Back

A Theoretical Framework for the Hemodynamic Role of Sarcomere Length Dynamics During the Isovolumic Phases of the Left Ventricle

KATO, S.; KISHIDA, K.; HIMENO, Y.; Amano, A.

2026-03-18 physiology
10.64898/2026.03.16.712012 bioRxiv
Show abstract

The left ventricle (LV) exhibits torsional deformation during systole, and mechanical relaxation begins during the isovolumic phase. Recent advances in imaging techniques, such as MRI, have revealed that myocardial tissue deformation and sarcomere length changes occur during the isovolumic relaxation phase, even when the chamber volume remains constant. Although such ventricular deformation during the isovolumic phase is considered important for blood ejection and filling efficiency, its mechanistic contribution to contraction and relaxation remains unresolved. In this study, we hypothesized that sarcomere length dynamics during the isovolumic phase affect the isovolumic contraction and relaxation time (IVCT and IVRT) by regulating the contraction force via the force-velocity relationship of ventricular myocytes. To investigate this hypothesis, we focused on experimentally reported differences in the relationship between sarcomere length and LV volume across the endocardial and epicardial layers, as described by Rodriguez et al. We constructed and compared two types of hemodynamic models within the same integrated framework consisting of a circulation model, a LV model, and a myocardial cell contraction model by Negroni-Lascano et al., which differ only in how sarcomere length is determined: a volume-based length model (VL model), in which sarcomere length is uniquely determined by LV volume, and a volume-force-coupled length model (VFL model), in which sarcomere length is determined by the balance between LV volume and contraction force. Simulation results showed that in the VFL model, compared to the VL model, sarcomere length changed during the isovolumic phase, leading to a decrease in contractile force and shortening of IVRT, which may contribute to improved hemodynamic efficiency. These results indicate that sarcomere length dynamics can mechanically regulate force decay during isovolumic relaxation, even under constant left ventricular volume. This study provides a theoretical framework for understanding the contributions of different layers within the LV wall to diastolic function during the isovolumic relaxation phase.

Matching journals

The top 8 journals account for 50% of the predicted probability mass.

1
Frontiers in Physiology
93 papers in training set
Top 0.1%
12.8%
2
Biomechanics and Modeling in Mechanobiology
25 papers in training set
Top 0.1%
8.6%
3
Scientific Reports
3102 papers in training set
Top 9%
8.6%
4
PLOS Computational Biology
1633 papers in training set
Top 5%
7.0%
5
PLOS ONE
4510 papers in training set
Top 33%
4.4%
6
Journal of the American Heart Association
119 papers in training set
Top 2%
4.3%
7
Mathematical Biosciences and Engineering
23 papers in training set
Top 0.1%
4.1%
8
Frontiers in Cardiovascular Medicine
49 papers in training set
Top 0.8%
4.1%
50% of probability mass above
9
Physiological Reports
35 papers in training set
Top 0.1%
3.7%
10
Computers in Biology and Medicine
120 papers in training set
Top 1%
2.8%
11
American Journal of Physiology-Heart and Circulatory Physiology
32 papers in training set
Top 0.4%
2.7%
12
International Journal of Molecular Sciences
453 papers in training set
Top 4%
2.4%
13
eLife
5422 papers in training set
Top 33%
2.4%
14
BioMed Research International
25 papers in training set
Top 1%
1.8%
15
JACC: Clinical Electrophysiology
11 papers in training set
Top 0.2%
1.7%
16
Human Brain Mapping
295 papers in training set
Top 3%
1.7%
17
Biochemical and Biophysical Research Communications
78 papers in training set
Top 0.8%
1.4%
18
Frontiers in Bioengineering and Biotechnology
88 papers in training set
Top 2%
1.0%
19
Biophysical Journal
545 papers in training set
Top 4%
1.0%
20
American Journal of Physiology-Regulatory, Integrative and Comparative Physiology
13 papers in training set
Top 0.3%
0.9%
21
Journal of Cellular Physiology
21 papers in training set
Top 0.6%
0.8%
22
Ultrasound in Medicine & Biology
10 papers in training set
Top 0.5%
0.8%
23
Function
15 papers in training set
Top 0.5%
0.8%
24
Journal of the Mechanical Behavior of Biomedical Materials
22 papers in training set
Top 0.3%
0.7%
25
iScience
1063 papers in training set
Top 33%
0.7%
26
IEEE Transactions on Medical Imaging
18 papers in training set
Top 0.6%
0.7%
27
Cells
232 papers in training set
Top 7%
0.7%
28
IEEE Access
31 papers in training set
Top 1%
0.7%
29
The Journal of Physiology
134 papers in training set
Top 2%
0.5%
30
Communications Biology
886 papers in training set
Top 31%
0.5%