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.

PubMed

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.