Walter Carmen, Oertel Bruno G, Felden Lisa, Nöth Ulrike, Deichmann Ralf, Lötsch Jörn
Institute of Clinical Pharmacology, Goethe - University, Theodor - Stern - Kai 7, 60590, Frankfurt am Main, Germany.
Fraunhofer Institute of Molecular Biology and Applied Ecology - Project Group Translational Medicine and Pharmacology (IME-TMP), Theodor - Stern - Kai 7, 60590, Frankfurt am Main, Germany.
IBRO Rep. 2019 Nov 13;7:117-128. doi: 10.1016/j.ibror.2019.11.004. eCollection 2019 Dec.
Cannabis proofed to be effective in pain relief, but one major side effect is its influence on memory in humans. Therefore, the role of memory on central processing of nociceptive information was investigated in healthy volunteers.
In a placebo-controlled cross-over study including 22 healthy subjects, the effect of 20 mg oral Δ-tetrahydrocannabinol (THC) on memory involving nociceptive sensations was studied, using a delayed stimulus discrimination task (DSDT). To control for nociceptive specificity, a similar DSDT-based study was performed in a subgroup of thirteen subjects, using visual stimuli.
For each nociceptive stimulus pair, the second stimulus was associated with stronger and more extended brain activations than the first stimulus. These differences disappeared after THC administration. The THC effects were mainly located in two clusters comprising the insula and inferior frontal cortex in the right hemisphere, and the caudate nucleus and putamen bilaterally. These cerebral effects were accompanied in the DSDT by a significant reduction of correct ratings from 41.61% to 37.05% after THC administration (rm-ANOVA interaction "drug" by "measurement": F (1,21) = 4.685, p = 0.042). Rating performance was also reduced for the visual DSDT (69.87% to 54.35%; rm-ANOVA interaction of "drug" by "measurement": F (1,12) = 13.478, p = 0.003) and reflected in a reduction of stimulus-related brain deactivations in the bilateral angular gyrus.
Results suggest that part of the effect of THC on pain may be related to memory effects. THC reduced the performance in DSDT of nociceptive and visual stimuli, which was accompanied by significant effects on brain activations. However, a pain specificity of these effects cannot be deduced from the data presented.
大麻已被证明在缓解疼痛方面有效,但一个主要副作用是其对人类记忆的影响。因此,在健康志愿者中研究了记忆在伤害性信息中枢处理中的作用。
在一项包括22名健康受试者的安慰剂对照交叉研究中,使用延迟刺激辨别任务(DSDT)研究了20毫克口服Δ-四氢大麻酚(THC)对涉及伤害性感觉的记忆的影响。为了控制伤害性特异性,在13名受试者的亚组中使用视觉刺激进行了一项类似的基于DSDT的研究。
对于每对伤害性刺激,第二个刺激比第一个刺激与更强和更广泛的脑激活相关。THC给药后这些差异消失。THC的影响主要位于两个集群,包括右半球的岛叶和额下回,以及双侧的尾状核和壳核。在DSDT中,THC给药后正确评分从41.61%显著降低到37.05%(rm-ANOVA交互作用“药物”ד测量”:F(1,21)=4.685,p=0.042)。视觉DSDT的评分表现也降低(从69.87%降至54.35%;“药物”ד测量”的rm-ANOVA交互作用:F(1,12)=13.478,p=0.003),并反映在双侧角回中与刺激相关的脑去激活减少。
结果表明,THC对疼痛的部分作用可能与记忆效应有关。THC降低了伤害性和视觉刺激的DSDT表现,这伴随着对脑激活的显著影响。然而,从所呈现的数据中无法推断出这些影响的疼痛特异性。