» Articles » PMID: 17293398

Interfilament Spacing is Preserved During Sarcomere Length Isometric Contractions in Rat Cardiac Trabeculae

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2007 Feb 13
PMID 17293398
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

It is generally assumed that the myofilament lattice in intact (i.e., nonskinned) striated muscle obeys constant volume. However, whether such is the case during the myocardial contraction is unknown. Accordingly, we measured interfilament spacing by x-ray diffraction in ultra-thin isolated rat right ventricular trabeculae during a short 10 ms shuttered exposure either just before electrical stimulation (diastole), or at the peak of the contraction (systole); sarcomere length (SL) was held constant throughout the contraction using an iterative feedback control system. SL was thus varied in a series of SL-clamped contractions; the relationship between SL and interfilament spacing was not different between diastole and systole within 1%; this was true also over a wide range of inotropic states induced by varied [Ca(2+)](o). We conclude that the cardiac myofilament lattice maintains constant volume, and thus constant interfilament spacing, during contraction.

Citing Articles

Load-dependence of the activation of myosin filaments in heart muscle.

Wang Y, Fusi L, Ovejero J, Hill C, Juma S, Paradine Cullup F J Physiol. 2024; 602(24):6889-6907.

PMID: 39552044 PMC: 11652228. DOI: 10.1113/JP287434.


Structural and functional impact of troponin C-mediated Ca sensitization on myofilament lattice spacing and cross-bridge mechanics in mouse cardiac muscle.

Gonzalez-Martinez D, Johnston J, Landim-Vieira M, Ma W, Antipova O, Awan O J Mol Cell Cardiol. 2018; 123:26-37.

PMID: 30138628 PMC: 6282743. DOI: 10.1016/j.yjmcc.2018.08.015.


Titin strain contributes to the Frank-Starling law of the heart by structural rearrangements of both thin- and thick-filament proteins.

Ait-Mou Y, Hsu K, Farman G, Kumar M, Greaser M, Irving T Proc Natl Acad Sci U S A. 2016; 113(8):2306-11.

PMID: 26858417 PMC: 4776536. DOI: 10.1073/pnas.1516732113.


Roles for cardiac MyBP-C in maintaining myofilament lattice rigidity and prolonging myosin cross-bridge lifetime.

Palmer B, Sadayappan S, Wang Y, Weith A, Previs M, Bekyarova T Biophys J. 2011; 101(7):1661-9.

PMID: 21961592 PMC: 3183797. DOI: 10.1016/j.bpj.2011.08.047.


Analysis of mitochondrial 3D-deformation in cardiomyocytes during active contraction reveals passive structural anisotropy of orthogonal short axes.

Yaniv Y, Juhaszova M, Wang S, Fishbein K, Zorov D, Sollott S PLoS One. 2011; 6(7):e21985.

PMID: 21779362 PMC: 3136939. DOI: 10.1371/journal.pone.0021985.


References
1.
Konhilas J, Irving T, de Tombe P . Frank-Starling law of the heart and the cellular mechanisms of length-dependent activation. Pflugers Arch. 2002; 445(3):305-10. DOI: 10.1007/s00424-002-0902-1. View

2.
Yagi N, Okuyama H, Toyota H, Araki J, Shimizu J, Iribe G . Sarcomere-length dependence of lattice volume and radial mass transfer of myosin cross-bridges in rat papillary muscle. Pflugers Arch. 2004; 448(2):153-60. DOI: 10.1007/s00424-004-1243-z. View

3.
Ter Keurs H, Rijnsburger W, van Heuningen R, Nagelsmit M . Tension development and sarcomere length in rat cardiac trabeculae. Evidence of length-dependent activation. Circ Res. 1980; 46(5):703-14. DOI: 10.1161/01.res.46.5.703. View

4.
Cecchi G, Griffiths P, Bagni M, Ashley C, Maeda Y . Time-resolved changes in equatorial x-ray diffraction and stiffness during rise of tetanic tension in intact length-clamped single muscle fibers. Biophys J. 1991; 59(6):1273-83. PMC: 1281207. DOI: 10.1016/S0006-3495(91)82342-6. View

5.
Farman G, Walker J, de Tombe P, Irving T . Impact of osmotic compression on sarcomere structure and myofilament calcium sensitivity of isolated rat myocardium. Am J Physiol Heart Circ Physiol. 2006; 291(4):H1847-55. DOI: 10.1152/ajpheart.01237.2005. View