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Neurotoxicological profile of the hallucinogenic compound 25I-NBOMe
4-Iodo-2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (25I-NBOMe) is a new psychoactive substance with strong hallucinogenic properties. Our previous data reported increased release of dopamine, serotonin, and glutamate after acute injections and a tolerance development in the neurotransmitters rel...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861095/ https://www.ncbi.nlm.nih.gov/pubmed/35190675 http://dx.doi.org/10.1038/s41598-022-07069-8 |
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author | Herian, Monika Wojtas, Adam Maćkowiak, Marzena Wawrzczak-Bargiela, Agnieszka Solarz, Anna Bysiek, Agnieszka Madej, Katarzyna Gołembiowska, Krystyna |
author_facet | Herian, Monika Wojtas, Adam Maćkowiak, Marzena Wawrzczak-Bargiela, Agnieszka Solarz, Anna Bysiek, Agnieszka Madej, Katarzyna Gołembiowska, Krystyna |
author_sort | Herian, Monika |
collection | PubMed |
description | 4-Iodo-2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (25I-NBOMe) is a new psychoactive substance with strong hallucinogenic properties. Our previous data reported increased release of dopamine, serotonin, and glutamate after acute injections and a tolerance development in the neurotransmitters release and rats’ behavior after chronic treatment with 25I-NBOMe. The recreational use of 25I-NBOMe is associated with severe intoxication and deaths in humans. There is no data about 25I-NBOMe in vivo toxicity towards the brain tissue. In this article 25I-NBOMe-crossing through the blood–brain barrier (BBB), the impact on DNA damage, apoptosis induction, and changes in the number of cortical and hippocampal cells were studied. The presence of 25I-NBOMe in several brain regions shortly after the drug administration and its accumulation after multiple injections was found. The DNA damage was detected 72 h after the chronic treatment. On the contrary, at the same time point apoptotic signal was not identified. A decrease in the number of glial but not in neural cells in the frontal (FC) and medial prefrontal cortex (mPFC) was observed. The obtained data indicate that 25I-NBOMe passes easily across the BBB and accumulates in the brain tissue. Observed oxidative DNA damage may lead to the glial cells’ death. |
format | Online Article Text |
id | pubmed-8861095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88610952022-02-23 Neurotoxicological profile of the hallucinogenic compound 25I-NBOMe Herian, Monika Wojtas, Adam Maćkowiak, Marzena Wawrzczak-Bargiela, Agnieszka Solarz, Anna Bysiek, Agnieszka Madej, Katarzyna Gołembiowska, Krystyna Sci Rep Article 4-Iodo-2,5-dimethoxy-N-(2-methoxybenzyl)phenethylamine (25I-NBOMe) is a new psychoactive substance with strong hallucinogenic properties. Our previous data reported increased release of dopamine, serotonin, and glutamate after acute injections and a tolerance development in the neurotransmitters release and rats’ behavior after chronic treatment with 25I-NBOMe. The recreational use of 25I-NBOMe is associated with severe intoxication and deaths in humans. There is no data about 25I-NBOMe in vivo toxicity towards the brain tissue. In this article 25I-NBOMe-crossing through the blood–brain barrier (BBB), the impact on DNA damage, apoptosis induction, and changes in the number of cortical and hippocampal cells were studied. The presence of 25I-NBOMe in several brain regions shortly after the drug administration and its accumulation after multiple injections was found. The DNA damage was detected 72 h after the chronic treatment. On the contrary, at the same time point apoptotic signal was not identified. A decrease in the number of glial but not in neural cells in the frontal (FC) and medial prefrontal cortex (mPFC) was observed. The obtained data indicate that 25I-NBOMe passes easily across the BBB and accumulates in the brain tissue. Observed oxidative DNA damage may lead to the glial cells’ death. Nature Publishing Group UK 2022-02-21 /pmc/articles/PMC8861095/ /pubmed/35190675 http://dx.doi.org/10.1038/s41598-022-07069-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Herian, Monika Wojtas, Adam Maćkowiak, Marzena Wawrzczak-Bargiela, Agnieszka Solarz, Anna Bysiek, Agnieszka Madej, Katarzyna Gołembiowska, Krystyna Neurotoxicological profile of the hallucinogenic compound 25I-NBOMe |
title | Neurotoxicological profile of the hallucinogenic compound 25I-NBOMe |
title_full | Neurotoxicological profile of the hallucinogenic compound 25I-NBOMe |
title_fullStr | Neurotoxicological profile of the hallucinogenic compound 25I-NBOMe |
title_full_unstemmed | Neurotoxicological profile of the hallucinogenic compound 25I-NBOMe |
title_short | Neurotoxicological profile of the hallucinogenic compound 25I-NBOMe |
title_sort | neurotoxicological profile of the hallucinogenic compound 25i-nbome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861095/ https://www.ncbi.nlm.nih.gov/pubmed/35190675 http://dx.doi.org/10.1038/s41598-022-07069-8 |
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