Neuronal nicotinic receptors in synaptic functions in humans and rats: physiological and clinical relevance

被引:82
作者
Albuquerque, EX
Pereira, EFR
Mike, A
Eisenberg, HM
Maelicke, A
Alkondon, M
机构
[1] Univ Maryland, Sch Med, Dept Pharmacol & Expt Therapeut, Baltimore, MD 21201 USA
[2] Univ Fed Rio de Janeiro, CCS, ICB, Dept Farmacol Basica & Clin, BR-21944 Rio De Janeiro, Brazil
[3] Univ Maryland, Sch Med, Dept Neurosurg, Baltimore, MD 21201 USA
[4] Univ Mainz, Sch Med, Mol Microbiol Lab, Inst Physiol Chem & Pathobiochem, D-55099 Mainz, Germany
关键词
acetylcholine; choline; GABA; hippocampus; cerebral cortex; slices; human; electrophysiology;
D O I
10.1016/S0166-4328(00)00208-4
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The present report describes the participation of nicotinic receptors (nAChRs) in controlling the excitability of local neuronal circuitries in the rat hippocampus and in the human cerebral cortex. The patch-clamp technique was used to record responses triggered by the non-selective agonist ACh and the alpha 7-nAChR-selective agonist choline in interneurons of human cerebral cortical acid rat hippocampal slices. Evidence is provided that functional alpha 7- and alpha 4 beta 2-like nAChRs are present on somatodendritic and/or preterminal/terminal regions of interneurons in the CA1 field of the rat hippocampus and in the human cerebral cortex and that activation of the different nAChR subtypes present in the preterminal/terminal areas of the interneurons triggers the tetrodotoxin-sensitive release of GABA. Modulation by nAChRs of GABAergic transmission, which can result either in inhibition or disinhibition of pyramidal neurons. depends both on the receptor subtype present in the interneurons and on the agonist acting upon these receptors. Not only do alpha 7 nAChRs desensitize faster than alpha 4 beta 2 nAChRs, but also alpha 7 nAChR desensitization induced by ACh lasts longer than that induced by choline. These mechanisms, which appear to be retained across species, might explain the involvement of nAChRs in cognitive functions and in such neurological disorders as Alzheimer's disease and schizophrenia. (C) 2000 Elsevicr Science B.V. All rights reserved.
引用
收藏
页码:131 / 141
页数:11
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