Mendelson W B, Martin J V, Perlis M, Wagner R
Department of Psychiatry and Behavioral Science, State University of New York at Stony Brook.
J Neural Transm. 1987;70(3-4):329-36. doi: 10.1007/BF01253607.
CL 218,872, which preferentially binds to benzodiazepine (BZ) type 1 receptors, and flurazepam, which is thought to bind to both types 1 and 2, were given alone and in combination to rats. CL 218,872 had little effect on sleep latency, but significantly increased total sleep time. As expected, flurazepam both shortened sleep latency and prolonged total sleep. Pretreatment with CL 218,872 had no effect on these alterations in sleep induced by flurazepam. The implications for possible significance of sub-typing of BZ receptors are discussed.
优先与1型苯二氮䓬(BZ)受体结合的CL 218,872以及被认为能与1型和2型受体都结合的氟西泮,被单独及联合给予大鼠。CL 218,872对睡眠潜伏期影响不大,但显著增加了总睡眠时间。正如预期的那样,氟西泮既缩短了睡眠潜伏期又延长了总睡眠时间。用CL 218,872进行预处理对氟西泮诱导的这些睡眠改变没有影响。文中讨论了BZ受体亚型可能具有的意义。