Vit K Flashcards
2 different types of Vit K and source
Phylloquinone - natural form found in food (K1) 10% of total liver stores
Menaquinone - made by intestinal bacteria (Ks Mk-4) 90% of total liver stores
Major storage for Vit K
Liver (most proteins that need it are here)
What is the function of Vit K
Blood Clotting and bone formation:
Post translation Modification of glutamic acid of calcium binding proteins to add a neg change (COO-) which allows calcium to bind
Vit K cycle
- Vit K uses NADPH to reduce quinone to hydroquinone (active)
- Vit-K carboxylase adds COO to Protein group (ex. Osteocalcin, prothrombin)
- Vit-K is now a Epoxide which uses Epoxide reductase to reduce back to Vit K
All factors are proteins made in the liver that need for K for?
modification, add 1-2 negatives which allow them to take on calcium
When will a protein become active that needs Vit K?
After addition of calcium
Osteocalcin
Glutamic acid rq vit K
Made from osteoblast - (vit D)
Found in kidney, lung, spleen
Bind to hydroxyapatite (mineralizes bone)
Matrix Gla Protein (MGP)
Rq. Vit-K, expressed in developing bone for bone organization
inhibits inappropriate calcification of epiphyseal growth plate
Protein S
Modulates cell proliferation
Gas6 Protein
Needed for neuronal development
Absorption of Vit K depends on
Bile salts and lipids in the jejunum
Is Vit K excreted in the urine?
No, in the feces in large quantities (from bacteria sources)
60-70% of phylloquinone absorbed will be excreted
Sources of Vit K
Intestinal bacterial synthesis (enough to meet the body needs)
Green leafy vegetables
Soybeans, beef, liver - low in poly high in mena
Olive, canola, soybean oil
Who is at risk for a Vit K deficiencies
Newborns: Hemorrhagic disease, VKDB (have no microbiome)
Adults: Antibiotic or anticoagulants/ malabsorption / biliary obstruction
Explain why infants are at risk for VKDB (Vit K deficiency bleeding)
Low at birth, and low precursors
limited placental transfer
several weeks to develop liver stores based on mothers milk