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首页> 外文期刊>The Journal of Physiology >Novel action of BAPTA series chelators on intrinsic K+ currents in rat hippocampal neurones.
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Novel action of BAPTA series chelators on intrinsic K+ currents in rat hippocampal neurones.

机译:BAPTA系列螯合剂对大鼠海马神经元内在K +电流的新作用。

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1. Whole-cell recordings were made from rat CA1 neurones in brain slices. When electrodes contained diazo-2 (2 mM) or dibromo BAPTA (1 mM) a large steady-state outward current (hundreds of picoamps) developed within 5 min of breakthrough at a VH of -60 mV. BAPTA itself (1 mM) caused qualitatively similar but smaller effects. 2. The outward current was accompanied by increased conductance with a null potential close to the calculated K+ equilibrium potential (EK) of -110 mV. Development of outward current occurred concurrently with progressive loss of slow AHP tail current (IsAHP) evoked by brief depolarizations. The peak latency of IsAHP increased during the onset of chelator action. 3. The persistent outward current was reversibly inhibited by noradrenaline (10 microM) or isoprenaline (2-5 microM), and completely prevented by 8-bromoadenosine 3',5' cyclic monophosphate (8-Br cAMP; 100 microM) or QX-314 (10 mM) in recording electrodes. After development of outward current, diazo-2 photolysis caused inward current and decreased conductance. Both flash- and noradrenergic-sensitive responses were inwardly rectifying outward currents with null potentials close to EK. 4. The outward current induced by dibromo BAPTA was not blocked by internal EGTA (10 mM). However, experiments incorporating Ca2+ influx or Ca2+ loading of the buffer indicate that Ca2+ facilitated the outward current. 5. The outward currents induced by dibromo BAPTA or diazo-2 were not associated with significant changes in resting [Ca2+]i. Regions of the cell contributing to the outward current were deduced from measurements of fura-2 diffusion. These were compared with regions of [Ca2+]i elevation during IsAHP. 6. These results are consistent with the hypothesis that the BAPTA series Ca2+ buffers can activate those Ca2+-activated K+ channels that underlie the slow AHP, without the predicted elevation of bulk [Ca2+]i. Therefore these results cannot be interpreted solely in terms of Ca2+ concentration changes, although the observations illustrate a novel, investigative role for these compounds in the study of Ca2+-dependent processes.
机译:1.从大鼠CA1神经元的脑切片中进行全细胞记录。当电极包含diazo-2(2 mM)或dibromo BAPTA(1 mM)时,在-60 mV的VH穿透后5分钟内会产生大的稳态向外电流(数百皮安)。 BAPTA本身(1 mM)造成了质量上相似但较小的影响。 2.向外电流伴随电导增加,其零电位接近于计算的K +平衡电位(EK)-110 mV。外来电流的发展与短暂的去极化引起的慢速AHP尾电流(IsAHP)的逐渐丧失同时发生。在螯合剂作用开始期间,IsAHP的峰值潜伏期增加。 3.去甲肾上腺素(10 microM)或异丙肾上腺素(2-5 microM)可逆地抑制持续的外向电流,并被8-溴腺苷3',5'环状单磷酸酯(8-Br cAMP; 100 microM)或QX-完全阻止在记录电极中为314(10 mM)。在产生向外电流之后,重氮2光解会引起向内电流并降低电导。闪光和去甲肾上腺素敏感的反应都向内整流具有接近EK的零电位的向外电流。 4.由二溴BAPTA感应的向外电流未被内部EGTA(10 mM)阻挡。但是,结合Ca2 +流入或缓冲液中Ca2 +加载的实验表明,Ca2 +促进了向外的电流。 5. Dibromo BAPTA或diazo-2诱导的外向电流与静止[Ca2 +] i的显着变化无关。从呋喃2扩散的测量值推导了有助于向外电流的细胞区域。将这些与IsAHP期间[Ca2 +] i升高的区域进行比较。 6.这些结果与BAPTA系列Ca2 +缓冲液可以激活慢AHP基础上的那些Ca2 +激活的K +通道,而没有预测的[Ca2 +] i升高的假设相一致。因此,尽管观察结果表明这些化合物在研究Ca2 +依赖性过程中具有新颖的研究作用,但不能仅根据Ca2 +浓度变化来解释这些结果。

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