Ischaemia and Infarction Flashcards

1
Q

Ischaemia is

A

inadequate local blood supply to a tissue.

-Causes hypoxia and reduced transfer of metabolic substances (eg glucose and catabolites)

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2
Q

Hypoxia is

A

deficiency of O2 which causes cell injury

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3
Q

ANoxia is

A

COmplete lack of O2

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4
Q

Infarction. Results from?

A

necrosis of a tissue due to ischaemia.

thrombosis/embolism, spasm, extrinsic compression of vessel

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5
Q

Possible causes of Ischaemia

A

Ext/int occlusion of vessels (bed sores or atherosclerosis)

Spasm of vessel
capillary block (sickle cell anaemia)
shock (low arterial BP)
Increased Demand (inc tissue mass, workload)
venous obstruction
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6
Q

Sensitivity of different cell types to Ischaemia from least to most

A
Fibroblasts & macrophages
Skeletal muscle
Myocardium
Renal proximal tubular epithelium
Neurons
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7
Q

Neutrophils sensitivity to ischaemia?

A

Right OFF the scale, and actually do better with ischaemia!!
Their resistance to apoptosis and necrosis is enhance by hypoxia!
A number of genes are turned on at the transcriptional level, which turn on many enzymes required for survival.

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8
Q

Main Transcription factor turned on by hypoxic neutrophils?

A

HIF which leads to survival.

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9
Q

Why is is the Neutrophils are enhanced in hypoxic environments?

A

The role of neutrophils is often required in hostile, damaged environments, therefore it makes sense that their survival is enhanced.

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10
Q

Effect of ischaemia on cells, If not severe or of long enough duration

A

still changes cell biology.

Reduced ATP availability (all energy mechanisms crippled).

More activation of signalling cascades> protect and repair

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11
Q

How does ischaemia cause lowered ATP?

A

Increased anaerobic glycolysis
low glycogen
lower pH
nuclear chromatin clumping

Decr Na+ pumps
influx of calcium, water and Na+
ER swelling, cell Swelling, loss of micro villi.

Protein breakdown

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12
Q

Do ischaemic cells usually die by apoptosis or necrosis?

A

Necrosis, due to the lowered ATP levels there’s not enough energy to allow the process of apoptosis to occur

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13
Q

Levels of ischaemic effect?

A
No effect
Functional defects (due to sub-optimal tissue perfusion)
Adaptation, atrophy and shut down
Apoptosis 
Infarction/necrosis

A LARGE RANGE, functional parenchyma more at risk

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14
Q

Other factors that influence the outcome for tissues of vessel occlusion

A

Anatomy, size of occlusion, speed of onset, repurfusion, metabolic demands, adequency

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15
Q

Red (haemorrhagic) infarcts may occur in?

A
  • tissue with dual blood supply (lung)
  • Tissues where blood flow is re-established after arterial occlusion

(pumping blood into dead tissue)

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16
Q

White (anaemic) infarcts occur in

A

-solid tissues supplied by a single artery, often wedge shaped.
(bc usually artery supplies wedge tissue)

17
Q

Coagulative necrosis

A

usual pattern after infarction in solid organs

18
Q

how to get ischaemia in ARTERY

A

1) artherosclerosis (turbulence and EC injury)
2) Vulnerable plaque gets damaged
3) thrombosis
4) Downstream ischaemia and infarction
5) repurfusion

19
Q

how to get ischaemia in VEIN

A

1) Venous stasis, EC injury and systemic factors
2) deep vein thrombosis forms
3) embolisation
4) distant ischaemia and infarction

20
Q

Ischaemia effect if coronary arteries were occluded

A

Angina
Chronic ischaemic heart disease with heart failure
MI > transmural or subendocardial infarction
Cerebral ischaemic injury

21
Q

Timing of a typical infarction

A

1) 24hr acute inflammation develops from viable margins
2) 1-3 days, macrophages and lymphocytes appear
3) Fibroblasts and endothelial cells then recruited > granulation tissue “organisation”
4) 6-8wks infarct organised > fibrous scar

** some tissues (liver) may attempt regeneration

22
Q

How to treat infarcts

A

Thrombolitic agents

Mechanical re-expansion

have to be done quickly before irreversible molecular events

23
Q

Complications of MI

A

mural thrombus (in heart)
Dysrhythmias
heart failure
Repurfusion injury

24
Q

Repurfusion injury

A

Short period ischaemia then repurfused : back to normal

Long period ischaemia then repurfused : additional damage due to accumulation of ROS in cells producing oxidative stress

25
Q

How exactly due free radicals damage cells in repurfusion

A
  • attack double bonds
  • oxidise sude chains > enzyme damage
  • DNA damage

autocatalytic chain of damage