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灰藓毒素I引起神经膜去极化的机制。

Mechanism of nerve membrane depolarization caused by grayanotoxin I.

作者信息

Narahashi T, Seyama I

出版信息

J Physiol. 1974 Oct;242(2):471-87. doi: 10.1113/jphysiol.1974.sp010718.

Abstract
  1. The mechanism of depolarization of squid axon membranes caused by grayanotoxin I has been studied by means of internal perfusion and voltage clamp techniques.2. The depolarization induced by either internal or external application of grayanotoxin I was reversed by decreasing the external sodium concentration from 449 to 1 mm.3. No depolarization was observed when both external and internal media were devoid of sodium ions, indicating that the depolarization by grayanotoxin I in normal media is due to a specific increase in resting sodium permeability.4. The resting sodium permeability as measured by voltage clamp was increased to 1.31 x 10(-6) cm/sec by internal application of 1 x 10(-5)m grayanotoxin I, an increase by a factor of about 90.5. The apparent dissociation constant of internally applied grayanotoxin I in increasing the resting sodium permeability was estimated to be 4.12 x 10(-5)m, and the toxin interacts with the membrane receptor on a one-to-one stoichiometric basis.6. Tetrodotoxin antagonized the action of grayanotoxin I in increasing the resting sodium permeability in a non-competitive manner.
摘要
  1. 利用内部灌注和电压钳技术研究了灰毒素I引起的乌贼轴突膜去极化机制。

  2. 通过将外部钠浓度从449 mM降至1 mM,可逆转由内部或外部施加灰毒素I所诱导的去极化。

  3. 当外部和内部介质均不含钠离子时,未观察到去极化现象,这表明在正常介质中灰毒素I引起的去极化是由于静息钠通透性的特异性增加。

  4. 通过电压钳测量,内部施加1×10⁻⁵ M灰毒素I可使静息钠通透性增加至1.31×10⁻⁶ cm/秒,增加了约90倍。

  5. 内部施加的灰毒素I在增加静息钠通透性方面的表观解离常数估计为4.12×10⁻⁵ M,且毒素与膜受体以一对一的化学计量关系相互作用。

  6. 河豚毒素以非竞争性方式拮抗灰毒素I增加静息钠通透性的作用。

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本文引用的文献

1
POTENTIAL, IMPEDANCE, AND RECTIFICATION IN MEMBRANES.膜的电位、阻抗和整流。
J Gen Physiol. 1943 Sep 20;27(1):37-60. doi: 10.1085/jgp.27.1.37.
4
ION FLUXES AND TRANSFERENCE NUMBER IN SQUID AXONS.乌贼轴突中的离子通量与迁移数
J Neurophysiol. 1965 May;28:526-44. doi: 10.1152/jn.1965.28.3.526.
7
Sodium permeability in toad nerve and in squid nerve.蟾蜍神经和鱿鱼神经中的钠通透性。
J Physiol. 1960 Jun;152(1):159-66. doi: 10.1113/jphysiol.1960.sp006477.

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