MEH Flashcards
Describe b12 absoprtion
- B12 binds haptocorrin secreted by salivary glands and the complex passes through the stomach
- In the small intestine, Vit B12 is released from haptocorrin and binds intrinsic factor (IF) produced by parietal cells in the stomach
- IF-B12 complex then binds to receptors in the terminal ileum, leading to absorption of B12 and destruction of intrinsic factor
perincous anameais is …
autoimmune disease afecting gastric parietal cells cauing lack of IF
link between b12 and folate
- Vitamin B12 is responsible for reactivating folic acid, back into tetrahydrofolate, the form of folic acid which the body can use.-so low B12 causes a functional folate deficiency
- THF is essential for: serine-glycine conversion, histidine catabolism, purine synthesis, and most importantly, thymidylate synthesis which is needed throughout the body for DNA synthesis
- On the other hand, vitamin B12 needs folic acid to reduce homocysteine MTHF gives off its methyl group to vitamin B12 (cobalamin), which becomes methylcobalamin.
- At the same time, the MTHF folic acid is converted back into its bioactive form, tetrahydrofolate
- Methylcobalamin then gives off its methyl group to homocysteine, to create methionine
- Methionine is converted to S-adenosyl methionine (SAM) – one of the most important things for the production of various neurotransmitters and for DNA methylation.
treatment of perincous anameia
intramusclular injection
hydroxycobalamine
INtravascular hameolysis
within blood vessels
extravascualr hameolyiss
in spleen or wider RES
inherited causes of hameolytic anameia
Pyruvate kinase def
G6pdh
Function of band 3
Facilitates Cl- and bicarbonate exchange across PM
Howell Jolly bodies in blood film indicates…
prob in spleen
asplenic
What is DIC
Bleeding and clotting occur at same time in patient - e.g. in malignacny, obstetric complications, trauma and sepssi, and thromobotic thrombocytopenic purpura - small thrombi form within microvascualture
lab findings in haemolytic anaemia
raised bilirubin
high reitculocytes
rasied LDH
what is cause of anaemia of chronic disease
problem with hepcidin causes a functional iron deficiency reduced erythropoiesis Iron dysregulation: iron not released for use in bone marrow -Marrow shows a lack of response to EPO -Reduced LS of rbc
what is sideroblastic anaemia
bone marrow produces rigid sideroblasts than normal healthy rbc. Rare inhertied Microcytic anameia,
Results from defects in haem synthetic pathway
what are crises in sickle cell
Vaso-occlusive
Aplastic (often triggered by parvovirus infection)
Haemolytic
Jaundice and gall stones
Splenic atrophy
what is stored iron
Ferritin
Haemosiderin