Kalivas P W, Horita A
J Pharmacol Exp Ther. 1980 Feb;212(2):203-10.
Possible neuroanatomical substrates mediating some of the effects seen with thyrotropin-releasing hormone (TRH) in the pentobarbital (PB) narcotized rat were examined. This was accomplished by microinjecting picomole concentrations of TRH into 20 different brain sites. The behavioural effects examined were the capacity of TRH to antagonize PB-induced narcosis and hypothermia as well as TRH-induced shaking behavior. Microinjection of TRH into the septum was found to be significantly more effective in the reversal of PB narcosis than any other site examined. In contrast, the temperature and shaking response were evoked with approximately equal efficacy by TRH microinjection into a number of brain sites; including the preoptic/anterior hypothalamus, medial thalamus, thalamic, periventricular gray, interpeduncular nucleus and locus ceruleus. These results demonstrate the septal region to be the site of action for TRH reversal of PB narcosis and suggest the involvement of the septohippocampal system. In addition, they indicate that the neurogenesis of the shaking response is similar to that of the temperature response and that this differs from the neurogenesis of the analeptic response.
研究了在戊巴比妥(PB)麻醉大鼠中,介导促甲状腺激素释放激素(TRH)所产生的某些效应的可能神经解剖学底物。这是通过将皮摩尔浓度的TRH微量注射到20个不同的脑区来实现的。所检测的行为效应包括TRH拮抗PB诱导的麻醉和体温过低的能力以及TRH诱导的颤抖行为。发现将TRH微量注射到隔区在逆转PB麻醉方面比所检测的任何其他部位都显著更有效。相比之下,通过将TRH微量注射到多个脑区,包括视前区/下丘脑前部、内侧丘脑、丘脑、脑室周围灰质、脚间核和蓝斑,诱发温度和颤抖反应的效力大致相同。这些结果表明隔区是TRH逆转PB麻醉的作用部位,并提示隔海马系统参与其中。此外,它们表明颤抖反应的神经发生与温度反应的神经发生相似,且这与苏醒反应的神经发生不同。