Pinprick-evoked brain potentials: a novel tool to assess central sensitization of nociceptive pathways in humans

被引:65
作者
Iannetti, G. D. [1 ]
Baumgaertner, U. [2 ]
Tracey, I. [3 ]
Treede, R. D. [2 ]
Magerl, W. [2 ]
机构
[1] UCL, Dept Neurosci Physiol & Pharmacol, London WC1E 6BT, England
[2] Heidelberg Univ, Ctr Biomed & Med Technol Mannheim CBTM, Chair Neurophysiol, Mannheim, Germany
[3] Univ Oxford, Dept Clin Neurol, FMRIB Ctr, Oxford, England
关键词
central sensitization; electrophysiology; human; neuropathic pain; pain; NEUROPATHIC PAIN; NEUROGENIC HYPERALGESIA; SECONDARY HYPERALGESIA; CEREBRAL POTENTIALS; CUTANEOUS PAIN; FIBER NOCICEPTORS; EFNS GUIDELINES; EEG RESPONSES; HEAT PAIN; CAPSAICIN;
D O I
10.1152/jn.00774.2012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although hyperalgesia to mechanical stimuli is a frequent sign in patients with inflammation or neuropathic pain, there is to date no objective electrophysiological measure for its evaluation in the clinical routine. Here we describe a technique for recording the electroencephalographic (EEG) responses elicited by mechanical stimulation with a flat-tip probe (diameter 0.25 mm, force 128 mN). Such probes activate A delta nociceptors and are widely used to assess the presence of secondary hyperalgesia, a psychophysical correlate of sensitization in the nociceptive system. The corresponding pinprick-evoked potentials (PEPs) were recorded in 10 subjects during stimulation of the right and left hand dorsum before and after intradermal injection of capsaicin into the right hand and in 1 patient with a selective lesion of the right spinothalamic tract. PEPs in response to stimulation of normal skin were characterized by a vertex negative-positive (NP) complex, with N/P latencies and amplitudes of 111/245 ms and 3.5/11 mu V, respectively. All subjects developed a robust capsaicin-induced increase in the pain elicited by pinprick stimulation of the secondary hyperalgesic area (+91.5%, P < 0.005). Such stimulation also resulted in a significant increase of the N-wave amplitude (+92.9%, P < 0.005), but not of the P wave (+6.6%, P = 0.61). In the patient, PEPs during stimulation of the hypoalgesic side were reduced. These results indicate that PEPs 1) reflect cortical activities triggered by somatosensory input transmitted in A delta primary sensory afferents and spinothalamic projection neurons, 2) allow quantification of experimentally induced secondary mechanical hyperalgesia, and 3) have the potential to become a diagnostic tool to substantiate mechanical hyperalgesia in patients with presumed central sensitization.
引用
收藏
页码:1107 / 1116
页数:10
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