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由于受体-递质相互作用的随机特性导致的内在量子变异性。

Intrinsic quantal variability due to stochastic properties of receptor-transmitter interactions.

作者信息

Faber D S, Young W S, Legendre P, Korn H

机构信息

Neurobiology Laboratory, State University of New York, Buffalo 14214.

出版信息

Science. 1992 Nov 27;258(5087):1494-8. doi: 10.1126/science.1279813.

Abstract

Synaptic events at the neuromuscular junction are integer multiples of a quantum, the postsynaptic response to transmitter released from one presynaptic vesicle. At central synapses where quanta are small, it has been suggested they are invariant due to occupation of all postsynaptic receptors, a concept neglecting inherent fluctuations in channel behavior. If this did occur, the quantal release model would not apply there and could not be used to localize sites of synaptic modification. Monte Carlo simulations of quanta include transmitter diffusion and interactions with postsynaptic receptors that are treated probabilistically. These models suggest that when there are few postsynaptic channels available at a synapse, their stochastic behavior produces significant intrinsic variance in response amplitude and kinetics, and saturation does not occur. These results were confirmed by analysis of inhibitory quanta in embryonic and adult Mauthner cells involving a small and large number of channels, respectively. The findings apply to excitatory synapses as well.

摘要

神经肌肉接头处的突触事件是量子的整数倍,量子是对从一个突触前囊泡释放的递质的突触后反应。在量子较小的中枢突触中,有人认为由于所有突触后受体都被占据,量子是不变的,这一概念忽略了通道行为中固有的波动。如果这种情况确实发生,量子释放模型将不适用于那里,也不能用于定位突触修饰位点。量子的蒙特卡罗模拟包括递质扩散以及与突触后受体的概率性相互作用。这些模型表明,当突触处可用的突触后通道很少时,它们的随机行为会在反应幅度和动力学上产生显著的内在变化,并且不会发生饱和。通过分别分析涉及少量和大量通道的胚胎和成年莫纳细胞中的抑制性量子,证实了这些结果。这些发现也适用于兴奋性突触。

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