Mephedrone – a synthetic derivative of cathinone

IF 0.4 Q3 MEDICINE, GENERAL & INTERNAL Current Issues in Pharmacy and Medical Sciences Pub Date : 2023-03-01 DOI:10.2478/cipms-2023-0011
Gabriela Bielecka-Papierz, E. Poleszak, Anna Serafko
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Abstract

Abstract Novel psychoactive substances (NPS) are a very diverse group of recreational drugs that mimic effects of classic drugs of abuse and, at least at the beginning, are not usually prohibited. Representative of this group is mephedrone – a cathinone derivative. It is widely used as a recreational drug, particularly among club guests. Mephedrone`s effects are compared to effects of cocaine and MDMA but are more short-lived and include: psychostimulation, enhanced empathy, reduced feeling of tiredness, euphoria, hallucinations. This drug also exerts adverse effects, such as: anxiety, delusions, paranoia, psychosis, increased body temperature, elevated blood pressure, sleep disturbances. According to surveys performed on mephedrone users, it may be addictive. Those findings confirms a growing number of behavioural and molecular studies on animals. Mephedrone acts mainly via increasing monoamine transmission through increasing release of dopamine, serotonin and noradrenaline into synaptic cleft, inhibiting their re-uptake and reducing their metabolism. However, participation of other transmitters, modulators and pathways are investigated, including glutamate and nitric oxide. Favorable routes of administering mephedrone is intranasal and per os. Moreover, most often drug users use it in a binge way, e.g. taking repeated doses of a drug in a short period of time. According to animal studies, this pattern of mephedrone use leaves more neural injuries than taking it regularly, but in smaller doses. Our aim was to present a short, but essential, overview of the current knowledge on mephedrone, focusing on its effects, mechanism of action, animal studies evaluating its influence on the brain structures, toxicity and pharmacokinetics.
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甲氧麻黄酮-卡西酮的合成衍生物
新型精神活性物质(NPS)是一类非常多样化的娱乐性药物,它们模仿经典药物的滥用效果,至少在开始时通常不被禁止。这类药物的代表是甲氧麻黄酮——卡西酮的衍生物。它被广泛用作消遣性毒品,尤其是在俱乐部客人中。与可卡因和MDMA相比,甲氧麻黄酮的效果更短暂,包括:精神刺激、增强同理心、减少疲惫感、欣快感和幻觉。这种药物也有副作用,如:焦虑、妄想、偏执、精神病、体温升高、血压升高、睡眠障碍。根据对甲氧麻黄酮使用者的调查,它可能会上瘾。这些发现证实了越来越多的动物行为和分子研究。甲氧麻黄酮主要通过增加多巴胺、血清素和去甲肾上腺素向突触间隙的释放增加单胺的传递,抑制它们的再摄取,降低它们的代谢。然而,其他递质、调节剂和途径的参与也被研究,包括谷氨酸和一氧化氮。给予甲氧麻黄酮的有利途径是鼻内和静脉注射。此外,大多数情况下,吸毒者以暴饮暴食的方式使用它,例如在短时间内重复服用一种药物。根据动物研究,这种使用甲氧麻黄酮的模式比定期服用更容易造成神经损伤,但剂量较小。我们的目的是对甲氧麻黄酮的现有知识进行简短但必要的概述,重点是其作用、作用机制、评估其对大脑结构影响的动物研究、毒性和药代动力学。
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来源期刊
Current Issues in Pharmacy and Medical Sciences
Current Issues in Pharmacy and Medical Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
0.80
自引率
0.00%
发文量
28
审稿时长
16 weeks
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