首页> 美国卫生研究院文献>The Journal of Physiology >The role of bicarbonate in GABAA receptor-mediated IPSPs of rat neocortical neurones.
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The role of bicarbonate in GABAA receptor-mediated IPSPs of rat neocortical neurones.

机译:碳酸氢盐在大鼠新皮层神经元的GABAA受体介导的IPSP中的作用。

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摘要

1. The ionic mechanism underlying the fast, GABAA receptor-mediated inhibitory postsynaptic potential (IPSPA) was examined in rat neocortical neurones using intracellular recording techniques. Synaptic responses were evoked by orthodromic stimulation applied to the subcortical white matter or to the pial surface. All experiments were carried out at a constant extracellular Cl- concentration. 2. The resting membrane potential was -76.2 +/- 1.0 mV (mean +/- S.E.M., n = 32) and in most cells IPSPA was depolarizing. The reversal potential of IPSPA (EIPSP-A) was -70.2 +/- 0.9 mV (n = 32) and that of a more slowly developing hyperpolarizing response (IPSPB) was -91.4 +/- 1.3 mV (n = 28). 3. An examination of the temporal relationships between excitatory postsynaptic potentials (EPSPs) and IPSPAs in different cells suggested that, despite partial overlap of these responses, EPSPs had little influence on the measured values of EIPSP-A. 4. Application of 20 mM trimethylamine (TriMA), a membrane-permeant weak base which is expected to produce a rise in pHi (and hence in intracellular HCO3-), induced a reversible positive shift in EIPSP-A of up to +9.0 mV (mean + 4.2 mV) at an extracellular pH (pHo) of 7.4. In some experiments, the shift in reversal potential was associated with a change in the polarity of IPSPA from hyperpolarizing to depolarizing. 5. Application of 20 mM lactate (a membrane-permeant weak acid which is expected to produce a fall in pHi and hence in intracellular HCO3-) at pHo 7.0 produced a hyperpolarizing shift in EIPS-A of up to -7.5 mV (mean -5.6 mV). In some experiments, exposure to lactate changed the polarity of IPSPA from depolarizing to hyperpolarizing. 6. Changes in pHo from 7.4 to 7.0 reduced the effect of TriMA and augmented that of lactate on EIPSP-A, as could be expected on the basis of the pHo-dependent change in the fraction of membrane permeable non-charged weak base or acid. 7. Under control conditions, a change in pHo from 7.4 to 7.0 produced a slight positive shift (< +2 mV) in EIPSP-A. In the presence of TriMA, a similar change in pHo gave rise to a negative shift (-1.8 to -2.7 mV). 8. The results obtained indicate that HCO3- ions contribute significantly to the IPSPA, thereby making EIPSP-A more positive than the Cl- equilibrium potential.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.使用细胞内记录技术在大鼠新皮层神经元中研究了快速的GABAA受体介导的抑制性突触后电位(IPSPA)的离子机制。施加于皮层下白质或脑膜表面的正畸刺激引起了突触反应。所有实验均在恒定的细胞外Cl-浓度下进行。 2.静息膜电位为-76.2 +/- 1.0 mV(平均+/- S.E.M.,n = 32),在大多数细胞中IPSPA消极化。 IPSPA(EIPSP-A)的反向电势为-70.2 +/- 0.9 mV(n = 32),发展较慢的超极化响应(IPSPB)的反向电势为-91.4 +/- 1.3 mV(n = 28)。 3.对不同细胞中兴奋性突触后电位(EPSPs)和IPSPAs之间的时间关系的研究表明,尽管这些反应部分重叠,但EPSPs对EIPSP-A的测量值几乎没有影响。 4.应用20 mM三甲胺(TriMA),一种膜渗透性弱碱,预期会导致pHi升高(因此会导致细胞内HCO3-升高),导致EIPSP-A的可逆正向移位高达+9.0 mV。 (平均+ 4.2毫伏)在7.4的细胞外pH(pHo)下。在某些实验中,反转电位的变化与IPSPA极性从超极化到去极化的变化有关。 5.在pHo 7.0时应用20 mM乳酸(一种可透过膜的弱酸,预期会导致pHi下降,从而导致细胞内HCO3-下降),在EIPS-A中产生的超极化位移高达-7.5 mV(均值- 5.6毫伏)。在某些实验中,暴露于乳酸会改变IPSPA的极性,从去极化变为超极化。 6. pHo从7.4更改为7.0降低了TriMA对EIPSP-A的作用,并增强了乳酸盐对EIPSP-A的作用,这是基于pHo依赖的膜渗透性不带电弱碱或酸部分的变化所预期的。 7.在对照条件下,pH值从7.4更改为7.0在EIPSP-A中产生了轻微的正移(<+2 mV)。在存在TriMA的情况下,pHo的类似变化会导致负移(-1.8至-2.7 mV)。 8.获得的结果表明,HCO3-离子对IPSPA的贡献很大,从而使EIPSP-A比Cl-平衡电位更强。(摘要截短了400字)

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