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多巴胺能受体激动剂和拮抗剂对新纹状体胆碱能系统活性的影响。

Effects of dopaminergic receptor agonists and antagonists on the activity of the neo-striatal cholinergic system.

作者信息

Guyenet P G, Javory A F, Beaujouan J C, Rossier B J, Glowinski J

出版信息

Brain Res. 1975 Feb 7;84(2):227-44. doi: 10.1016/0006-8993(75)90978-6.

Abstract

The effects of various neuroleptics and of apomorphine on the metabolism of ACh were examined in the neostriatum of the rat. For this purpose, a specific radio-enzymatic assay for brain ACh was used. This method is based on the preliminary purification of the choline esters by liquid cation exchange, separation of choline and ACh on thin layer chromatography plates, hydrolysis of ACh then reactylation of the choline moiety with a purified and stabilized rat brain choline acetyltransferase. The rat neostriatal ACh levels were decreased by neuroleptics of the phenothiazine and butyrophenone type and increased by apomorphine. An "in vivo" estimation of the rate of utilization of ACh was obtained by measuring the decline in neostriatal ACh content following the local microinjection of hemicholinium-3. This compound blocked almost totally the synthesis of ACh in these conditions. Chlorpromazine (15 mg/kg) enhanced neo-striatal ACh utilization and apomorphine (10 mg/kg) antagonized this effect. Neuroleptics did not effect ACh levels in the parietal cerebral cortex and the hippocampal formation. The modifications of the activity of neostriatal cholinergic neurons by chlorpromazine and apomorphine were still observed following the degeneration of the nigro-neostriatal dopaminergic fibers induced by the injection of 6-hydroxydopamine into the substantia nigra. The results strongly suggest that dopaminergic receptors as defined by their pharmacological interaction with neuroleptics and apomorphine are localized on neostriatal ACh neurons.

摘要

在大鼠新纹状体中研究了各种抗精神病药物和阿扑吗啡对乙酰胆碱(ACh)代谢的影响。为此,采用了一种针对脑ACh的特异性放射酶测定法。该方法基于通过液相阳离子交换对胆碱酯进行初步纯化,在薄层色谱板上分离胆碱和ACh,水解ACh,然后用纯化并稳定化的大鼠脑胆碱乙酰转移酶使胆碱部分再乙酰化。吩噻嗪类和丁酰苯类抗精神病药物可降低大鼠新纹状体ACh水平,而阿扑吗啡则使其升高。通过测量局部微量注射3-羟甲基胆碱后新纹状体ACh含量的下降,获得了ACh利用速率的“体内”估计值。在这些条件下,该化合物几乎完全阻断了ACh的合成。氯丙嗪(15mg/kg)增强了新纹状体ACh的利用,而阿扑吗啡(10mg/kg)则拮抗了这种作用。抗精神病药物对顶叶大脑皮质和海马结构中的ACh水平没有影响。在向黑质注射6-羟基多巴胺诱导黑质-新纹状体多巴胺能纤维变性后,仍观察到氯丙嗪和阿扑吗啡对新纹状体胆碱能神经元活性的改变。结果强烈表明,通过其与抗精神病药物和阿扑吗啡的药理相互作用所定义的多巴胺能受体定位于新纹状体ACh神经元上。

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