Session 4: Phagocytosis, Complement, Oedema Flashcards

1
Q

What happens to a microbe following adherence to a phagocyte?

A

The microbe is ingested into a phagosome (phagocytic vesicle) which fuses with a lysosome to form a phagolysosome.
The microbe is ingested by enzymes within the lysosome.
Indigested material is discharged from the phagocyte.

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2
Q

Complement consists of a group of serum proteins that activates what?

A
  • Inflammation
  • Destruction of cells
  • Opsonisation
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3
Q

Are the enzyme precursors normally active?

A

No, they are normally active

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4
Q

Enzyme precursors are activated mainly by which pathway?

A

The “classic pathway”

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5
Q

What is the “class pathway” activated by?

A

Antigen-antibody reaction

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6
Q

The “classic pathway” is the C1 or the C3b pathway?

A

C1

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7
Q

The “C3b” pathway is known as the what?

What is it activated by?

A

The alternative pathway

Activated by reaction with antigens such as bacterial cell wall

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8
Q

True or false: Both the classic and alternative pathways follow the same sequence after C3

A

True

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9
Q

What happens following activation of C3?

A
  • Inflammation
  • Opsonisation
  • Membrane attack complexes causes cell lysis
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10
Q

What is oedema?

A

Accumulation of an excessive amount of watery fluid in cells, tissues or serous cavities

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11
Q

What is lymphoedema?

A

Swelling (especially in subcutaneous tissues) as a result of obstruction of lymphatic vessels or lymph nodes and the accumulation of large amounts of lymph in the affected region

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12
Q

Is lymphoedema pitting or non-pitting?

A

It is initially pitting, but non-pitting after initial stages

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13
Q

Why does lymphoedema become non-pitting?

A

The fluid cannot move into tissues when pressed as it becomes segregated off by fibroblasts into compartments

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14
Q

Is ferrous oxide (FeO) red or brown?

A

Red

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15
Q

Is Ferric Oxide (Fe203) red or brown?

A

Brown

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16
Q

During phagocytosis, macrophages oxidise _____________________ to ______________________

A

Ferrous oxide

Ferric oxide

17
Q

Is Capillary Hydrostatic Pressure (CHP) highest at the arteriole or venous end?

A

Arteriole end

18
Q

Is Capillary Oncotic Pressure (COP) highest at the arteriole or the venous end?

A

Venous end

19
Q

Does high hydrostatic pressure cause fluid to leave or to enter the capillary?

A

To leave to capillary and move into interstitial fluid

20
Q

Does high oncotic pressure cause fluid to leave or to enter the capillaries?

A

To enter the capillary from the interstitial fluid

21
Q

Midcapillary, is the net movement of fluid in or out of the capillary? Why?n

A

There is no net movement midcapillary, as the hydrostatic pressure=the oncotic pressure

22
Q

What, in terms of fluid movement, is the result of the differences in hydrostatic and oncotic pressure at the arteriole end, the middle of the capillary and the venous end?

A

The arteriole end: filtration out of the capillary
Midcapillary: No net movement
The venous end: Reabsorption of fluid into the capillary

23
Q

What is normal arteriolar capillary hydrostatic pressure?

A

35mmHg

24
Q

What is the normal venular capillary hydrostatic pressure?

A

15mmHg

25
Q

Normal blood colloid oncotic pressure is what?

A

25mmHg

26
Q

Hypoproteinemia (low blood protein) leads to what in terms of oncotic pressure?

A

This leads to lowering of capillary oncotic pressure which causes fluid to leave the capillary and move into interstitial fluid, presenting as oedema

27
Q

At the arteriole end _______, _________ and other nutrients have the greatest concentrations in the blood and so they move ____________ by diffusion.

A

Oxygen
Glucose
Out

28
Q

At the venous end __________ and other waste products have greatest concentrations in ________________ so they move out by ______________.

A

Carbon dioxide
Interstitial fluid
Diffusion