Sarlis N J, Kaniaris P K
Department of Medicine, Westminster Hospital, University of London, England.
Middle East J Anaesthesiol. 1991 Oct;11(3):271-88.
As fast-acting, water-soluble compounds, like midazolam (MID) are increasingly used in anesthetic practice, the need for quick and effective reversal of benzodiazepine actions in accidental overdoses is obvious. Quite a few drugs have been used in both animal models and clinically towards this aim, including: physostigmine (PHYS), naloxone (NAL), aminophylline, doxapram, in the past and, more recently, flumazenil (FLU) or Ro-15-1788. In the present study we assessed the relative potency, safety and efficacy of the antagonistic actions of PHYS (0.06 and 0.6 mg/kg), NAL (2 mg/kg) and FLU (2.5 mg/kg) on the state of sleep induced by MID (2.5 mg/kg) in 50 male, drug-naive rats. Time of induction of anesthesia and duration of sleep were measured with digital chronometer. Level of consciousness was determined by pain reactivity, spontaneous motor activity and computer-aided analysis of cumulative EEG patterns. Times obtained were integrated as mean values and statistical analysis was made using the t-test (Student's criterion). Rats were given MID followed 30 min later by an i.p. injection of either vehicle (VEH = water for injection = control group) or low-dose PHYS or high-dose PHYS or NAL or FLU (n = 10 in each group). We measured the duration of anesthesia following the injection of each antagonist. The following results were obtained: [table: see text] Thus, the relative potency scale of MID antagonism in this series of experiments is: FLU = High-dose PHYS greater than low-dose PHYS much greater than NAL VEH. Although FLU has a strong duration and rapid awakening action, this action is of short duration and the animals are resedated after 33.3 +/- 7.14 min. PHYS does not appear to show this resedation effect, while in high doses is equipotent to FLU. Nevertheless, in these excessive doses, the animals become restless and excited, showing phenomena of an acute, severe nicotinic crisis. In conclusion, FLU appears to have much more specific and reliable effects upon reversing MID-induced anesthesia in comparison to either PHYS or NAL. In fact, PHYS must reach toxic levels to counteract MID effects, while FLU is very safe. The existence of the resedation effect is due to the short t1/2 of FLU and can be overcome by continuous i.v. infusions or repeated bolus injections.
作为起效迅速的水溶性化合物,如咪达唑仑(MID)在麻醉实践中越来越常用,显然在意外用药过量时需要快速有效地逆转苯二氮䓬类药物的作用。过去有不少药物已用于动物模型和临床以实现这一目的,包括:毒扁豆碱(PHYS)、纳洛酮(NAL)、氨茶碱、多沙普仑,最近还有氟马西尼(FLU)或Ro-15-1788。在本研究中,我们评估了PHYS(0.06和0.6 mg/kg)、NAL(2 mg/kg)和FLU(2.5 mg/kg)对50只未用过药的雄性大鼠中由MID(2.5 mg/kg)诱导的睡眠状态的拮抗作用的相对效力、安全性和有效性。用数字计时器测量麻醉诱导时间和睡眠时间。通过疼痛反应性、自发运动活动以及累积脑电图模式的计算机辅助分析来确定意识水平。所获得的时间整合为平均值,并使用t检验(学生准则)进行统计分析。给大鼠注射MID,30分钟后腹腔注射溶剂(VEH = 注射用水 = 对照组)或低剂量PHYS或高剂量PHYS或NAL或FLU(每组n = 10)。我们测量了注射每种拮抗剂后的麻醉持续时间。得到以下结果:[表格:见原文] 因此,在这一系列实验中MID拮抗作用的相对效力顺序为:FLU = 高剂量PHYS > 低剂量PHYS >> NAL > VEH。虽然FLU具有强烈的持续时间和快速唤醒作用,但这种作用持续时间短,动物在33.3 ± 7.14分钟后会再次入睡。PHYS似乎没有这种再次入睡的效果,而高剂量时与FLU等效。然而,在这些过量剂量下,动物会变得烦躁不安和兴奋,表现出急性、严重的烟碱样危象现象。总之,与PHYS或NAL相比,FLU在逆转MID诱导的麻醉方面似乎具有更特异和可靠的效果。事实上,PHYS必须达到中毒水平才能抵消MID的作用,而FLU非常安全。再次入睡效果的存在是由于FLU的半衰期短,可以通过持续静脉输注或重复推注来克服。