Abstract
The Frank-Starling law of the heart describes the interrelationship between end-diastolic volume and cardiac ejection volume, a regulatory system that operates on a beat-to-beat basis. The main cellular mechanism that underlies this phenomenon is an increase in the responsiveness of cardiac myofilaments to activating Ca2+ ions at a longer sarcomere length, commonly referred to as myofilament length-dependent activation. This review focuses on what molecular mechanisms may underlie myofilament length dependency. Specifically, the roles of inter-filament spacing, thick and thin filament based regulation, as well as sarcomeric regulatory proteins are discussed. Although the "Frank-Starling law of the heart" constitutes a fundamental cardiac property that has been appreciated for well over a century, it is still not known in muscle how the contractile apparatus transduces the information concerning sarcomere length to modulate ventricular pressure development.
Original language | English |
---|---|
Pages (from-to) | 851-858 |
Number of pages | 8 |
Journal | Journal of Molecular and Cellular Cardiology |
Volume | 48 |
Issue number | 5 |
DOIs | |
Publication status | Published - May 2010 |
Externally published | Yes |
Keywords
- Frank-Starling Law of The Heart
- Length-Tension Relationship
- Regulation
- Sarcomere length