Cardiac Muscle Structure & Function Flashcards
1
Q
Composition of contractile protein
A
- myosin: 2 heavy chains, 4 light chains
- actin: similar to skeletal muscle actin; binds tropomyosin and troponin
- thin filament regulatory proteins:
i. TN-C: one Ca2+ binding site
ii. TH-I: N-terminal regulated by phosporylation (PK sites)
iii. TN-T: Isoforms are developmentally & pathologically regulated
iv. TM: only alpha isoform
2
Q
Cardiac muscle structure
A
- interconnected mono-nucleated cells w/in collagen
- cells w/large number of myofibrils
- majority of cell volume=mitochondria
- cells coupled both electrically and mechanically
3
Q
Regulation of calcium flow w/in muscle cells
A
- depolarization –> L-type channels open –> calcium influx
- calcium influx –> calcium release from SR via ryanodine receptors (CICR)
- calcium binding to TN-C triggers contraction
- calcium removed by SR Ca2+-ATPase
4
Q
Cross-bridge cycle of cardiac muscle contraction
A
- @ rest: low intracell Ca2+ –> TN-TM complex inhibits actin-myosin combination
- increase myoplasmic Ca2+: TN releases inhibition, moves TM out of actin groove, myosin binds –> myosin head undergoes power stroke –> myofilaments shorten
5
Q
Cardiac output=
A
Stroke volume x heart rate
6
Q
Regulators of stroke volume
A
- pre-load
- afterload
- contractility
7
Q
Molecular mechanism of length-tension relationship
A
xxx
8
Q
Pre-load effects on stroke volume
A
- based on length-tension relationship –>
- stimulating contraction at low lengths (i.e. when heart chamber is empty) generates less tension when stimulated at increased muscle lengths (i.e. when heart chambers are full)
9
Q
Afterload effects on stroke volume
A
- related to aortic (systemic) pressure
- pressure ventricles need to generate to eject blood from chamber
- inverse relationship between shortening velocity and afterload
10
Q
Contractility definition/effects on stroke volume
A
- force w/which heart contracts
- regulated by norepinerphine
- “ionotropes” (positive or negative) change contractility
11
Q
Frank-Starling Law
A
- stroke volume of heart increases in response to an increase in the volume of blood filling the heart (=end diastolic volume)
- i.e. increase in pre-load = increase in stroke volume
12
Q
Factors that may contribute to Starlings Law
A
- Cardiac titin isoform is very stiff
- Ca2+-sensitivity of myofilaments increases as sarcomeres are stretched
- closer lattice spacing: stretched sarcomeres have altered spacing between actin and myosin
13
Q
Hypertrophy impact on cardiac muscle
A
- cell growth:
i. concentric
ii. upregulation of fetal gene program - changes in contractility (mainly calcium sensitivity)
14
Q
Dilation impact on cardiac muscle
A
- cell growth:
i. eccentric
ii. upregulation of fetal gene program - changes in contractility: changes in force output (maximal)
15
Q
Mechanism of changes in contractility
A
- translational changes:
i. sarcomeric proteins (upregulation of fetal proteins)
ii. changes in signaling proteins - post-translational changes of sarcomeric proteins