Changes in regional cerebral blood flow during acute electroconvulsive therapy in patients with depression - Positron emission tomographic study

被引:59
作者
Takano, H.
Motohashi, N.
Uema, T.
Ogawa, K.
Ohnishi, T.
Nishikawa, M.
Kashima, H.
Matsuda, H.
机构
[1] Natl Ctr Neurol & Psychiat, Natl Ctr Hosp Mental Nervous & Muscular Disorders, Dept Psychiat, Tokyo, Japan
[2] Keio Univ, Sch Med, Dept Neuropsychiat, Tokyo, Japan
[3] Natl Ctr Neurol & Psychiat, Natl Ctr Hosp Mental Nervous & Muscular Disorders, Dept Anaesthesiol, Tokyo, Japan
[4] Natl Ctr Neurol & Psychiat, Natl Ctr Hosp Mental Nervous & Muscular Disorders, Dept Radiol, Tokyo, Japan
[5] Keio Univ, Sch Med, Dept Neuropsychiat, Tokyo 108, Japan
[6] Yokohama City Univ, Sch Med, Dept Anaesthesiol, Yokohama, Kanagawa 232, Japan
关键词
D O I
10.1192/bjp.bp.106.023036
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background Although electroconvulsive therapy (FCT) is widely used to treat psychiatric disorders such as depression, its precise neural mechanisms remain unknown. Aims To investigate the time course of changes in cerebral blood flow during acute ECT. Method Cerebral blood flow was quantified serially prior to, during and after acute ECT in six patients with depression under anaesthesia using [O-15]H2O positron emission tomography (PET). Results Cerebral blood flow during ECT increased particularly in the basal ganglia, brain-stem, diencephalon, amygdala, vermis and the frontal, temporal and parietal cortices compared with that before ECT The flow increased in the thalamus and decreased in the anterior cingulate and medial frontal cortex soon after ECT compared with that before ECT. Conclusions These results suggest a relationship between the centrencephalic system and seizure generalisation. Further, they suggest that some neural mechanisms of action of ECT are mediated via brain regions including the anterior cingulate and medial frontal cortex and thalamus.
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收藏
页码:63 / 68
页数:6
相关论文
共 27 条
[11]   PATTERNS OF HUMAN LOCAL CEREBRAL GLUCOSE-METABOLISM DURING EPILEPTIC SEIZURES [J].
ENGEL, J ;
KUHL, DE ;
PHELPS, ME .
SCIENCE, 1982, 218 (4567) :64-66
[12]  
FROMM GH, 1991, JPN J PSYCHIAT NEUR, V45, P229
[13]   Thresholding of statistical maps in functional neuroimaging using the false discovery rate [J].
Genovese, CR ;
Lazar, NA ;
Nichols, T .
NEUROIMAGE, 2002, 15 (04) :870-878
[14]   A RATING SCALE FOR DEPRESSION [J].
HAMILTON, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1960, 23 (01) :56-62
[15]  
HERSCOVITCH P, 1983, J NUCL MED, V24, P782
[16]  
Kajimura N, 1999, J NEUROSCI, V19, P10065
[17]   Regional metabolic effects of fluoxetine in major depression: Serial changes and relationship to clinical response [J].
Mayberg, HS ;
Brannan, SK ;
Tekell, JL ;
Silva, JA ;
Mahurin, RK ;
McGinnis, S ;
Jerabek, PA .
BIOLOGICAL PSYCHIATRY, 2000, 48 (08) :830-843
[18]   Diagnostic and Statistical Manual of Mental Disorders [J].
Mittal, Vijay A. ;
Walker, Elaine F. .
PSYCHIATRY RESEARCH, 2011, 189 (01) :158-159
[19]  
NOBLER MS, 1994, ARCH GEN PSYCHIAT, V51, P884
[20]  
Penfield W., 1954, EPILEPSY FUNCTIONAL, DOI DOI 10.1097/00007611-195407000-00024