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培养的大鼠神经元中γ-氨基丁酸A型(GABAA)受体复合物上锌的新型调节性结合位点。

A novel modulatory binding site for zinc on the GABAA receptor complex in cultured rat neurones.

作者信息

Smart T G

机构信息

School of Pharmacy, Department of Pharmacology, London.

出版信息

J Physiol. 1992 Feb;447:587-625. doi: 10.1113/jphysiol.1992.sp019020.

Abstract
  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)
摘要
  1. 运用膜片钳记录技术,在离体培养的大鼠交感神经元和小脑神经元上,研究了γ-氨基丁酸A(GABAA)受体-离子通道复合物的特性以及与过渡金属锌的相互作用。2. 锌对交感神经元上GABA诱导的膜电流的拮抗作用受发育影响。使用急性培养24 - 72小时的胚胎交感神经元,与同期培养的成年神经元相比,GABA反应受锌的抑制作用更强。对于在体内发育的神经元,出生后48.2天,锌对胚胎神经元GABA反应的抑制百分比估计下降50%。3. 与培养较短时间(体外培养10 - 20天)的神经元相比,在培养中维持较长时间(体外培养40 - 50天)的胚胎交感神经元对锌的敏感性降低。体外培养的神经元锌抑制作用的降低以每天0.55%的明显速率进行。4. 蝇蕈醇(0.2 - 2微摩尔)激活GABA受体也受到锌(50 - 100微摩尔)的拮抗。5. 降低灌注的Krebs溶液的pH值不影响锌对交感神经元GABA反应的抑制作用。6. 一些苯二氮䓬类药物、一种巴比妥酸盐、一种基于孕烷醇酮的类固醇或拮抗剂荷包牡丹碱和印防己毒素对GABAA受体的调节,不干扰锌对交感神经元的拮抗作用。提出了锌在GABAA受体上的一个新结合位点。7. 对交感神经元上GABA激活电流噪声的分析揭示,功率谱有两个动力学成分,需要双洛伦兹拟合。描述快速成分的时间常数(τ2,2.1毫秒)不受锌的影响,而慢速成分时间常数(τ1,21.7毫秒)略有降低至17.1毫秒。8. 从功率谱(γs = 22.7皮安)以及平均GABA诱导的内向电流与电流方差之间的关系(γv = 24皮安)确定了GABA激活离子通道的表观单通道电导。锌(25 - 100微摩尔)不影响单通道电导。9. 从大的小脑神经元胞体获取的外向膜片上记录到了单个GABA激活的离子通道。单个GABA通道能够激活到多个电流幅度,这些幅度被评估为以下电导水平:8、18、23、29和34皮安。(摘要截短于400字)

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