The P300 in pain evoked potentials

被引:82
作者
Zaslansky, R
Sprecher, E
Tenke, CE
Hemli, JA
Yarnitsky, D
机构
[1] TECHNION ISRAEL INST TECHNOL, RAMBAM MED CTR, INST CLIN NEUROPHYSIOL, SCH MED, HAIFA, ISRAEL
[2] TECHNION ISRAEL INST TECHNOL, RAMBAM MED CTR, DEPT NEUROL, HAIFA, ISRAEL
[3] NEW YORK STATE PSYCHIAT INST & HOSP, DEPT BIOPSYCHOL, NEW YORK, NY 10032 USA
关键词
pain evoked potentials; pain; laser; P300; oddball;
D O I
10.1016/0304-3959(96)03020-5
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Pain evoked potentials (EPs) have been used in the last two decades as means of obtaining objective measures of pain, in clinical and experimental setups. The possibility that the pain EP wave contains elements of the endogenous P300 potential rather than being a neurophysiological correlate of pain has been raised by a number of authors, but the issue has not been resolved, In this study, two experiments were performed to study the effect of non-modality-specific factors on the laser EP: (1) a stimulus attend as opposed to a stimulus-ignore condition and (2) counterbalanced oddball and task P300 stimulus presentations. The latter was to permit full examination of the separate and combined influences of each condition on the EP. Stimuli were given to the radial hand of 10 healthy volunteers using a CO2 laser. The positive component of the laser EP was affected by both manipulations relating to (1) attention (P = 0.0146) and (2) the frequency condition (P = 0.003) in the P300 paradigm. The task condition in the second paradigm did not affect the positive wave on its own, although its effect was visible in interaction with frequency (P = 0.033), In conclusion, although the presence of a somatic component in the laser EP cannot be ruled out, we suggest that the laser EP contains a definite non-modality-specific P300 component, and is not a pure neurophysiological correlate of pain intensity.
引用
收藏
页码:39 / 49
页数:11
相关论文
共 39 条
[1]  
[Anonymous], HUMAN EVENT RELATED
[2]  
[Anonymous], 1989, HUMAN BRAIN ELECTROP
[3]  
ARENDTNIELSEN L, 1990, J NEUROL NEUROSUR PS, V53, P398, DOI 10.1136/jnnp.53.5.398
[4]   IDENTIFICATION OF PAIN, INTENSITY AND P300 COMPONENTS IN THE PAIN EVOKED-POTENTIAL [J].
BECKER, DE ;
YINGLING, CD ;
FEIN, G .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1993, 88 (04) :290-301
[5]   ARGON-LASER INDUCED SINGLE CORTICAL RESPONSES - A NEW METHOD TO QUANTIFY PRE-PAIN AND PAIN PERCEPTIONS [J].
BJERRING, P ;
ARENDTNIELSEN, L .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1988, 51 (01) :43-49
[6]   PRINCIPAL COMPONENT ANALYSIS OF PAIN-RELATED CEREBRAL POTENTIALS TO MECHANICAL AND ELECTRICAL-STIMULATION IN MAN [J].
BROMM, B ;
SCHAREIN, E .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1982, 53 (01) :94-103
[7]  
BROMM B, 1991, REV NEUROL-FRANCE, V147, P625
[8]   EFFECTS OF ACETAMINOPHEN AND ANTIPYRINE ON NONINFLAMMATORY PAIN AND EEG ACTIVITY [J].
BROMM, B ;
FORTH, W ;
RICHTER, E ;
SCHAREIN, E .
PAIN, 1992, 50 (02) :213-221
[9]   HUMAN CEREBRAL POTENTIALS-EVOKED BY CO2-LASER STIMULI CAUSING PAIN [J].
BROMM, B ;
TREEDE, RD .
EXPERIMENTAL BRAIN RESEARCH, 1987, 67 (01) :153-162
[10]  
BROMM B, 1984, METHOD FIND EXP CLIN, V6, P405