Carhart-Harris R L, Wall M B, Erritzoe D, Kaelen M, Ferguson B, De Meer I, Tanner M, Bloomfield M, Williams T M, Bolstridge M, Stewart L, Morgan C J, Newbould R D, Feilding A, Curran H V, Nutt D J
Division of Brain Sciences, Faculty of Medicine, Imperial College London, Centre for Neuropsychopharmacology, London, UK.
Institute of Neurology, University College London, London, UK.
Int J Neuropsychopharmacol. 2014 Apr;17(4):527-40. doi: 10.1017/S1461145713001405. Epub 2013 Dec 17.
3,4-methylenedioxymethamphetamine (MDMA) is a potent monoamine-releaser that is widely used as a recreational drug. Preliminary work has supported the potential of MDMA in psychotherapy for post-traumatic stress disorder (PTSD). The neurobiological mechanisms underlying its putative efficacy are, however, poorly understood. Psychotherapy for PTSD usually requires that patients revisit traumatic memories, and it has been argued that this is easier to do under MDMA. Functional magnetic resonance imaging (fMRI) was used to investigate the effect of MDMA on recollection of favourite and worst autobiographical memories (AMs). Nineteen participants (five females) with previous experience with MDMA performed a blocked AM recollection (AMR) paradigm after ingestion of 100 mg of MDMA-HCl or ascorbic acid (placebo) in a double-blind, repeated-measures design. Memory cues describing participants' AMs were read by them in the scanner. Favourite memories were rated as significantly more vivid, emotionally intense and positive after MDMA than placebo and worst memories were rated as less negative. Functional MRI data from 17 participants showed robust activations to AMs in regions known to be involved in AMR. There was also a significant effect of memory valence: hippocampal regions showed preferential activations to favourite memories and executive regions to worst memories. MDMA augmented activations to favourite memories in the bilateral fusiform gyrus and somatosensory cortex and attenuated activations to worst memories in the left anterior temporal cortex. These findings are consistent with a positive emotional-bias likely mediated by MDMA's pro-monoaminergic pharmacology.
3,4-亚甲基二氧甲基苯丙胺(摇头丸)是一种强效单胺释放剂,被广泛用作娱乐性药物。初步研究支持了摇头丸在创伤后应激障碍(PTSD)心理治疗中的潜力。然而,其假定疗效背后的神经生物学机制却知之甚少。PTSD的心理治疗通常要求患者重温创伤记忆,有人认为在摇头丸作用下更容易做到这一点。功能磁共振成像(fMRI)被用于研究摇头丸对最喜欢和最糟糕的自传体记忆(AMs)回忆的影响。19名有摇头丸使用经历的参与者(5名女性)在双盲、重复测量设计中,在摄入100毫克盐酸摇头丸或抗坏血酸(安慰剂)后,进行了一个分组自传体记忆回忆(AMR)范式实验。他们在扫描仪中阅读描述其自传体记忆的记忆线索。与服用安慰剂相比,服用摇头丸后,最喜欢的记忆被评为明显更生动、情感更强烈且更积极,而最糟糕的记忆被评为负面程度更低。来自17名参与者的功能磁共振成像数据显示,在已知参与自传体记忆回忆的区域对自传体记忆有强烈激活。记忆效价也有显著影响:海马区域对最喜欢的记忆表现出优先激活,而执行区域对最糟糕的记忆表现出优先激活。摇头丸增强了双侧梭状回和体感皮层对最喜欢记忆的激活,并减弱了左前颞叶皮层对最糟糕记忆的激活。这些发现与摇头丸的促单胺能药理学可能介导的积极情绪偏向一致。