Hemoglobin
Hemoglobin
Van den Bergh reaction (Jaundice test)
“Indirect reactingbilirubin = Unconjugated bilirubin”:
Both start with vowels, so they go together: Indirect & Unconjugated.
Heme synthesis: amino acid precursors to basic unit ofporphyrins , heme (pyrrole ring)
“Dracula wants to Suck a Co-ed’s blood [think heme] with his Glystening teeth!”:
Succinyl CoA and Glycine are precursor amino acids topyrrole rings, which is the basic unit of porphyrins and heme.
Hemoglobin binding curve: causes of shift to right
“CADET, face right!”:
Porphyrias : acute intermittent porphyria symptoms
5 P’s:
Sickle cell anemia: mutation
“HbS isn’t Very Good”:
At Sixth position ofHB beta chain , Valine is present instead of Glutamic acid.
Sickle cell diseasepathophysiology
SICKle cell disease is due to a Substitution of the SICKsth amino acid of the B chain.
Vitamin K dependent cofactors
“Several Tend To Nicely Stop Clots”:
Factor Seven, Ten, Two, Nine.
Protein S, Protein C.
Coagulation common pathway: factors in order
10 + 5 – 2 = 13
Coagulation common pathway:
Factor X to Factor V to Factor II to Factor XIII
“Indirect reacting
Both start with vowels, so they go together: Indirect & Unconjugated.
Heme synthesis: amino acid precursors to basic unit of
“Dracula wants to Suck a Co-
Succinyl CoA and Glycine are precursor amino acids to
Hemoglobin binding curve: causes of shift to right
“CADET, face right!”:
- CO2
- Acid
- 2,3-DPG (aka 2,3 BPG)
- Exercise
- Temperature
5 P’s:
- Pain in abdomen
- P
olyneuropathy - P
sychologial abnormalities - Pink urine
- Precipitated by drugs (
eg barbiturates, oral contraceptives,sulpha drugs)
Sickle cell anemia: mutation
“
At Sixth position of
Sickle cell disease
SICK
Vitamin K dependent cofactors
“Several Tend To Nicely Stop Clots”:
Factor Seven, Ten, Two, Nine.
Protein S, Protein C.
Coagulation common pathway: factors in order
10 + 5 – 2 = 13
Coagulation common pathway:
Factor X to Factor V to Factor II to Factor XIII
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