Shalinsky Mark H, Magistretti Jacopo, Ma Li, Alonso Angel A
Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec H3A 2B4, Canada.
J Neurophysiol. 2002 Sep;88(3):1197-211. doi: 10.1152/jn.2002.88.3.1197.
The effects of muscarinic stimulation on the membrane potential and current of in situ rat entorhinal-cortex layer-II principal neurons were analyzed using the whole cell, patch-clamp technique. In current-clamp experiments, application of carbachol (CCh) induced a slowly developing, prolonged depolarization initially accompanied by a slight decrease or no significant change in input resistance. By contrast, in a later phase of the depolarization input resistance appeared consistently increased. To elucidate the ionic bases of these effects, voltage-clamp experiments were then carried out. In recordings performed in nearly physiological ionic conditions at the holding potential of -60 mV, CCh application promoted the slow development of an inward current deflection consistently associated with a prominent increase in current noise. Similarly to voltage responses to CCh, this inward-current induction was abolished by the muscarinic antagonist, atropine. Current-voltage relationships derived by applying ramp voltage protocols during the different phases of the CCh-induced inward-current deflection revealed the early induction of an inward current that manifested a linear current/voltage relationship in the subthreshold range and the longer-lasting block of an outward K(+) current. The latter current could be blocked by 1 mM extracellular Ba(2+), which allowed us to study the CCh-induced inward current (I(CCh)) in isolation. The extrapolated reversal potential of the isolated I(CCh) was approximately 0 mV and was not modified by complete substitution of intrapipette K(+) with Cs(+). Moreover, the extrapolated I(CCh) reversal shifted to approximately -20 mV on removal of 50% extracellular Na(+). These results are consistent with I(CCh) being a nonspecific cation current. Finally, noise analysis of I(CCh) returned an estimated conductance of the underlying channels of approximately 13.5 pS. We conclude that the depolarizing effect of muscarinic stimuli on entorhinal-cortex layer-II principal neurons depends on both the block of a K(+) conductance and the activation of a "noisy" nonspecific cation current. We suggest that the membrane current fluctuations brought about by I(CCh) channel noise may facilitate the "theta" oscillatory dynamics of these neurons and enhance firing reliability and synchronization.
采用全细胞膜片钳技术分析了毒蕈碱刺激对原位大鼠内嗅皮层II层主要神经元膜电位和电流的影响。在电流钳实验中,应用卡巴胆碱(CCh)可诱导缓慢发展、持续时间较长的去极化,最初伴有输入电阻轻微降低或无显著变化。相比之下,在去极化的后期阶段,输入电阻持续增加。为了阐明这些效应的离子基础,随后进行了电压钳实验。在接近生理离子条件下于-60 mV的钳制电位进行的记录中,应用CCh促进了内向电流偏转的缓慢发展,该偏转始终伴随着电流噪声的显著增加。与对CCh的电压反应类似,这种内向电流诱导被毒蕈碱拮抗剂阿托品消除。在CCh诱导的内向电流偏转的不同阶段应用斜坡电压方案得出的电流-电压关系显示,早期诱导出的内向电流在阈下范围内表现出线性电流/电压关系,以及对外向K(+)电流的持续阻断。后一种电流可被1 mM细胞外Ba(2+)阻断,这使我们能够单独研究CCh诱导的内向电流(I(CCh))。分离出的I(CCh)的外推反转电位约为0 mV,并且在用Cs(+)完全替代微电极内的K(+)时未发生改变。此外,在去除50%细胞外Na(+)后,外推的I(CCh)反转电位移至约-20 mV。这些结果与I(CCh)是一种非特异性阳离子电流一致。最后,对I(CCh)的噪声分析得出基础通道的估计电导约为13.5 pS。我们得出结论,毒蕈碱刺激对内嗅皮层II层主要神经元的去极化作用既取决于K(+)电导的阻断,也取决于“嘈杂”的非特异性阳离子电流的激活。我们认为,由I(CCh)通道噪声引起的膜电流波动可能促进这些神经元的“theta”振荡动力学,并提高放电可靠性和同步性。