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替马西泮和咪达唑仑在戊巴比妥依赖大鼠中的替代作用。

Substitution of temazepam and midazolam in pentobarbital-dependent rats.

作者信息

Yutrzenka G J, Patrick G A, Rosenberger W

机构信息

Department of Physiology and Pharmacology, University of South Dakota School of Medicine, Vermillion.

出版信息

Physiol Behav. 1989 Jul;46(1):55-60. doi: 10.1016/0031-9384(89)90321-1.

DOI:10.1016/0031-9384(89)90321-1
PMID:2573097
Abstract

The ability of temazepam and midazolam to substitute for pentobarbital and thus maintain the physical dependence state was used to assess the potential dependence liability of these two benzodiazepine compounds. Male Sprague-Dawley rats, weighing 175-200 g and having ad lib access to food and water, were determined to be dependent on pentobarbital following 12 days of continuous, intraperitoneal infusion of pentobarbital using an escalating drug infusion schedule. On day 13 (substitution phase) the pentobarbital was replaced with either temazepam, midazolam or vehicle and the rats were infused for an additional 24 hours. This was followed on Day 14 (withdrawal phase) by a 24 hr saline infusion period. Rats were observed for changes in overt behavior and alterations of body weight during both Day 13 and Day 14. Preliminary potency estimation studies had indicated that both drugs were more potent and longer acting than was pentobarbital. Temazepam, in doses of 32.5, 65 and 130 mg/kg/24 hr, was demonstrated to substitute for pentobarbital and provided dose-dependent suppression of overt behavioral signs indicative of withdrawal. Temazepam also suppressed the weight loss typically observed during withdrawal. Substitution of saline for temazepam resulted in an increased incidence of withdrawal signs and an approximate 10% decline in body weight. Midazolam, in doses of 60 and 120 mg/kg/24 hr, also substituted for pentobarbital and suppressed both overt behavior and weight loss. Following saline substitution on Day 14, a mild withdrawal syndrome was evident although body weight was noted to remain near control values.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

使用替马西泮和咪达唑仑替代戊巴比妥并维持身体依赖状态的能力,来评估这两种苯二氮卓类化合物的潜在依赖倾向。体重175 - 200克、可自由获取食物和水的雄性斯普拉格-道利大鼠,在采用递增药物输注方案连续腹腔输注戊巴比妥12天后,被确定对戊巴比妥产生了依赖。在第13天(替代阶段),将戊巴比妥替换为替马西泮、咪达唑仑或赋形剂,并对大鼠再输注24小时。随后在第14天(戒断阶段)进行24小时的生理盐水输注期。在第13天和第14天观察大鼠明显行为的变化和体重改变。初步效价估计研究表明,这两种药物都比戊巴比妥更有效且作用时间更长。剂量为32.5、65和130毫克/千克/24小时的替马西泮,被证明可替代戊巴比妥,并能剂量依赖性地抑制表明戒断的明显行为体征。替马西泮还抑制了戒断期间通常观察到的体重减轻。用生理盐水替代替马西泮导致戒断体征发生率增加,体重下降约10%。剂量为60和120毫克/千克/24小时的咪达唑仑也可替代戊巴比妥,并抑制明显行为和体重减轻。在第14天用生理盐水替代后,尽管注意到体重仍接近对照值,但出现了轻度戒断综合征。(摘要截短至250字)

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