Very late pain-related activity identified with topographically mapped frequency domain analysis of evoked potentials

被引:3
作者
Becker, DE
Noss, RS
Fein, G
Yingling, CD
机构
[1] Univ Calif San Francisco, Dept Anesthesia, San Francisco, CA 94143 USA
[2] Univ Bern, Dept Psychiat, CH-3012 Bern, Switzerland
[3] Univ Calif San Francisco, Vet Affairs Med Ctr, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Otolaryngol, San Francisco, CA 94143 USA
来源
EVOKED POTENTIALS-ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY | 1998年 / 108卷 / 04期
关键词
pain; pain-evoked potential; somatosensory evoked potential; topographic mapping; complex demodulation; frequency domain analysis;
D O I
10.1016/S0168-5597(98)00011-2
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Objective: To identify low-frequency activity in the pain-evoked potential at very late latencies, consistent with C-fiber transmission velocities, Methods: Brief (1 ms) painful (intracutaneous) and two levels of non-painful (mild and strong) electrical pulses were applied to the index and middle fingers of the left hand. Evoked potentials (EPs) were recorded from 30 electrodes covering the entire scalp. Data from the 3 stimulus conditions (approximately 60 trials per condition per subject) were compared using the frequency domain technique of complex demodulation applied to single trial data. Subjects were 14 normal right-handed male human volunteers, aged 19-36 years. Results: Using descriptive probability mapping, pain versus strong non-pain differences were found in grand average data as well as in 8 of 14 subjects, consisting of greater low-frequency power at latencies from 700 to 1100 ms at electrodes near the contralateral central sulcus and at the vertex. Conclusions: There are topographically focal, pain versus non-pain differences in the 700-1100 ms latency range that can be seen using frequency-domain analytic techniques. These differences were not seen with traditional time domain analyses. They may be due to a C-fiber-related mechanism or to very late activity triggered by faster fibers. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:398 / 405
页数:8
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