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巴氯芬对体外培养的大鼠孤束核神经元及突触传递的作用。

The actions of baclofen on neurones and synaptic transmission in the nucleus tractus solitarii of the rat in vitro.

作者信息

Brooks P A, Glaum S R, Miller R J, Spyer K M

机构信息

Department of Physiology, Royal Free Hospital School of Medicine, London.

出版信息

J Physiol. 1992 Nov;457:115-29. doi: 10.1113/jphysiol.1992.sp019367.

Abstract
  1. Intracellular and whole-cell patch recordings were made from sixty-seven neurones located in the nucleus tractus solitarii (NTS) in transverse slices of rat brainstem. 2. Baclofen at concentrations of 2-20 microM caused hyperpolarization from normal resting membrane potentials (Vm). This response was associated with a decrease in input resistance (Rm) tested by current pulses in discontinuous current clamp mode when membrane potential was restored to control level by current injection. In single electrode discontinuous voltage clamp mode, baclofen at these concentrations caused a small (< 50 pA) outward current associated with increased membrane conductance measured by voltage steps from holding potentials (Vh) of -50 or -60 mV. Current-voltage relations at these Vhs and the results of varying Vh between -50 and -110 mV during responses to baclofen gave a reversal potential of -73 mV. The amplitudes of baclofen responses were related to K+ concentration tested by comparing responses in media containing 1-24 mM extracellular K+, indicating that postsynaptically baclofen acts via a K+ conductance. 3. These effects were still apparent in the presence of tetrodotoxin (which did not abolish all spontaneous synaptic activity) and also in medium containing a combination of Co2+, the excitatory amino acid antagonist 6-cyano-7-nitro-quinoxaline-2,3-dione (CNQX) and the GABAA antagonist bicuculline which blocked synaptic activity. 4. The amplitude and frequency of spontaneous postsynaptic potentials (spPSPs) and spontaneous postsynaptic currents (spPSCs) were reduced by baclofen at concentrations (1 microM or less) which had no effect on membrane potential or holding current in current or voltage clamp recordings respectively. 5. The amplitude of evoked excitatory (evEPSPs/evEPSCs) and inhibitory (evIPSPs/evIPSCs) synaptic events elicited by electrical stimulation in the vicinity of the tractus solitarius (TS) was reduced by low concentrations of baclofen (250 nM-1 microM) which did not produce discernible postsynaptic responses. 6. In order to examine the effects of baclofen on excitatory synaptic events without contamination with inhibitory events, stimulation of the TS was carried out in the presence of bicuculline. Conversely to investigate actions on purely inhibitory synaptic responses experiments were carried out with CNQX in the bathing solution. Inhibitory synaptic responses could still be evoked, presumably by stimulation of interneurones in the vicinity of the TS. IPSPs/IPSCs were more sensitive to baclofen than EPSPs/EPSCs. 7. The effects of baclofen on membrane potential or holding current and PSP/PSCs were antagonized by 2-hydroxysaclofen (400 microM) confirming that baclofen was acting at gamma-aminobutyric acid (GABA)B receptors.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 采用细胞内和全细胞膜片钳记录技术,对大鼠脑干横切片中孤束核(NTS)的67个神经元进行记录。2. 浓度为2 - 20微摩尔的巴氯芬可使正常静息膜电位(Vm)发生超极化。当通过电流注入将膜电位恢复到对照水平时,在不连续电流钳模式下,用电流脉冲测试发现这种反应与输入电阻(Rm)降低有关。在单电极不连续电压钳模式下,这些浓度的巴氯芬会引起一个小的(<50皮安)外向电流,该电流与从 - 50或 - 60毫伏的钳制电位(Vh)进行电压阶跃测量得到的膜电导增加有关。在这些Vh下的电流 - 电压关系以及在对巴氯芬反应期间将Vh在 - 50至 - 110毫伏之间变化的结果得出反转电位为 - 73毫伏。通过比较含1 - 24毫摩尔细胞外钾离子的培养基中的反应,发现巴氯芬反应的幅度与钾离子浓度有关,这表明巴氯芬在突触后通过钾离子电导起作用。3. 在存在河豚毒素(其并未消除所有自发突触活动)的情况下以及在含有钴离子、兴奋性氨基酸拮抗剂6 - 氰基 - 7 - 硝基喹喔啉 - 2,3 - 二酮(CNQX)和GABAA拮抗剂荷包牡丹碱的培养基中(该培养基可阻断突触活动),这些效应仍然明显。4. 巴氯芬在浓度为1微摩尔或更低时,可降低自发突触后电位(spPSPs)和自发突触后电流(spPSCs)的幅度和频率,而这些浓度分别对电流钳或电压钳记录中的膜电位或钳制电流没有影响。5. 低浓度的巴氯芬(25纳摩尔 - 1微摩尔)可降低在孤束(TS)附近通过电刺激诱发的兴奋性(evEPSPs/evEPSCs)和抑制性(evIPSPs/evIPSCs)突触事件的幅度,且这些低浓度不会产生可察觉的突触后反应。6. 为了在不受抑制性事件干扰的情况下研究巴氯芬对兴奋性突触事件的影响,在荷包牡丹碱存在下对TS进行刺激。相反,为了研究对纯抑制性突触反应的作用,在浴液中加入CNQX进行实验。仍然可以诱发抑制性突触反应,推测是通过刺激TS附近的中间神经元。IPSPs/IPSCs比EPSPs/EPSCs对巴氯芬更敏感。7. 2 - 羟基巴氯芬(400微摩尔)可拮抗巴氯芬对膜电位或钳制电流以及PSP/PSCs 的作用,这证实巴氯芬作用于γ - 氨基丁酸(GABA)B受体。(摘要截取自400字)

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