Magnusson T, Carlsson A, Fisher G H, Chang D, Folkers K
J Neural Transm. 1976;38(2):89-93. doi: 10.1007/BF01262967.
Synthetic substance P has been discovered to stimulate significantly the formation of dopa in the limbic, striatum, hemisphere and diencephalon regions of the brain and the lower brain stem. There was no effect upon 5-hydroxytryptophan formation or on tryptophan or tyrosine levels. After inhibition of monoamine synthesis by N'-(DL-SERYL)-N2-(2, 3, 4-trihydroxybenzyl)hydrazine, substance P significantly accelerated the disappearance of dopamine, noradrenaline and 5-hydroxytryptamine. Substance P appears to stimulate monoaminergic neurons in the brain and to serve as an excitatory transmitter in nerve terminals impinging upon dopaminergic cell bodies. A similar stimulation of noradrenaline and 5-hydroxytryptamine indicate a similar transmitter role for noradrenergic and serotonergic neurons. These data strengthen questions about the possible clinical influence of substance P in disease states involving monoaminergic mechanisms including Parkinsonism and schizophrenia.
已发现合成的P物质能显著刺激大脑边缘系统、纹状体、半球、间脑区域以及脑干下部中多巴胺的形成。对5-羟色氨酸的形成、色氨酸或酪氨酸水平没有影响。在用N'-(DL-丝氨酰)-N2-(2,3,4-三羟基苄基)肼抑制单胺合成后,P物质显著加速了多巴胺、去甲肾上腺素和5-羟色胺的消失。P物质似乎能刺激大脑中的单胺能神经元,并在作用于多巴胺能细胞体的神经末梢中充当兴奋性递质。对去甲肾上腺素和5-羟色胺的类似刺激表明去甲肾上腺素能和5-羟色胺能神经元具有类似的递质作用。这些数据强化了关于P物质在涉及单胺能机制的疾病状态(包括帕金森病和精神分裂症)中可能产生的临床影响的疑问。