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2C-B(4-溴-2,5-二甲氧基苯乙胺)对大鼠的行为、神经化学和药物脑电图特征。

Behavioral, neurochemical and pharmaco-EEG profiles of the psychedelic drug 4-bromo-2,5-dimethoxyphenethylamine (2C-B) in rats.

机构信息

Prague Psychiatric Center, Ústavní 91, 181 03 Bohnice, Prague 8, Czech Republic.

出版信息

Psychopharmacology (Berl). 2013 Jan;225(1):75-93. doi: 10.1007/s00213-012-2797-7. Epub 2012 Jul 29.

DOI:10.1007/s00213-012-2797-7
PMID:22842791
Abstract

RATIONALE AND OBJECTIVES

Behavioral, neurochemical and pharmaco-EEG profiles of a new synthetic drug 4-bromo-2,5-dimethoxyphenethylamine (2C-B) in rats were examined.

MATERIALS AND METHODS

Locomotor effects, prepulse inhibition (PPI) of acoustic startle reaction (ASR), dopamine and its metabolite levels in nucleus accumbens (NAc), EEG power spectra and coherence in freely moving rats were analysed. Amphetamine was used as a reference compound.

RESULTS

2C-B had a biphasic effect on locomotion with initial inhibitory followed by excitatory effect; amphetamine induced only hyperlocomotion. Both drugs induced deficits in the PPI; however they had opposite effects on ASR. 2C-B increased dopamine but decreased 3,4-dihydroxyphenylacetic acid (DOPAC) in the NAc. Low doses of 2C-B induced a decrease in EEG power spectra and coherence. On the contrary, high dose of 2C-B 50 mg/kg had a temporally biphasic effect with an initial decrease followed by an increase in EEG power; decrease as well as increase in EEG coherence was observed. Amphetamine mainly induced an increase in EEG power and coherence in theta and alpha bands. Increases in the theta and alpha power and coherence in 2C-B and amphetamine were temporally linked to an increase in locomotor activity and DA levels in NAc.

CONCLUSIONS

2C-B is a centrally active compound similar to other hallucinogens, entactogens and stimulants. Increased dopamine and decreased DOPAC in the NAc may reflect its psychotomimetic and addictive potential and monoaminoxidase inhibition. Alterations in brain functional connectivity reflected the behavioral and neurochemical changes produced by the drug; a correlation between EEG changes and locomotor behavior was observed.

摘要

目的和背景

研究了一种新型合成药物 4-溴-2,5-二甲氧基苯乙胺(2C-B)在大鼠体内的行为、神经化学和药物脑电图特征。

材料和方法

分析了自由活动大鼠的运动效应、听觉惊跳反应(ASR)的前脉冲抑制(PPI)、伏隔核(NAc)中的多巴胺及其代谢物水平、脑电图功率谱和相干性。使用安非他命作为参考化合物。

结果

2C-B 对运动有双相作用,初始抑制,随后兴奋;安非他命仅引起过度运动。两种药物均导致 PPI 缺陷;然而,它们对 ASR 有相反的影响。2C-B 增加了多巴胺,但减少了 NAc 中的 3,4-二羟基苯乙酸(DOPAC)。2C-B 的低剂量导致脑电图功率谱和相干性降低。相反,高剂量 2C-B(50mg/kg)在时间上具有双相作用,初始减少,随后增加 EEG 功率;观察到 EEG 相干性的降低和增加。安非他命主要引起 theta 和 alpha 频段 EEG 功率和相干性增加。2C-B 和安非他命中 theta 和 alpha 功率和相干性的增加与运动活动和 NAc 中多巴胺水平的增加时间相关。

结论

2C-B 是一种中枢活性化合物,类似于其他致幻剂、快感增强剂和兴奋剂。NAc 中多巴胺的增加和 DOPAC 的减少可能反映了其致幻和成瘾潜力以及单胺氧化酶抑制作用。脑功能连接的改变反映了药物引起的行为和神经化学变化;观察到 EEG 变化与运动行为之间的相关性。

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