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假定的新皮质递质物质的组织化学与功能意义:综述

Histochemistry and functional significance of putative neocortical transmitter substances: a review.

作者信息

Mihály A

出版信息

Z Mikrosk Anat Forsch. 1982;96(6):916-36.

PMID:6190322
Abstract
  1. Intrinsic neuronal chains of the neocortex communicate most probably with amino acid transmitters. These involve both excitatory (glutamate, aspartate--Nadler et al. 1976) both inhibitory (GABA--Ribak 1978) amino acids, and ensure fast, ionotropic postsynaptic actions (Eccles, McGeer 1979). 2. Some interneurons of the neocortex seemingly operate with the peptide transmitter VIP (Lorén et al. 1979). Presumably, this is a metabotropic, slowly acting substance (Dodd, Kelly and Said 1979). 3. The existence of intrinsic cholinergic neurons in the neocortex is a matter of question (Krnjevic and Silver 1965). It is worth to mention that in the periphery, cholinergic terminals also contain and release VIP (Hökfelt et al. 1980). It is not known, whether this transmitter dualism can be found in neocortex, too. An ascending cholinergic system projecting from the basal forebrain to the neocortex exists and exerts profound influence on cortical function (Shute and Lewis 1967). 4. Diffusely terminating, ascending monoamine axons innervate the neocortex and modulate interneuronal transmission (Thiery et al. 1977; Morrison et al. 1981, Lidov et al. 1981). 5. The neuropeptide SP excites cortical neurons (Phillis and Limacher 1974), and its presence in thin axons can be demonstrated immunohistochemically (Hökfelt et al. 1976). 6. Neocortical efferents to the thalamus and striatum seemingly use glutamate or aspartate (Fonnum et al. 1981). The transmitters of other corticofugal projections are not known. 7. The transmitters of specific thalamic afferents and those of callosal and association projections are unknown, too. 8. The main task of future histochemistry is to explore the synaptology of neocortical neurons and afferent systems with identified or evidenced transmitters, viz. to explore the neurochemical subsystems of cortical organization. The tool for it could be the immunohistochemistry, and future development depends mainly on the synthesis and purification of suitable antigens. The knowledge on the synaptology of identified neurochemical units of the cortex would be the basis of the understanding at least partly of the pharmacological effects exerted by the putative neocortical transmitters.
摘要
  1. 新皮层的内在神经元链很可能通过氨基酸递质进行通信。这些氨基酸包括兴奋性氨基酸(谷氨酸、天冬氨酸——纳德勒等人,1976年)和抑制性氨基酸(γ-氨基丁酸——里巴克,1978年),并确保快速的离子型突触后作用(埃克尔斯、麦吉尔,1979年)。2. 新皮层的一些中间神经元似乎利用肽类递质血管活性肠肽(洛伦等人,1979年)发挥作用。据推测,这是一种促代谢型、作用缓慢的物质(多德、凯利和赛义德,1979年)。3. 新皮层中是否存在内在胆碱能神经元尚存在疑问(克尔涅维奇和西尔弗,1965年)。值得一提的是,在周围神经系统中,胆碱能终末也含有并释放血管活性肠肽(霍克费尔特等人,1980年)。尚不清楚这种递质二元性在新皮层中是否也存在。存在一个从基底前脑投射到新皮层的上行胆碱能系统,它对皮层功能有深远影响(舒特和刘易斯,1967年)。4. 弥散性终末的上行单胺能轴突支配新皮层并调节中间神经元的传递(蒂埃里等人,1977年;莫里森等人,1981年,利多夫等人,1981年)。5. 神经肽P物质能兴奋皮层神经元(菲利斯和利马彻,1974年),其在细轴突中的存在可通过免疫组织化学方法证实(霍克费尔特等人,1976年)。6. 新皮层向丘脑和纹状体的传出纤维似乎利用谷氨酸或天冬氨酸(丰努姆等人,1981年)。其他皮质传出投射的递质尚不清楚。7. 特异性丘脑传入纤维以及胼胝体和联合投射的递质也不清楚。8. 未来组织化学的主要任务是探索新皮层神经元和具有已确定或已证实递质的传入系统的突触学,即探索皮层组织的神经化学亚系统。实现这一目标的工具可能是免疫组织化学,未来的发展主要取决于合适抗原的合成和纯化。了解皮层中已确定的神经化学单位的突触学知识将至少部分成为理解假定的新皮层递质所产生药理作用的基础。

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