Ovsepian Saak V
Department of Pharmacology and Therapeutics, Trinity College Dublin, Dublin 2, Ireland.
Neurosci Res. 2008 May;61(1):92-8. doi: 10.1016/j.neures.2008.01.015. Epub 2008 Feb 6.
Recent studies have highlighted a variety of cognitive effects caused by cholinolytic drug injections into different cortical structures. These findings were largely interpreted as evidence for location-specific cholinergic modulation of synaptic encoding mechanisms. Here, using evoked field responses in anaesthetized rat dorsal hippocampus we show that in addition to reinforcement of synaptic connections (long-term potentiation, LTP), endogenous acetylcholine also regulates firing gain of CA1 pyramidal neurons (EPSP-spike potentiation). Gain augmentation upon increase in cholinergic drive involves evoked synchronous firing at both apical and basal afferent projections, unlike enhancement of activity-induced LTP constrained to the basal afferent system. These data indicate that acetylcholine can act as an effective input and gain controller in the hippocampus. Modulation of synaptic plasticity would determine the relative dominance of afferent inputs while the facilitation of synchronous firing is likely to promote a more generalized spread of excitation and long range communication within the limbic cortex.
最近的研究强调了向不同皮质结构注射抗胆碱能药物所引起的多种认知效应。这些发现大多被解释为突触编码机制存在位置特异性胆碱能调节的证据。在此,我们利用麻醉大鼠背侧海马体中的诱发场反应表明,除了强化突触连接(长时程增强,LTP)外,内源性乙酰胆碱还调节CA1锥体神经元的放电增益(EPSP-峰电位增强)。胆碱能驱动增加时增益增强涉及顶叶和基底传入投射的诱发同步放电,这与局限于基底传入系统的活动诱导LTP增强不同。这些数据表明乙酰胆碱可作为海马体中有效的输入和增益控制器。突触可塑性的调节将决定传入输入的相对优势,而同步放电的促进可能会促进边缘皮质内更广泛的兴奋传播和长距离通信。