# Conceptualizing myocardial contractility as an emergent property that characterizes myocardial contraction

**Authors:** Serena Y. Kuang, Gorune Geloian

PMC · DOI: 10.3389/fphys.2025.1499536 · Frontiers in Physiology · 2025-04-16

## TL;DR

This paper redefines myocardial contractility using a new three-domain framework to clarify its complex and dynamic nature for better clinical and research applications.

## Contribution

A novel three-domain functional framework for myocardial contractility emphasizing dynamic interactions and clinical implications.

## Key findings

- The three-domain framework (capacity/resource, adaptability, and ability) clarifies myocardial contractility and resolves definitional inconsistencies.
- Interventions targeting myocardial contractility may have non-linear effects, suggesting a focus on optimizing resource use rather than maximizing outputs.
- System-level emergent properties like contraction efficiency and history-dependence are identified with implications for research and clinical practice.

## Abstract

Myocardial contractility (MC) is a fundamental concept that is widely used to describe the cardiac muscles’ mechanical function, yet its definitions in textbooks and literature are vague, inconsistent, and often contradictory. In this article, we categorize these many issues into five groups and conducts a conceptual analysis to redefine MC from a broader, more comprehensive perspective. We propose a functional, three-domain framework of MC consisting of capacity/resource, adaptability, and ability (force (F) and/or velocity (V) generated during muscle contraction), emphasizing the dynamic, non-linear interactions among the three domains and their clinical significance. Specifically, we highlight how interventions targeting MC may produce non-linear effects, suggesting a shift toward optimizing resource use rather than maximizing outputs (i.e., F and/or V of myocardial contraction, the outputs of the ability domain), which could potentially reduce the complications of positive inotropic interventions. We also discuss the implications of several new conceptual developments as the byproducts of the three-domain MC framework. Additionally, we identify system-level emergent properties of MC briefly, including contraction efficiency, circadian rhythm-dependence, temperature-dependence, and history-dependence, with implications for cardiac muscle research, exercise training, and clinical decision-making. The three-domain functional framework of MC resolves the inconsistencies in definitions, differentiates MC from cardiac performance, and offers a structured perspective for facilitating both experimental studies and therapeutic strategies.

## Full-text entities

- **Genes:** BCAR1 (BCAR1 scaffold protein, Cas family member) [NCBI Gene 9564] {aka CAS, CAS1, CASS1, CRKAS, P130Cas}, MYH14 (myosin heavy chain 14) [NCBI Gene 79784] {aka DFNA4, DFNA4A, FP17425, MHC16, MYH17, NMHC II-C}
- **Diseases:** ischemic injury (MESH:D017202), heart failure (MESH:D006333), microvascular dysfunction (MESH:D017566), MC (MESH:D009202), left ventricular outflow tract obstruction (MESH:D000092242), cardiac muscle (MESH:D006331), stroke (MESH:D020521), systolic heart failure (MESH:D054143), atrophy (MESH:D001284), hypertrophic cardiomyopathy (MESH:D002312), ischemic myocardium (MESH:D017682), muscle contraction (MESH:C536214), myocardial disease (MESH:D004194), systole (MESH:D000092244), hypercalcemia (MESH:D006934), ischemia (MESH:D007511)
- **Chemicals:** FL (MESH:D005459), nitric oxide (MESH:D009569), OM (MESH:C547293), cardiac glycosides (MESH:D002301), glucose (MESH:D005947), calcium (MESH:D002118), Levosimendan (MESH:D000077464), O2 (MESH:D010100), fatty acid (MESH:D005227), 3-imEFs (-), Mava (MESH:C000605992), lactate (MESH:D019344), ATP (MESH:D000255)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12040998/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12040998/full.md

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Source: https://tomesphere.com/paper/PMC12040998