Ilkjaer S, Petersen K L, Brennum J, Wernberg M, Dahl J B
Department of Anaesthesiology, Skejby University Hospital, Aarhus, Denmark.
Br J Anaesth. 1996 Jun;76(6):829-34. doi: 10.1093/bja/76.6.829.
Ketamine reduces nociception by binding noncompetitively to the N-methyl-D-aspartate (NMDA) receptor, activation of which increases spinal hypersensitivity. We studied 19 healthy, unmedicated male volunteers, aged 20-31 yr. Burn injuries were produced on the medial surface of the dominant calf with a 25 x 50 mm rectangular thermode. On 3 separate days, at least 1 week apart, subjects received a bolus of either ketamine 0.15 mg kg-1, ketamine 0.30 mg kg-1 or placebo, delivered by a mechanical infusion pump over 15 min. The bolus was followed by continuous infusion of ketamine 0.15 mg kg-1 h-1, ketamine 0.30 mg kg-1 h-1 or placebo, respectively, for 135 min. Ketamine reduced the magnitude of both primary and secondary hyperalgesia, and also pain evoked by prolonged noxious heat stimulation, in a dose-dependent manner. In contrast, ketamine did not alter phasic heat pain perception (perception of transient, painful, thermal stimuli) in undamaged skin. The analgesic effects of ketamine in the burn injury model are in agreement with results from experimental studies, and can be distinguished from those of local anaesthetics and opioids. Side effects caused by continuous infusion of ketamine 0.15 and 0.30 mg kg-1 h-1 were frequent but clinically acceptable.
氯胺酮通过与N-甲基-D-天冬氨酸(NMDA)受体非竞争性结合来减轻伤害感受,NMDA受体的激活会增加脊髓超敏反应。我们研究了19名年龄在20至31岁之间、未接受过药物治疗的健康男性志愿者。使用一个25×50毫米的矩形热刺激器在优势小腿的内侧表面造成烧伤。在3个不同的日子里,间隔至少1周,受试者通过机械输液泵在15分钟内接受一次剂量为0.15毫克/千克、0.30毫克/千克的氯胺酮或安慰剂推注。推注后分别以0.15毫克/千克·小时、0.30毫克/千克·小时的氯胺酮或安慰剂持续输注135分钟。氯胺酮以剂量依赖的方式降低了原发性和继发性痛觉过敏的程度,以及长时间有害热刺激诱发的疼痛。相比之下,氯胺酮并未改变未受损皮肤的阶段性热痛觉(对短暂、疼痛的热刺激的感觉)。氯胺酮在烧伤模型中的镇痛作用与实验研究结果一致,并且可以与局部麻醉药和阿片类药物的作用相区分。持续输注0.15毫克/千克·小时和0.30毫克/千克·小时氯胺酮引起的副作用很常见,但在临床上是可以接受的。