Blood Flashcards

1
Q

whats the ph of blood?

A

7.35-7.45

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2
Q

what percent of bodyweight does blood make up?

A

about 8%

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3
Q

what is blood composed of?

A

55% plasma
45% cells and cell fragments

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4
Q

what is blood plasma composed of?

A

water 91.5%
proteins 7%
other solutes 1.5%

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5
Q

what proteins are contained in blood plasma? what do they each do? where are they produced?

A

albumins - osmotic balance by binding to lipophilic molecules
globulins - alpha and beta transport chemicals like iron and contribute to blood clotting, produced by liver and then gamma
fibrinogen
other proteins

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6
Q

give examples of other solutes found in blood plasma

A

-ions such as Na+ and Ca2+
-nutrients like glucose and amino acids
-waste produces like urea
-dissolved gasses like o2
-hormones

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7
Q

how is the the blood pH chemically balanced, give the chemical equations

A

check optom useful screenshots folder

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8
Q

Give some functions of blood plasma

A

-regulation of body temp
-regulation of cells water content
-blood clotting via fibrinogen

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9
Q

give examples of how proteins in the blood aid in transport of small molecules

A

-alpha and beta globulins by providing clotting factors
-gamma globulins which are immunoglobulins produced by lymphocytes

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10
Q

What cells/ cell fragments are in the blood and say their main function

A

-erythrocytes (red blood cells) - transport o2 to cells and remove c02
-leucocytes (white blood cells) - immunity, allergic reactions and phagocytosis
-thrombocytes (thrombocytes) - blood clotting

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11
Q

What is hematopoeisis?

A

The production of erythrocytes, leucocytes and platelets via stem cell division

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12
Q

give 3 features of erythrocytes

A

-bioconcave disks
-lack a nucleus and mitochondria
-carry o2 and co2 associated with haemoglobin

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13
Q

what is erythropoietic protoporphyria?

A

a disease caused by a lack of iron bound to the haem group of haemoglobin

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14
Q

give four features of leucocytes

A
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15
Q

what are the 5 different types of leucocytes and are they granular or agranular

A

agranular - lymphocytes and monocytes

granular- neutrophils ( account for most of the leucocytes), basophils and eosinophils

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16
Q

what do neutrophils do?

A

Respond to first bacterial invasion, phagocytic and so release lysozyme, important un controlling inflammation

17
Q

what do basophils do?

A

Synthesise, store the vasodilator histamine and the anticoagulant heparin. Librate histamine, heparin and serotonin un allergic reactions that intensify the overall inflammatory response

18
Q

what do eosinophils do?

A

-counteract the affects of histamine in allergic reactions
-phagocytise antigen-antibody complexes
-help break down blood clots and destroy certain parasitic worms

19
Q

what do monocytes do?

A

-Release white blood cell growth factors causing population increase in white blood cells
-become macrophages and so phagocytose microbes, antigen-antibody complexes

20
Q

what do lymphocytes do?

A

Provide an immune response through:
-b cells
-T cells: helper T cells and cytotoxic T cells
-natural killer cells

21
Q

give 4 characteristics of leucocytes

A

-do chemotaxis
-amoeboid movements by forming temporary projections in order to move
-capability of diapedesis
-phagocytic

22
Q

give the features of thrombocytes

A

-formed from cell fragmentation
-have no nucleus
-involved with clotting
-functional for 7-10 days before being removed by macrophages in the liver and spleen
-make up 55% of the blood

23
Q

how do thrombocytes regulate homeostasis? Use the example of prevention of blood loss from a broken vessel

A

-vascular spasm: reduces blood flow by causing vasoconstriction of the injured vessel
-formation of a platelet plug where platelets aggregate at the point of vessel rupture

24
Q

how do thrombocytes carry out coagulation?

A
  1. Platelet adhesion
  2. Platelet releases ADP and thromboxane
  3. Platelet aggregation triggered
25
Q

give examples of bleeding disorders

A

-haemophillia: blood clotting ability is severely reduced, caused by genetic defect
-thrombocytopenia abnormally low platelet count, many have idiopathic thrombocytopenia while in others it’s an autoimmune disease

26
Q

Give three fibrinogen disorders

A

-afibrinogenemia: lack of
-hypofibrinogenemia: reduced levels
-dysfibrinogenemia: dysfunctional

27
Q

give examples of inapporpriate blood clotting and what can this cause

A

-thrombus: clot formed in an intact vessel possibly due to atherosclerosis, slow moving blood and formation of small fibrin quantities that accumulate
-embolus: a moving clot

These cause risk of stroke, heart attack and pulmonary embolism

28
Q

what is clot retraction?

A

Where as the wound heals, the contraction of platelets trapped within the clot shrinks fibrin meshwork pulling the edges of damaged vessels closer together - dissolution

29
Q

give the pathway of fibrinolysis

A

-plasminogen binds to fibrinogen and fibrin and is incorporated into a clot as it’s formed
-plasminogen is activated by tissue plasminogen activator (tPA) and urokinase to become the protease plasmin
-plasmin then breaks down the fibrin mesh work and phagocytic leucocytes remove the products if the clot dissolution

30
Q

What is haemoglobin made of?

A

A quaternary protein molecule made of 4 polypeptides (two of which are alpha polypeptides and 2 are beta polypeptides) where each one is associated with a haem group which contains an Fe2+ ion.

31
Q

Where do oxygen molecules mind on a heamoglobin?

A

The bind to the Fe2+ of each polypeptide so each haemoglobin molecule can carry for O2 molecules

32
Q

Give examples of types of people that have increased risk of elevated plasma fibrinogen levels.

A

-pregnancy
-menopause
-coronary artery disease
-diabetes
-hypertension
-smoking

33
Q

what cells circulating in the blood can go through unruptured blood vessels into tissues?

A

neutrophils

34
Q

how many leucocytes are normally present in the average mm of human blood?

A

5-10 million

35
Q

what is the role of tissue plasminogen activator in fibrinolysis?

A

-it activates plasminogen
-it activates a protease which breaks down the fibrin in the clot