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联合增强/抑制的突触关联:海马体的超微结构研究

Synaptic correlates of associative potentiation/depression: an ultrastructural study in the hippocampus.

作者信息

Desmond N L, Levy W B

出版信息

Brain Res. 1983 Apr 11;265(1):21-30. doi: 10.1016/0006-8993(83)91329-x.

DOI:10.1016/0006-8993(83)91329-x
PMID:6850319
Abstract

Brief high-frequency trains delivered to the monosynaptic entorhinal cortical input to the dentate gyrus result in both increases and decreases of synaptic strength as a function of whether a particular afferent is active during conditioning (associative potentiation/depression). The present report concerns the effect of such brief, high-frequency conditioning trains upon the asymmetric synapses of the rat dentate gyrus molecular layer. Only those animals whose responses increased at least 50% following conditioning stimulation were included in the study. Additional animals were used for one-dimensional current source density analyses to localize the activated synaptic region. Double blind scoring procedures were used to classify and quantify electron micrographic data. Asymmetric synapses were scored as a function of their position in the molecular layer, spine head size and shape, and postsynaptic density length. All data were treated as inherently matched comparisons between the conditioned and control sides of each animal. The number of large, concave spine synapses with large postsynaptic densities significantly increases in the central zone of synaptic activation. Bordering this zone are regions with increases in synaptic number following conditioning, primarily due to an increased number of small spine synapses. The increased number of large, concave spine synapses in the central zone is postulated to mediate associative potentiation. The many small spine heads just adjacent to the zone of strongest synaptic activation may reflect synaptic depression evoked at synapses inactive during conditioning.

摘要

向齿状回的单突触内嗅皮质输入传递短暂的高频串刺激,会导致突触强度增加或降低,这取决于特定传入神经在条件刺激期间是否活跃(联合增强/抑制)。本报告关注此类短暂的高频条件刺激串对大鼠齿状回分子层不对称突触的影响。只有那些在条件刺激后反应至少增加50%的动物才被纳入研究。另外使用动物进行一维电流源密度分析,以定位激活的突触区域。采用双盲评分程序对电子显微镜数据进行分类和量化。不对称突触根据其在分子层中的位置、棘突头部大小和形状以及突触后致密长度进行评分。所有数据都被视为每只动物条件刺激侧和对照侧之间本质上匹配的比较。在突触激活的中心区域,具有大突触后致密的大的、凹陷棘突突触的数量显著增加。在这个区域的边界是条件刺激后突触数量增加的区域,主要是由于小棘突突触数量的增加。推测中心区域大的、凹陷棘突突触数量的增加介导联合增强。紧邻最强突触激活区域的许多小棘突头部可能反映了在条件刺激期间不活跃的突触处诱发的突触抑制。

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