1-Striated Muscle Cardiac Flashcards

1
Q

development sequence

A
  1. pluripotent stem cells
  2. mesoderm/mesenchymal cells
  3. myogenic progenitor cells
  4. cardiomyocyte via transcription factors and epigenetic regulation
  5. embryonic cardiomyocytes
  6. fetal cardiomyocytes
  7. neonatal
  8. adult
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2
Q

cardiac muscle cell

characteristics

A
  • aggregate but not fuse like skeletal cells but still repeating format
    -smaller than skeletal
    -branched
    -one or two nuclei
    adjacents are connected by intercalated discs
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3
Q

intercalated disc components

A

desmosomes + fascia adherens

gap junctions facilitate spread of ions so coordinated contraction (syncytium)

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4
Q

layers of CT

A
  1. basement membrane
  2. endomysium
  3. perimysium
  4. epimysium
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5
Q

sarcomeric structure

A
  1. bounded by z discs/lines
  2. thick myosin filaments interact with thin actin
  3. titin span 1/2 sarcomere from M to Z line
  4. costameres @ z discs link cytoskeleton to basal lamina

same as skeletal

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6
Q

causes of heart failure

A

-highest percentage is from dilated cardiomyopathy aka muscle pathology

from familial mutations of cardiac genes for dystrophin, actin, myosin, desmosomal proteins, titin

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7
Q

remodeling in heart disease

A

long term mechanical stress from high arterial pressure or ischemic =
-inc size of myocytes
-activation of myofibroblasts to inc secretion of ECM to promote fibrosis
-change mechanical properties of heart

aka heart becomes fibrotic and hypertrophic

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8
Q

renin-angiotensin system

A

another way to inc ECM and become fibrotic

from chronic activation of innate mechanisms /endogenous hormonal signaling

activation = inc angiotensin II > TGF beta and CT growth factor pathways activate > fibroblast differentiate to myofibros and inc deposition of ECM

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9
Q

action potential transmission

A

og @ SA node then propogate to cardiac muscle cells rapidly via gap junctions

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10
Q

neurotransmission

calcium induced calcium release

A
  1. T tubules transmit AP from suface of cardiac muscle cell
  2. depolarization = open voltage gated calcium channels, L type
  3. influx of extracellular Ca into cell
  4. Ca binds ryanodine receptor RYR on membrane of SR
  5. conformational change in RYR so release Ca from inside SR
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11
Q

Calcium in SR

A

bound by calsequestrin @ region adj to RYR by junctin and triadin proteins

come back by pumps (SERCA, Na/Ca exchanger)

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12
Q

modulating force

A

inc force = inc length of muscle prior to contraction

either by inc Ca sensitivity or titin helps inc muscle tension

helps inc amount of blood pumping

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13
Q

catecholamines

A

aka epinephrine or norepinephrine = inc calcium release and force production

bind to beta-adrenorecptors > adenylate cyclase > inc cAMP > activate PKA > phosphorylate LTCC and RYR to enhance CICR

or PKA can relax muscle by phos proteins that reg calcium reuptake

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14
Q

muscarinic agonists

A

aka acetylcholine have oppo effect of catecholamines

Gi mechanism so inhibits adenylate cyclase and dec phos of phospholamban, troponin I, RYR, voltage gate calcium channels

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15
Q

metabolic characteristics

A

ATP from oxidation of fatty acids (beta) and TCA cycle/oxidative phosphorylation

majority of acetyl CoA from beta oxidation and rest from lactate/pyruvate oxidation

creatine phosphate important for actin-myosin interactions bc rapidly regenerates ATP from ADP

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