Robledo P, Lumeng L, Li T K, Ehlers C L
Department of Neuropharmacology, Scripps Research Institute, La Jolla, California 92037.
Alcohol Clin Exp Res. 1994 Apr;18(2):363-8. doi: 10.1111/j.1530-0277.1994.tb00026.x.
The selectively bred alcohol-preferring (P) and alcohol-nonpreferring (NP) rats have been shown to possess a number of behavioral and electrophysiological differences in response to alcohol. We sought to evaluate whether or not P and NP rats would respond differently to other sedative-hypnotic drugs related to ethanol. EEG recordings were conducted following systemic administration of the NMDA receptor antagonist MK 801 (0.1 mg/kg, ip) and the GABA/benzodiazepine receptor complex agonist diazepam (1.5 mg/kg, ip). Nine P and nine NP rats was implanted with bipolar stainless steel electrodes in the frontal cortex, the dorsal hippocampus, the ventral thalamus, and the anterior amygdala. In the vehicle condition, P rats showed significantly greater power of the EEG in the slow frequencies as compared with NP rats in the frontal cortex. Furthermore, P rats were found to have lower peak theta frequency (6-8 Hz) than NP rats in the frontal cortex, the dorsal hippocampus, and the ventral thalamus. MK 801 produced a significantly greater increase in the mean power of the EEG in NP rats in the 8-16 Hz than in P rats, whereas diazepam was found to decrease theta peak frequency (6-8 Hz), but more so in NP rats that in P rats. These data suggest that, in addition to differential responsiveness to alcohol, P and NP rats also differ in response to drugs that modify GABA and glutamate neurotransmission.
选择性培育的嗜酒(P)大鼠和不嗜酒(NP)大鼠已被证明在对酒精的反应方面存在许多行为和电生理差异。我们试图评估P大鼠和NP大鼠对与乙醇相关的其他镇静催眠药物的反应是否不同。在全身给予NMDA受体拮抗剂MK 801(0.1 mg/kg,腹腔注射)和GABA/苯二氮䓬受体复合物激动剂地西泮(1.5 mg/kg,腹腔注射)后进行脑电图记录。将9只P大鼠和9只NP大鼠在额叶皮质、背侧海马体、腹侧丘脑和前杏仁核植入双极不锈钢电极。在给予赋形剂的情况下,与额叶皮质中的NP大鼠相比,P大鼠在慢频率下脑电图的功率显著更高。此外,发现在额叶皮质、背侧海马体和腹侧丘脑中,P大鼠的θ波峰值频率(6 - 8 Hz)低于NP大鼠。MK 801使NP大鼠脑电图在8 - 16 Hz的平均功率增加幅度显著大于P大鼠,而地西泮被发现可降低θ波峰值频率(6 - 8 Hz),但NP大鼠的降低幅度大于P大鼠。这些数据表明,除了对酒精的反应不同外,P大鼠和NP大鼠对改变GABA和谷氨酸神经传递的药物的反应也不同。