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Related Concept Videos

Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

Dysrhythmia management involves a multifaceted approach, incorporating pharmacological treatments, medical procedures, surgical interventions, lifestyle modifications, and patient education.Pharmacological ManagementAntiarrhythmic Drugs:Class I (Sodium Channel Blockers): This class includes quinidine and procainamide, which reduce the speed of impulse conduction in the heart, stabilize the cardiac membrane, and control arrhythmias. Quinidine and procainamide are Class IA agents that prolong the...
Heart Failure V: Medical Management01:30

Heart Failure V: Medical Management

Medical Management of Acute Decompensated Heart Failure (ADHF)The primary goals of therapy for patients hospitalized with acute decompensated heart failure (ADHF) include:Relieving symptomsOptimizing volume statusSupporting oxygenation and ventilationMaintaining cardiac output (CO) and end-organ perfusionIdentifying and addressing the cause of ADHFPreventing complicationsProviding patient education on factors precipitating HF exacerbationPlanning for dischargeOngoing monitoring and assessment...
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers01:12

Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers

Class III antiarrhythmic drugs are a group of medications that can prolong action potentials in the heart. They achieve this by blocking potassium channels or enhancing inward currents from sodium channels. However, these drugs have a unique property of "reverse use-dependence," which is most pronounced at slower heart rates and can lead to torsades de pointes—a specific type of arrhythmia. However, it is essential to note that excessive QT interval prolongation—a measure of the heart's...
Transducer Mechanism: Enzyme-Linked Receptors01:27

Transducer Mechanism: Enzyme-Linked Receptors

Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:

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Related Experiment Video

Updated: Jul 4, 2026

Impact of Intracardiac Neurons on Cardiac Electrophysiology and Arrhythmogenesis in an Ex Vivo Langendorff System
06:40

Impact of Intracardiac Neurons on Cardiac Electrophysiology and Arrhythmogenesis in an Ex Vivo Langendorff System

Published on: May 22, 2018

Endogenous digitalis: pathophysiologic roles and therapeutic applications.

Alexei Y Bagrov1, Joseph I Shapiro

  • 1Hypertension Unit at Laboratory of Cardiovascular Science, Intramural Research Program, National Institute on Aging, NIH, Baltimore 21224, MD, USA. bagrova@mail.nih.gov

Nature Clinical Practice. Nephrology
|June 11, 2008
PubMed
Summary

Endogenous cardiotonic steroids, like ouabain, play key roles in cardiovascular health and disease. Research highlights their involvement in essential hypertension, heart failure, and kidney disease, paving the way for new therapies.

Related Experiment Videos

Last Updated: Jul 4, 2026

Impact of Intracardiac Neurons on Cardiac Electrophysiology and Arrhythmogenesis in an Ex Vivo Langendorff System
06:40

Impact of Intracardiac Neurons on Cardiac Electrophysiology and Arrhythmogenesis in an Ex Vivo Langendorff System

Published on: May 22, 2018

Area of Science:

  • Physiology
  • Endocrinology
  • Cardiovascular Medicine

Background:

  • Endogenous digitalis-like factors, or cardiotonic steroids, have been studied for decades.
  • Ouabain and marinobufagenin are identified human cardiotonic steroids signaling via the sodium/potassium-transporting ATPase.
  • Their roles extend beyond renal sodium transport to cell growth, apoptosis, and fibrosis.

Purpose of the Study:

  • To review the role of endogenous cardiotonic steroids in major cardiovascular and renal diseases.
  • To explore potential therapeutic strategies based on cardiotonic steroid function.

Main Methods:

  • Literature review focusing on endogenous cardiotonic steroids.
  • Analysis of their involvement in pathophysiology of hypertension, heart failure, ESRD, and pre-eclampsia.

Main Results:

  • Cardiotonic steroids are implicated in essential hypertension, congestive heart failure, end-stage renal disease, and pre-eclampsia.
  • Established effector mechanisms involve the sodium/potassium-transporting ATPase.

Conclusions:

  • Endogenous cardiotonic steroids are significant factors in cardiovascular and renal pathophysiology.
  • Understanding their regulation and actions offers novel therapeutic avenues.