功能磁共振成像
脑岛
岛叶皮质
神经科学
医学
内脏痛
脑干
肠易激综合征
后扣带
扣带回前部
扣带皮质
神经影像学
孤束
功能成像
孤核
丘脑
心理学
伤害
内科学
中枢神经系统
认知
受体
作者
Abraham B. Beckers,Lukas Van Oudenhove,Zsa Zsa R. M. Weerts,Heidi I.L. Jacobs,Nikos Priovoulos,Benedikt A. Poser,Dimo Ivanov,Ali Gholamrezaei,Qasim Aziz,Sigrid Elsenbruch,Ad Masclee,Dániel Keszthelyi
出处
期刊:Pain
[Ovid Technologies (Wolters Kluwer)]
日期:2021-11-15
卷期号:163 (8): 1520-1529
被引量:8
标识
DOI:10.1097/j.pain.0000000000002538
摘要
Abstract Neuroimaging studies have revealed important pathomechanisms related to disorders of brain–gut interactions, such as irritable bowel syndrome and functional dyspepsia. More detailed investigations aimed at neural processing in the brainstem, including the key relay station of the nucleus of the solitary tract (NTS), have hitherto been hampered by technical shortcomings. To ascertain these processes in more detail, we used multiecho multiband 7T functional magnetic resonance imaging and a novel translational experimental model based on a nutrient-derived intestinal chemonociceptive stimulus. In a randomized cross-over fashion, subjects received duodenal infusion of capsaicin (the pungent principle in red peppers) and placebo (saline). During infusion, functional magnetic resonance imaging data and concomitant symptom ratings were acquired. Of 26 healthy female volunteers included, 18 were included in the final analysis. Significantly increased brain activation over time during capsaicin infusion, as compared with placebo, was observed in brain regions implicated in pain processing, in particular the NTS. Brain activation in the thalamus, cingulate cortex, and insula was more pronounced in subjects who reported abdominal pain (visual analogue scale > 10 mm), as compared with subjects who experienced no pain. On the contrary, activations at the level of the NTS were independent of subjective pain ratings. The current experimental paradigm therefore allowed us to demonstrate activation of the principal relay station for visceral afferents in the brainstem, the NTS, which was engaged irrespective of the conscious pain response. These findings contribute to understanding the fundamental mechanism necessary for developing novel therapies aimed at correcting disturbances in visceral afferent pain processing.
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