Bromm B, Ganzel R, Herrmann W M, Meier W, Scharein E
Neuropsychobiology. 1986;16(2-3):152-6. doi: 10.1159/000118317.
Somatosensory (SEP), auditory evoked potentials (AEP) and power spectral density of ongoing EEG (PSD) were investigated under different drug conditions: the opioid pentazocine (30 mg), the centrally acting non-narcotic analgesic flupirtine (80 mg) and placebo were administered i.v. in a double-blind cross-over study (intersession interval 7 days) with 20 healthy male subjects. Intracutaneous electrical stimuli were applied to the finger tip with randomized intensities of two- and threefold individual pain threshold. One stimulus block consisted of 80 trials. Mean values of two stimulus blocks per session were analyzed: one block before and one block 30 min after treatment. Pentazocine significantly reduced the peak-to peak amplitude of the late SEP components (N150-P240) from pretreatment to posttreatment blocks, and flupirtine diminished this amplitude to nearly the same degree. With placebo no substantial reduction was found. In contrast to these drug-induced changes in SEP, the AEP components showed no significant alterations after any treatment. The PSD under pentazocine showed a reduction of total power. This effect was mainly due to a reduced power in the alpha band. The PSD under flupirtine showed slight increases in power of theta, alpha and beta activity. Again, under placebo no changes from pretreatment to posttreatment conditions occurred. The difference in EEG change might suggest different sites of action of the two analgesics.
在不同药物条件下,对体感诱发电位(SEP)、听觉诱发电位(AEP)和脑电图(EEG)的功率谱密度(PSD)进行了研究:在一项双盲交叉研究(间隔期为7天)中,对20名健康男性受试者静脉注射阿片类药物喷他佐辛(30毫克)、中枢性非麻醉性镇痛药氟吡汀(80毫克)和安慰剂。将皮内电刺激以两倍和三倍个体疼痛阈值的随机强度施加于指尖。一个刺激组由80次试验组成。分析每次试验中两个刺激组的平均值:治疗前一组和治疗后30分钟一组。喷他佐辛显著降低了从治疗前组到治疗后组的SEP晚期成分(N150 - P240)的峰峰值幅度,氟吡汀将该幅度降低到几乎相同程度。使用安慰剂未发现幅度有实质性降低。与这些药物引起的SEP变化相反,任何治疗后AEP成分均未显示出显著改变。喷他佐辛作用下的PSD显示总功率降低。这种效应主要是由于α波段功率降低。氟吡汀作用下的PSD显示θ、α和β活动功率略有增加。同样,使用安慰剂时,从治疗前到治疗后条件未发生变化。脑电图变化的差异可能表明这两种镇痛药的作用部位不同。