NONSYNAPTIC MODULATION OF NEURONAL-ACTIVITY IN THE BRAIN - ELECTRIC CURRENTS AND EXTRACELLULAR IONS

被引:493
作者
JEFFERYS, JGR
机构
[1] Neuronal Networks Group, St. Mary's Hospital Medical School, Imp. Coll. Sci., Technol., and Med., London
[2] Neuroscience Group, Dept. of Physiology, University of Birmingham, Edgbaston
基金
英国惠康基金;
关键词
D O I
10.1152/physrev.1995.75.4.689
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Nonsynaptic interactions between neurons have been eclipsed by our increasingly detailed understanding of chemical synapses, but they do play significant roles in the nervous system. This review considers four classes of nonsynaptic interaction, mainly in mammalian brain. 1) Electrotonic (and chemical) coupling through gap junctions has effects during development and under some, often pathological, conditions in the mature brain. 2) Ephaptic transmission is mediated by electrical coupling between specific neuronal elements in the absence of specialized contacts, notably in the cerebellum, and in axon tracts affected by demyelination, 3) Field effect interactions are mediated by large extracellular currents and potential fields generated by the hippocampus and other cortical structures. Both endogenous and applied electric fields alter neuronal excitability at field strengths over a few millivolts per millimeter. Weaker fields have more subtle effects, for instance, on axonal growth during development and repair and, more controversially, in behavioral responses to environmental fields. 4) There are fluctuations in extracellular ions such as K+, which are released during neuronal activity and which alter neuronal excitability, Field effects and ion fluctuations probably have modest effects during physiological activity but have a significant impact on epileptic seizures, and can sustain them in the absence of synaptic transmission.
引用
收藏
页码:689 / 723
页数:35
相关论文
共 198 条
  • [1] Abraham W.C., Bliss T.V.P., Goddard G.V., Heterosynaptic changes accompany long-term but not short-term potentiation of the perforant path in the anaesthetized rat, J. Physiol. Lond., 363, pp. 335-349, (1985)
  • [2] Agopyan N., Avoli M., Synaptic and non-synaptic mechanisms underlying low calcium bursts in the in vitro hippocampal slice, Exp. Brain Res., 73, pp. 533-540, (1988)
  • [3] Albrecht D., Heinemann U., Low calcium-induced epileptiform activity in hippocampal slices from infant rats, Dev. Brain Res., 48, pp. 316-320, (1989)
  • [4] Albrecht D., Rausche G., Heinemann U., Reflections of low calcium epileptiform activity from area CA1 into dentate gyrus in the rat hippocampal slice, Brain Res., 480, pp. 393-396, (1989)
  • [5] Alford S., Frenguelli B.G., Schofield J.G., Collingridge G.L., Characterization of Ca<sup>2+</sup> signals induced in hippocampal CA1 neurones by the synaptic activation of NMDA receptors, J. Physiol. Lond., 469, pp. 693-716, (1993)
  • [6] Allen P.J., Fish D.R., Smith S.J.M., Very high-frequency rhythmic activity during SEEG suppression in frontal lobe epilepsy, Electroencephalogr. Clin. Neurophysiol., 82, pp. 155-159, (1992)
  • [7] Altschuler S.M., Bao X.M., Miselis R.R., Dendritic architecture of nucleus ambiguus motoneurons projecting to the upper alimentary tract in the rat, J. Comp. Neurol., 309, pp. 402-414, (1991)
  • [8] Amir R., Devor M., Axonal cross-excitation in nerve-end neuromas: Comparison of A- and C-fibers, J. Neurophysiol., 68, pp. 1160-1166, (1992)
  • [9] Andersen P., Gjerstad L., Langmoen I.A., A cortical epilepsy model in vitro, Abnormal Neuronal Discharges, pp. 29-36, (1978)
  • [10] Anderson W.W., Lewis D.V., Swartzwelder H.S., Wilson W.A., Magnesium-free medium activates seizure-like events in the rat hippocampal slice, Brain Res., 398, pp. 215-219, (1986)