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体外培养的豚鼠三叉神经运动神经元中N-甲基-D-天冬氨酸诱导的爆发性放电

NMDA-induced burst discharge in guinea pig trigeminal motoneurons in vitro.

作者信息

Kim Y I, Chandler S H

机构信息

Department of Physiological Science, University of California at Los Angeles 90024, USA.

出版信息

J Neurophysiol. 1995 Jul;74(1):334-46. doi: 10.1152/jn.1995.74.1.334.

Abstract
  1. The responses of guinea pig trigeminal motoneurons (TMNs) to N-methyl-D,L-aspartate (NMA) were studied using brain stem slice preparations and whole cell patch-clamp (n = 89) or conventional microelectrode (n = 22) recording techniques. The primary goals of this study were to determine whether N-methyl-D-aspartate (NMDA) receptor activation would produce spontaneous bursting activity in TMNs and, if so, the underlying mechanisms responsible for the generation of these bursts. 2. Bath-applied NMA (100-300 microM, n = 80) in standard perfusion medium elicited depolarization, increase in apparent input resistance (Rinp), and rhythmic burst discharges (1-90 s in duration) from TMNs. These effects were blocked by the NMDA receptor antagonist DL-2-amino-5-phosphonopentanoic acid (AP5, 30 microM, n = 6), but not by the non-NMDA receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX, 5-10 microM, n = 10). Furthermore, the burst-inducing effect of NMA was not mimicked by the non-NMDA receptor agonists kainate (KA, 5-10 microM, n = 6) and (+/-)-alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA, 5-10 microM, n = 5). 3. In tetrodotoxin (TTX) treatment conditions (n = 13), NMA elicited depolarization, an increase in apparent Rinp, and rhythmic membrane potential oscillations without action potential bursts (i.e., plateau potentials), suggesting that the effects of NMA observed in the TTX-free condition resulted from activation of postsynaptic NMDA receptors. 4. Graded depolarization of neurons (n = 20) by intracellular direct current injection generally led to a graded increase in frequency and duration of the NMA-induced bursts and plateau potentials until these rhythmic events eventually became transformed into continuous spike discharge and maintained depolarization, respectively. Removal of Mg2+ from the perfusion medium (n = 11) also turned the bursts and plateau potentials into continuous spike discharge and maintained depolarization, respectively. 5. The effects of NMA on the current-voltage (I-V) curve after a depolarizing ramp voltage-clamp command (15-20 mV/s) were examined (n = 40). Under NMA (100-300 microM) conditions, the I-V relationship exhibited a region of negative slope conductance (NSC) between -60 and -35 mV, thus making the I-V relationship N-shaped. The NSC was abolished by AP5 (30 microM, n = 8), but not by CNQX (5-10 microM, n = 6). The I-V relationship in AMPA (3-10 microM, n = 5) or KA (3-10 microM, n = 5) was almost linear between -80 and -30 mV.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 采用脑干切片标本和全细胞膜片钳(n = 89)或传统微电极(n = 22)记录技术,研究豚鼠三叉神经运动神经元(TMNs)对N-甲基-D,L-天冬氨酸(NMA)的反应。本研究的主要目的是确定N-甲基-D-天冬氨酸(NMDA)受体激活是否会在TMNs中产生自发性爆发活动,如果是,负责产生这些爆发的潜在机制。2. 在标准灌流液中浴加NMA(100 - 300 μM,n = 80)可引起TMNs去极化、表观输入电阻(Rinp)增加以及节律性爆发放电(持续时间1 - 90秒)。这些效应被NMDA受体拮抗剂DL-2-氨基-5-膦酰基戊酸(AP5,30 μM,n = 6)阻断,但未被非NMDA受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX,5 - 10 μM,n = 10)阻断。此外,非NMDA受体激动剂海人藻酸(KA,5 - 10 μM,n = 6)和(±)-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸(AMPA,5 - 10 μM,n = 5)不能模拟NMA的爆发诱导效应。3. 在河豚毒素(TTX)处理条件下(n = 13),NMA引起去极化、表观Rinp增加以及无动作电位爆发的节律性膜电位振荡(即平台电位),表明在无TTX条件下观察到的NMA效应是由突触后NMDA受体激活引起的。4. 通过细胞内直流注入对神经元(n = 20)进行分级去极化通常会导致NMA诱导的爆发和平台电位的频率和持续时间分级增加,直到这些节律性事件最终分别转变为连续的动作电位发放和持续去极化。从灌流液中去除Mg2+(n = 11)也分别将爆发和平台电位转变为连续的动作电位发放和持续去极化。5. 在去极化斜坡电压钳制指令(15 - 20 mV/s)后,研究了NMA对电流-电压(I-V)曲线的影响(n = 40)。在NMA(100 - 300 μM)条件下,I-V关系在-60至-35 mV之间呈现负斜率电导(NSC)区域,从而使I-V关系呈N形。NSC被AP5(30 μM,n = 8)消除,但未被CNQX(5 - 10 μM,n = 6)消除。在AMPA(3 - 10 μM,n = 5)或KA(3 - 10 μM,n = 5)条件下,I-V关系在-80至-30 mV之间几乎呈线性。(摘要截断于400字)

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