Lecture 6: Cardiomyocyte Growth Physiology Flashcards

1
Q

When does calcium peak?

A

Starts before contraction and peaks before cell shortens

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2
Q

What receptor activates the Na/H exchanger and what does this cause?

A

Alpha 1, makes cell more alkaline - increased contraction

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3
Q

What do AT1/AT2 promote?

A

Rapid contractile response, fibroblast collagen production, repair, growth, fibrosis

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4
Q

What does Mas downregualte?

A

Fibrosis, BP, hypertrophy

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5
Q

What effect does beta 1 have on calcium?

A

Increase calcium entry

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6
Q

What effect does alpha 1 have on calcium?

A

Increase calcium sensitivity

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7
Q

What effect do Ang II and ET-1 have on calcium?

A

Increase sensitivity and entry

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8
Q

What are levels of Ang II related to?

A

Heart mass - thicker walls and larger individual muscle cells

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9
Q

What activates AT1 and AT2?

A

Ang II

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10
Q

What activates Mas?

A

Ang I-VII

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11
Q

What do oncogenes do?

A

Initiate growth response

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12
Q

When is AT2 most abundant and what is it important for?

A

Pre and neonatally - important for remodelling of the heart

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13
Q

What do AT1 receptors signal?

A

Miocene growth postnatally

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14
Q

What do AT1 & AT2 mediate?

A

Apoptosis

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15
Q

What is a whole heart replacement/abicor?

A

Whole heart inserted and major vessels reattached - operates at 5-9k revs /min as opposed to 60 revs /min by a normal heart.

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16
Q

What was the problem with whole heart replacement?

A

Patients couldn’t feel a heart beat, hard to get interface between existing and artificial vessels - lots of clot formation

17
Q

What are the features of the 1st gen VADs?

A

Pulsatile pumps, many moving parts, large

18
Q

What are the features of the 2nd gen VADs?

A

Continuous flow, small, need anticoagulation, only for patients with severe at rest symptoms who do not respond to therapy within 60 days

19
Q

What are the advantages of 2nd gen VADs?

A

Only one moving part, no wearing surfaces, reliable, 7-10L blood/min, small

20
Q

What are the disadvantages of 2nd gen VADs?

A

Infection risks with percutaneous leads to external battery, device malfunction, patient cannot be removed from battery at any time, weak or no pulse

21
Q

What are the risks of mechanical heart devices?

A

Thrombus, heparin coating, endothelial tissue growth of blood contacting surfaces, not economically viable

22
Q

When are mechanical device used?

A

As a bridge to transplant or as a last resort if transplant is not possible

23
Q

What happens when there is a sustained increased cardiac workload?

A

Alkalinity maintained, calcium levels increased, oncogenes activated, structural and functional adaptation of the heart