{"title":"Effects of Short-Term 5-MeO-DiPT Exposure on the Brain Metabolome of Zebrafish (Danio rerio).","authors":"Yin Tang, Yanjiao Wang, Liang Meng, Sen Zhao","doi":"10.1002/jat.70178","DOIUrl":null,"url":null,"abstract":"<p><p>5-MeO-DiPT (5-methoxy-N,N-diisopropyltryptamine) has been preliminarily reported to exhibit short-term hallucinogenic effects on humans. However, the connection between its toxic mechanism and behavioral changes remains unexplored. Therefore, this study used zebrafish as the research subject to investigate the metabolic characteristics of 5-MeO-DiPT and its perturbation effects on the metabolic network of organisms and verified the specific impacts of this perturbation through behavioral studies. It is shown that 27 metabolites with significant changes were detected in the brain of zebrafish after being exposed to 5-MeO-DiPT for a short period. The concentration of eight metabolites is increased, whereas the other 19 show a downward trend. Additionally, nine core metabolic pathways were significantly perturbed (p < 0.05). It is indicated that 5-MeO-DiPT disrupted the homeostasis of neurotransmitters, interfered with amino acid metabolism and lipid peroxidation reactions, causing a series of damages to the organism's neural conduction, immune response, and energy metabolism. Its potential carcinogenic risk and the mechanism of inducing metabolic syndrome deserve attention. Filling the theoretical gap in the research of the metabolic mechanism of this drug provides a reference basis for the next step of its research direction.</p>","PeriodicalId":15242,"journal":{"name":"Journal of Applied Toxicology","volume":" ","pages":"4175-4185"},"PeriodicalIF":3.1000,"publicationDate":"2026-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/jat.70178","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/4/8 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
5-MeO-DiPT (5-methoxy-N,N-diisopropyltryptamine) has been preliminarily reported to exhibit short-term hallucinogenic effects on humans. However, the connection between its toxic mechanism and behavioral changes remains unexplored. Therefore, this study used zebrafish as the research subject to investigate the metabolic characteristics of 5-MeO-DiPT and its perturbation effects on the metabolic network of organisms and verified the specific impacts of this perturbation through behavioral studies. It is shown that 27 metabolites with significant changes were detected in the brain of zebrafish after being exposed to 5-MeO-DiPT for a short period. The concentration of eight metabolites is increased, whereas the other 19 show a downward trend. Additionally, nine core metabolic pathways were significantly perturbed (p < 0.05). It is indicated that 5-MeO-DiPT disrupted the homeostasis of neurotransmitters, interfered with amino acid metabolism and lipid peroxidation reactions, causing a series of damages to the organism's neural conduction, immune response, and energy metabolism. Its potential carcinogenic risk and the mechanism of inducing metabolic syndrome deserve attention. Filling the theoretical gap in the research of the metabolic mechanism of this drug provides a reference basis for the next step of its research direction.
据初步报道,5-MeO-DiPT(5-甲氧基- n, n -二异丙基色胺)对人类具有短期致幻作用。然而,其毒性机制与行为改变之间的联系仍未被探索。因此,本研究以斑马鱼为研究对象,研究5-MeO-DiPT的代谢特性及其扰动对生物体代谢网络的影响,并通过行为学研究验证这种扰动的具体影响。结果表明,短时间暴露于5-MeO-DiPT后,斑马鱼大脑中检测到27种代谢物发生了显著变化。8种代谢物浓度呈上升趋势,其余19种呈下降趋势。此外,9个核心代谢途径明显受到干扰(p
期刊介绍:
Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.