Klockgether T, Schwarz M, Turski L, Sontag K H
Max-Planck-Institute for Experimental Medicine, Göttingen, Federal Republic of Germany.
Exp Brain Res. 1988;70(2):445-7. doi: 10.1007/BF00248371.
To investigate the behavioural role of mesocortical dopamine innervation we performed bilateral microinjections of haloperidol into various parts of the rat frontal cortex and into adjacent subcortical forebrain structures. Haloperidol (2.5 micrograms/0.5 microliter) locally injected into the medial prefrontal cortex or into the rostral part of the neostriatum resulted in the development of catalepsy as measured in the bar test. In contrast, injections of haloperidol into the nucleus accumbens, more caudal parts of the neostriatum, anterior cingulate cortex, rostral and lateral parts of the prefrontal cortex and into the lateral ventricles failed to induce catalepsy. It is concluded that blockade of dopamine receptors located in the rostral neostriatum and in the medial prefrontal cortex contributes to the development of haloperidol induced catalepsy.
为研究中皮质多巴胺神经支配的行为作用,我们将氟哌啶醇双侧微量注射到大鼠额叶皮质的不同部位以及相邻的皮质下前脑结构中。将氟哌啶醇(2.5微克/0.5微升)局部注射到内侧前额叶皮质或新纹状体的前部,在棒测试中可导致僵住症的出现。相比之下,将氟哌啶醇注射到伏隔核、新纹状体更靠尾侧的部分、前扣带回皮质、前额叶皮质的前部和外侧部分以及侧脑室中,均未能诱发僵住症。得出的结论是,位于新纹状体前部和内侧前额叶皮质的多巴胺受体被阻断,有助于氟哌啶醇诱发僵住症的发展。