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猫脊髓三叉神经核胶状质小球中的树突轴突突触。

Dendroaxonic synapses in the substantia gelatinosa glomeruli of the spinal trigeminal nucleus of the cat.

作者信息

Gobell S

出版信息

J Comp Neurol. 1976 May 15;167(2):165-76. doi: 10.1002/cne.901670204.

Abstract

The glomeruli in the substantia gelatinosa layer of the spinal trigeminal nucleus of the cat contain three kinds of dendritic processes. One of these, the type 2 dendrite, contains large synaptic vesicles in its spine heads and in its shafts. The type 2 dendrite receivers axodendritic synapses from primary trigeminal afferent (C) axons and an occasional axodendritic synapse from small axonal (P) endings with small synaptic vesicles. The type 2 dendrites in turn form dendroaxonic synapses on the C endings. The dendroaxonic synapse and the axodendritic synapse of the C ending typically occur in reciprocal pairs. The axodendritic synapse usually lies in the depths of scalloped depressions in the surface of the C ending while the dendroaxonic synapse is found on the rim of the depression. Type 1 spines, i.e., dendritic spines receiving axodendritic synapses from the primary ending and lacking synaptic vesicles, also receive dendrodentritic synapses from type 2 dendrites. The type 2 dendrite with its large, rounded synaptic vesicles is considered to be excitatory at its dendroaxonic and dendrodendritic synapses. The type 2 dendrites course from glomerulus to glomerulus receiving their excitatory input through the axodendritic synapses of C axons. A type 2 dendrite, in response to C axon excitation would activate type 1 spines directly through their dendrodendritic synapses (C leads to 2 leads to 1) and indirectly by increasing transmitter release at the axodendritic synapses of the C axonal endings through their dendroaxonic synapses (2 leads to C leads to 1). The type 2 dendrites could serve two functions. First, they may prolong transmitter release from the axodendritic synapses of C axonal endings beyond the time of arrival of incoming potentials because of the reciprocal pairing of dendroaxonic and axodendritic synapses (C in equilibrium 2). Second, they may extend the spatial range of the excitatory output of active primary afferent axons to type 1 spines of glomeruli whose primary afferent axons may be inactive (C leads to 2 leads to 1).

摘要

猫三叉神经脊束核胶状质层中的肾小球包含三种树突状突起。其中一种,即2型树突,在其棘突头部和轴突中含有大型突触小泡。2型树突接受来自三叉神经初级传入(C)轴突的轴-树突触,偶尔也接受来自带有小型突触小泡的小轴突(P)末梢的轴-树突触。2型树突反过来在C末梢上形成树-轴突触。C末梢的树-轴突触和轴-树突触通常以相互配对的形式出现。轴-树突触通常位于C末梢表面扇贝状凹陷的深处,而树-轴突触则位于凹陷的边缘。1型棘突,即接受来自初级末梢的轴-树突触且缺乏突触小泡的树突棘,也接受来自2型树突的树-树突触。具有大型圆形突触小泡的2型树突在其树-轴突触和树-树突触处被认为是兴奋性的。2型树突从一个肾小球延伸到另一个肾小球,通过C轴突的轴-树突触接受其兴奋性输入。一个2型树突,响应C轴突的兴奋,将直接通过它们的树-树突触激活1型棘突(C导致2导致1),并通过它们的树-轴突触增加C轴突末梢的轴-树突触处的递质释放而间接激活1型棘突(2导致C导致1)。2型树突可以起到两种作用。首先,由于树-轴突触和轴-树突触的相互配对(C处于平衡2),它们可能会使C轴突末梢的轴-树突触释放递质的时间延长到传入电位到达之后。其次,它们可能会将活跃的初级传入轴突的兴奋性输出的空间范围扩展到其初级传入轴突可能不活跃的肾小球的1型棘突(C导致2导致1)。

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