Fuchs V, Burbes E, Coper H
Drug Alcohol Depend. 1984 Oct;14(2):179-86. doi: 10.1016/0376-8716(84)90043-7.
Four groups of rats were given free choice between water and solutions of either 3 micrograms/ml etonitazene, 5% ethanol (v/v), 0.1 mg/ml diazepam or 3 mg/ml barbital for 10-14 days. With the exception of barbital, some rats spontaneously preferred the drug solutions to water. This preference was reduced by addition of 7 micrograms/ml haolperidol. In a forced drug fluid consumption procedure, the daily administration of 15 mg/kg i.p. of the gamma-aminobutyric acid (GABA)-transaminase blocker aminooxyacetic acid (AOAA) led to a reduction of ethanol and diazepam intake, but not of etonitazene and barbital. It is suggested that the diminished consumption of ethanol and diazepam as caused by GABA-T-inhibition may also be mediated by dopamine which seems to act indirectly, via benzodiazepine receptors and GABA neurons.
将四组大鼠置于水与浓度分别为3微克/毫升依托尼秦、5%乙醇(体积/体积)、0.1毫克/毫升地西泮或3毫克/毫升巴比妥的溶液之间,任其自由选择,持续10 - 14天。除巴比妥外,一些大鼠自发地更喜欢药物溶液而非水。添加7微克/毫升氟哌啶醇后,这种偏好降低。在强制药物液体消耗实验中,腹腔注射15毫克/千克的γ-氨基丁酸(GABA)转氨酶抑制剂氨氧乙酸(AOAA),每日给药,导致乙醇和地西泮摄入量减少,但依托尼秦和巴比妥的摄入量未减少。研究表明,GABA转氨酶抑制引起的乙醇和地西泮消耗量减少可能也由多巴胺介导,多巴胺似乎通过苯二氮䓬受体和GABA神经元间接发挥作用。