Giorgi O, Corda M G, Fernandez A, Biggio G
Department of Experimental Biology, University of Cagliari, Italy.
Pharmacol Biochem Behav. 1989 Mar;32(3):671-5. doi: 10.1016/0091-3057(89)90016-6.
The aim of the present study was to investigate the ability of different benzodiazepine recognition site antagonists (Ro 15-1788 and ZK 93426) and inverse agonists (Ro 15-4513, FG 7142 and CGS 8216) to induce abstinence signs in diazepam-dependent cats. Different groups of cats were challenged with each of the benzodiazepine recognition site ligands under investigation 24 hours after the last dose of chronic treatment with diazepam (7 mg/kg, IP at 8.00 a.m. and 8.00 p.m. for 21 consecutive days). The benzodiazepine derivatives Ro 15-4513 and Ro 15-1788 precipitated an abstinence syndrome within minutes after IP administration. The pyrazoloquinoline derivative CGS 8216 also induced withdrawal signs that were less severe and had a longer latency than those elicited by Ro 15-4513 and Ro 15-1788. Abstinence signs included tremors, increased muscle tone, irritability, fear, arched-back posture, pupillary dilation and vocalizations. On the other hand, the beta-carboline derivatives ZK 93426 and FG 7142 failed to precipitate abstinence signs in diazepam-dependent cats when given at doses that prevented the acute effects of diazepam. Our results demonstrate that the ability to induce withdrawal signs in diazepam-dependent cats depends on the chemical structure of the challenge drug (i.e., benzodiazepine or pyrazoloquinoline), since beta-carboline antagonists like ZK 93426 and partial inverse agonists like FG 7142 lack this property.
本研究的目的是调查不同的苯二氮䓬识别位点拮抗剂(Ro 15 - 1788和ZK 93426)及反向激动剂(Ro 15 - 4513、FG 7142和CGS 8216)在依赖地西泮的猫中诱发戒断症状的能力。在最后一剂地西泮(7 mg/kg,腹腔注射,上午8点和晚上8点,连续21天)慢性治疗后24小时,用所研究的每种苯二氮䓬识别位点配体对不同组的猫进行激发试验。苯二氮䓬衍生物Ro 15 - 4513和Ro 15 - 1788在腹腔注射后数分钟内引发了戒断综合征。吡唑并喹啉衍生物CGS 8216也诱发了戒断症状,但其严重程度低于Ro 15 - 4513和Ro 15 - 1788,且潜伏期更长。戒断症状包括震颤、肌张力增加、易怒、恐惧、弓背姿势、瞳孔散大和鸣叫。另一方面,β-咔啉衍生物ZK 93426和FG 7142在给予能阻止地西泮急性效应的剂量时,未能在依赖地西泮的猫中引发戒断症状。我们的结果表明,在依赖地西泮的猫中诱发戒断症状的能力取决于激发药物的化学结构(即苯二氮䓬或吡唑并喹啉),因为像ZK 93426这样的β-咔啉拮抗剂和像FG 7142这样的部分反向激动剂缺乏这种特性。