Division of Neurology, Department of Internal Medicine, Faculty of Medicine, University of Manitoba Winnipeg, MB, Canada.
Front Hum Neurosci. 2013 May 1;7:170. doi: 10.3389/fnhum.2013.00170. eCollection 2013.
Limitations of known anatomical circuit rules necessitate the identification of supplementary rules. This is essential for explaining how associative sensory stimuli induce nervous system changes that generate internal sensations of memory, concurrent with triggering specific motor activities in response to specific cue stimuli. A candidate mechanism is rapidly reversible, yet stabilizable membrane hemi-fusion formed between the closely apposed postsynaptic membranes of different neurons at locations of convergence of sensory inputs during associative learning. The lateral entry of activity from the cue stimulus-activated postsynapse re-activates the opposite postsynapse through the hemi-fused area and induces the basic units of internal sensation (namely, semblions) as a systems property. Working, short-term and long-term memories can be viewed as functions of the number of re-activatible hemi-fusions present at the time of memory retrieval. Blocking membrane hemi-fusion either by the insertion of the herpes simplex virus (HSV) glycoproteins or by the deposition of insoluble intermediates of amyloid protein in the inter-postsynaptic extracellular matrix (ECM) space leads to cognitive impairments, supporting this mechanism. The introduction of membrane fusion blockers into the postsynaptic cell cytoplasm that attenuates long-term potentiation (LTP), a correlate of behavioral motor activities in response to memory retrieval, provides further support. The lateral spread of activity through the inter-postsynaptic membrane is capable of contributing to oscillating neuronal activity at certain neuronal orders. At the resting state these oscillations provide sub-threshold activation to many neurons at higher orders, including motor neurons maintaining them at a low initiation threshold for motor activity.
已知解剖学电路规则的局限性需要确定补充规则。这对于解释联想感觉刺激如何诱导神经系统变化,从而产生记忆的内部感觉,同时针对特定的提示刺激触发特定的运动活动是至关重要的。一个候选机制是快速可逆的,但可稳定化的膜半融合,在联想学习期间感觉输入的会聚处,在不同神经元的紧密贴合的突触后膜之间形成。来自提示刺激激活的突触后膜的活性的侧向进入通过半融合区域重新激活相反的突触后膜,并诱导内部感觉的基本单元(即 semblions)作为系统属性。工作记忆、短期记忆和长期记忆可以被视为在记忆检索时存在的可重新激活半融合的数量的函数。通过插入单纯疱疹病毒(HSV)糖蛋白或在突触后细胞外基质(ECM)空间中沉淀不溶性淀粉样蛋白中间物来阻断膜半融合会导致认知障碍,支持这种机制。将膜融合抑制剂引入突触后细胞质中,会减弱长时程增强(LTP),这是对记忆检索反应的行为运动活动的相关物,这提供了进一步的支持。通过突触后膜的侧向扩散的活性能够在某些神经元阶次引起振荡神经元活动。在静止状态下,这些振荡为更高阶次的许多神经元提供亚阈值激活,包括运动神经元,使它们处于低启动阈值以维持运动活动。