首页> 美国卫生研究院文献>The Journal of Physiology >A novel modulatory binding site for zinc on the GABAA receptor complex in cultured rat neurones.
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A novel modulatory binding site for zinc on the GABAA receptor complex in cultured rat neurones.

机译:培养的大鼠神经元中GABAA受体复合物上锌的新型调节结合位点。

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摘要

1. The properties of gamma-aminobutyric acidA (GABAA) receptor-ion channel complexes and the interaction with the transition metal zinc, were studied on rat sympathetic and cerebellar neurones in dissociated culture using patch clamp recording techniques. 2. The antagonism of GABA-induced membrane currents by zinc on sympathetic neurones was subject to developmental influence. Using embryonic sympathetic neurones acutely cultured for 24-72 h, GABA responses were more depressed by zinc when compared to responses evoked on adult neurones cultured for the same period. For neurones developing in vivo, the percentage inhibition of GABA responses produced by zinc in embryonic neurones was estimated to decline by 50% after 48.2 days following birth. 3. Embryonic sympathetic neurones maintained in culture for prolonged periods (40-50 days in vitro, DIV) became less sensitive to zinc when compared to neurones cultured for shorter periods (10-20 DIV). The decrease in the zinc inhibition for neurones maintained in vitro proceeded at an apparent rate of 0.55% per day. 4. Activation of the GABA receptor by muscimol (0.2-2 microM) was also antagonized by zinc (50-100 microM). 5. Lowering the pH of the perfusing Krebs solution did not affect the inhibition of GABA responses by zinc on sympathetic neurones. 6. Modulation of the GABAA receptor by some benzodiazepines, a barbiturate, a steroid based on pregnanolone, or antagonists bicuculline and picrotoxinin, did not interfere with the antagonism exerted by zinc on sympathetic neurones. A novel binding site for zinc on the GABAA receptor is proposed. 7. Analysis of the GABA-activated current noise on sympathetic neurones revealed two kinetic components to the power spectra requiring a double Lorentzian fit. The time constant describing the fast component (tau 2, 2.1 ms) was unaffected by zinc, whereas the slow component time constant (tau 1, 21.7 ms) was slightly reduced to 17.1 ms. 8. The apparent single-channel conductance for GABA-activated ion channels was determined from the power spectra (gamma s = 22.7 pS) and also from the relationship between the mean GABA-induced inward current and the variance of the current (gamma v = 24 pS). Zinc (25-100 microM) did not affect the single-channel conductance. 9. Single GABA-activated ion channels were recorded from outside-out patches taken from the soma of large cerebellar neurones. Single GABA channels were capable of activation to multiple current amplitudes which were assessed into the following conductance levels: 8, 18, 23, 29 and 34 pS.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.使用膜片钳记录技术研究了分离培养的大鼠交感神经和小脑神经元的γ-氨基丁酸A(GABAA)受体离子通道复合物的性质以及与过渡金属锌的相互作用。 2.锌对交感神经元的GABA诱导的膜电流的拮抗作用受到发育的影响。与急性培养的成年神经元诱发的反应相比,使用急性培养24-72小时的胚胎交感神经元,锌对GABA反应的抑制作用更大。对于体内发育的神经元,据估计,锌在胚胎神经元中产生的GABA反应抑制百分比在出生后48.2天后下降了50%。 3.与培养时间较短(10-20 DIV)的神经元相比,长期培养(40-50天体外培养,DIV)的胚胎交感神经元对锌的敏感性降低。体外维持的神经元对锌的抑制作用的降低以每天0.55%的表观速率进行。 4. muscimol(0.2-2 microM)对GABA受体的激活也被锌(50-100 microM)拮抗。 5.降低灌注的Krebs溶液的pH值不会影响锌对交感神经元对GABA反应的抑制作用。 6.一些苯二氮卓类,巴比妥类,一种基于孕烯醇酮的类固醇或拮抗剂双小分子和苦瓜毒素对GABAA受体的调节不会干扰锌对交感神经元的拮抗作用。提出了锌在GABA A受体上的新结合位点。 7.对交感神经元上GABA激活的电流噪声的分析表明,功率谱有两个动力学分量,需要双重洛伦兹拟合。锌不会影响描述快速组分的时间常数(τ2,2.1 ms),而缓慢组分的时间常数(τ1,21.7 ms)略微降低到17.1 ms。 8. GABA活化离子通道的表观单通道电导率是根据功率谱(γs = 22.7 pS)以及平均GABA诱导的内向电流与电流方差之间的关系确定的(γv = 24 ps)。锌(25-100 microM)不会影响单通道电导。 9.单个GABA激活的离子通道是从大脑小脑神经元的体表中向外记录的。单个GABA通道能够激活多个电流幅度,这些电流幅度经评估为以下电导级别:8、18、23、29和34 pS。(截短为400字的抽象)

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