Bromm B, Seide K
Institute of Physiology, Universitäts-Krankenhaus Eppendorf, 2000 Hamburg 20 G.F.R.
Pain. 1982 Mar;12(3):247-258. doi: 10.1016/0304-3959(82)90156-7.
Pain rating, withdrawal reflex and skin resistance reaction upon electrical skin stimuli were studied on 15 male volunteers under placebo, tilidine and prazepam. Tilidine (Valoron) is an orally applicable narcotic analgesic, with a mode of pain relief presumably similar to morphine; the tranquilizer prazepam (Demetrin) belongs to the benzodiazepine group. Significant reduction in all measured reaction amplitudes was found under tilidine, whereas prazepam reduced significantly only the skin resistance reaction. The relative drug-induced changes in reaction amplitudes, related to the corresponding placebo value, were independent of stimulus intensity for all investigated reactions. Therefore, fitted power functions re = a . Sn between reaction amplitudes re and stimulus intensity S showed a decrease in parameter a under the investigated drugs, whereas the exponent n remained constant. High correlations between parameters a and corresponding reciprocal threshold currents could be shown for all reactions measured. Furthermore the drug-induced changes of withdrawal reflex amplitude and of subjective estimation were found to be correlated over subjects. In contrast, no correlations were found between variations in skin resistance reaction and magnitude estimation due to the selected drugs, i.e., the influence of the drugs on the sensory component of pain sensation and on the skin resistance reaction were independent effects.
在15名男性志愿者身上,研究了他们在服用安慰剂、替利定和普拉西泮时对皮肤电刺激的疼痛评分、退缩反射和皮肤电阻反应。替利定(瓦洛伦)是一种口服麻醉性镇痛药,其镇痛方式可能与吗啡相似;镇静剂普拉西泮(去甲羟基安定)属于苯二氮䓬类药物。服用替利定后,所有测量的反应幅度均显著降低,而普拉西泮仅显著降低皮肤电阻反应。与相应安慰剂值相关的药物诱导的反应幅度相对变化,对于所有研究的反应来说,与刺激强度无关。因此,反应幅度re与刺激强度S之间的拟合幂函数re = a·Sn表明,在所研究的药物作用下,参数a降低,而指数n保持不变。对于所有测量的反应,参数a与相应的反向阈值电流之间显示出高度相关性。此外,发现不同受试者之间,药物引起的退缩反射幅度变化与主观估计之间存在相关性。相比之下,由于所选药物,未发现皮肤电阻反应变化与强度估计之间存在相关性,即药物对痛觉感觉成分和皮肤电阻反应的影响是独立的效应。