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胰高血糖素、哇巴因和去甲肾上腺素的变力性反应比较。

Comparison of the inotropic response to glucagon, ouabain and noradrenaline.

作者信息

Spilker B

出版信息

Br J Pharmacol. 1970 Nov;40(3):382-95. doi: 10.1111/j.1476-5381.1970.tb10620.x.

Abstract
  1. The inotropic activity of glucagon was compared with catecholamines and cardiac glycosides by in vitro procedures which were able to differentiate between the activities of the latter two groups.2. The frequency-force curve for glucagon resembled that of noradrenaline at low stimulation frequencies (1 and 2/min) and that of ouabain at more rapid frequencies of stimulation.3. Noradrenaline and adrenaline increased the amplitude of contraction of cat papillary muscles and markedly shortened the time to reach peak tension. Ouabain and glucagon increased tension without any change in the time to peak tension.4. Noradrenaline caused a rapid onset and rate of rise of contraction of cat aortic strips, whereas the response to ouabain was slow in onset and rate of development. Glucagon had no effect on this preparation, even at high concentrations.5. Manganese ions caused a shift of the dose-response curve to ouabain and glucagon, but not to noradrenaline or calcium. In 0.5 mM Ca media, the response to ouabain was abolished and the curve to noradrenaline shifted.6. When glucagon was added to an atrial preparation, the time to the initial increase in tension and the time to maximal tension was intermediate between that necessary for noradrenaline and that necessary for cardiac glycosides.7. Propranolol blocked the inotropic response to noradrenaline, but not to either ouabain or glucagon.8. A relative measure of contraction-dependency was described. Cardiac glycosides exhibited a greater degree of contraction-dependency than either noradrenaline or glucagon.9. Adrenaline elevated the depressed plateau of the action potential from calf and sheep Purkinje fibres, but ouabain and glucagon were without effect.10. Electrophysiological measurements demonstrated that moderate concentrations of glucagon exerted only a small effect in prolonging atrial and ventricular action potentials.11. Several pharmacological blocking drugs and other inotropic agents did not potentiate or block the inotropic response to glucagon. Reserpine pretreatment increased the response to glucagon.12. It was concluded that glucagon has its own spectrum of inotropic activity and does not completely mimic the effects of either ouabain or noradrenaline.
摘要
  1. 通过能够区分后两组活性的体外实验程序,比较了胰高血糖素与儿茶酚胺和强心苷的变力活性。

  2. 胰高血糖素的频率-张力曲线在低刺激频率(1次/分钟和2次/分钟)时类似于去甲肾上腺素,在更快的刺激频率时类似于哇巴因。

  3. 去甲肾上腺素和肾上腺素增加了猫乳头肌的收缩幅度,并显著缩短了达到峰值张力的时间。哇巴因和胰高血糖素增加了张力,但达到峰值张力的时间没有变化。

  4. 去甲肾上腺素使猫主动脉条带的收缩迅速开始并上升,而对哇巴因的反应开始和发展速度较慢。即使在高浓度下,胰高血糖素对该制剂也没有影响。

  5. 锰离子使哇巴因和胰高血糖素的剂量-反应曲线发生偏移,但对去甲肾上腺素或钙没有影响。在0.5 mM钙培养基中,对哇巴因的反应被消除,而去甲肾上腺素的曲线发生偏移。

  6. 当将胰高血糖素添加到心房制剂中时,张力最初增加的时间和达到最大张力的时间介于去甲肾上腺素所需时间和强心苷所需时间之间。

  7. 普萘洛尔阻断了对去甲肾上腺素的变力反应,但对哇巴因或胰高血糖素均无阻断作用。

  8. 描述了收缩依赖性的相对测量方法。强心苷表现出比去甲肾上腺素或胰高血糖素更大程度的收缩依赖性。

  9. 肾上腺素升高了小牛和绵羊浦肯野纤维动作电位的降低平台,但哇巴因和胰高血糖素没有作用。

  10. 电生理测量表明,中等浓度的胰高血糖素在延长心房和心室动作电位方面仅产生很小的作用。

  11. 几种药理阻断药物和其他变力药物既不增强也不阻断对胰高血糖素的变力反应。利血平预处理增加了对胰高血糖素的反应。

  12. 得出的结论是,胰高血糖素具有其自身的变力活性谱,并不完全模拟哇巴因或去甲肾上腺素的作用。

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3
Contraction dependency of the positive inotropic action of cardiac glycosides.
Circ Res. 1967 Nov;21(5):727-40. doi: 10.1161/01.res.21.5.727.
8
Influence of manganese and ouabain on the rate of action of calcium on atrial contractions.
Am J Physiol. 1969 Feb;216(2):244-8. doi: 10.1152/ajplegacy.1969.216.2.244.

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