Chronic Cardiac Adaptation Flashcards

1
Q

Cardiac dilation

A

Myocyte length increase&raquo_space; myocyte width increase
Extensive fibrosis
Myocyte death
Advanced cardiac dysfunction

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2
Q

Pathological hypertrophy

A

Myocyte length increase < myocyte width increase
Fibrosis
Maybe cardiac dysfunction

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3
Q

Physiologic hypertrophy

A

Myocyte length increase > myocyte width increase
No fibrosis
No cardiac dysfunction

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4
Q

What types of MHC exist? What do they form and how do they differ?

A
There are alpha and beta isoforms
Form heterodimers (aa, ab, and bb) 
Have distinct ATPase activity (and some other functional properties)
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5
Q

Biochemical property of pathological hypertrophy

A

Decrease in ATPase and increase in bb MHC

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6
Q

Biochemical property of physiological hypertrophy

A

Increase in ATPase activity and aa MHC

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7
Q

The heart has not only _____ plasticity but also _____ plasticity

A

phenotypic, genetic

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8
Q

The functional adaptations of the heart are generally ____ but can result in ventricular dysfunction over time

A

adaptive

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9
Q

LVH –> CHF phenotype

A

Heart becomes more stiff, concentrically hypertrophied = pathologic hypertrophy

LVH:
At same EDV, less CO because heart is ejecting against increased afterload

CHF:
As heart fails, PV curve shifts right (dilated cardiomyopathy)

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10
Q

Cellular mechanisms of LVH

A
  1. Increase in Ca current via L-type Ca channel
  2. Reduced SR pump fxn via increased PLB/SERCA2 ratio
  3. Impaired myofilament relaxation
  4. Altered (increased) cytosolic calcium and new steady-state
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11
Q

____ gene transfer is sufficient to correct mechanical defects in cadiocytes from animals with HF

A

SERCA2

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12
Q

Calcineurin & NFAT to demonstrate that genes really can lead to LVH or other remodeling

A

Calcineurin dephospho NFAT
NFAT translocates into nucleus & influences gene transcrption ofcardiac growth and remodeling genes = some master regulatory switches.

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13
Q

Explain the animal testing of LV function following an acute insult

A

Give animal heart attack
EF drops, heart function fails…
Over time things got worse despite attempts to use P4H

Why? Series of positive feedback loops. If you don’t do something to interrupt them, you will see progressive decline in cardiac fxn. Current therapy is trying to interrupt.

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