.
References
1.Venhuis, B.J. et al. Scientific opinion on the regulatory status of 1,3-dimethylamylamine (DMAA). Eur J Food Res Rev 2012, 2, 93–100.
2.Rodrigues, A.N. et al Pharmacokinetic and toxicological aspects of 1,3-dimethylamylamine with clinical and forensic relevance. Psychoactives 2023, 2, 222–241, doi: 10.3390/psychoactives2030015.
3.Small, C. et al. The alkylamine stimulant 1,3-dimethylamylamine exhibits substrate-like regulation of dopamine transporter function and localization. J Pharmacol Exp Ther 2023, 386, 266–273, doi: 10.1124/jpet.122.001573.
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Copyright (c) 2026 Maria Mexia-de-Almeida , Andreia Machado Brito-da-Costa , Cláudia Ribeiro, Ricardo Jorge Dinis-Oliveira , Diana Dias da Silva
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