Related Experiment Video
Updated: May 12, 2026

Simultaneous Assessment of Cardiomyocyte DNA Synthesis and Ploidy: A Method to Assist Quantification of Cardiomyocyte Regeneration and Turnover
Published on: May 23, 2016
A computational model of age-dependent cardiomyocyte apoptosis
Elena Kutumova1,2,3, Ilya Kiselev3, Fedor Kolpakov1,2,3
1Department of Computational Biology, Sirius University of Science and Technology, Sirius, Krasnodar Region, Russia.
Insights
Targeting cardiac apoptosis pathways can improve survival in patients with heart pressure overload. Losartan suppresses cardiomyocyte apoptosis, with greater molecular benefits in conditions causing water and sodium retention.
Area of Science:
- Cardiovascular research
- Cellular biology
- Pharmacology
Background:
- Hypertension and aging increase arterial stiffness, leading to cardiac overload and left ventricular hypertrophy.
- Cardiomyocyte apoptosis is a key adaptive response to pressure overload, and anti-hypertensive drugs may offer cardioprotection by inhibiting this process.
- Losartan, an angiotensin II receptor blocker, is used for hypertension and cardiac remodeling and may inhibit cardiomyocyte apoptosis.
Purpose of the Study:
- To investigate the impact of apoptotic signals in left ventricular (LV) myocytes on patient survival.
- To model the effects of losartan treatment on cardiomyocyte apoptosis and patient survival.
- To integrate cardiorenal processes with biochemical mechanisms of cell death using a mathematical model.
Main Methods:
- Utilized a previously developed mathematical model of human cardiovascular and renal systems.
- Extended the model to incorporate mechanisms of CD95-induced cardiomyocyte apoptosis.
- Simulated patient survival with and without losartan treatment under various conditions.
Main Results:
- The model predicted that interventions targeting cardiac apoptotic pathways significantly improve survival in patients with cardiac pressure overload.
- Losartan was shown to suppress cardiomyocyte apoptosis, primarily via effects on LV hemodynamic function.
- In conditions promoting water and sodium accumulation, losartan's therapeutic effect on molecular apoptotic processes may exceed its hemodynamic impact.
Conclusions:
- Targeting cardiac apoptotic pathways offers a promising therapeutic strategy for improving survival in pressure overload conditions.
- Losartan's cardioprotective effects involve suppressing cardiomyocyte apoptosis, with its molecular impact being particularly relevant in fluid and electrolyte imbalances.
- Mathematical modeling provides valuable insights into complex cardiorenal interactions and the mechanisms of drug action.
Abstract:
Hypertension and ageing are risk factors for arterial stiffness, which increases cardiac overload and causes left ventricular (LV) hypertrophy. Cardiomyocyte apoptosis acts as a regulatory mechanism that participates in the adaptive response of the heart to pressure overload. Anti-hypertensive drugs can exert anti-apoptotic effects on cardiomyocytes, which are important therapeutic targets for cardio protection. The angiotensin II receptor blocker losartan, used in hypertension and cardiac remodelling, may inhibit cardiomyocyte apoptosis, possibly by reducing Bax expression. To study the effect of apoptotic signals in LV myocytes on patient survival with and without losartan treatment we used a previously developed mathematical model of the human cardiovascular and renal systems. Here we extended this model to include mechanisms of CD95-induced cardiomyocyte apoptosis. Our model is the first to integrate a mechanistic view of cardiorenal processes with biochemical mechanisms of cell death. The model predicted that therapeutic intervention on cardiac apoptotic pathways could significantly improve the survival in patients with cardiac pressure overload pathology. Although the modelling results showed that losartan suppresses cardiomyocyte apoptosis primarily through its effects on LV haemodynamic function, the model demonstrated that in diseases that promote water and sodium accumulation in the body, the therapeutic effect of losartan on molecular apoptotic processes may be more significant than its effects on LV haemodynamics. KEY POINTS: Therapeutic interventions that target cardiac apoptotic pathways have the potential to markedly improve the survival of patients with cardiac pressure overload pathology. The findings of the modelling suggest that losartan suppresses cardiomyocyte apoptosis primarily through its effect on left ventricular haemodynamic function. In diseases that result in the accumulation of water and sodium within the body the therapeutic efficacy of losartan on molecular apoptotic processes may prove to be more significant than its effects on left ventricular haemodynamics.
More Related Videos
08:54Creating a Structurally Realistic Finite Element Geometric Model of a Cardiomyocyte to Study the Role of Cellular Architecture in Cardiomyocyte Systems Biology
Published on: April 18, 2018
05:06Model of Ischemic Heart Disease and Video-Based Comparison of Cardiomyocyte Contraction Using hiPSC-Derived Cardiomyocytes
Published on: May 5, 2020
Related Concept Videos
Apoptosis
Cellular Injury V: Apoptosis and Autophagy