Brain activity during biofeedback relaxation - A functional neuroimaging investigation

被引:130
作者
Critchley, HD
Melmed, RN
Featherstone, E
Mathias, CJ
Dolan, RJ
机构
[1] UCL, Inst Neurol, Wellcome Dept Cognit Neurol, London WC1N 3BG, England
[2] Natl Hosp Neurol & Neurosurg, Auton Unit, London WC1N 3BG, England
[3] Univ London Imperial Coll Sci Technol & Med, Sch Med, St Marys Hosp, Dept Neurovasc Med, London, England
[4] UCL, Univ Coll Hosp, Sch Med, Royal Free Hosp, London, England
[5] Hadassah Univ Hosp, Dept Med, IL-91240 Jerusalem, Israel
关键词
autonomic; biofeedback; relaxation; positron emission tomography; electrodermal activity;
D O I
10.1093/brain/124.5.1003
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The mechanisms by which cognitive processes influence states of bodily arousal are important for understanding the pathogenesis and maintenance of stress-related morbidity. We used PET to investigate cerebral activity relating to the cognitively driven modulation of sympathetic activity. Subjects were trained to perform a biofeedback relaxation exercise that reflected electrodermal activity and were subsequently scanned performing repetitions of four tasks: biofeedback relaxation, relaxation without biofeedback and two corresponding control conditions in which the subjects were instructed not to relax. Relaxation was associated with significant increases in left anterior cingulate and globus pallidus activity, whereas no significant increases in activity were associated with biofeedback compared with random feedback. The interaction between biofeedback and relaxation, highlighting activity unique to biofeedback relaxation, was associated with enhanced anterior cingulate and cerebellar vermal activity. These data implicate the anterior cingulate cortex in the intentional modulation of bodily arousal and suggest a functional neuroanatomy of how cognitive states are integrated with bodily responses. The findings have potential implications for a mechanistic account of how therapeutic interventions, such as relaxation training in stress-related disorders, mediate their effects.
引用
收藏
页码:1003 / 1012
页数:10
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