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雄蜂光感受器中钠通道对小信号放大所涉及的膜电导。

Membrane conductances involved in amplification of small signals by sodium channels in photoreceptors of drone honey bee.

作者信息

Vallet A M, Coles J A, Eilbeck J C, Scott A C

机构信息

INSERM U176, Bordeaux, France.

出版信息

J Physiol. 1992 Oct;456:303-24. doi: 10.1113/jphysiol.1992.sp019338.

Abstract
  1. Voltage signals of about 1 mV evoked in photoreceptors of the drone honey bee by shallow modulation of a background illumination of an intensity useful for behaviour are thought to be amplified by voltage-dependent Na+ channels. To elucidate the roles of the various membrane conductances in this amplification we have studied the effects of the Na+ channel blocker tetrodotoxin (TTX) and various putative K+ channel blockers on the membrane potential, Vm. 2. Superfusion of a slice of retina with 0.5-10 mM-4-aminopyridine (4-AP) depolarized the membrane and, in fifty of sixty-three cells induced repetitive action potentials. Ionophoretic injection of tetraethylammonium produced similar effects. 3. In order to measure the depolarization caused by 4-AP, action potentials were prevented by application of TTX: 4-AP was applied when the membrane was depolarized to different levels by light. 4-AP induced an additional depolarization at all membrane potentials tested (-64 to -27 mV). We conclude that there are 4-AP-sensitive K+ channels that are open at constant voltage over this range. 4. 4-AP slowed down the recovery phase of the action potential induced by a light flash by a factor that ranged from 0.51 to 0.16. This reduction could be accounted for by the reduction in a voltage-independent K+ conductance estimated from the steady-state depolarization. 5. After the voltage-gated Na+ channels had been blocked by TTX, exposure to 4-AP further changed the amplitude of the response to a small (approximately 10%) decremental light stimulus. The change was an increase when the background illumination brought Vm to potentials more negative than about -40 mV; it was a decrease when Vm > -40 mV. The data could be fitted by a circuit representation of the membrane with a light-activated conductance and a K+ conductance (EK = -66 mV) that was partly blocked by 4-AP. The voltage range studied was from -52 to -27 mV; neither conductance in the model was voltage dependent. 6. The responses to small changes in light intensity in the absence of TTX were mimicked by a model. We conclude that a voltage-dependent Na+ conductance described by the Hodgkin-Huxley equations can amplify small voltage changes in a cell membrane that is also capable of generating action potentials; the magnitude of the K+ conductance is critical for optimization of signals while avoiding membrane instability.
摘要
  1. 强度适宜于行为的背景光照进行浅调制时,在雄蜂感光细胞中诱发的约1 mV电压信号被认为是由电压依赖性Na⁺通道放大的。为了阐明各种膜电导在这种放大过程中的作用,我们研究了Na⁺通道阻滞剂河豚毒素(TTX)和各种假定的K⁺通道阻滞剂对膜电位Vm的影响。2. 用0.5 - 10 mM的4 - 氨基吡啶(4 - AP)灌流视网膜切片会使膜去极化,并且在63个细胞中的50个细胞中诱发重复动作电位。离子电泳注入四乙铵产生类似的效果。3. 为了测量由4 - AP引起的去极化,通过应用TTX来阻止动作电位:当膜被光去极化到不同水平时施加4 - AP。在所有测试的膜电位(-64至-27 mV)下,4 - AP都诱导了额外的去极化。我们得出结论,存在对4 - AP敏感的K⁺通道,它们在这个范围内的恒定电压下是开放的。4. 4 - AP使光闪诱发的动作电位的恢复阶段减慢,减慢因子范围为0.51至0.16。这种降低可以由根据稳态去极化估计的非电压依赖性K⁺电导的降低来解释。5. 在电压门控Na⁺通道被TTX阻断后,暴露于4 - AP进一步改变了对小的(约10%)递减光刺激的反应幅度。当背景光照使Vm达到比约-40 mV更负的电位时,变化是增加;当Vm > -40 mV时,变化是减少。数据可以用具有光激活电导和部分被4 - AP阻断的K⁺电导(EK = -66 mV)的膜电路模型来拟合。研究的电压范围是从-52至-27 mV;模型中的两种电导都不依赖于电压。6. 在没有TTX的情况下对小的光强度变化的反应由一个模型模拟。我们得出结论,由霍奇金 - 赫胥黎方程描述的电压依赖性Na⁺电导可以放大细胞膜中能够产生动作电位的小电压变化;K⁺电导的大小对于优化信号同时避免膜不稳定至关重要。

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