Avoli M, Köhling R, Barbarosie M
Montreal Neurological Institute, McGill University, Quebec, Canada.
Neuroscience. 1996 Dec;75(4):999-1002. doi: 10.1016/0306-4522(96)00429-0.
Field potential and (K+)o recordings were made in rat hippocampal slices during application of 4-aminopyridine (50 microM) and ionotropic excitatory amino acid receptor antagonists, to establish whether anoxia modified the mechanisms that regulate GABA release from inhibitory interneurons. Synchronous, negative-going field potentials (amplitude = 1.41 +/- 0.64 mV, mean +/- S.D.; interval = 40.9 +/- 15.7 s; n = 10) occurred spontaneously in the CA3 stratum radiatum under control conditions. These events were associated with transient elevations in (K+)o (peak values = 5.3 +/- 0.7 mM; duration = 23.4 +/- 3.5 s; n = 5 slices) and were abolished by the GABAA, receptor antagonist bicuculline methiodide (10 microM; n = 5), the GABAB receptor agonist baclofen (100 microM; n = 6) or the mu-opioid receptor agonist (D-Ala2-N-Me-Phe, Gly-ol)enkephalin (10 microM; n = 4). Hence they represented monosynaptic field inhibitory postsynaptic potentials. Brief (4-5 min) episodes of anoxia induced a reversible, slow elevation of the baseline (K+)o to 5.2 +/- 0.3 mM (n = 5), while the rate of the field inhibitory postsynaptic potentials increased by an average of 130.7% (n = 10). Oxygen interruption during application of either baclofen (n = 6) or (D-Ala2-N-Me-Phe,Gly-ol)enkephalin (n = 4) blocked the depressant action of both drugs on the field inhibitory postsynaptic potential. These findings demonstrate that hippocampal monosynaptic field inhibitory postsynaptic potentials are resistant to brief anoxic episodes and that oxygen deprivation readily blocks the presynaptic control of GABA release exerted by GABAB and mu-opioid receptors at inhibitory interneuron terminals.
在应用4-氨基吡啶(50微摩尔)和离子型兴奋性氨基酸受体拮抗剂期间,对大鼠海马切片进行场电位和细胞外钾离子([K⁺]o)记录,以确定缺氧是否改变了调节抑制性中间神经元释放γ-氨基丁酸(GABA)的机制。在对照条件下,CA3辐射层中自发出现同步的负向场电位(幅度 = 1.41 ± 0.64毫伏,平均值 ± 标准差;间隔 = 40.9 ± 15.7秒;n = 10)。这些事件与细胞外钾离子的短暂升高有关(峰值 = 5.3 ± 0.7毫摩尔;持续时间 = 23.4 ± 3.5秒;n = 5个切片),并且被GABAA受体拮抗剂甲磺酸荷包牡丹碱(10微摩尔;n = 5)、GABAB受体激动剂巴氯芬(100微摩尔;n = 6)或μ-阿片受体激动剂(D-丙氨酸²-N-甲基苯丙氨酸,甘氨醇)脑啡肽(10微摩尔;n = 4)消除。因此,它们代表单突触场抑制性突触后电位。短暂(4 - 5分钟)的缺氧发作导致基线细胞外钾离子可逆性缓慢升高至5.2 ± 0.3毫摩尔(n = 5),而场抑制性突触后电位的频率平均增加130.7%(n = 10)。在应用巴氯芬(n = 6)或(D-丙氨酸²-N-甲基苯丙氨酸,甘氨醇)脑啡肽(n = 4)期间中断氧气供应,会阻断两种药物对场抑制性突触后电位的抑制作用。这些发现表明,海马单突触场抑制性突触后电位对短暂缺氧发作具有抗性,并且缺氧容易阻断GABAB和μ-阿片受体在抑制性中间神经元终末对GABA释放的突触前控制。