BIOL 2420 Lecture Notes - Lecture 4: Hereditary Spherocytosis, Fetal Hemoglobin, Bilirubin

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Unit 3 Lecture 4
RBCs Live About 4 Months
- red blood cells live for about 120 +/- 20 days
- increasing fragile older red blood cells may rupture as they try to squeeze through narrow
capillaries
o they also could be ingested by scavenging macrophages as they pass through the spleen
- many components of the destroyed cells are recycled
o amino acids from the globin chains are incorporated into new proteins
o some iron from the heme groups is reused to make new heme groups
- the spleen and liver convert remnants of the heme groups to a colored pigment (bilirubin)
o bilirubin is carried by plasma albumin to the liver
in the liver bilirubin is incorporated into a secretion called bile
o bile is secreted into the digestive tract
o bilirubin metabolites leave the body in the feces
- small amounts of other bilirubin metabolites are filtered from the blood in the kidneys they
contribute to the yellow color of urine
- bilirubin levels in the blood can become elevated
o jaundice: the increased levels of bilirubin cause skin and whites of eyes to take on a
yellow color
o accumulation of bilirubin can occur for several reasons
newborns fetal hemoglobin is being broken down and replaced with adult
hemoglobin are particularly susceptible to bilirubin toxicity
they are monitored in the first few weeks of life for bilirubin toxicity
liver disease the liver is unable to process or excrete bilirubin
RBC Disorders Decrease Oxygen Transport
- hemoglobin plays a critical role in oxygen transport
o red blood cell count and hemoglobin context of the body are important
o anemia: a condition occurring when hemoglobin content is too low
the blood cannot transport enough oxygen to the tissues
people with this condition are usually tired and weak (especially during exercise)
Table 16.3 causes of anemia
Accelerated Red Blood Cell Loss
Blood loss: cells are normal in size and hemoglobin content but low in number
Hemolytic anemias: cells rupture at an abnormally high rate
Hereditary
Membrane defects (example: hereditary spherocytosis)
Enzyme defects
Abnormal hemoglobin (example: sickle cell anemia)
Acquired
Parasitic infections (example: malaria)
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