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人脑中5-羟色胺1D受体的个体发生发育:一项放射自显影研究。

Ontogenetic development of 5-HT1D receptors in human brain: an autoradiographic study.

作者信息

del Olmo E, del Arco C, Díaz A, Pascual J, Mengod G, Palacios J M, Pazos A

机构信息

Department of Physiology and Pharmacology, University of Cantabria, Santander, Spain.

出版信息

Eur J Neurosci. 1996 Jan;8(1):53-60. doi: 10.1111/j.1460-9568.1996.tb01166.x.

Abstract

The pattern of pre- and postnatal appearance of 5-HT1D receptors throughout the different areas of the human brain was studied by quantitative in vitro autoradiography, using [125I]GTI (serotonin O-carboxymethyl-glycyl-[125I]tyrosinamide) as a ligand. The anatomical distribution of 5-HT1D receptors in neonatal, infant and children's brain was in good agreement with that observed in the adult, the basal ganglia and substantia nigra being the most intensely labelled areas. The development of these receptors throughout the human brain was mainly postnatal: low densities of [125I]GTI binding sites were observed at the fetal/neonatal stage in most regions analyzed, in contrast with the high levels of labelling found in infant and children's brains. Indeed, in a number of regions, including the globus pallidus, substantia nigra and visual cortex, a peak of overexpression of 5-HT1D receptors was observed in the first decade of life. Such overexpression could support a regulatory role for 5-HT1D receptors in advanced periods of the CNS developmental process. Our results also indicate that the administration of drugs acting on 5-HT1D receptors during the early postnatal period of life could result in modifications of their properties, as these receptors are already functional in this period.

摘要

采用定量体外放射自显影技术,以[125I]GTI(5-羟色胺O-羧甲基-甘氨酰-[125I]酪氨酰胺)为配体,研究了5-HT1D受体在人脑中不同区域的产前和产后出现模式。5-HT1D受体在新生儿、婴儿和儿童脑中的解剖分布与在成人脑中观察到的情况高度一致,基底神经节和黑质是标记最强烈的区域。这些受体在整个人脑中的发育主要发生在出生后:在分析的大多数区域,胎儿/新生儿阶段观察到[125I]GTI结合位点的低密度,这与婴儿和儿童脑中发现的高水平标记形成对比。事实上,在包括苍白球、黑质和视觉皮层在内的许多区域,在生命的第一个十年中观察到5-HT1D受体的过表达峰值。这种过表达可能支持5-HT1D受体在中枢神经系统发育过程后期的调节作用。我们的结果还表明,在生命的产后早期给予作用于5-HT1D受体的药物可能会导致其性质的改变,因为这些受体在这个时期已经具有功能。

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