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Titlebook: Cardiac Glycosides 1785–1985; Biochemistry — Pharm Erland Erdmann,K. Greef,J. C. Skou Conference proceedings 1986 Springer-Verlag Berlin He

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The “endogenous cardiac glycoside”ular Na.-concentration may also mediate hormonal effects on cellular processes (66). Provided this concept is right, the sodium pump must also be considered as a receptor of hormones and as a mediator of hormonal action (3). Alterations of the intracellular sodium concentration are considered to be
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Electrophysiological effects of cardiac glycosidesf s. r. function such as caffeine and ryanodine. As well as these oscillations of [Ca.]. which follow repolarization, there are also spontaneous oscillations in the absence of stimulation. These spontaneous oscillations, which also result from release of Ca from the sarcoplasmic reticulum, interfere
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Rat cardiac hypertrophy: contribution of heteregeneous digitalis receptor formsduced hypertrophied rat hearts working under isovolumic conditions in the presence of 0.25 mM [Ca]...Under these conditions, as compared to normal hearts, the inotropic response of hypertrophied hearts to ouabain appeared to be depressed and mainly prolonged. This delayed recovery of normal contract
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Digitalis receptors in normal and hypertrophied rat hearts. Differential effects of a Ca2+ free perfts. The pressure-overload induced hypertrophy represented a suitable model in that the movements of Ca. appeared to be slowed..When the heart was maintained at a physiological calcium level (2.5 mM), hypertrophied and normal cardiac preparations had heterogeneous ouabain binding sites: H. A. (K. 3 ×
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Biphasic contractile response to ouabain: Species specific? Calcium dependent? Altered sensitivity?onse to high ouabain concentrations was identical in both exposures. In Langendorff perfused rat heart preparations the “low-dose” response was not diminished by repeated ouabain exposure and .H-ouabain binding was not altered. The “low-dose” effect was not present in rat atrial strip preparations..
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