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Updated: May 9, 2026

Murine Isolated Heart Model of Myocardial Stunning Associated with Cardioplegic Arrest
Published on: August 6, 2015
[Effects of cardioplegic solutions on coronary and myocardial ultrastructure. Preliminary note]
Insights
The University of Alabama cardioplegic solution preserved myocardial ultrastructure, while the St. Thomas Hospital solution caused endothelial damage. Solution composition, not cardiac arrest, dictates coronary arterial endothelium injury.
Area of Science:
- Cardiovascular Research
- Cell Biology
- Histology
Context:
- Cardiac surgery requires myocardial protection during ischemic arrest.
- Cardioplegic solutions (CPS) are used to preserve heart function during surgery.
- Evaluating the ultrastructural effects of different CPS on myocardium and endothelium is crucial.
Purpose:
- To compare the ultrastructural effects of two cardioplegic solutions (University of Alabama and St. Thomas Hospital) versus Krebs' solution on guinea pig myocardium and coronary endothelium.
- To determine if cardiac arrest, perfusion solutions, or myocardial damage contribute to endothelial injury.
Summary:
- Cold perfusion with University of Alabama CPS maintained myocardial ultrastructure, unlike Krebs' solution which caused severe myocardial damage.
- St. Thomas Hospital CPS induced significant coronary arterial endothelial damage, including layer interruption and cell bulging.
- Krebs' solution and University of Alabama CPS did not cause vascular changes, suggesting CPS composition is key to endothelial integrity.
Impact:
- Findings indicate that cardioplegic solution composition, specifically the St. Thomas Hospital formulation, can cause endothelial injury independent of cardiac arrest or myocardial damage.
- This research highlights the importance of selecting cardioplegic solutions to minimize both myocardial and vascular damage during cardiac procedures.
- The study provides critical ultrastructural evidence for guiding the development of safer and more effective cardioplegic solutions.
Abstract:
Ultrastructural changes of the myocardium and the coronary arterial endothelium were studied following cold perfusion with two different cardioplegic solutions (CPS) (the University of Alabama and the St. Thomas Hospital solutions), and with Krebs' solution as a control (CS). Guinea pig heart-lung preparations (HLP) were subjected to cardiac arrest by perfusion under CPS or CS (4 ml/Kg/min. X 4 min.). The duration of the cardiac arrest was 60 minutes, and additional amounts of cold solution were perfused after the first 30 minutes. In a second experimental group, HLP were reperfused with blood following 60 minutes of cardioplegic arrest, and maintained under full activity for the next 30 minutes. At the end of the study, specimens of coronary artery and myocardium were obtained and observed by Scanning (SEM) and Trasmission (TEM) electron microscopy. All the specimens were compared with additional specimens obtained from control hearts not subjected to cardiac arrest. The myocardial ultrastructure of hearts arrested with CPS was well preserved, whereas severe myocardial damage, consisting in the absence of glycogen granules, intracellular edema and myofibrillar contraction, was following CS-induced cardiac arrest. In contrast, perfusion with the St. Thomas CPS produced severe vascular damage, characterized by interruption of the endothelial layer, and bulging of endothelial cells into the lumen; no vascular changes were observed following cardiac arrest with CS or Alabama CPS. We conclude that the damage to the coronary arterial endothelium is not related to cardiac arrest, or to perfusion with cristalloid solution, or to myocardial damage, but appears to depend on the composition of the CPS.
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