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在豚鼠心肌中,具有心脏活性的甾体类药物不依赖扩散作用的起效速度有多快?

How fast do cardioactive steroids act independently of diffusion in guinea-pig myocardium?

作者信息

Ebner F

机构信息

Institut für Pharmakologie und Toxikologie, Technischen Universität München, Federal Republic of Germany.

出版信息

Br J Pharmacol. 1987 Aug;91(4):763-71. doi: 10.1111/j.1476-5381.1987.tb11274.x.

DOI:10.1111/j.1476-5381.1987.tb11274.x
PMID:3664077
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1853575/
Abstract

1 The rate of onset of the inotropic effect of different cardioactive steroids (in order of increasing potency: dihydroouabain, digoxigenin, digoxin, ouabain, digitoxin) was studied in guinea-pig papillary muscles stimulated at 0.5 Hz. For an estimate of diffusion rate the time to defined levels of effect was evaluated in relation to the diameter of cylindrical muscles. 2 The dependence of onset rates on muscle diameter was more pronounced with a highly potent steroid, e.g., digitoxin, than with a less potent compound, e.g., dihydroouabain; that is, the apparent rate of diffusion was inversely correlated with the inotropic potency. Reduction of the ratio of receptor to steroid concentration with increase of ouabain or K+ concentration enhanced the apparent rate of diffusion. 3 Extrapolation to negligibly short diffusion distance indicated that the effects of the various steroids develop faster in the absence of diffusion. The effect of 50 mumol l-1 of dihydroouabain appeared more quickly than with ouabain in the perfused heart. The time courses of the inotropic effect in perfused hearts and in papillary muscles of diameters less than 0.75 mm were superimposable, indicating that the onset of the dihydroouabain effect was not controlled by diffusion. 4 After the interference of diffusion had been excluded, the rates of onset of action correlated inversely with the inotropic potencies of the steroids. The dissociation rate of the drug-receptor complex appeared to be related to the different receptor affinities.

摘要
  1. 在以0.5Hz频率刺激的豚鼠乳头肌中,研究了不同强心甾体类药物(效力递增顺序为:双氢哇巴因、洋地黄毒苷元、地高辛、哇巴因、洋地黄毒苷)正性肌力作用的起效速率。为了估算扩散速率,根据圆柱形肌肉的直径评估达到特定效应水平所需的时间。2. 与效力较低的化合物(如双氢哇巴因)相比,效力高的甾体类药物(如洋地黄毒苷)的起效速率对肌肉直径的依赖性更明显;也就是说,表观扩散速率与正性肌力效力呈负相关。随着哇巴因或钾离子浓度的增加,受体与甾体浓度之比降低,表观扩散速率加快。3. 外推至可忽略不计的短扩散距离表明,在不存在扩散的情况下,各种甾体类药物的效应发展得更快。在灌注心脏中,50μmol/L双氢哇巴因的效应比哇巴因出现得更快。灌注心脏和直径小于0.75mm的乳头肌中正性肌力作用的时间进程是重叠的,这表明双氢哇巴因效应的起效不受扩散控制。4. 在排除扩散干扰后,作用起效速率与甾体类药物的正性肌力效力呈负相关。药物-受体复合物的解离速率似乎与不同的受体亲和力有关。

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How fast do cardioactive steroids act independently of diffusion in guinea-pig myocardium?在豚鼠心肌中,具有心脏活性的甾体类药物不依赖扩散作用的起效速度有多快?
Br J Pharmacol. 1987 Aug;91(4):763-71. doi: 10.1111/j.1476-5381.1987.tb11274.x.
2
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Diffusion characteristics dissociate ouabain binding from inotropic effect in guinea-pig myocardium.在豚鼠心肌中,扩散特性使哇巴因结合与变力作用相分离。
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Naunyn Schmiedebergs Arch Pharmacol. 1986 Dec;334(4):475-9. doi: 10.1007/BF00569389.
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Br J Pharmacol. 1988 Dec;95(4):1063-74. doi: 10.1111/j.1476-5381.1988.tb11740.x.

引用本文的文献

1
Diffusion characteristics dissociate ouabain binding from inotropic effect in guinea-pig myocardium.在豚鼠心肌中,扩散特性使哇巴因结合与变力作用相分离。
Br J Pharmacol. 1988 Oct;95(2):399-404. doi: 10.1111/j.1476-5381.1988.tb11659.x.
2
EP 171: a high affinity thromboxane A2-mimetic, the actions of which are slowly reversed by receptor blockade.EP 171:一种高亲和力的血栓素A2模拟物,其作用可通过受体阻断缓慢逆转。
Br J Pharmacol. 1989 Apr;96(4):875-87. doi: 10.1111/j.1476-5381.1989.tb11898.x.

本文引用的文献

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The inhibition by (+/-)-propranolol of the positive inotropic effects of (+/-)-isoprenaline and (-)-noradrenaline. Competitive antagonism and saturable uptake.(±)-普萘洛尔对(±)-异丙肾上腺素和(-)-去甲肾上腺素正性肌力作用的抑制。竞争性拮抗和可饱和摄取。
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The rate of action of atropine.阿托品的作用速率。
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Frequent stimulation of the guinea-pig myocardium raises the inotropic efficacy of tissue-bound ouabain.频繁刺激豚鼠心肌可提高组织结合型哇巴因的正性肌力作用。
Naunyn Schmiedebergs Arch Pharmacol. 1986 Dec;334(4):475-9. doi: 10.1007/BF00569389.
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Diffusion-controlled receptor occupancy determines the rate of inotropic action of some cardioactive steroids.扩散控制的受体占有率决定了某些强心甾体类药物的变力作用速率。
J Mol Cell Cardiol. 1985 Nov;17(11):1115-26. doi: 10.1016/s0022-2828(85)80127-9.
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Sodium pump inhibition, enhanced calcium influx via sodium-calcium exchange, and positive inotropic response in cultured heart cells.钠泵抑制、通过钠钙交换增强钙内流以及培养的心脏细胞中的正性肌力反应。
Circ Res. 1985 Feb;56(2):231-41. doi: 10.1161/01.res.56.2.231.
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The reaction of ouabain with the sodium pump of guinea-pig myocardium in relation to its inotropic effect.哇巴因与豚鼠心肌钠泵的反应及其变力作用
J Physiol. 1986 Oct;379:187-203. doi: 10.1113/jphysiol.1986.sp016247.
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The role of uptake of noradrenaline of its positive inotropic effect in relation to muscle geometry. Statistical evaluation.
Naunyn Schmiedebergs Arch Pharmacol. 1978 May;303(1):1-6. doi: 10.1007/BF00496179.
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Increase in dissociation rate constants of cardiotonic steroid-brain (Na+ + K+)-ATPase complexes by reduction of the unsaturated lactone.通过还原不饱和内酯增加强心甾类-脑(钠+钾)-ATP酶复合物的解离速率常数。
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