Procurement and preservation of neonatal porcine cardiac tissue

The porcine and human heart are remarkably similar in cardiac physiology and biochemistry. Translational research involving the porcine biomedical model is becoming increasingly applicable for the study of human cardiac function in health and disease. Presently, few protocols exist for collecting experimentally viable cardiac tissue from large animal models, particularly during neonatal maturation. To address this deficiency, we have developed a technique to procure and preserve ventricular tissue from neonatal piglets at <i>day 3</i> (<i>n</i> = 4) and <i>day 30</i> (<i>n</i> = 6) postpartum. Piglets were subjected to a strict sedation, anesthesia, and analgesia regimen. During surgery, cardiopulmonary indices of electrocardiogram, heart rate, systolic and diastolic blood pressure, respiration rate, peripheral O<sub>2</sub> saturation, and end-tidal CO<sub>2</sub> were monitored continuously to ensure normal cardiac function. Before cardiectomy, each heart was perfused with an intravenous administration of heparin (10 mL/kg) and ice-cold Custodiol HTK cardioplegia solution (10 mL/kg). After cardiac explantation, myocardial samples (dimensions: 1 × 1 × 1 cm) were dissected from the left and right ventricles and snap-frozen in liquid nitrogen. Analysis via SDS-PAGE densitometry demonstrated that myofibrillar proteins are stable and undegraded. Western Blots showed full expression of protein. These results suggest that the detailed cardiac tissue procurement technique preserves the experimental viability of the cardiac tissue and prevents the degradation of myofibrillar proteins.<b>NEW & NOTEWORTHY</b> This project's objective was to develop a technique for procuring and preserving cardiac tissue from a porcine model. Porcine is a rapidly emerging animal model to study cardiovascular disease and has recently been popularized due to advancements in CRISPR-cas9 technology. The technique, originally derived from human heart transplant protocols, involves full anesthetic and analgesic regimens and the use of saline heparin and cardioplegia solution to preserve tissue integrity.

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Publication Details

Journal
American Journal of Physiology-Heart and Circulatory Physiology
Published
2024-10-25
DOI
https://doi.org/10.1152/ajpheart.00362.2024
Primary Topic
Tissue Engineering and Regenerative Medicine
Type
article
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article

Procurement and preservation of neonatal porcine cardiac tissue

Mallery Larson, Laís M Malavasi, Luis M. Pereira, A. Bradshaw et al.
American Journal of Physiology-Heart and Circulatory Physiology
Tissue Engineering and Regenerative Medicine
article

Procurement and preservation of neonatal porcine cardiac tissue

Mallery Larson, Laís M Malavasi, Luis M. Pereira, A. Bradshaw, Daniel P. Fitzsimons, Alyssa Marre, Lauren M. Gilbertsen, Jennifer A Sexton, Jeff Olivarez, Tara L. Goertzen, Raney L Hazan, Georgia F Patyna, Abigail H Thomas, Emma S. Scudder
article en

Abstract

The porcine and human heart are remarkably similar in cardiac physiology and biochemistry. Translational research involving the porcine biomedical model is becoming increasingly applicable for the study of human cardiac function in health and disease. Presently, few protocols exist for collecting experimentally viable cardiac tissue from large animal models, particularly during neonatal maturation. To address this deficiency, we have developed a technique to procure and preserve ventricular tissue from neonatal piglets at <i>day 3</i> (<i>n</i> = 4) and <i>day 30</i> (<i>n</i> = 6) postpartum. Piglets were subjected to a strict sedation, anesthesia, and analgesia regimen. During surgery, cardiopulmonary indices of electrocardiogram, heart rate, systolic and diastolic blood pressure, respiration rate, peripheral O<sub>2</sub> saturation, and end-tidal CO<sub>2</sub> were monitored continuously to ensure normal cardiac function. Before cardiectomy, each heart was perfused with an intravenous administration of heparin (10 mL/kg) and ice-cold Custodiol HTK cardioplegia solution (10 mL/kg). After cardiac explantation, myocardial samples (dimensions: 1 × 1 × 1 cm) were dissected from the left and right ventricles and snap-frozen in liquid nitrogen. Analysis via SDS-PAGE densitometry demonstrated that myofibrillar proteins are stable and undegraded. Western Blots showed full expression of protein. These results suggest that the detailed cardiac tissue procurement technique preserves the experimental viability of the cardiac tissue and prevents the degradation of myofibrillar proteins.<b>NEW & NOTEWORTHY</b> This project's objective was to develop a technique for procuring and preserving cardiac tissue from a porcine model. Porcine is a rapidly emerging animal model to study cardiovascular disease and has recently been popularized due to advancements in CRISPR-cas9 technology. The technique, originally derived from human heart transplant protocols, involves full anesthetic and analgesic regimens and the use of saline heparin and cardioplegia solution to preserve tissue integrity.

American Journal of Physiology-Heart and Circulatory PhysiologyVol. 327(6)
University of Idaho (US), Washington State University (US)
Good health and well-being
Openalex Percentile: Top 64%
Tissue Engineering and Regenerative Medicine
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