Red Blood Cells Flashcards

1
Q

What are RBC’s also known as?

A

Erythrocytes

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2
Q

How are Erythrocytes Produced?

A

via erythropoiesis

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3
Q

Where are Erythrocytes Produced and How?

A

in the bone marrow
- cell size decreases, loses RNA and DNA
- colour change from blue to red
- leaves bone marrow
- nuclei destroyed by macrophages

cell becomes a reticulocyte
after couple days = erthrocyte

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4
Q

Which Hormone Enhances Erythropoiesis?

A

Testosterone

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5
Q

Which Vitamins are Particularly Needed in Erythropoiesis?

A

Vitamin B12+B9

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6
Q

List Features and their Advantages from the Morphology of Erythrocytes. (5)

A
  • haemoglobin - carry oxygen
  • no mitochondria - more volume for Haemoglobin
  • no nucleus - same
  • biconcave shape - surface area and flexibility
  • 2 alpha chains, 2 beta chains, 4 haem groups
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7
Q

How Large are Erythrocytes and Why?

A

7.5micrometers in diameter when capillaries are 8micrometers
- allows more surface area for gaseous exchnage

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8
Q

What is a ‘Porphyrin’?

A

the ring like compound, how erythrocytes are structured
- iron sits in the middle

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9
Q

What are the 3 Types of Haemoglobin?

A

HbA = most common
HbA2 = small amounts
HbF = foetal haemoglobin

when oxygenated = red
when deoxygenated = blue

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10
Q

What is the Life Span of Erythrocytes?

A

100-120 days

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11
Q

What is the name for RBC death?

A

Eryptosis

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12
Q

What Hormone is Released when Erythrocytes are being Destroyed, Why and Where From?

A

Erythropoietin is released from the kidneys

  • in response to hypoxia
  • it stimulates rapid maturation of RBC’s
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13
Q

Describe Eryptosis. (4)

A
  • change on the erythrocyte membrane
  • detected and engulfed by macrophages
  • divided into globin and haem
  • destroyed by macrophages in liver, spleen and bone marrow
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14
Q

What Happens to the Globin during Eryptosis?

A

broken down into it’s amino acids and reused

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15
Q

What Happens to the Haem during Eryptosis and How does it Leave the Body?

A

broken down into Biliverdin, CO2 and Fe by haem oxidase
- Biliverdin appears green in bruises

Biliverdin broken down into Bilirubin
- in the liver
- stored in the gall bladder

Bilirubin released into the intestines
- transformed into urobilinogen by bacteria

some remains as sterocobilin
- excreted in faeces
some sent to kidneys as urobilin
- excreted as urine

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16
Q

Iron is Released from Haem During Eryptosis, what Happens to it?

A

binds to tranferrin
- becomes unreactive
- transported to the liver
- becomes ferritin
- binds to aluminum and stored in the gall bladder
- moves out and recirculated

17
Q

Define Anaemia

A

decrease in a number of red blood cells or less than the normal quantity

18
Q

What are the 3 Main Causes of Anaemia?

A
  • excess blood loss
  • excess RBC destruction
  • deficient RBC production
19
Q

What are the Common Underlying Causes behind Anaemia (5)

A
  • dietary
  • blood loss
  • malabsorption
  • pregnancy
  • parasitosis
20
Q

Give some Signs and Symptoms to Anaemia (8)

A
  • fatigue
  • paleness
  • irritable
  • light headed
  • poor wound healing
  • candida infections
  • glossitis
  • recurring mouth ulcers
21
Q

Define Pernicious Anaemia.

A

RBC count drops as intestines cannot properly absorb vitamin B12

22
Q

What are the Common Causes of Pernicious Anaemia (4)

A
  • autoimmune disease
  • tapeworm
  • diet
  • celiac
23
Q

What are the Symptoms of Pernicious Anaemia? (8)

A
  • tired
  • parasthesia
  • dyspepsia
  • depression
  • weight loss
  • neurological
  • glossitis
  • angular cheilitis
24
Q

How do you Treat Pernicious Anaemia?

A
  • B12 injections
  • oral supplements
25
Q

What is Haemoglobinopathies?

A

a group of recessively inherited genetic conditions affecting the haemoglobin component of blood

26
Q

What is Sickle Cell Anaemia?

A
  • haemoglobin is abnormal
    = red blood cells = hard and sticky
  • look like a C-shape called a “sickle”
27
Q

How does Sickle Cell Anaemia affect Haemoglobin?

A

change in amino acid from Glutamine to Valine on position 6

on the beta chain of chromosome 11

= sickle cell

28
Q

What are the Problems of Sickle Cell Anaemia?

A
  • cause haem molecules to polymerise and clumo
  • cant carry oxygen
29
Q

How is Sickle Cell Anaemia Inherited? How does this Affect Malaria?

A

autosomal recessive

  • if you are a heterozygote, offers protection against malaria as you cant carry infection
30
Q

How is Sickle Cell Anaemia Treated?

A

Hydroxyurea to increase HbF production

31
Q

Difference between Sickle Cell Anaemia and Thallassaemia

A

SCA = qualitative
Th = quantitative

32
Q

What is Thalassaemia and the Two Types?

A

inherited when the body doesn’t make enough haemoglobin

alpha - reduction of alpha unit production
alpha unit = 2 genes, 4 alleles
lose 1 = no problem
lose 2 = mild anaemia
lose 3 = severe anaemia
lose 4 = incompatible with life

beta - reduction of beta unit production
beta unit = 1 gene, 2 alelles
- varying severity

  • when the extra units clump together = abnormal RBC
33
Q

What is Haemolytic Anaemia?

A

when there is more destruction of RBC than production