Differential changes of laser evoked potentials, late auditory evoked potentials and P300 under morphine in chronic pain patients

Jürgen Lorenz , Helge Beck , Burkhart Bromm
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引用次数: 43

Abstract

The present study investigates the differential behavior of laser evoked brain potentials (LEPs), late auditory evoked potentials (AEP) and the endogenous P300 in response to morphine treatment, examined in 6 chronic pain patients. The main result was that in parallel with marked clinical pain relief, amplitudes of the long latency LEP positivity (P400) were significantly reduced under morphine. One patient suffering from extremely painful osteoporosis for 20 years exhibited a large middle latency component (N170) which was prominently attenuated by morphine. In contrast to LEP amplitude reductions, auditory N1 and P2 potentials appeared either unchanged or even enlarged during morphine treatment. Also P300 amplitude was slightly increased under morphine. Reaction time and mood scales also failed to indicate any sedation. Obviously, LEPs reflected specifically the analgesic morphine effect in this study, while stability or enhancement of AEPs and P300 during morphine treatment indicated lack of sedation or even improved perception and concentration due to the removal of persistent pain as a disruptive perceptual-cognitive stressor.

吗啡作用下慢性疼痛患者激光诱发电位、晚期听觉诱发电位及P300的差异变化
研究了6例慢性疼痛患者的激光诱发脑电位(LEPs)、晚期听觉诱发电位(AEP)和内源性P300在吗啡治疗后的差异行为。主要结果是,在明显的临床疼痛缓解的同时,吗啡组长潜伏期LEP阳性(P400)的振幅显著降低。一名患有20年极度痛苦的骨质疏松症的患者表现出较大的中潜伏期成分(N170),吗啡明显减弱。与LEP振幅降低相反,吗啡治疗期间,听觉N1和P2电位没有变化甚至增大。吗啡组P300振幅略有增加。反应时间和情绪量表也没有显示任何镇静。显然,LEPs在本研究中专门反映了吗啡的镇痛作用,而吗啡治疗期间AEPs和P300的稳定或增强表明,由于持续疼痛作为破坏性感知-认知应激源的消除,缺乏镇静甚至改善了感知和注意力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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