Martin W R, Sloan J W, Wala E
Department of Pharmacology, University of Kentucky College of Medicine, Lexington.
J Pharmacol Exp Ther. 1990 Nov;255(2):744-55.
The ability of graded doses of flumazenil (2, 6, 18, 36 and 72 mg/kg) and a lactose placebo to precipitate abstinence was studied in dogs treated chronically with diazepam, nordiazepam, flunitrazepam, alprazolam, oxazepam, halazepam and lorazepam by oral dosing. A scale comprised of 10 precipitated abstinence signs, the Benzodiazepine Precipitated Abstinence Scale, was developed, which yielded linear flumazenil log-dose response lines with significant slopes in dogs dependent on diazepam, nordiazepam and flunitrazepam. The effects of 18, 36 and 72 mg/kg of flumazenil in otherwise drug naive dogs were studied. In naive dogs, the most prominent effect of flumazenil was to reduce activity. All benzodiazepines studied produced dependence that was characterized by signs of precipitated abstinence; however, the intensity and quality of abstinence varied from one benzodiazepine to another. Precipitated abstinence in dogs treated chronically with diazepam and flunitrazepam was characterized by a dose-related increase in clonic convulsions and Benzodiazepine Precipitated Abstinence Scale scores. This pattern differed from that seen in nordiazepam- and alprazolam-dependent dogs, which showed a comparable flumazenil dose-related increase in clonic convulsion but only a modest increase in Benzodiazepine Precipitated Abstinence Scale scores. Oxazepam and lorazepam produced dependence that was less intense than that seen with the other benzodiazepines. Plasma levels of the benzodiazepines and their metabolites were repeatedly determined after single doses and during addiction cycles. Nordiazepam accumulated in diazepam- and nordiazepam-dependent dogs and alpha-OH alprazolam accumulated in alprazolam-dependent dogs. Other drugs and metabolites did not. These observations suggest that: 1) different benzodiazepines or their metabolites produce different types of physical dependence, suggesting that they or their metabolites have different mechanisms and sites of action; 2) plasma cumulation of the benzodiazepines or their active metabolites is an important factor in the genesis of physical dependence; and 3) metabolism of benzodiazepines plays an important role in their dependence-producing capacity, and because of differences in the way species metabolize benzodiazepines, the type of dependence produced in different species may differ.
通过口服给药,对长期接受地西泮、去甲西泮、氟硝西泮、阿普唑仑、奥沙西泮、哈拉西泮和劳拉西泮治疗的犬,研究了不同剂量(2、6、18、36和72mg/kg)的氟马西尼和乳糖安慰剂引发戒断反应的能力。开发了一个由10个戒断反应体征组成的量表,即苯二氮䓬类戒断反应量表,该量表在依赖地西泮、去甲西泮和氟硝西泮的犬中产生了具有显著斜率的氟马西尼对数剂量反应线。研究了18、36和72mg/kg氟马西尼对原本未接触过药物的犬的影响。在未接触过药物的犬中,氟马西尼最显著的作用是降低活动水平。所研究的所有苯二氮䓬类药物均产生了以戒断反应体征为特征的依赖性;然而,不同苯二氮䓬类药物的戒断反应强度和性质各不相同。长期接受地西泮和氟硝西泮治疗的犬的戒断反应表现为阵挛性惊厥和苯二氮䓬类戒断反应量表评分与剂量相关的增加。这种模式与去甲西泮和阿普唑仑依赖的犬不同,后者阵挛性惊厥的氟马西尼剂量相关增加相当,但苯二氮䓬类戒断反应量表评分仅适度增加。奥沙西泮和劳拉西泮产生的依赖性比其他苯二氮䓬类药物弱。单次给药后及成瘾周期中反复测定苯二氮䓬类药物及其代谢物的血浆水平。去甲西泮在依赖地西泮和去甲西泮的犬中蓄积,α-羟基阿普唑仑在依赖阿普唑仑的犬中蓄积。其他药物及其代谢物则没有。这些观察结果表明:1)不同的苯二氮䓬类药物或其代谢物产生不同类型的身体依赖性,表明它们或其代谢物具有不同的作用机制和部位;2)苯二氮䓬类药物或其活性代谢物的血浆蓄积是身体依赖性产生的一个重要因素;3)苯二氮䓬类药物的代谢在其产生依赖性的能力中起重要作用,并且由于不同物种代谢苯二氮䓬类药物的方式不同,不同物种产生的依赖性类型可能不同。