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血清素并非在下丘脑背内侧核的神经元中合成,而是在其中特异性转运。

Serotonin is not synthesized, but specifically transported in the neurons of the hypothalamic dorsomedial nucleus.

作者信息

Vanhatalo S, Soinila S

机构信息

Department of Anatomy, Institute of Biomedicine, University of Helsinki, Finland.

出版信息

Eur J Neurosci. 1998 May;10(5):1930-5. doi: 10.1046/j.1460-9568.1998.00217.x.

Abstract

A small group of neurons in the hypothalamic dorsomedial nucleus (DMN) have been reported to contain serotonin after pharmacological treatments enhancing brain serotonin levels. This study aimed at elucidating whether these neurons are able to synthesize serotonin de novo, and whether they possess a specific serotonin transport mechanism. Serotonin content in these neurons was raised by administration of L-tryptophan and pargyline. Double immunostaining for serotonin and tryptophan hydroxylase (TpOH), the serotonin synthesizing enzyme, revealed that none of the serotonin-containing neuronal somata expressed TpOH. Intracerebroventricular colchicine treatment did not result in TpOH-IR in these neurons. Fluoxetine, a specific serotonin transport inhibitor, prevented the accumulation of serotonin in these neurons. The present results thus indicate that the serotonin-containing DMN neurons are not able to synthesize serotonin. Instead, they take up exogenous serotonin via a specific serotonin transport mechanism. As serotonin and DMN are associated with various physiological functions, such as regulation of food intake and modulation of fear and anxiety, the mechanisms revealed in the present study may participate in these clinically important brain functions.

摘要

据报道,在采用提高脑血清素水平的药物治疗后,下丘脑背内侧核(DMN)中的一小群神经元含有血清素。本研究旨在阐明这些神经元是否能够从头合成血清素,以及它们是否具有特定的血清素转运机制。通过给予L-色氨酸和帕吉林来提高这些神经元中的血清素含量。对血清素和血清素合成酶色氨酸羟化酶(TpOH)进行双重免疫染色,结果显示,含血清素的神经元胞体均未表达TpOH。脑室内注射秋水仙碱对这些神经元未产生TpOH免疫反应。特异性血清素转运抑制剂氟西汀可阻止血清素在这些神经元中蓄积。因此,目前的结果表明,含血清素的DMN神经元无法合成血清素。相反,它们通过特定的血清素转运机制摄取外源性血清素。由于血清素和DMN与多种生理功能相关,如食物摄入调节以及恐惧和焦虑调节,本研究揭示的机制可能参与这些具有临床重要性的脑功能。

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