Mimura M, Namiki A, Kishi R, Ikeda T, Miyake H, Iwasaki H
Department of Anesthesiology, Sapporo Medical College, Japan.
Acta Anaesthesiol Scand. 1992 Jul;36(5):460-2. doi: 10.1111/j.1399-6576.1992.tb03497.x.
Ketamine sometimes produces posthypnotic emergency reactions, such as prolonged hallucination or delirium. In a previous paper, we showed that physostigmine, an anticholinesterase agent, counteracts the manifestation of effects of ketamine at some doses. In the present study, we investigated the mechanism of the antagonistic effect of physostigmine on ketamine anesthesia. At first, rats were given ketamine 75 mg/kg. Immediately after the loss of righting reflex, the four groups of rats were given one of the three central cholinergic agents, physostigmine 0.1 mg/kg, oxotremorine 0.05 mg/kg, 4-aminopyridine 3 mg/kg, or saline as the control. The sleeping times were 10.7 +/- 1.0, 12.3 +/- 0.9, 11.4 +/- 1.3 and 21.2 +/- 0.7 min, respectively. The three cholinergic agents antagonized ketamine anesthesia. In the other groups of rats, the central anticholinergic agent, l-hyoscyamine, 0.5 mg/kg, was given subcutaneously for premedication before the above-mentioned procedure. The sleeping times were 16.3 +/- 1.2 min in the physostigmine group, 18.7 +/- 1.0 min in the oxotremorine group and 18.6 +/- 0.8 min in the 4-aminopyridine group. The sleeping time was significantly longer in the premedicated group than in the non-premedicated group, in the case of the three central cholinergic agents. The sleeping time in the saline group, 20.0 +/- 0.4 min, was not significantly different from that of the control in the non-premedicated case. It is, therefore, considered that the central cholinergic action produces antagonism to ketamine anesthesia.
氯胺酮有时会产生催眠后紧急反应,如幻觉或谵妄持续时间延长。在之前的一篇论文中,我们表明抗胆碱酯酶药物毒扁豆碱在某些剂量下可抵消氯胺酮的作用表现。在本研究中,我们调查了毒扁豆碱对氯胺酮麻醉拮抗作用的机制。首先,给大鼠注射75mg/kg氯胺酮。在翻正反射消失后,四组大鼠分别注射三种中枢胆碱能药物之一:0.1mg/kg毒扁豆碱、0.05mg/kg氧化震颤素、3mg/kg 4-氨基吡啶,或注射生理盐水作为对照。睡眠时间分别为10.7±1.0、12.3±0.9、11.4±1.3和21.2±0.7分钟。这三种胆碱能药物均拮抗氯胺酮麻醉。在其他几组大鼠中,在上述操作前皮下注射0.5mg/kg中枢抗胆碱能药物l-莨菪碱进行预处理。毒扁豆碱组的睡眠时间为16.3±1.2分钟,氧化震颤素组为18.7±1.0分钟,4-氨基吡啶组为18.6±0.8分钟。对于这三种中枢胆碱能药物,预处理组的睡眠时间明显长于未预处理组。在未预处理的情况下,生理盐水组的睡眠时间为20.0±0.4分钟,与对照组无显著差异。因此,可以认为中枢胆碱能作用对氯胺酮麻醉产生拮抗作用。