Bennett D A
Research Department, CIBA-GEIGY Corporation Summit, NJ 07901.
Psychopharmacol Ser. 1988;4:85-94. doi: 10.1007/978-3-642-73223-2_7.
Benzodiazepines produce discriminative stimuli that are stereospecific and antagonized by specific benzodiazepine receptor antagonists. The potency of these stimuli correlate with the ability of these compounds to bind to the benzodiazepine receptor complex. These data indicate that benzodiazepine stimuli are transduced via the benzodiazepine receptor. The underlying basis of these stimuli is unclear. Results with novel compounds that produce preclinical anxiolytic effects without the sedation and muscle relaxation of the classical benzodiazepines suggest that muscle relaxation may contribute to these stimuli. A direct comparison of discriminative stimuli established on a classical benzodiazepine agonist with the stimuli established on a partial benzodiazepine agonist supports the possibility that the classical benzodiazepine cue is mediated by a muscle relaxant effect, while the partial agonist cue is related to the anxioselectivity of the compound.
苯二氮䓬类药物产生的辨别性刺激具有立体特异性,并被特定的苯二氮䓬受体拮抗剂所拮抗。这些刺激的效力与这些化合物与苯二氮䓬受体复合物结合的能力相关。这些数据表明苯二氮䓬类刺激是通过苯二氮䓬受体转导的。这些刺激的潜在基础尚不清楚。新型化合物产生临床前抗焦虑作用但无经典苯二氮䓬类药物的镇静和肌肉松弛作用,其结果表明肌肉松弛可能导致这些刺激。对基于经典苯二氮䓬类激动剂建立的辨别性刺激与基于部分苯二氮䓬类激动剂建立的刺激进行直接比较,支持了经典苯二氮䓬类线索由肌肉松弛作用介导,而部分激动剂线索与化合物的抗焦虑选择性相关的可能性。