Cognitive and subjective dose-response effects of acute oral Δ9-tetrahydrocannabinol (THC) in infrequent cannabis users

Cognitive and subjective dose-response effects of acute oral Δ9-tetrahydrocannabinol (THC) in infrequent cannabis users
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DOI:
10.1007/s00213-002-1169-0
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发表时间:
2002-10-01
期刊:
影响因子:
3.4
通讯作者:
Henry, J
Henry, J
中科院分区:
医学3区
文献类型:
--
作者:
Curran, HV;Brignell, C;Henry, J

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基本原理:虽然已知记忆功能的某些方面会受到Delta(9)-tetrahydrocannabinol(Delta(9)-THC;大麻的主要活性成分)的严重损害,但对记忆其他方面的影响尚不清楚,功能损害的时间过程也不清楚。目的:本研究旨在详细说明Delta(9)-THC对偶尔使用大麻者的急性和残留认知影响。研究方法:在15名男性志愿者中,使用平衡的双盲交叉设计来比较7.5 mg和15 mg Delta(9)-THC与匹配的安慰剂的效果。在给药前和给药后1、2、4、6、8、24和48 h对参与者进行评估。结果:Delta(9)-THC 15 mg在血浆浓度峰值时(给药后2 h)损害了两项外显记忆任务的表现。在同一时间点,内隐记忆任务的表现保持不变。较高剂量的Delta(9)-THC导致在2小时的三次试验选择性提醒任务中没有任何学习发生。工作记忆通常不受Delta(9)-THC的影响。在几项任务中,Delta(9)-THC增加了速度和错误率,反映了“更高风险”的速度-准确性权衡。主观效应在2小时时也最明显,但通常持续时间更长,参与者将自己评为“石头”8小时。参与者经历了强烈的药物作用,喜欢这种效果,直到4小时,想要更多的口服Delta(9)-THC。在摄入后24或48小时未发现Delta(9)-THC的影响,表明口服Delta(9)-THC的残留影响极小。结论:这些数据表明,口服Delta(9)-THC以剂量依赖性方式损害情景记忆和学习,同时保留感知启动和工作记忆。
Rationale: Although some aspects of memory functions are known to be acutely impaired by Delta(9)-tetrahydrocannabinol (Delta(9)-THC; the main active constituent of marijuana), effects on other aspects of memory are not known and the time course of functional impairments is unclear. Objective: The present study aimed to detail the acute and residual cognitive effects of Delta(9)-THC in infrequent cannabis users. Methods: A balanced, double-blind cross-over design was used to compare the effects of 7.5 mg and 15 mg Delta(9)-THC with matched placebo in 15 male volunteers. Participants were assessed pre and 1, 2, 4, 6, 8, 24 and 48 h post-drug. Results: Delta(9)-THC 15 mg impaired performance on two explicit memory tasks at the time of peak plasma concentration (2 h post-drug). At the same time point, performance on an implicit memory task was preserved intact. The higher dose of Delta(9)-THC resulted in no learning whatsoever occurring over a three-trial selective reminding task at 2 h. Working memory was generally unaffected by Delta(9)-THC. In several tasks, Delta(9)-THC increased both speed and error rates, reflecting "riskier" speed-accuracy trade-offs. Subjective effects were also most marked at 2 h but often persisted longer, with participants rating themselves as "stoned" for 8 h. Participants experienced a strong drug effect, liked this effect and, until 4 h, wanted more oral Delta(9)-THC. No effects of Delta(9)-THC were found 24 or 48 h following ingestion indicating that the residual effects of oral Delta(9)-THC are minimal. Conclusions: These data demonstrate that oral Delta(9)-THC impairs episodic memory and learning in a dose-dependent manner whilst sparing perceptual priming and working memory.