Digitalis antagonism. I.

AMA Arch Intern Med

Published: May 1958

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http://dx.doi.org/10.1001/archinte.1958.00260170005002DOI Listing

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Cardiac rhythm regulated by micro-macroscopic structures of heart. Pacemaker abnormalities or disruptions in electrical conduction, lead to arrhythmic disorders may be benign, typical, threatening, ultimately fatal, occurs in clinical practice, patients on digitalis, anaesthesia or acute myocardial infarction. Both traditional and genetic animal models are: In-vitro: Isolated ventricular Myocytes, Guinea pig papillary muscles, Patch-Clamp Experiments, Porcine Atrial Myocytes, Guinea pig ventricular myocytes, Guinea pig papillary muscle: action potential and refractory period, Langendorff technique, Arrhythmia by acetylcholine or potassium.

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Cloning of the "Na pump" (Na,K-ATPase or NKA) and identification of a circulating ligand, endogenous ouabain (EO), a cardiotonic steroid (CTS), triggered seminal discoveries regarding EO and its NKA receptor in cardiovascular function and the pathophysiology of heart failure (HF) and hypertension. Cardiotonic digitalis preparations were a preferred treatment for HF for two centuries, but digoxin was only marginally effective in a large clinical trial (1997). This led to diminished digoxin use.

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Article Synopsis
  • Cardiac glycosides, like digitoxin and digoxin, are traditionally used to treat heart conditions but may also have anti-cancer properties and affect angiogenesis, the formation of new blood vessels.
  • Research focused on how these drugs impact the early stages of angiogenesis in human umbilical vein endothelial cells (HUVECs), assessing cell viability, migration, and tube formation.
  • Results showed that digitoxin significantly inhibited HUVEC migration and angiogenesis without harming cell viability and suggested its potential as an anti-angiogenic treatment in conditions characterized by abnormal blood vessel growth.
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Background: Immunoneutralization of elevated circulating levels of endogenous digitalis-like Na/K-ATPase inhibitors (i.e. cardiotonic steroids (CTS)) represents a novel approach in the treatment of preeclampsia (PE).

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Treatment of heart failure with preserved ejection fraction: have we been pursuing the wrong paradigm?

Mayo Clin Proc

June 2011

Division of Cardiovascular Medicine, University Hospitals of Cleveland, Case Medical Center, Cleveland, OH, USA.

Heart failure with preserved ejection fraction (HF-PEF) is the clinical syndrome of heart failure associated with normal or near-normal systolic function. Because inhibition of the adrenergic and renin-angiotensin-aldosterone systems has been so effective in the treatment of systolic heart failure, these same therapies have been the subject of recent clinical trials of HF-PEF. In this review, we examine the current evidence about treatment of HF-PEF, with particular emphasis on reviewing the literature for large-scale randomized clinical studies.

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