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急性分离的齿状回颗粒神经元中钙电流的多个成分

Multiple components of calcium current in acutely dissociated dentate gyrus granule neurons.

作者信息

Eliot L S, Johnston D

机构信息

Division of Neuroscience, Baylor College of Medicine, Houston, Texas 77030.

出版信息

J Neurophysiol. 1994 Aug;72(2):762-77. doi: 10.1152/jn.1994.72.2.762.

Abstract
  1. Specific Ca2+ channel blocker were used to isolate and characterize different components of whole cell Ba2+ current in granule neurons acutely dissociated from guinea pig hippocampal slices. 2. Granule cell Ba2+ current peaked around +5 mV, whether elicited by step or ramp commands, and was completely blocked by 100 microM Cd2+. 3. Saturating doses (> or = 5 microM) of the dihydropyridine antagonist, nimodipine, blocked 39% of the total current, and the inhibition was partially reversible. Nimodipine had a greater effect on current at the end of a depolarizing step, suggesting some voltage dependence of its action. 4. Saturating doses (> or = 3 microM) of omega-conotoxin-GVIA irreversibly blocked 21% of the total current and did not occlude subsequent nimodipine inhibition. 5. High concentrations (> or = 100 nM) of omega-agatoxin-IVA irreversibly blocked another 20% of the total current. The effect of omega-Aga-IVA was quite slow, but saturated after several minutes at 200 nM concentration. A high dose (1 microM) produced rapid effects that were used to quantify the magnitude of block. 6. When applied together, all three blockers inhibited nearly the same amount of total current (77%) as would be expected from the sum of each blocker applied individually (80%), suggesting that the three antagonists blocked different channel types. 7. Quantitatively similar results were obtained for the effect of each blocker alone and in combination on currents elicited by depolarizing ramp commands. Ramp currents blocked by each antagonist (difference ramps) all peaked near the same potential as the initial control ramp, indicating very similar activation properties for the three current components. Difference currents elicited by step commands similarly showed little difference among the three components in their kinetics of inactivation during relatively brief (30 ms) depolarizations. With longer steps, however, the omega-CgTX-GVIA-sensitive component showed some inactivation, whereas the omega-Aga-IVA-sensitive current did not inactivate. 8. The component of current resistant to all three blockers (approximately 23% of total current) was not inhibited by omega-conotoxin-MVIIC, but was half blocked by 50 microM Ni2+. This Ni(2+)-sensitive component showed relatively rapid inactivation and peaked at a somewhat lower potential (-10 mV) than the control current. The resistant current was also inactivated by approximately 50% by holding at -60 compared with -80 mV.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 运用特异性钙离子通道阻滞剂,对从豚鼠海马切片中急性分离出的颗粒神经元全细胞钡离子电流的不同成分进行分离和特性鉴定。2. 无论通过阶跃指令还是斜坡指令引发,颗粒细胞钡离子电流在约+5 mV时达到峰值,并被100微摩尔/升的镉离子完全阻断。3. 饱和剂量(≥5微摩尔)的二氢吡啶拮抗剂尼莫地平可阻断39%的总电流,且这种抑制作用部分可逆。尼莫地平对去极化阶跃末期的电流影响更大,表明其作用存在一定电压依赖性。4. 饱和剂量(≥3微摩尔)的ω-芋螺毒素-GVIA不可逆地阻断21%的总电流,且不影响随后尼莫地平的抑制作用。5. 高浓度(≥100纳摩尔)的ω-阿加毒素-IVA不可逆地阻断另外20%的总电流。ω-阿加毒素-IVA的作用相当缓慢,但在200纳摩尔浓度下几分钟后达到饱和。高剂量(1微摩尔)产生快速作用,用于量化阻断程度。6. 当三种阻滞剂共同应用时,它们抑制的总电流量(77%)与单独应用每种阻滞剂预期的总和(80%)相近,表明这三种拮抗剂阻断的是不同的通道类型。7. 对于每种阻滞剂单独及联合应用对去极化斜坡指令引发的电流的影响,获得了定量相似的结果。每种拮抗剂阻断的电流(差异电流)在峰值电位附近均与初始对照斜坡电流相近,表明三种电流成分的激活特性非常相似。阶跃指令引发的差异电流在相对短暂(30毫秒)的去极化过程中,三种成分的失活动力学也显示出很小的差异。然而,在较长阶跃时,ω-芋螺毒素-GVIA敏感成分表现出一定失活,而ω-阿加毒素-IVA敏感电流则未失活。8. 对所有三种阻滞剂均有抗性的电流成分(约占总电流的23%)不受ω-芋螺毒素-MVIIC抑制,但被50微摩尔/升的镍离子阻断一半。这种镍离子敏感成分表现出相对快速的失活,且峰值电位(-10 mV)略低于对照电流。与-80 mV相比,在-60 mV钳制时,抗性电流也失活约50%。(摘要截选至400字)

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