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
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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
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3
Q

Regulation of calcium flow w/in muscle cells

A
  1. depolarization –> L-type channels open –> calcium influx
  2. calcium influx –> calcium release from SR via ryanodine receptors (CICR)
  3. calcium binding to TN-C triggers contraction
  4. calcium removed by SR Ca2+-ATPase
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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
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5
Q

Cardiac output=

A

Stroke volume x heart rate

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6
Q

Regulators of stroke volume

A
  • pre-load
  • afterload
  • contractility
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7
Q

Molecular mechanism of length-tension relationship

A

xxx

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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)
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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
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10
Q

Contractility definition/effects on stroke volume

A
  • force w/which heart contracts
  • regulated by norepinerphine
  • “ionotropes” (positive or negative) change contractility
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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
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12
Q

Factors that may contribute to Starlings Law

A
  1. Cardiac titin isoform is very stiff
  2. Ca2+-sensitivity of myofilaments increases as sarcomeres are stretched
  3. closer lattice spacing: stretched sarcomeres have altered spacing between actin and myosin
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13
Q

Hypertrophy impact on cardiac muscle

A
  1. cell growth:
    i. concentric
    ii. upregulation of fetal gene program
  2. changes in contractility (mainly calcium sensitivity)
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14
Q

Dilation impact on cardiac muscle

A
  1. cell growth:
    i. eccentric
    ii. upregulation of fetal gene program
  2. changes in contractility: changes in force output (maximal)
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15
Q

Mechanism of changes in contractility

A
  1. translational changes:
    i. sarcomeric proteins (upregulation of fetal proteins)
    ii. changes in signaling proteins
  2. post-translational changes of sarcomeric proteins
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