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Open AccessJournal ArticleDOI

Comparison of the inotropic response to glucagon, ouabain and noradrenaline

B. A. Spilker
- 01 Nov 1970 - 
- Vol. 40, Iss: 3, pp 382-395
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TLDR
It was concluded that glucagon has its own spectrum of inotropic activity and does not completely mimic the effects of either ouabain or noradrenaline.
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.

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Effects of Beta- and Alpha-Adrenoceptor Activators and Adrenergic Transmitter Releasing Agents on the Mechanical Activity of the Heart

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References
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Journal ArticleDOI

The dependence of slow inward current in Purkinje fibres on the extracellular calcium-concentration

TL;DR: In sodium‐free solution electrical constants of short Purkinje fibres were similar to those in Tyrode solution, and Alterations in the extracellular calcium concentration had no appreciable effect on these constants.
Journal ArticleDOI

Differences in Na and Ca Spikes As Examined by Application of Tetrodotoxin, Procaine, and Manganese Ions

TL;DR: The results suggest that the plateau phase of the ventricular action potential is related to the conductance increase in the membrane to Ca ions even though Na conductance change may also contribute to the plateau.
Journal ArticleDOI

Glucagon Its Enhancement of Cardiac Performance in the Cat and Dog and Persistence of its Inotropic Action Despite Beta-Receptor Blockade with Propranolol

TL;DR: In the dog, myocardial performance was markedly augmented by the administration of glucagon, 50 μg/kg iv, as indicated by an average increase of 72.2±18.8% in force recorded by a strain gauge arch, despite an average decrease of 3.8±1.2 cm H2O (P < 0.02) in left ventricular end-diastolic pressure.
Journal Article

Studies on the pharmacology of glucagon.

TL;DR: The quantitative data presented indicate that the biological effects observed here are due to the same substance, presumably glucagon, and are most probably not caused by an impurity which contaminates crystalline glucagon.
Journal ArticleDOI

Cardiovascular Effects of Glucagon in Man

TL;DR: Glucagon benefits cardiac performance in man, and with its demonstrated action in the absence of catecholamines and in the presence of full digitalization, may be useful to treat acute heart failure.
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