McCown T J, Moray L J, Kizer J S, Breese G R
Pharmacol Biochem Behav. 1986 May;24(5):1269-74. doi: 10.1016/0091-3057(86)90183-8.
When rats were pretreated with ethanol (3.0 g/kg, IP), subsequent microinjection of thyrotropin-releasing hormone (TRH) (500 or 1000 ng) into the medial septum, 30 minutes later, significantly shortened the time necessary for the rats to regain their righting reflex. Conversely, microinjection of TRH into the nucleus accumbens (1000 ng/side) or the area of the raphe obscurus (1000 ng) had no effect on ethanol-induced depression, although both of these structures mediate specific TRH effects in the CNS. In order to determine if this antagonism was due to a specific TRH interaction, TRH Fab fragments were microinjected into the medial septum just prior to the microinjection of TRH. Under these conditions, TRH did not alter ethanol's depressant actions. Finally, this TRH antagonism of ethanol-induced depression appears attributable to a net increase in neuronal activity, because electrical stimulation (160 microA, 120 Hz, 1.5 msec duration) of the medial septum antagonized ethanol's impairment of the righting reflex. These results are discussed in relationship to a potential CNS site for the action of ethanol.
当给大鼠腹腔注射乙醇(3.0克/千克)进行预处理后,30分钟后向其内侧隔区微量注射促甲状腺激素释放激素(TRH)(500或1000纳克),能显著缩短大鼠恢复翻正反射所需的时间。相反,向伏隔核(每侧1000纳克)或中缝隐核区域(1000纳克)微量注射TRH,对乙醇诱导的抑制作用没有影响,尽管这两个结构在中枢神经系统中介导特定的TRH效应。为了确定这种拮抗作用是否归因于特定的TRH相互作用,在微量注射TRH之前,先将TRH Fab片段微量注射到内侧隔区。在这些条件下,TRH并未改变乙醇的抑制作用。最后,TRH对乙醇诱导的抑制作用的这种拮抗作用似乎归因于神经元活动的净增加,因为对内侧隔区进行电刺激(160微安、120赫兹、1.5毫秒持续时间)可拮抗乙醇对翻正反射的损害。结合乙醇作用的潜在中枢神经系统部位对这些结果进行了讨论。