Herve D, Tassin J P, Studler J M, Dana C, Kitabgi P, Vincent J P, Glowinski J, Rostene W
Proc Natl Acad Sci U S A. 1986 Aug;83(16):6203-7. doi: 10.1073/pnas.83.16.6203.
In the rat brain, destruction of dopaminergic cell groups by injections of 6-hydroxydopamine into the ventral mesencephalic tegmentum results in large decreases in the number of neurotensin binding sites in the mesencephalon and the striatum. In contrast, these lesions produce an increase in the number of 125I-labeled neurotensin binding sites in the lateral part of the prefrontal cortex despite a large decrease in cortical dopamine levels. Increases in the number of 125I-labeled neurotensin binding sites in this cortical area as well as in the entorhinal cortex, the nucleus accumbens, and the central part of the striatum were also obtained after chronic blockade of dopamine neurotransmission by a long-acting neuroleptic pipotiazine palmitic ester. We propose that dopamine inputs regulate the density of postsynaptic neurotensin binding sites through cortical and subcortical dopamine receptors. Therefore, some of the clinical effects of neuroleptics in schizophrenic patients could be partly related to changes in neurotensin neurotransmission.
在大鼠脑中,向腹侧中脑被盖区注射6-羟基多巴胺破坏多巴胺能细胞群,会导致中脑和纹状体中神经降压素结合位点数量大幅减少。相比之下,尽管皮质多巴胺水平大幅下降,但这些损伤会使前额叶皮质外侧部分125I标记的神经降压素结合位点数量增加。通过长效抗精神病药物棕榈酸哌泊噻嗪长期阻断多巴胺神经传递后,该皮质区域以及内嗅皮质、伏隔核和纹状体中央部分的125I标记神经降压素结合位点数量也会增加。我们认为,多巴胺输入通过皮质和皮质下多巴胺受体调节突触后神经降压素结合位点的密度。因此,抗精神病药物对精神分裂症患者的一些临床作用可能部分与神经降压素神经传递的变化有关。