Cardioprotective effect of histidine-containing dipeptides in pharmacological cold cardioplegia

L A Bokeriya1, A A Boldyrev, R R Movsesyan

  • 1A. N. Bakulev Institute of Cardiovascular Surgery, Russian Academy of Medical Sciences, Moscow.

Insights

Histidine-containing dipeptides in cardioplegic solutions enhance heart protection during hypothermic ischemia. These natural dipeptides increase myocardial buffer capacity, providing an additional anti-ischemic effect for prolonged procedures.

Area of Science:

  • Cardiology
  • Biochemistry
  • Physiology

Background:

  • Cardioplegic solutions are crucial for myocardial protection during cardiac surgery.
  • Ischemia and hypothermia pose significant risks to heart tissue.
  • Histidine-containing dipeptides are known for their buffering properties.

Purpose of the Study:

  • To evaluate the cardioprotective effects of a cardioplegic solution utilizing histidine-containing dipeptides.
  • To assess the impact of these dipeptides on isolated rat hearts subjected to hypothermia and prolonged ischemia.

Main Methods:

  • Isolated rat heart model.
  • Application of a cardioplegic solution containing histidine-containing dipeptides.
  • Induction of hypothermia and long-term ischemia.

Main Results:

  • The cardioplegic solution demonstrated cardioprotective effects.
  • Use of natural dipeptides increased the buffer capacity of myocardial cells.
  • An additional anti-ischemic effect was observed under prolonged ischemia and hypothermia.

Conclusions:

  • Cardioplegic solutions based on histidine-containing dipeptides offer significant cardioprotection.
  • These dipeptides enhance myocardial resilience against ischemic and hypothermic injury.
  • Natural dipeptides represent a promising strategy for improving cardiac surgical outcomes.

Related Concept Videos

Cardiopulmonary Resuscitation IV: Pharmacological Management01:25

Cardiopulmonary Resuscitation IV: Pharmacological Management

Pharmacologic intervention is crucial in treating cardiac arrest patients during ACLS or Advanced Cardiovascular Life Support. The ACLS algorithms guide the administration of specific drugs based on the patient's cardiac arrest rhythm, which includes pulseless ventricular tachycardia (VT), ventricular fibrillation (VF), asystole, and pulseless electrical activity (PEA).EpinephrineIndication: Epinephrine is the first-line drug for all cardiac arrest rhythms.Mechanism of Action: Epinephrine...
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,...
Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
Myocarditis III: Medical Management01:14

Myocarditis III: Medical Management

Myocarditis: Comprehensive Medical ManagementMyocarditis, the heart muscle inflammation, requires a comprehensive medical management strategy that addresses the underlying cause, provides supportive care, manages symptoms, and reduces cardiac workload.Infections and Autoimmune CausesAdminister appropriate antimicrobial therapy when an infectious agent causes myocarditis. For instance, penicillin treats infections caused by Group A Streptococcus. In cases where autoimmune processes are...
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...