Suppr超能文献

大鼠中5-羟色胺能神经元发育的免疫组织化学研究:上行通路和终末区

An immunohistochemical study of serotonin neuron development in the rat: ascending pathways and terminal fields.

作者信息

Lidov H G, Molliver M E

出版信息

Brain Res Bull. 1982 Apr;8(4):389-430. doi: 10.1016/0361-9230(82)90077-6.

Abstract

The ontogeny of the serotonergic axonal projections may be divided into three periods: one of initial axon elongation (E12-E16), the development of selective pathways (E15-E19) and terminal field development (E19-E21). All serotonergic axons that enter the prosencephalon ascend in the medial forebrain bundle From this bundle fascicles of immunoreactive axons enter several well-defined fiber tracts: specifically, the fasciculus retroflexus, stria medullaris, external capsule, fornix, and supracallosal stria. Axons from these pathways form terminal arborizations in the thalamus, hypothalamus, basal and limbic forebrain, and cerebral cortex. Serotonergic axons appear to be guided by pre-existing non-serotonergic tracts in reaching targets in the forebrain. Innervation of the cerebral cortex is a prolonged process extending from E19 through PND21. Axons enter directly into the marginal and intermediate zones of the immature cortex, at the medial, frontal and lateral edges of the hemisphere, and subsequently spread tangentially to cover the hemispheres. Terminal ramifications then arise from the bilaminar axons and fill in the middle cortical layers. This growth pattern gives rise to tangential and radial gradients in innervation density. While the growth of serotonin axons across the forebrain appears to be a continuous, sequential process, the development of terminal innervation is highly heterogeneous, occurring at different times and at different rates from region to region. Serotonergic axons do not innervate immature, primarily proliferative neuronal populations. The delay in serotonin innervation of the suprachiasmatic nucleus, striatum, and middle cortical layers long after the axons have reached these structures suggests that the formation of serotonin axon terminals is dependent on maturation of other elements in local neuronal circuitry.

摘要

血清素能轴突投射的个体发生可分为三个时期

一是轴突初始伸长阶段(胚胎第12天至第16天),二是选择性通路发育阶段(胚胎第15天至第19天),三是终末场发育阶段(胚胎第19天至第21天)。所有进入前脑的血清素能轴突都在内侧前脑束中上行。从该束中,免疫反应性轴突束进入几条明确的纤维束:具体而言,有回返束、髓纹、外囊、穹窿和胼胝体上纹。来自这些通路的轴突在丘脑、下丘脑、基底前脑和边缘前脑以及大脑皮层形成终末分支。血清素能轴突似乎在前脑到达靶标的过程中由预先存在的非血清素能束引导。大脑皮层的神经支配是一个从胚胎第19天持续到出生后第21天的漫长过程。轴突直接进入未成熟皮层的边缘区和中间区,位于半球的内侧、额叶和外侧边缘,随后沿切线方向扩散以覆盖半球。然后,双层层状轴突产生终末分支并填充皮质中间层。这种生长模式导致神经支配密度出现切线和径向梯度。虽然血清素轴突在前脑的生长似乎是一个连续的、有序的过程,但终末神经支配的发育高度异质,在不同时间和不同区域以不同速率发生。血清素能轴突不会支配未成熟的、主要是增殖性的神经元群体。在轴突到达视交叉上核、纹状体和皮质中间层后很长时间,血清素对这些结构的神经支配才出现延迟,这表明血清素轴突终末的形成依赖于局部神经元回路中其他元件的成熟。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验