Jahn U, Mixich G
Psychopharmacologia. 1976 Mar 16;46(2):191-6. doi: 10.1007/BF00421391.
Wet dog shake (WDS) behavior in rats, well known as morphine-withdrawal syndrome, could be elicited without concomitant symptoms for the first time chemically in non-morphine-addicted animals. The capability to produce WDS was correlated with a specific chemical structure among the title-compounds. The threshold-dose of the most effective agents was 25-50 mg/kg, rather independent of the mode of application. Maximal response of 10-20 WDS per min and animal were reached after application of 100-200 mg/kg. WDS behavior appeared within the first minutes after dose and lasted up to several hours. Detailed information is given on WDS-action of the substance Sgd 8473 = alpha [(4chlorobenzylideneamino)-oxy]-isobutyric acid and the influence by different pharmacologie agents thereon. Inhibition of WDS was produced by: narcotic analgesics, narcotic antagonists, psychosedativ drugs, yohimbine, dl-amphetamine, cocaine, apomorphine and clonidine. Without influence on WDS were: physostigmine, atropine, ganglionic- or adrenergic-blocking drugs, Dopa, MAO-inhibitors, serotonin- and histamin-antagonists and nonnarcotic analgesics. To some extent chemically induced WDS seemed to be susceptible like precipitated WDS. So Sgd 8473 could be qualified for differentiating narctic analgesics, for a "quasiabstinence" agent in research of dependence mechanisms and for a tool in neuroanatomical studies of the CNS.
大鼠的湿狗样抖动(WDS)行为,即众所周知的吗啡戒断综合征,首次能够在未成瘾的动物身上通过化学方法诱发,且不伴有其他症状。产生WDS的能力与标题化合物中的特定化学结构相关。最有效药物的阈值剂量为25 - 50毫克/千克,与给药方式无关。给予100 - 200毫克/千克后,每分钟每只动物可达到10 - 20次WDS的最大反应。WDS行为在给药后的最初几分钟内出现,并持续数小时。文中详细介绍了物质Sgd 8473 = α - [(4 - 氯亚苄基氨基)-氧基]-异丁酸的WDS作用以及不同药理剂对其的影响。抑制WDS的药物有:麻醉性镇痛药、麻醉性拮抗剂、精神安定药、育亨宾、右旋苯丙胺、可卡因、阿扑吗啡和可乐定。对WDS无影响的药物有:毒扁豆碱、阿托品、神经节或肾上腺素能阻断药、多巴、单胺氧化酶抑制剂、血清素和组胺拮抗剂以及非麻醉性镇痛药。在某种程度上,化学诱导的WDS似乎与戒断诱发的WDS一样敏感。因此,Sgd 8473可用于区分麻醉性镇痛药,作为研究依赖机制的“准戒断”剂以及中枢神经系统神经解剖学研究的工具。