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成年和老年大鼠中枢神经系统中胆囊收缩素-多巴胺受体相互作用的证据。对其功能意义的研究。

Evidence for cholecystokinin-dopamine receptor interactions in the central nervous system of the adult and old rat. Studies on their functional meaning.

作者信息

Agnati L F, Fuxe K, Giardino L, Calza L, Zoli M, Battistini N, Benfenati F, Vanderhaeghen J J, Guidolin D, Ruggeri M

出版信息

Ann N Y Acad Sci. 1985;448:315-33. doi: 10.1111/j.1749-6632.1985.tb29927.x.

DOI:10.1111/j.1749-6632.1985.tb29927.x
PMID:2862827
Abstract

Evidence has been presented for the existence of interactions between CCK and DA receptors both in striatal and limbic membranes. A similar type of modulation by CCK-8 of DA receptors also exists after chronic neuroleptic treatment indicating that supersensitive DA receptors are also modulated by this peptide. As seen from simulation curves, CCK-8 increases the binding of [3H]DA agonists and reduces the binding of [3H]DA antagonists in striatal membranes, suggesting that CCK-8 may increase striatal DA transmission. Results of this type may underlie some of the non-neuroleptic effects of CCK-8. In the aged brain, the ability of CCK-8 to modulate DA antagonist binding sites is changed such that the binding of [3H]DA antagonists is increased. Thus, in the aged brain, receptor-receptor interactions may be altered, leading to a derangement of heterostatic mechanisms (mechanisms changing chemical transmission without interfering with synaptic homeostasis). It was also demonstrated that during aging there is a preferential disappearance of CCK-like immunoreactivity versus TH immunoreactivity in the nigral DA neurons, especially in the medially located nigral DA cells; furthermore, co-existence in the TH/CCK co-storing terminals in the nucleus accumbens was reduced during aging. Such alterations should also lead to changes in heterostatic regulation because the CCK co-modulation line controlling the DA receptors may be preferentially affected.

摘要

已有证据表明,在纹状体和边缘系统膜中,胆囊收缩素(CCK)与多巴胺(DA)受体之间存在相互作用。长期使用抗精神病药物治疗后,CCK-8对DA受体也存在类似的调节作用,这表明超敏DA受体也受该肽调节。从模拟曲线可以看出,CCK-8增加纹状体膜中[3H]DA激动剂的结合,并减少[3H]DA拮抗剂的结合,这表明CCK-8可能增加纹状体DA传递。这类结果可能是CCK-8某些非抗精神病药物作用的基础。在老年大脑中,CCK-8调节DA拮抗剂结合位点的能力发生改变,使得[3H]DA拮抗剂的结合增加。因此,在老年大脑中,受体-受体相互作用可能发生改变,导致异稳态机制(在不干扰突触稳态的情况下改变化学传递的机制)紊乱。研究还表明,在衰老过程中,黑质DA神经元中CCK样免疫反应性相对于酪氨酸羟化酶(TH)免疫反应性优先消失,尤其是在内侧黑质DA细胞中;此外,衰老过程中伏隔核中TH/CCK共储存终末的共存减少。这些改变也应导致异稳态调节的变化,因为控制DA受体的CCK共调节线路可能受到优先影响。

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