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乙酰胆碱和氨甲酰胆碱对鱿鱼神经纤维中轴突和施万细胞电位的影响。

Effects of acetylcholine and carbamylcholine on the axon and Schwann cell electrical potentials in the squid nerve fibre.

作者信息

Villegas J

出版信息

J Physiol. 1974 Nov;242(3):647-59. doi: 10.1113/jphysiol.1974.sp010728.

DOI:10.1113/jphysiol.1974.sp010728
PMID:4449050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1330656/
Abstract
  1. The effect of acetylcholine and carbamylcholine on the axon and Schwann cell membrane potential have been studied in the giant nerve fibre of the squid. The addition of carbamylcholine (10(-6)M) to the external sea-water medium has no appreciable effects on the resting and action potentials of the axon. However, it induces a long-lasting hyperpolarization in the surrounding Schwann cells of the unstimulated intact or slit nerve fibres which is completely blocked by D-tubocurarine (10(-9)M). Eserine (10(-9)M) prolongs the Schwann cell hyperpolarizations induced by a 1 min exposure of the unstimulated nerve fibres to acetylcholine (10(-7)M).2. The addition of carbamylcholine (10(-6)M) to the external medium increases the relative permeability of the Schwann cell membrane to the potassium ion in slit nerve fibres. Yet, a hundredfold reduction in external sodium concentration has no appreciable effect on the hyperpolarization of the Schwann cells of the slit nerve fibre under similar conditions.3. Tetrodotoxin at a concentration of 5 x 10(-8)M has no appreciable effects on either the Schwann cell electrical potential or on the hyperpolarizing action of carbamylcholine on the Schwann cells of the unstimulated intact nerve fibres.4. These findings indicate the presence of acetylcholine receptors in the plasma membrane of the Schwann cell in these nerve fibres and give further support to the hypothesis on the role of the cholinergic system in the genesis of the long-lasting Schwann cell hyperpolarizations caused by the conduction of nerve impulse trains by the axon.
摘要
  1. 已在鱿鱼的巨大神经纤维中研究了乙酰胆碱和氨甲酰胆碱对轴突和施万细胞膜电位的影响。向外部海水介质中添加氨甲酰胆碱(10⁻⁶M)对轴突的静息电位和动作电位没有明显影响。然而,它会在未受刺激的完整或切断神经纤维周围的施万细胞中诱导持久的超极化,这种超极化会被D - 筒箭毒碱(10⁻⁹M)完全阻断。毒扁豆碱(10⁻⁹M)会延长未受刺激的神经纤维暴露于乙酰胆碱(10⁻⁷M)1分钟所诱导的施万细胞超极化。

  2. 向外部介质中添加氨甲酰胆碱(10⁻⁶M)会增加切断神经纤维中施万细胞膜对钾离子的相对通透性。然而,在类似条件下,外部钠浓度降低一百倍对切断神经纤维的施万细胞超极化没有明显影响。

  3. 浓度为5×10⁻⁸M的河豚毒素对施万细胞电位或氨甲酰胆碱对未受刺激的完整神经纤维施万细胞的超极化作用均无明显影响。

  4. 这些发现表明这些神经纤维的施万细胞质膜中存在乙酰胆碱受体,并进一步支持了胆碱能系统在轴突传导神经冲动序列所引起的施万细胞持久超极化发生过程中作用的假说。

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Effects of acetylcholine and carbamylcholine on the axon and Schwann cell electrical potentials in the squid nerve fibre.乙酰胆碱和氨甲酰胆碱对鱿鱼神经纤维中轴突和施万细胞电位的影响。
J Physiol. 1974 Nov;242(3):647-59. doi: 10.1113/jphysiol.1974.sp010728.
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Effects of tubocurarine and eserine on the axon-Schwann cell relationship in the squid nerve fibre.筒箭毒碱和毒扁豆碱对鱿鱼神经纤维中轴突-施万细胞关系的影响。
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Effects of cholinergic compounds on the axon-Schwann cell relationship in the squid nerve fiber.胆碱能化合物对鱿鱼神经纤维中轴突-施万细胞关系的影响。
Fed Proc. 1975 Apr;34(5):1370-3.
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Characterization of acetylcholine receptors in the Schwann cell membrane of the squid nerve fibre.鱿鱼神经纤维施万细胞膜中乙酰胆碱受体的特性研究
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本文引用的文献

1
The antagonism between tubocurarine and substances which depolarize the motor end-plate.筒箭毒碱与使运动终板去极化的物质之间的拮抗作用。
J Physiol. 1960 Jul;152(2):309-24. doi: 10.1113/jphysiol.1960.sp006489.
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Schwann cell and axon electrical potential differences. Squid nerve structure and excitable membrane location.施万细胞与轴突的电位差。鱿鱼神经结构与可兴奋膜的位置。
J Gen Physiol. 1963 May;46(5):1047-64. doi: 10.1085/jgp.46.5.1047.
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Nature of the Schwann cell electrical potential. Effects of the external ionic concentrations and a cardiac glycoside.施万细胞电位的性质。外部离子浓度和一种强心苷的影响。
J Gen Physiol. 1968 Jan;51(1):47-64. doi: 10.1085/jgp.51.1.47.
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Axon-Schwann cell interaction in the squid nerve fibre.鱿鱼神经纤维中的轴突-施万细胞相互作用。
J Physiol. 1972 Sep;225(2):275-96. doi: 10.1113/jphysiol.1972.sp009940.
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Effects of tubocurarine and eserine on the axon-Schwann cell relationship in the squid nerve fibre.筒箭毒碱和毒扁豆碱对鱿鱼神经纤维中轴突-施万细胞关系的影响。
J Physiol. 1973 Jul;232(1):193-208. doi: 10.1113/jphysiol.1973.sp010264.
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Acetylcholinesterase localization in the giant nerve fiber of the squid.乙酰胆碱酯酶在鱿鱼巨大神经纤维中的定位。
J Ultrastruct Res. 1974 Jan;46(1):149-63. doi: 10.1016/s0022-5320(74)80028-6.