Previous work from this laboratory has shown that rostral nucleus tractus solitarii (rNTS) neurons can be separated into four different classes on the basis of responses to a current injection paradigm consisting of membrane hyperpolarization immediately followed by a depolarizing pulse. These classes have been termed Group I, II, III, and IV neurons. The regular repetitive firing discharge pattern of Group I cells is changed into an irregular spike train by membrane hyperpolarization. Hyperpolarization of Group II neurons delays the firing discharge induced by depolarization. Hyperpolarization had the least effect on the discharge pattern of Group III neurons. The discharge pattern of Group IV neurons consisted of a short burst of spikes. We used whole-cell recordings and pharmacological channel blockers in an in vitro brain stem slice preparation to determine the ionic basis for the repetitive firing properties of rNTS neurons. 2. Application of 4-aminopyridine (4-AP, 1 mM) decreased input resistance and increased action potential duration in all groups of neurons. However, the discharge pattern of Group I, III, and IV neurons was either unaltered or slightly modified by 4-AP. In contrast the delay in firing of Group II cells induced by hyperpolarization was strongly reduced and in some cases completely suppressed by application of 4-AP. This suggests that a 4-AP-sensitive conductance primarily underlies the firing pattern of Group II cells. 3. Voltage-clamp recordings revealed that the delay in Group II neurons is due to a transient outward potassium current that is partially inactivated around the resting membrane potential. Hyperpolarization removed this inactivation, causing a delay in the firing of the cell. The potassium current was blocked by 4-AP. A similar current was occasionally seen in neurons of the other groups. On the basis of its voltage and pharmacological dependence this current was presumed to be an A-current (IKA). 4. Blockade of calcium currents by a low-calcium (0.5 mM) saline containing 2 mM Co2+ depressed the excitability of rNTS cells. For Group II neurons the delay in firing activity was increased. In the other groups the repetitive firing pattern was suppressed. In addition the amplitude of the afterhyperpolarization occurring after a short train of action potentials was substantially reduced. This indicates that calcium currents (ICa) and calcium-activated potassium currents (IKCa) contribute to the repetitive firing properties of rNTS neurons. 5. In about half of Group I, III, and IV neurons an additional property was found.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
本实验室之前的研究表明,延髓孤束核吻侧部(rNTS)神经元可根据对一种电流注入模式的反应分为四类,该模式包括先进行膜超极化紧接着施加去极化脉冲。这些类别被称为I、II、III和IV组神经元。I组细胞的规则重复放电模式通过膜超极化转变为不规则的尖峰序列。II组神经元的超极化延迟了去极化诱导的放电。超极化对III组神经元放电模式的影响最小。IV组神经元的放电模式由短串尖峰组成。我们在体外脑干切片制备中使用全细胞膜片钳记录和药理学通道阻滞剂来确定rNTS神经元重复放电特性的离子基础。2. 应用4-氨基吡啶(4-AP,1 mM)降低了所有组神经元的输入电阻并增加了动作电位持续时间。然而,4-AP对I、III和IV组神经元的放电模式要么没有改变,要么只有轻微改变。相反,超极化诱导的II组细胞放电延迟被4-AP强烈降低,在某些情况下完全被抑制。这表明一种对4-AP敏感的电导主要是II组细胞放电模式的基础。3. 电压钳记录显示,II组神经元的延迟是由于一种瞬时外向钾电流,该电流在静息膜电位附近部分失活。超极化消除了这种失活,导致细胞放电延迟。钾电流被4-AP阻断。在其他组的神经元中偶尔也能看到类似的电流。基于其电压和药理学依赖性,该电流被推测为A电流(IKA)。4. 用含有2 mM Co2+的低钙(0.5 mM)盐溶液阻断钙电流会降低rNTS细胞的兴奋性。对于II组神经元,放电活动的延迟增加。在其他组中,重复放电模式受到抑制。此外,在短串动作电位后出现的超极化后电位的幅度大幅降低。这表明钙电流(ICa)和钙激活钾电流(IKCa)对rNTS神经元的重复放电特性有贡献。5. 在大约一半的I、III和IV组神经元中发现了另一种特性。(摘要截断于400字)