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用于评估新型精神活性物质毒性的表观遗传学研究:聚焦合成大麻素和卡西酮

Epigenetic Studies for Evaluation of NPS Toxicity: Focus on Synthetic Cannabinoids and Cathinones.

作者信息

Mazdai Leila, Fabbri Matteo, Tirri Micaela, Corli Giorgia, Arfè Raffaella, Marchetti Beatrice, Bilel Sabrine, Bergamin Eva, Gaudio Rosa Maria, Rubini Michele, De-Giorgio Fabio, Marti Matteo

机构信息

Department of Neurosciences and Rehabilitation, Section of Medical Biochemistry, Molecular Biology and Genetics, University of Ferrara, 44121 Ferrara, Italy.

Department of Translational Medicine, Section of Legal Medicine, LTTA Center, University of Ferrara, 44121 Ferrara, Italy.

出版信息

Biomedicines. 2022 Jun 13;10(6):1398. doi: 10.3390/biomedicines10061398.


DOI:10.3390/biomedicines10061398
PMID:35740419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9219842/
Abstract

In the recent decade, numerous new psychoactive substances (NPSs) have been added to the illicit drug market. These are synthetized to mimic the effects of classic drugs of abuse (i.e., cannabis, cocaine, etc.), with the purpose of bypassing substance legislations and increasing the pharmacotoxicological effects. To date, research into the acute pharmacological effects of new NPSs is ongoing and necessary in order to provide an appropriate contribution to public health. In fact, multiple examples of NPS-related acute intoxication and mortality have been recorded in the literature. Accordingly, several in vitro and in vivo studies have investigated the pharmacotoxicological profiles of these compounds, revealing that they can cause adverse effects involving various organ systems (i.e., cardiovascular, respiratory effects) and highlighting their potential increased consumption risks. In this sense, NPSs should be regarded as a complex issue that requires continuous monitoring. Moreover, knowledge of long-term NPS effects is lacking. Because genetic and environmental variables may impact NPS responses, epigenetics may aid in understanding the processes behind the harmful events induced by long-term NPS usage. Taken together, "pharmacoepigenomics" may provide a new field of combined study on genetic differences and epigenetic changes in drug reactions that might be predictive in forensic implications.

摘要

在最近十年里,非法药物市场新增了大量新型精神活性物质(NPSs)。这些物质被合成出来以模仿传统滥用药物(如大麻、可卡因等)的效果,目的是规避药物立法并增强药物毒理学效应。迄今为止,对新型NPSs急性药理作用的研究仍在进行且很有必要,以便为公共卫生做出适当贡献。事实上,文献中已记录了多个与NPSs相关的急性中毒和死亡案例。相应地,多项体外和体内研究调查了这些化合物的药物毒理学特征,揭示它们可导致涉及多个器官系统的不良反应(如心血管、呼吸方面的影响),并凸显出其潜在的更高消费风险。从这个意义上讲,NPSs应被视为一个需要持续监测的复杂问题。此外,目前尚缺乏对NPSs长期影响的了解。由于基因和环境变量可能影响对NPSs的反应,表观遗传学可能有助于理解长期使用NPSs所引发有害事件背后的机制。综上所述,“药物表观基因组学”可能为药物反应中基因差异和表观遗传变化的联合研究提供一个新领域,这在法医层面可能具有预测意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d10/9219842/4daa8c97cb57/biomedicines-10-01398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d10/9219842/b09dfa32deb1/biomedicines-10-01398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d10/9219842/4daa8c97cb57/biomedicines-10-01398-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d10/9219842/b09dfa32deb1/biomedicines-10-01398-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d10/9219842/4daa8c97cb57/biomedicines-10-01398-g002.jpg

相似文献

[1]
Epigenetic Studies for Evaluation of NPS Toxicity: Focus on Synthetic Cannabinoids and Cathinones.

Biomedicines. 2022-6-13

[2]
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[3]
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[4]
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[6]
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[7]
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[8]
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[9]
Sex and Gender Differences in the Effects of Novel Psychoactive Substances.

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[10]
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[1]
Modern perspectives on psychoses: dissociation, automatism, and temporality across exogenous and endogenous dimensions.

Front Psychiatry. 2025-3-20

[2]
Rethinking Mental Automatism: De Clérambault's Theory in the Age of Novel Psychoactive Drugs: Psychotropic Effects and Synthetic Psychosis.

Healthcare (Basel). 2024-6-10

[3]
Mutuality of epigenetic and nanoparticles: two sides of a coin.

Heliyon. 2023-12-13

[4]
Geospatiotemporal and Causal Inferential Study of European Epidemiological Patterns of Cannabis- and Substance-Related Congenital Orofacial Anomalies.

J Xenobiot. 2023-2-1

本文引用的文献

[1]
In vitro and in vivo pharmaco-dynamic study of the novel fentanyl derivatives: Acrylfentanyl, Ocfentanyl and Furanylfentanyl.

Neuropharmacology. 2022-5-15

[2]
Ethanol enhanced MDPV- and cocaine-induced aggressive behavior in mice: Forensic implications.

Drug Alcohol Depend. 2021-12-1

[3]
Current and Future Perspectives of Noncoding RNAs in Brain Function and Neuropsychiatric Disease.

Biol Psychiatry. 2022-1-15

[4]
Rescuing effect of folates on methotrexate cytotoxicity in human trophoblast cells.

Clin Exp Rheumatol. 2022-7

[5]
In vitro metabolic profile of mexedrone, a mephedrone analog, studied by high- and low-resolution mass spectrometry.

Drug Test Anal. 2022-2

[6]
Worsening of the Toxic Effects of (±)-4,4'-DMAR Following Its Co-Administration with (±)-4,4'-DMAR: Neuro-Behavioural, Physiological, Immunohistochemical and Metabolic Studies in Mice.

Int J Mol Sci. 2021-8-16

[7]
Adolescent cannabinoid exposure modulates the vulnerability to cocaine-induced conditioned place preference and DNMT3a expression in the prefrontal cortex in Swiss mice.

Psychopharmacology (Berl). 2021-11

[8]
In Vitro and In Vivo Pharmaco-Toxicological Characterization of 1-Cyclohexyl-x-methoxybenzene Derivatives in Mice: Comparison with Tramadol and PCP.

Int J Mol Sci. 2021-7-17

[9]
Evaluation of Cytotoxic and Mutagenic Effects of the Synthetic Cathinones Mexedrone, α-PVP and α-PHP.

Int J Mol Sci. 2021-6-12

[10]
Molecular and clinical aspects of potential neurotoxicity induced by new psychoactive stimulants and psychedelics.

Exp Neurol. 2021-9

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