Components and function of the blood (Theme 2) Flashcards

1
Q

Methods of transporting CO2 in the blood.

A

Most of it is in bicarbonate form, 68%.

22% as carbaminohaemoglobin

10% dissolved in plasma (more soluble that O2)

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2
Q

Fetal haemoglobin (HbF)

A

HbF contains 2 alpha and 2 gamma units.

HbF has a very low affinity to 2,3-DPG, this maintains the T state, retaining for oxygen.

HbF has a much higher affinity to O2 than adult haemoglobin (HbA)

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3
Q

Oxygen transport in the blood

A

Oxygen is poorly soluble in plasma: only 0.003ml of O2 is present per 100ml of plasma/ mm Hg.

Most of O2 is carried in haemoglobin (Hb): 1.39ml of O2 is carried by Hb/ g of blood.

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4
Q

Haemoglobin

A

Quaternary protein that is the primary mode of transport for O2 in the blood. Makes up 95% of RBC dry weight.

Structure:
4 polypeptide chains- 2 alpha, 2 beta.
One Fe2+ in the haem group, the group gives it colour.

Mechanism with O2:
Each unit carries one O2 molecule. Binding of one O2 causes confirmation change= cooperativity of other units.

Release of one O2 molecule from one unit also triggers the release from other units.

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5
Q

Average amount of Hb in adults.

A

In males: 13-17 g/dL

In females: 12-16 g/dL

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6
Q

Myoglobin

A

Oxygen storage in muscles.

Only has one polypeptide change so does not undergo cooperativity.

Has higher affinity to O2 than HbA but lower than HbF.

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7
Q

Respiratory control of O2 in the blood.

A

Respiratory control is either triggered by fall in O2 lower than 88% or a rise in H+ in the cerebrospinal fluid (CSF)
O2 below 90% is clinically significant so CSF control is more mandatory.

CO2 reacts with water in the CSF, producing H+. This is picked up in medullary receptors.

H+ in the blood is only picked up by chemoreceptors in the aortic and carotid bodies.

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8
Q

Erythrocytes

A

Red blood cells produced via erythropoiesis (branch from haemopoiesis).

Cells is biconcave and anucleate.

Life span- mature RBC last 120 days.

Contain Hb which is the primary transport of O2 in the blood.

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9
Q

Average hematocrit in adults

A

Haematocrit- the ratio of volume RBCs to total blood volume

Males: 40-52%

Females: 36- 48%

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10
Q

Mean corpuscular volume

A

Volume of red blood cells

80-100 fL (femtolitre)

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11
Q

Erythropoiesis

A

The development of red blood cells.

During embryogenesis: occurs in the liver, spleen, lymph nodes and yolk sac.
After birth occurs in the bone marrow.
After 20 years, occurs in membranous bones.

Development from stem cells-
1. Derive from hematopoietic MULTIPOTENT stem cells.

  1. Become multipotent myeloid progenitor cells.
  2. Cell becomes committed and undergoes maturity into erythrocytes under terminal differentiation.
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12
Q

General development of mature cells from stem cells.

A
  1. Derived from MULTIPOTENT stem cells
  2. Become multipotent progenitor cells.
  3. Undergo commitment and become lineage-committed progenitor cells.
  4. Proliferates then undergoes terminal differentiation to form mature cells.
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13
Q

Erythropoietin

A

Cytokine made in the kidneys used especially in the early haematopoietic stages, in the bone marrow .

Used as a drug to combat anaemia in the forms: Epogen/Procrit, Aranesp.

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14
Q

Methemoglobinemia

A

Anaemia where O2 cannot sufficiently bind to Hb due to Fe2+ in the haem group (ferrous), being oxidised to Fe3+ (ferric).

Causes:
Hereditary decrease of NADH (reducing agent)
Congenital mutation of Hb
Toxic substances

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15
Q

CO poisoning

A

CO has affinity to Hb 250x stronger than O2.

Low levels of CO displaces O2, as it prevents O2 from binding.
Symptoms:
Dizziness, nausea, headaches.

Treatment: 95 % O2 (compared to usual 21%) and 5 % CO2.

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16
Q

Reticulocytes

A

Immature RBCs, precursor of erythrocytes.

Life span= 2 days.

Reticulocyte indications: bone marrow activity
Low count= Erythropoiesis is low,
High count= haemolytic anaemia (erythrocytes are dying so bone marrow compensates by making more reticulocytes).

17
Q

Polycythaemia

A

Blood is very viscous due to very high RBC count.

This can clog vessels and cause stroke/ ischaemia.

Physiological polycythaemia:
Increase in RBCs due to living in higher altitudes. Homeostatic response to low O2 levels.
Endurance athletes train at higher altitudes to increase RBCs, increasing O2 carrying capacity.

Polycythemia vera:
Blood cancer that causes bone marrow to produce too many RBCs.
Likelihood of developing increases with age.
Treatment: venesection (phlebotomy), essential controlled blood letting, with a needle.

18
Q

Pernicious anaemia

A

Malabsorption of vitamin B12 due to loss of intrinsic factor from gastric parietal cells.

Intrinsic factor is vital for the absorption of vit B12 in the gut.

19
Q

Megaloblastic anaemia

A

Bone marrow produces megaloblast, large immature red blood cells.

Can occur as a result of B12 or folic acid deficiency

20
Q

Microcytic hypochromic anaemia

A

Anaemia, presented as very small RBCs. Mean corpuscular volume is <80 fL.

Cause: iron deficiency, unable to make haem group, causing it to be ‘hypochromic’

21
Q

Vitamin B12

A

Vitamin that forms thymidine, essential for the synthesis of DNA.

Essential in RBCs, skin and gametogenesis.

Deficiency can cause anaemia, like pernicious anaemia.
Deficiency risk factors:
Old Age
Veganism
Lymphoma
Haemolytic anaemia
Pregnancy
22
Q

Folic acid

A

Folic acid is a B vitamin essential for the body to make DNA, RNA, and metabolise amino acids for cell division.

Can only be obtained from diet/ supplement.

Deficiency can cause anemia, such as megaloblastic anaemia.

23
Q

Role of iron in red blood cells.

A

65% of iron is stored in RBCs, in haem.

30% are in intracellular storage:
Ferritin
Hemosiderin

Storage in the reticuloendothelial system:
Liver, spleen, RBC, bone marrow, macrophages, monocytes

Iron deficiency can lead to anaemia- like microcytic hypochromic anaemia

24
Q

Mean cell haemoglobin (MCH)

A

The average amount of Hb in each red blood cell.

Average = 27-34 pcg