Hansen Tine Maria, Olesen Anne Estrup, Graversen Carina, Drewes Asbjørn Mohr, Frøkjaer Jens Brøndum
Mech-Sense, Department of Radiology, Aalborg University Hospital, Aalborg, Denmark.
Mech-Sense, Department of Gastroenterology & Hepatology, Aalborg University Hospital, Aalborg, Denmark.
Basic Clin Pharmacol Toxicol. 2015 Nov;117(5):316-22. doi: 10.1111/bcpt.12415. Epub 2015 May 29.
Knowledge about cerebral mechanisms underlying pain perception and effect of analgesic drugs is important for developing methods for diagnosis and treatment of pain. The aim was to explore altered brain activation before and after morphine treatment using functional magnetic resonance imaging recorded during experimental painful heat stimulation. Functional magnetic resonance imaging data were recorded and analysed in 20 healthy volunteers (13 men and 7 women, 24.9 ± 2.6 years) in a randomized, double-blind, placebo-controlled, cross-over study. Painful stimulations were applied to the right forearm using a contact heat evoked potential stimulator (CHEPS) before and after treatment with 30 mg oral morphine and placebo. CHEPS stimulations before treatment induced activation in the anterior cingulate cortex, secondary somatosensory cortex/insula, thalamus and cerebellum (n = 16, p < 0.05). In response to morphine treatment, the spatial extent of these pain-specific areas decreased (n = 20). Reduced pain-induced activation was seen in the right insula, anterior cingulate cortex and inferior parietal cortex after morphine treatment compared to before treatment (n = 16, p < 0.05), and sensory ratings of pain perception were significantly reduced after morphine treatment (p = 0.02). No effect on pain-induced brain activation was seen after placebo treatment compared to before treatment (n = 12, p > 0.05). In conclusion, heat stimulation activated areas in the 'pain matrix' and a clinically relevant dose of orally administered morphine revealed significant changes in brain areas where opioidergic pathways are predominant. The method may be useful to investigate the mechanisms of analgesics.
了解疼痛感知背后的大脑机制以及镇痛药的作用,对于开发疼痛诊断和治疗方法至关重要。本研究旨在利用实验性热痛刺激期间记录的功能磁共振成像,探索吗啡治疗前后大脑激活的变化。在一项随机、双盲、安慰剂对照、交叉研究中,对20名健康志愿者(13名男性和7名女性,年龄24.9±2.6岁)进行了功能磁共振成像数据的记录和分析。在口服30毫克吗啡和安慰剂治疗前后,使用接触式热诱发电位刺激器(CHEPS)对右前臂进行疼痛刺激。治疗前CHEPS刺激可诱导前扣带回皮质、次级体感皮质/脑岛、丘脑和小脑激活(n = 16,p < 0.05)。与吗啡治疗前相比,这些疼痛特异性区域的空间范围在吗啡治疗后缩小(n = 20)。与治疗前相比,吗啡治疗后右侧脑岛、前扣带回皮质和下顶叶皮质中疼痛诱导的激活减少(n = 16,p < 0.05),吗啡治疗后疼痛感知的感觉评分显著降低(p = 0.02)。与治疗前相比,安慰剂治疗后对疼痛诱导的大脑激活没有影响(n = 12,p > 0.05)。总之,热刺激激活了“疼痛矩阵”中的区域,临床相关剂量的口服吗啡显示在阿片能通路占主导的脑区有显著变化。该方法可能有助于研究镇痛药的作用机制。