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芬太尼和纳洛酮对人体躯体及听觉诱发电位成分的影响。

Effect of fentanyl and naloxone on human somatic and auditory-evoked potential components.

作者信息

Velasco M, Velasco F, Castañeda R, Sánchez R

出版信息

Neuropharmacology. 1984 Mar;23(3):359-66. doi: 10.1016/0028-3908(84)90199-0.

Abstract

The effect of fentanyl (a morphine agonist) and naloxone (a morphine antagonist) on early and late components of somatic (SEP)- and auditory (AEP)-evoked potentials was studied in patients undergoing minor surgical procedures, in which these compounds were used in producing and regulating a state of neuroleptanalgesia. Fentanyl (2.5, 5.0 and 10.0 micrograms/kg), naloxone (1.5 and 3.0 micrograms/kg) and isotonic saline (for comparative purposes) were injected just before surgery, intravenously through a catheter and following a single blind procedure and three different pharmacological paradigms with four consecutive conditions each: (1) Initial baseline (C), first saline (S), second saline (S') and late baseline (C'). (2) C, First fentanyl (F), second naloxone (N') and C. (3) C, First naloxone (N), second fentanyl (F') and C'. Special care was taken in controlling the constancy of the muscular and cochlear receptor activation concomitant to somatic-evoked potentials and auditory-evoked potentials, determined by the amplitude of the muscular response at the tenar muscles (MP) and component I of the brain stem potentials ( ABSP ). Evaluation by the patients pain, topognoses and hearing and other somatic and autonomic indicators of the level of the analgesic response were also controlled. Fentanyl significantly reduced, while naloxone increased, the amplitude of late components P150 of somatic-evoked potentials and auditory-evoked potentials. Concomitantly, fentanyl increased, while naloxone decreased, the spatial threshold (two point discrimination test) at finger tip and arm. These effects were observed in patients taking various doses, although they were more consistent with larger doses of these compounds.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在接受小型外科手术的患者中,研究了芬太尼(一种吗啡激动剂)和纳洛酮(一种吗啡拮抗剂)对躯体诱发电位(SEP)和听觉诱发电位(AEP)的早期和晚期成分的影响。在这些手术中,这些化合物用于产生和调节神经安定镇痛状态。芬太尼(2.5、5.0和10.0微克/千克)、纳洛酮(1.5和3.0微克/千克)和等渗盐水(用于对比)在手术前通过导管静脉注射,采用单盲程序和三种不同的药理学范式,每种范式有四个连续条件:(1)初始基线(C)、首次注射盐水(S)、第二次注射盐水(S')和晚期基线(C')。(2)C、首次注射芬太尼(F)、第二次注射纳洛酮(N')和C。(3)C、首次注射纳洛酮(N)、第二次注射芬太尼(F')和C'。特别注意控制与躯体诱发电位和听觉诱发电位同时发生的肌肉和耳蜗受体激活的稳定性,这由鱼际肌的肌肉反应幅度(MP)和脑干电位的I成分(ABSP)确定。还控制了患者对疼痛、疼痛部位、听力以及镇痛反应水平的其他躯体和自主指标的评估。芬太尼显著降低了躯体诱发电位和听觉诱发电位晚期成分P150的幅度,而纳洛酮则使其增加。同时,芬太尼增加了指尖和手臂的空间阈值(两点辨别试验),而纳洛酮则使其降低。在服用不同剂量这些化合物的患者中均观察到了这些效应,尽管在较大剂量时这些效应更为一致。(摘要截取自250词)

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