Pircio A W, Gylys J A, Cavanagh R L, Buyniski J P, Bierwagen M E
Arch Int Pharmacodyn Ther. 1976 Apr;220(2):231-57.
Butorphanol, a new, totally synthetic morphinan, which is chemically related to naloxone, has been demonstrated to have both analgesic and narcotic antagonist properties. In rodent antiwrithing analgesic tests, butorphanol was 4 to 30 times more potent than morphine and dl-pentazocine, respectively. As an antagonist, butorphanol was about equivalent to nalorphine and 30 times more potent than dl-pentazocine. On the basis of the naloxone-induced mouse jumping test and the lack of substitution in withdrawn morphine-dependent mice, it is estimated that the potential for physical dependence of butorphanol will be less than that of dl-pentazocine but greater than that of nalorphine and dl-cyclazocine. Animal data also show that agonistic actions of butorphanol, such as respiratory depression and miosis, reach ceiling effects which are lower than those seen with morphine with an increase in dosage. Thus, butorphanol differed from morphine which exhibited agonist effects in a dose-related manner. Butorphanol showed weak to moderate central depressant properties at doses which were considerably higher (greater than 100 X) than those producing analgesia. Minimal cardiovascular and respiratory effects were seen with butorphanol in conscious dogs.
布托啡诺是一种全新的、完全合成的吗啡喃,在化学结构上与纳洛酮相关,已证实它兼具镇痛和麻醉拮抗特性。在啮齿动物扭体镇痛试验中,布托啡诺的效力分别比吗啡和消旋喷他佐辛强4至30倍。作为拮抗剂,布托啡诺的效力与纳洛芬相当,比消旋喷他佐辛强30倍。基于纳洛酮诱发的小鼠跳跃试验以及对戒断吗啡依赖小鼠无替代作用,据估计布托啡诺产生身体依赖性的可能性小于消旋喷他佐辛,但大于纳洛芬和消旋环唑辛。动物实验数据还表明,布托啡诺的激动作用,如呼吸抑制和瞳孔缩小,随着剂量增加会达到极限效应,且低于吗啡所产生的效应。因此,布托啡诺与吗啡不同,吗啡的激动效应呈剂量相关。布托啡诺在比产生镇痛作用的剂量高得多(大于100倍)的剂量下表现出弱至中度的中枢抑制特性。清醒犬使用布托啡诺时,对心血管和呼吸的影响极小。