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钾离子对犬离体静脉肾上腺素能神经传递的抑制作用。

Inhibition of adrenergic neurotransmission in isolated veins of the dog by potassium ions.

作者信息

Lorenz R R, Vanhoutte P M

出版信息

J Physiol. 1975 Mar;246(2):479-500. doi: 10.1113/jphysiol.1975.sp010900.

Abstract
  1. In the intact organism, an increase in K+ concentration decreases the reactivity of blood vessels to sympathetic stimulation. The present experiments were designed to determine whether or not K+ interferes with adrenergic neurotransmission. 2. Helical strips cut from dogs' saphenous veins were incubated (4 hr) in Krebs-Ringer solution containing [7-3H]norepinephrine (5 times 10(-8) g/ml). The preparations were mounted for superfusion and isometric tension recording; the superfusate was collected for estimation of total radioactivity and for chromatographic separation of 3H-labelled norepinephrine and metabolites. 3. Supramaximal electric stimulation (5 Hz, 9 V, 2 msec) increased the tension and the [3H]norepinephrine efflux. Increasing the K+ concentration from 5-9 to 1, 15, and 20 m-equiv/l. caused a progressive depression of these contractions and diminished the total 3H efflux in proportion to the relaxation; the decrease in 3H efflux reflected a decrease in intact [3H]norepinephrine. The same increase in K+ concentration did not alter basal tension or basal 3H efflux. 4. Addition of tyramine (4 times 10(-6) g/ml. min) to the superfusate augmented both the tension and the efflux, but these actions were not depresesd by increasing the K+ concentration. 5. Cocaine, phentolamine, and phenoxybenzamine did not prevent the depression by K+ of the response to electric stimulation. 6. These experiments show that K+ causes relaxation of venous smooth muscle constricted by sympathetic stimulation and does so by inhibiting the release of norepinephrine from nerve endings. By contrast, K+ does not inhibit norepinephrine release in response to tyramine. 7. During submaximal electric stimulation (5 Hz, 1-8--3 V, 2 msec), increasing the K+ concentration from 5-9 to 10 and 15 m-equiv/l. potentiated the contractions and increased the [3H]norepinephrine efflux; at 20 m-equil/l, K+ caused transient increases in tension and 3H efflux followed by relaxation and decreased norepinephrine release. After addition of cocaine (10(-5) g/ml. min), K+ only caused relaxation and decrease in 3H efflux, showing that, in addition to inhibition of norepinephrine release, K+ also inhibits the reuptake process. 8. In higher concentrations (40 m-equil/l.), K+ caused both a liberation of norepinephrine and a direct activation of the smooth muscle cells.
摘要
  1. 在完整机体中,钾离子浓度升高会降低血管对交感神经刺激的反应性。本实验旨在确定钾离子是否干扰肾上腺素能神经传递。2. 从犬隐静脉切取的螺旋条在含[7 - 3H]去甲肾上腺素(5×10⁻⁸ g/ml)的 Krebs - Ringer 溶液中孵育(4 小时)。制备物安装用于灌流和等长张力记录;收集灌流液以估计总放射性,并用于对 3H 标记的去甲肾上腺素及其代谢产物进行色谱分离。3. 超最大电刺激(5Hz,9V,2 毫秒)可增加张力和[3H]去甲肾上腺素外流。将钾离子浓度从 5 - 9 毫当量/升增加到 1、15 和 20 毫当量/升,会使这些收缩逐渐减弱,并使总 3H 外流按松弛比例减少;3H 外流的减少反映了完整的[3H]去甲肾上腺素的减少。相同的钾离子浓度增加并未改变基础张力或基础

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