Department of Psychiatry, University of Illinois at Chicago, Chicago, USA.
Department of Pharmacy Practice and Department of Psychiatry & Behavioral Neuroscience, Wayne State University, Detroit, USA.
Neuropsychopharmacology. 2019 Sep;44(10):1769-1777. doi: 10.1038/s41386-019-0416-6. Epub 2019 May 16.
The neural mechanisms and durability of Δ9-tetrahydrocannabinol (THC) impact on threat processing in humans are not fully understood. Herein, we used functional MRI and psychophysiological tools to examine the influence of THC on the mechanisms of conditioned threat extinction learning, and the effects of THC on extinction memory retention when assessed 1 day and 1 week from learning. Healthy participants underwent threat conditioning on day 1. On day 2, participants were randomized to take one pill of THC or placebo (PBO) 2-h before threat extinction learning. Extinction memory retention was assessed 1 day and 1 week after extinction learning. We found that THC administration increased amygdala and ventromedial prefrontal cortex (vmPFC) activation during early extinction learning with no significant impact on skin conductance responses (SCR). When extinction memory retention was tested 24 h after learning, the THC group exhibited lower SCRs to the extinguished cue with no significant extinction-induced activations within the extinction network. When extinction memory retention was tested 1 week after learning, the THC group exhibited significantly decreased responses to the extinguished cues within the vmPFC and amygdala, but significantly increased functional coupling between the vmPFC, hippocampus, and dorsal anterior cingulate cortex during this extinction retention test. Our results are the first to report a long-term impact of one dose of THC on the functional activation of the threat extinction network and unveil a significant change in functional connectivity emerging after a week from engagement. We highlight the need for further investigating the long-term impact of THC on threat and anxiety circuitry.
Δ9-四氢大麻酚(THC)对人类威胁处理的神经机制和持久性尚不完全清楚。在此,我们使用功能磁共振成像和心理生理工具来研究 THC 对条件性威胁消退学习机制的影响,以及在学习后 1 天和 1 周评估时 THC 对消退记忆保留的影响。健康参与者在第 1 天进行威胁条件反射。第 2 天,参与者被随机分配在威胁消退学习前 2 小时服用一片 THC 或安慰剂(PBO)。消退记忆保留在消退学习后 1 天和 1 周进行评估。我们发现,THC 给药增加了杏仁核和腹内侧前额叶皮层(vmPFC)在早期消退学习期间的激活,而对皮肤电反应(SCR)没有显著影响。当在学习后 24 小时进行消退记忆保留测试时,与无显著消退诱导激活的消退网络内相比,THC 组在消退线索上表现出较低的 SCR。当在学习后 1 周进行消退记忆保留测试时,与无显著消退诱导激活的消退网络内相比,THC 组在 vmPFC 和杏仁核内对消退线索的反应显著降低,但在该消退保留测试中 vmPFC、海马体和背侧前扣带皮层之间的功能连接显著增加。我们的结果是首次报道单次 THC 剂量对威胁消退网络的功能激活的长期影响,并揭示了从接触后一周开始出现的功能连接的显著变化。我们强调需要进一步研究 THC 对威胁和焦虑回路的长期影响。