blood Flashcards

1
Q

what are the components of blood?

A

Plasma (55%).

Cells/cell fragments (45%)

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2
Q

Albumins

A

maintain a normal plasma osmotic

pressure (formed in the liver)

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3
Q

Globulins

A

antibodies, transport of hormones

formed in the liver

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4
Q

Inorganic salts ( Fe, Ca) required for:

A

Cell formation
Transmission of nerve impulses
Muscle contraction
Maintenance of blood pH (7.35-7.45)

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5
Q

Hormones Synthesised and secreted into blood by

A

endocrine glands

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6
Q

Nutrients are absorbed into the blood via…

A

the capillary system surrounding the GI tract

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7
Q

what is oxygen carried in combination with

A

haemoglobin

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8
Q

what is Carbon dioxide mostly carried as

A

bicarbonate ions in plasma

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9
Q

what are the waste products of protein metabolism

A

Urea
Uric acid
Creatinine

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10
Q

cells in blood

A

Erythrocytes (red cells)
Leukocytes (white cells)
Thrombocytes

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11
Q

what are Erythrocytes: Red Cells Facilitated by

A

carbonic anhydrase

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12
Q

Erythrocytes: Red Cells STRUCTURE

A

Circular bi-concave discs
• 7 micrometers in diameter
• No nucleus

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13
Q

WHAT IS THE FORMATION OF Erythrocytes: Red Cells CALLED

A

-erythropoiesis

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14
Q

reticulocytes

A

Immature red blood cells

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15
Q

what organ secretes erythropoietin

A

kidneys

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16
Q

haemoglobin(Hb) molecule Consists of …

A

4 polypeptide

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17
Q

what does each polypeptide attach to

A

haeme

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18
Q

how many molecules oxygen can bind to each haeme

19
Q

where are Erythrocytes broken down

A

Spleen
Liver
Bone marrow.

20
Q

Average life of erthrocytes

21
Q

Diseases related to erythrocytes

A
Anaemia
• Iron deficiency
• Megaloblastic
• Hypoplastic
• Haemolytic
• Normocytic
22
Q

Leukocytes –white blood cells

A

Defence against pathogenic organisms

23
Q

Neutrophils

A

phagocytosis of pathogens

24
Q

Basophils

A

secrete histamine, seratonin

25
Eosinophils
parasitic defence and allergy
26
Monocytes
phagocytosis
27
Thrombocytes
Small, non nucleated discs Role in blood clotting life span is 8-11 days
28
Functions of blood
heat regulation transport through the body of molecules and ions defence of the body against infections and other foreign materials. All the WBCs participate in these defences
29
4 processes of Haemostasis
Vasoconstriction Platelet plug formation Coagulation Fibrinolysis
30
Vasoconstriction
``` Platelets come into contact with damaged endothelium of blood vessels Release: • Serotonin • Which causes vasoconstriction Damaged blood vessels release vasoconstrictors themselves e.g. thromboxane ```
31
Platelet Plug Formation
Platelets become sticky and cling to each other Platelets release substances which encourage other platelets to adhere to them
32
Function of platelet plug formation
Forms a temporary seal
33
Coagulation
Transformation of a liquid into a semisolid or | solid mass
34
what initiates coagulation
clotting factors
35
what is fibrinogen (soluble plasma protein) converted into?
fibrin (insoluble)
36
what strengthens a blood clot in coagulation
• Blood cells become entangled in the fibrin | mesh which strengthens the clot further
37
Fibrinolysis
Breakdown of a clot | First stage of healing
38
what is Plasminogen in blood is converted into
plasmin
39
what does plasmin break down
fibrin into soluble products that are removed by phagocytosis
40
Control of Coagulation
``` Smooth endothelium of blood vessels mean platelets do not adhere to it in normal circumstances • Natural anticoagulants in the blood • Thrombin binds to receptors lining blood vessels which inactivate it ```
41
Von Willebrands Disease
``` Decreased Von Willebrands factor • Von Willebrands factor helps platelets aggregate and stabilises factor VIII • Formation of platelet plug affected • Coagulation cascade affected • Same management as haemophilia patients ```
42
Medication affecting coagulation
Aspirin • Warfarin • Heparin • Clopidogrel
43
Aspirin
Inhibits platelet aggregation | • Lasts 7-10 days