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松鼠猴每日重复口服阿普唑仑、地西泮、氟硝西泮或奥沙西泮后出现戒断反应。

Precipitated withdrawal in squirrel monkeys after repeated daily oral administration of alprazolam, diazepam, flunitrazepam or oxazepam.

作者信息

Martin J R, Moreau J L, Jenck F

机构信息

Pharma Division, E. Hoffmann-La Roche Ltd., Basel, Switzerland.

出版信息

Psychopharmacology (Berl). 1995 Apr;118(3):273-9. doi: 10.1007/BF02245955.

Abstract

The lowest dose of alprazolam, diazepam, flunitrazepam and oxazepam consistently to induce loss of righting reflex in squirrel monkeys or vehicle was orally administered to monkeys on 18 consecutive days: 2 mg/kg alprazolam (n = 4), 30 mg/kg diazepam (n = 4), 1 mg/kg flunitrazepam (n = 4), 280 mg/kg oxazepam (n = 5), or vehicle (n = 4). Tolerance developed rapidly for loss of righting reflex, more slowly for sleep and only minimally for muscle relaxation observed during the period immediately following daily oral administration. Injection of the specific benzodiazepine receptor antagonist flumazenil (10 mg/kg i.v.) 5 h after the ninth daily oral treatment produced signs of precipitated withdrawal (tremor, vomiting and/or convulsions) in one alprazolam-, four diazepam-, one flunitrazepam- and four oxazepam-treated monkeys, but not in the vehicle-treated monkeys. Physiological saline injected intravenously several days later under these same experimental conditions failed to provoke a precipitated withdrawal reaction. When flumazenil-induced precipitated withdrawal was again evaluated after the 18th daily oral treatment, withdrawal signs were observed in all alprazolam- and all diazepam-treated monkeys, as well as in three flunitrazepam- and three oxazepam-treated monkeys, but not in the vehicle-treated monkeys (convulsions were observed in one alprazolam-, two diazepam-, one flunitrazepam- and two oxazepam-treated monkeys). No signs of spontaneous withdrawal were observed in any of the monkeys during a subsequent 3-week drug-free period. Thus, repeated administration of approximately equieffective doses of these four benzodiazepines resulted in a similar development of tolerance and physical dependence (indicated by the occurrence of a precipitated withdrawal reaction).

摘要

将阿普唑仑、地西泮、氟硝西泮和奥沙西泮能持续使松鼠猴出现翻正反射消失的最低剂量或赋形剂,连续18天口服给予猴子:2mg/kg阿普唑仑(n = 4)、30mg/kg地西泮(n = 4)、1mg/kg氟硝西泮(n = 4)、280mg/kg奥沙西泮(n = 5)或赋形剂(n = 4)。翻正反射消失的耐受性迅速形成,睡眠耐受性形成较慢,而在每日口服给药后立即观察到的肌肉松弛耐受性形成极小。在第9次每日口服治疗后5小时静脉注射特异性苯二氮䓬受体拮抗剂氟马西尼(10mg/kg),在1只接受阿普唑仑治疗、4只接受地西泮治疗、1只接受氟硝西泮治疗和4只接受奥沙西泮治疗的猴子中出现了戒断反应加剧的体征(震颤、呕吐和/或惊厥),但在接受赋形剂治疗的猴子中未出现。在相同实验条件下,数天后静脉注射生理盐水未能引发戒断反应加剧。在第18次每日口服治疗后再次评估氟马西尼诱导的戒断反应加剧时,在所有接受阿普唑仑和地西泮治疗的猴子中,以及3只接受氟硝西泮和3只接受奥沙西泮治疗的猴子中观察到了戒断体征,但在接受赋形剂治疗的猴子中未观察到(在1只接受阿普唑仑治疗、2只接受地西泮治疗、1只接受氟硝西泮治疗和2只接受奥沙西泮治疗的猴子中观察到惊厥)。在随后3周的无药期内,任何猴子均未观察到自发戒断体征。因此,重复给予这四种苯二氮䓬类药物的近似等效剂量导致了相似的耐受性和身体依赖性发展(通过戒断反应加剧的发生来表明)。

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