Suppr超能文献

海马体兴奋性突触后电位频率增强过程中的突触后膜移位。

Postsynaptic membrane shifts during frequency potentiation of the hippocampal EPSP.

作者信息

Pitler T A, Landfield P W

机构信息

Department of Physiology and Pharmacology, Bowman Gray School of Medicine, Wake Forest University, Winston-Salem, North Carolina 27103.

出版信息

J Neurophysiol. 1987 Oct;58(4):866-82. doi: 10.1152/jn.1987.58.4.866.

Abstract
  1. In some classes of central neurons, repetitive synaptic stimulation induces substantial changes in the postsynaptic membrane, in conjunction with robust frequency potentiation of the excitatory postsynaptic potential (EPSP). However, the nature and time course of these postsynaptic membrane shifts, or their possible contributions to EPSP frequency potentiation (e.g., by altering driving force or current pathways), have not been examined extensively. We therefore studied the simultaneous patterns of change in composite EPSP amplitude, postsynaptic input resistance (Rin), and postsynaptic membrane potential during a 4-min train of 10-Hz monosynaptic stimulation in CA1 neurons of hippocampal slices. Slices were maintained in media containing either control (4 mM) or high (6.5 mM) concentrations of K+. 2. Potentiation of the EPSP, hyperpolarization of the membrane, and a decline of Rin, all developed rapidly during 10-Hz synaptic stimulation; these responses reached maximal levels by 5-15 s of the stimulation train. In most cells, a membrane depolarization phase occurred between 15 and 45 s of stimulation, followed by rehyperpolarization by 1 min of stimulation. During the depolarization phase, both EPSP potentiation and the decline in Rin remained near maximal. No significant differences were seen as a function of K+ concentrations. 3. These results show that hyperpolarization is not invariably associated temporally with EPSP frequency potentiation. Moreover, if driving force and membrane conductance changes are assumed to be approximately similar in large dendrites and soma, then the increase in driving force due to membrane hyperpolarization was not sufficient to account for the three- and fourfold increases in EPSP amplitude seen during frequency potentiation. Further, based on similar assumptions and on dendritic models of EPSP attenuation, the decline in Rin should reduce EPSP amplitude at the dendritic synaptic site and, to a proportionately greater extent, at the soma. 4. Studies in which the membrane was hyperpolarized with injected current to approximately the IPSP reversal potential, or in which bicuculline methiodide was applied to the slices, indicated that depression of the IPSP by repetitive stimulation did not account for frequency potentiation of EPSP amplitude. 5. These data are therefore consistent with the conclusion that the frequency potentiation of composite EPSPs in central neurons depends on presynaptic mechanisms, rather than on generalized postsynaptic changes. However, our findings do not rule out localized postsynaptic changes in receptors or spines as possible contributing factors.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在某些中枢神经元类别中,重复性突触刺激会在突触后膜诱导出显著变化,同时伴有兴奋性突触后电位(EPSP)的强劲频率增强。然而,这些突触后膜变化的性质和时间进程,或者它们对EPSP频率增强的可能贡献(例如,通过改变驱动力或电流通路),尚未得到广泛研究。因此,我们研究了在海马切片CA1神经元中,10赫兹单突触刺激的4分钟序列期间,复合EPSP幅度、突触后输入电阻(Rin)和突触后膜电位的同步变化模式。切片维持在含有对照(4 mM)或高浓度(6.5 mM)钾离子的培养基中。2. 在10赫兹突触刺激期间,EPSP增强、膜超极化和Rin下降均迅速发展;这些反应在刺激序列的5 - 15秒时达到最大水平。在大多数细胞中,在刺激的15至45秒之间出现膜去极化阶段,随后在刺激1分钟时再次超极化。在去极化阶段,EPSP增强和Rin下降均保持在接近最大值的水平。未观察到钾离子浓度对其有显著差异。3. 这些结果表明,超极化在时间上并非总是与EPSP频率增强相关。此外,如果假设在大树突和胞体中驱动力和膜电导变化大致相似,那么由于膜超极化导致的驱动力增加不足以解释在频率增强期间EPSP幅度增加三到四倍的现象。此外,基于相似假设和EPSP衰减的树突模型,Rin下降应会降低树突突触部位的EPSP幅度,并且在胞体处降低的程度更大。4. 用注入电流将膜超极化至近似抑制性突触后电位(IPSP)反转电位的研究,或者向切片施加荷包牡丹碱甲碘化物的研究表明,重复性刺激导致的IPSP抑制并不能解释EPSP幅度的频率增强。5. 因此,这些数据与中枢神经元中复合EPSP频率增强取决于突触前机制而非普遍的突触后变化这一结论一致。然而,我们的发现并不排除受体或棘突处局部突触后变化作为可能的促成因素。(摘要截断于400字)

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