Key result
Hypertril administration significantly increased survival to 95% compared to 30% in the control group at 45 days in rats with doxorubicin-induced chronic heart failure.
Why the study?
The study aimed to compare the efficiency of various beta-blockers with the new potential drug Hypertril in improving parameters in modeled doxorubicin chronic heart failure.
Does Hypertril improve survival and biochemical markers in a rat model of doxorubicin-induced chronic heart failure compared to standard beta-blockers?
Does Hypertril improve survival and biochemical markers in a rat model of doxorubicin-induced chronic heart failure compared to standard beta-blockers?
Hypertril demonstrated significant cardioprotective effects, improving survival and reducing biomarkers of myocardial damage in a rat model of doxorubicin-induced heart failure, outperforming standard beta-blockers.
β-adrenergic blockers have been actively used in the treatment of heart failure, which relieve excessive sympathetic stimulation of the myocardium, reduce calcium overload of cardiomyocytes, reduce the heart's oxygen demand, inhibit lipid peroxidation and stabilize cell membranes, have an antiarrhythmic effect. The aim: to compare efficiency of various drugs with new potential "Hypertril" in the conditions of modeling doxorubicin chronic heart failure (CHF) to improve parameters. Objective: CHF was modeled on 85 white outbred rats weighing 190–220g by administering doxorubicin at a cumulative dose of 15 mg/kg. Material and metods: Nebivalol, Carvedilol, Bisoprolol, Metoprolol and Hypertril were administered intragastrically once a day in the form of a suspension of 1% starch mucus for 30 days after a 14-day administration of doxorubicin. To determine damage, we used the solid-phase immunosorbent sandwich ELISA method, enzyme immunoassay and the immunoturbodimetric method. Result and discussion: Administration of Hypertril to rats with CHF led to a decrease in the blood of the main molecular markers of CHF to the values of intact animals, which indicated its significant cardioprotective effect in comparison with other drugs. Hypertril reduces manifestations of mitochondrial dysfunction, protects the myocardium and positively affects the morphological and functional parameters of cardiomyocytes, inhibits apoptosis
No takes yet. Share an insight, caveat, or question.
Беленичев et al. (2023) studied Doxorubicin-induced chronic heart failure (n=85). Hypertril vs. Control (untreated CHF) and standard beta-blockers was evaluated on Survival at 45 days (p=<0.05). Hypertril administration significantly increased survival to 95% compared to 30% in the control group at 45 days in rats with doxorubicin-induced chronic heart failure.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: