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P物质改变6-羟基多巴胺诱导的中枢去甲肾上腺素能神经元产后发育的改变。

Substance P modifies the 6-hydroxydopamine induced alteration of postnatal development of central noradrenaline neurons.

作者信息

Jonsson G, Hallman H

出版信息

Neuroscience. 1982;7(11):2909-18. doi: 10.1016/0306-4522(82)90113-0.

Abstract

Systemic treatment of new-born rats with the catecholamine neurotoxin 6-hydroxydopamine leads to a permanent and selective alteration of the postnatal development of the central noradrenaline neurons, in particular of the locus coeruleus system. The changes involve a pronounced and permanent degeneration of distant nerve terminal projections (e.g. in the cerebral cortex and spinal cord) and a hyperinnervation of regions close to the noradrenaline perikarya (e.g. in the cerebellum and pons-medulla). Substance P administered intracisternally was found to counteract significantly both the 6-hydroxydopamine-induced denervation and hyperinnervation, as monitored by measuring endogenous noradrenaline levels and [3H]noradrenaline uptake in vitro. The counteracting effect of substance P disclosed a clear dose-response relationship and was most effective when injected on postnatal days one and two, while practically no effects were observed after injection on postnatal days three and four. Substance P treatment alone of new-born rats had no effect on the postnatal development of the regional monoamine levels. Binding studies employing radioligand technique showed substance P treatment to abolish the 6-hydroxydopamine-induced increase in beta-receptor binding in the frontal cortex, suggesting the 'spared' noradrenaline terminals to be functionally active. Substance P was shown to increase the utilization of noradrenaline in the neonatal stage. The results indicate that the counteracting effect of substance P may be due to a prevention of degeneration, growth stimulation and/or trophic influences on central noradrenaline neurons, possibly related to an excitatory effect of substance P on noradrenaline neurons.

摘要

用儿茶酚胺神经毒素6-羟基多巴胺对新生大鼠进行全身治疗,会导致中枢去甲肾上腺素能神经元产后发育的永久性和选择性改变,特别是蓝斑系统。这些变化包括远距离神经末梢投射(如在大脑皮层和脊髓中)的明显且永久性退化,以及去甲肾上腺素能神经元胞体附近区域(如在小脑和脑桥-延髓中)的神经支配过度。通过体外测量内源性去甲肾上腺素水平和[3H]去甲肾上腺素摄取来监测发现,脑池内注射P物质可显著对抗6-羟基多巴胺诱导的去神经支配和神经支配过度。P物质的对抗作用呈现出明显的剂量反应关系,在出生后第1天和第2天注射时最为有效,而在出生后第3天和第4天注射后几乎没有观察到效果。单独用P物质治疗新生大鼠对区域单胺水平的产后发育没有影响。采用放射性配体技术的结合研究表明,P物质治疗可消除6-羟基多巴胺诱导的额叶皮层β受体结合增加,表明“保留”的去甲肾上腺素能末梢具有功能活性。结果表明,P物质的对抗作用可能是由于其对中枢去甲肾上腺素能神经元的变性预防、生长刺激和/或营养影响,这可能与P物质对去甲肾上腺素能神经元的兴奋作用有关。

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