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J Physiol. 1990 Apr;423:363-80. doi: 10.1113/jphysiol.1990.sp018027.
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本文引用的文献

1
Effect of "calcium antagonist" D-600 on the postsynaptic membrane.“钙拮抗剂”D - 600对突触后膜的作用。
J Physiol (Paris). 1980 Sep;76(5):515-22.
2
Membrane-potential effects on an inhibitory post-synaptic conductance in Aplysia buccal ganglia.膜电位对海兔口腔神经节中抑制性突触后电导的影响。
J Physiol. 1980 Jul;304:165-80. doi: 10.1113/jphysiol.1980.sp013317.
3
The relationship between agonist occupation and the permeability response of the cholinergic receptor revealed by bound cobra alpha-toxin.结合的眼镜蛇α-毒素揭示的激动剂占据与胆碱能受体通透性反应之间的关系。
J Biol Chem. 1980 Nov 10;255(21):10144-56.
4
A cholinergic chloride conductance in neurones of Helix aspersa.皱襞蛞蝓神经元中的一种胆碱能氯电导。
J Physiol. 1983 Nov;344:119-35. doi: 10.1113/jphysiol.1983.sp014928.
5
The acetylcholine receptor at the neuromuscular junction.神经肌肉接头处的乙酰胆碱受体。
Physiol Rev. 1982 Oct;62(4 Pt 1):1271-340. doi: 10.1152/physrev.1982.62.4.1271.
6
Quantal release of acetylcholine examined by current fluctuation analysis at an identified neuro-neuronal synapse of Aplysia.通过电流波动分析在海兔一个已鉴定的神经-神经元突触处检测乙酰胆碱的量子释放。
Proc Natl Acad Sci U S A. 1980 Mar;77(3):1661-5. doi: 10.1073/pnas.77.3.1661.
7
The statistical nature of the acetycholine potential and its molecular components.乙酰胆碱电位及其分子成分的统计学性质。
J Physiol. 1972 Aug;224(3):665-99. doi: 10.1113/jphysiol.1972.sp009918.
8
Voltage clamp analysis of acetylcholine produced end-plate current fluctuations at frog neuromuscular junction.对乙酰胆碱在青蛙神经肌肉接头处产生的终板电流波动进行电压钳分析。
J Physiol. 1973 Dec;235(3):655-91. doi: 10.1113/jphysiol.1973.sp010410.
9
Completely isolated neurons in the mollusc, Lymnaea stagnalis. A new objective for nerve cell biology investigation.在软体动物椎实螺中完全分离的神经元。神经细胞生物学研究的一个新目标。
Comp Biochem Physiol A Comp Physiol. 1974 Sep 1;49(1A):89-100. doi: 10.1016/0300-9629(74)90544-1.
10
Acetylcholine receptor activation by a site-selective ligand: nature of brief open and closed states in BC3H-1 cells.位点选择性配体激活乙酰胆碱受体:BC3H-1细胞中短暂开放和关闭状态的性质
J Physiol. 1986 Jan;370:357-79. doi: 10.1113/jphysiol.1986.sp015939.

静水椎实螺神经元膜受体 - 通道复合物的一些功能特性。

Some characteristics of the functioning of membrane receptor-channel complexes of Limnaea stagnalis neurones.

作者信息

Panarin V A, Kondratyev V A, Rayevsky O A

机构信息

Institute of Physiologically Active Compounds, USSR Academy of Sciences, Moscow.

出版信息

J Physiol. 1990 Apr;423:363-80. doi: 10.1113/jphysiol.1990.sp018027.

DOI:10.1113/jphysiol.1990.sp018027
PMID:1696986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1189762/
Abstract
  1. Limnaea stagnalis neurones have been used to study the functioning of membrane receptor-channel complexes. The experiments were performed using a fixed membrane potential (E) and the intracellular perfusion technique. The cells employed responded to acetylcholine (ACh) by changing only their Cl- conductance. 2. ACh-induced currents, their fluctuations and relaxations resulting from a jump of E were studied. 3. The following facts have been established based on analysis of ACh currents, their fluctuations and relaxations: (1) the characteristic time of the exponential decay of the autocorrelation function, tau N, is in the range of 15-20 ms; (2) the characteristic relaxation time, tau R, equals 50-60 ms (ACh concentration = 0.25 microM, desensitization is not observed); (3) E does not exert any functionally significant effect upon tau N or tau R which could have governed the non-linearity of the membrane voltage-current characteristic; (4) variation of ACh concentration from 0.25 to 1 microM has a significant effect on tau R but not on tau N; (5) lowering of the ACh solution temperature from 22 to 8.5 degrees C results in a 20% increase of the ACh current, a 3- to 4-fold decrease of the single-channel conductance (gamma), a 20% increase in tau N and a 3- to 4-fold increase in tau R. 4. The suberylcholine (SCh)-induced membrane current has approximately the same value as the ACh-induced current at equal concentrations of ACh and SCh (0.25 microM); the tau N and gamma values were also quite close, but tau R was 2.3 times lower for SCh than for ACh. 5. An essentially two-stage scheme of functioning of membrane receptor-channel complexes is proposed. The scheme has two distinguishable and measurable stages and involves five closed states and one open state; it offers an explanation for our experimental data as well as the results of other workers.
摘要
  1. 椎实螺神经元已被用于研究膜受体 - 通道复合物的功能。实验采用固定膜电位(E)和细胞内灌注技术进行。所使用的细胞仅通过改变其氯离子电导来响应乙酰胆碱(ACh)。2. 研究了ACh诱导的电流、其波动以及由E的跃变引起的弛豫。3. 基于对ACh电流、其波动和弛豫的分析,已确定以下事实:(1)自相关函数指数衰减的特征时间tau N在15 - 20毫秒范围内;(2)特征弛豫时间tau R等于50 - 60毫秒(ACh浓度 = 0.25微摩尔,未观察到脱敏现象);(3)E对tau N或tau R没有任何功能上显著的影响,而tau N或tau R可能控制膜电压 - 电流特性的非线性;(4)ACh浓度从0.25微摩尔变化到1微摩尔对tau R有显著影响,但对tau N没有影响;(5)将ACh溶液温度从22摄氏度降低到8.5摄氏度会导致ACh电流增加20%,单通道电导(gamma)降低3至4倍,tau N增加20%,tau R增加3至4倍。4. 在ACh和琥珀酰胆碱(SCh)浓度相等(0.25微摩尔)时,琥珀酰胆碱(SCh)诱导的膜电流与ACh诱导的电流值大致相同;tau N和gamma值也相当接近,但SCh的tau R比ACh低2.3倍。5. 提出了膜受体 - 通道复合物功能的一个基本上分为两个阶段的方案。该方案有两个可区分和可测量的阶段,涉及五个关闭状态和一个开放状态;它为我们的实验数据以及其他研究者的结果提供了解释。