L12 - Blood as transport system Flashcards

1
Q

What are the main components of blood?

A
  • Plasma:
  • Plasma proteins: albumins, globulins + fibrinogen
  • Serum
  • Blood cells:
  • Erythrocytes (RBC)
  • Leucocytes (WBC)
  • Platelets
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2
Q

What is Haematopoiesis?

A

The formation of blood cellular components

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3
Q

What is plasma?

A
  • Makes up 55% of normal blood by volume
  • Water is 90% of plasma by volume
  • Many different solutes in plasma - dissolved organic + inorganic substances
  • It is the intravascular part of extracellular fluid.
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4
Q

What are the components of plasma?

A
  • Albumin => pH buffer + osmotic pressure
  • Globulins => binding proteins + antibodies
  • Fibrinogen + prothrombin => clotting proteins
  • Other proteins => enzymes, hormones, etc.
  • Nutrients => glucose, fatty acids, amino acids, cholesterol, vitamins
  • Electrolytes - Na+, K+, Ca2+, Mg2+, Cl-, phosphate, sulphate, bicarbonate, etc.
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5
Q

What are erythrocytes?

A
  • AKA red blood cells (RBC)
  • Function => O2 + CO2 transport
  • Shape => biconcave disk with flexible membrane – large surface area for diffusion of gases
  • No: nucleus, DNA, RNA, mitochondria, other organelles — no cell division of mature RBCs, hence short life span of 120 days
  • Contains enzymes => Haemoglobin , Glycolytic enzymes + carbonic anhydrase (CO2 conversion)
  • Produced in red bone marrow - process called Erythropoiesis - then filtered by spleen + liver
  • Hormone erythropoietin (from kidneys) triggers differentiation of stem cells to erythrocytes.
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6
Q

What is haemoglobin (Hb)?

A
  • Iron-containing oxygen-transport protein present in erythrocytes
  • Oxyhaemoglobin = O2 bound to iron
  • Deoxyhaemoglobin = no O2 bound to iron
  • Carbaminohaemoglobin = CO bound to polypeptide chain (not iron)
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7
Q

What is the oxygen-haemoglobin Bohr Effect?

A

The Bohr effect describes haemoglobin’s lower affinity for oxygen secondary to increases in the partial pressure of carbon dioxide and/or decreased blood pH.

This lower affinity, in turn, enhances the unloading of oxygen into tissues to meet the oxygen demand of the tissue.

  • CO2/H+ are affecting the affinity of Hb for O2
  • Dissociation curve = effects of pH described
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8
Q

What is the oxygen-haemoglobin Haldane Effect?

A

Oxygenation of blood in the lungs displaces carbon dioxide from haemoglobin, increasing the removal of carbon dioxide. Consequently, oxygenated blood has a reduced affinity for carbon dioxide.

  • O2 is affecting the affinity for Hb for CO2/H+
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9
Q

What are the requirements for erythrocyte production?

A
  • Iron
  • Folic acid
  • Vitamin B12
  • Deficiencies of any = a type of anaemia
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10
Q

What are the 3 of the main erythrocyte disorders?

A
  • Haemorrhagic anaemia => loss of blood from bleeding (wound, ulcers, etc)
  • Haemolytic anaemia => erythrocytes rupture (haemoglobin/transfusion problems, infection)
  • Aplastic anaemia => red marrow problems (cancer treatment, marrow disease, etc)
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11
Q

What are the anaemias that is caused by decrease in haemoglobin?

A
  • Iron-deficiency anaemia => low iron levels (diet; absorption, bleeding, etc)
  • Pernicious anaemia => low Vitamin B12 (diet; low in intrinsic factor for vitamin B12 absorption)
  • Megaloblastic anaemia => low folic acid levels or low vitamin B12
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12
Q

Morphological classification of anaemia

A
  • Microcytic (Hypochromic) anaemia:
  • low MCV + MCH (chronic)
  • cause – low iron levels

*Macrocytic (Hyperchromic) anaemia:
- aka Megablastic anaemia
- high MCV + MCH
- cause – low B12 or low folic acid

MCV = mean cell volume
MCH = mean cell height

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13
Q

How are the erythrocytes filtered and destroyed?

A
  • Spleen - filters + removes old erythrocytes
  • Liver - metabolises by-products from the breakdown of erythrocytes
  • Iron - recycled for new Hb
    - transported in blood bound to transferrin to red bone marrow (site of Hb production)
    - stored bound to ferritin in liver, spleen + small intestines (until needed for new Hb)
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14
Q

How does the spleen filter + destroy old erythrocytes?

A
  • Macrophages - filter blood by phagocytosis of old fragile RBCs — mechanisms or recognition (T-antigen exposure)
  • Hb is catabolised — iron removed + haeme converted to bilirubin
  • Bilirubin - in blood, travels to liver for further metabolism — products secreted in bile (part of GI)
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15
Q

What are leukocytes (white blood cells)?

A
  • Classified as granulocytes and agranulocytes based on the presence and absence of microscopic granules in their cytoplasm when stained with Giemsa or Leishman stains
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16
Q

What are neutrophils?

A
  • Type of granulocytes
  • Destroy/ingest (causes lysis) – bacteria + fungi
  • How? - antibiotic-like proteins (granules)
  • Polymorphonuclear - many-lobed nuclei
  • Most numerous WBC
17
Q

What are eosinophils?

A
  • Type of granulocytes
  • Phagocytosis — antigens + antigen/antibody complex
  • Contains granules of digestive enzymes
  • Two-lobed, purplish nucleus
  • Only 1-4% of all WBC
18
Q

What are basophils?

A
  • Type of granulocytes
  • Defend your body against:
    Allergens.
    Bacterial, fungal and viral infections (pathogens).
    Blood clotting.
    Parasites.
  • Contains basophilic (blue) granules with histamine
  • Deep purple U or S shaped nucleus
  • Rarest of all WBC (0.5%)
19
Q

What are the different types of Agranulocytes?

A
  • T lymphocytes => (in thymus) respond against virus infected cells + tumour cells
  • B lymphocytes => (in bone) differentiate into different “plasma cells” which each produce antibodies against different antigens
  • Monocytes => differentiate to become macrophages (largest of all WBC - 18 microns)