Postprandial cardiac hypertrophy is sustained by mechanics, epigenetic, and metabolic reprogramming in pythons

Constricting pythons, known for their ability to consume infrequent, massive meals, exhibit rapid and reversible cardiac hypertrophy following feeding. Our primary goal was to investigate how python hearts achieve this adaptive response after feeding. Isolated myofibrils increased force after feeding without changes in sarcomere ultrastructure and without increasing energy cost. Ca<sup>2+</sup> transients were prolonged after feeding with no changes in myofibril Ca<sup>2+</sup> sensitivity. Feeding reduced titin-based tension, resulting in decreased cardiac tissue stiffness. Feeding also reduced the activity of sirtuins, a metabolically linked class of histone deacetylases, and increased chromatin accessibility. Transcription factor enrichment analysis on transposase-accessible chromatin with sequencing revealed the prominent role of transcription factors Yin Yang1 and NRF1 in postfeeding cardiac adaptation. Gene expression also changed with the enrichment of translation and metabolism. Finally, metabolomics analysis and adenosine triphosphate production demonstrated that cardiac adaptation after feeding not only increased energy demand but also energy production. These findings have broad implications for our understanding of cardiac adaptation across species and hold promise for the development of innovative approaches to address cardiovascular diseases.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2024-08-19
DOI
https://doi.org/10.1073/pnas.2322726121
Citations
7
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
2.29

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article

Postprandial cardiac hypertrophy is sustained by mechanics, epigenetic, and metabolic reprogramming in pythons

Cierra J. Walker, Stefano Perni, Christopher D. Ozeroff, Kathleen C. Woulfe et al.
7 citations
Proceedings of the National Academy of Sciences
Adipose Tissue and Metabolism
2.29
article

Postprandial cardiac hypertrophy is sustained by mechanics, epigenetic, and metabolic reprogramming in pythons

Cierra J. Walker, Stefano Perni, Christopher D. Ozeroff, Kathleen C. Woulfe, Claudia Crocini, Mary A. Allen, Cortney E. Wilson, Leslie Anne Leinwand, Joseph F. Cardiello, Kristi S. Anseth
article en
7 citations

Abstract

Constricting pythons, known for their ability to consume infrequent, massive meals, exhibit rapid and reversible cardiac hypertrophy following feeding. Our primary goal was to investigate how python hearts achieve this adaptive response after feeding. Isolated myofibrils increased force after feeding without changes in sarcomere ultrastructure and without increasing energy cost. Ca<sup>2+</sup> transients were prolonged after feeding with no changes in myofibril Ca<sup>2+</sup> sensitivity. Feeding reduced titin-based tension, resulting in decreased cardiac tissue stiffness. Feeding also reduced the activity of sirtuins, a metabolically linked class of histone deacetylases, and increased chromatin accessibility. Transcription factor enrichment analysis on transposase-accessible chromatin with sequencing revealed the prominent role of transcription factors Yin Yang1 and NRF1 in postfeeding cardiac adaptation. Gene expression also changed with the enrichment of translation and metabolism. Finally, metabolomics analysis and adenosine triphosphate production demonstrated that cardiac adaptation after feeding not only increased energy demand but also energy production. These findings have broad implications for our understanding of cardiac adaptation across species and hold promise for the development of innovative approaches to address cardiovascular diseases.

Proceedings of the National Academy of SciencesVol. 121(36)
University of Colorado Boulder (US), Deutsches Herzzentrum der Charité (DE), University of Colorado Anschutz Medical Campus (US), Charité - Universitätsmedizin Berlin (DE)
Howard Hughes Medical Institute, American Heart Association, Human Frontier Science Program, University of Colorado School of Medicine, Anschutz Medical Campus
Affordable and clean energy
Openalex Percentile: Top 11%
Adipose Tissue and Metabolism
2.29
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