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[4-氨基吡啶对软体动物神经元快速钾电流通道的主要阻断作用]

[Predominant blocking of fast potassium current channels in mollusk neurons by 4-aminopyridine].

作者信息

Vislobokoe A I, Krylov B V, Akoev G N

出版信息

Fiziol Zh SSSR Im I M Sechenova. 1983 Nov;69(11):1420-6.

PMID:6317474
Abstract

Blocking effects of 4-aminopyridine (4-AP) on ionic currents were studied in Lymnaea stagnalies neurones using the suction pipette method for voltage clamp and internal perfusion. When applied externally, 4-AP blocks transient potassium current as well as early inward and delayed outward currents, apparent dissociation constants being 0.4 mM (E = -40-- -30 mV); 6.5 mM (E = -10-- -20 mV); 24 mM (E = 20 mV), resp. Intracellular 4-AP changes the constants to 0.85, 77, 55 mM. An experimental study of a possible role of the transient potassium channels in the regulation of molluscan unit activity seems to be effective when 4-AP is applied internally as it blocks then the transient potassium channels in a selective manner.

摘要

采用电压钳吸液管法和内部灌注法,研究了4-氨基吡啶(4-AP)对椎实螺神经元离子电流的阻断作用。当从外部施加时,4-AP可阻断瞬时钾电流以及早期内向电流和延迟外向电流,表观解离常数分别为0.4 mM(E = -40-- -30 mV);6.5 mM(E = -10-- -20 mV);24 mM(E = 20 mV)。细胞内4-AP可将这些常数分别变为0.85、77、55 mM。当内部应用4-AP时,对瞬时钾通道在调节软体动物单位活动中可能作用的实验研究似乎是有效的,因为此时它以选择性方式阻断瞬时钾通道。

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