10/9 Flashcards
Main pathway for production of NADPH
PPP
Iodoacetate
Non-specific inhibitor for Glyceraldehyde-3-P DH
PFK-1 inhibitors
ATP, Citrate
PFK-1 Activators
AMP, ADP, F-2,6-BisP
MCAD Deficiency
Medium-chain Acyl-CoA Dehydrogenase Deficiency
- most common inborn error of ß-oxidation
- can’t oxidize 6-10C FA’s
- severe hypoglycemia and hypoketonemia
- treated by avoiding fasting
Diabetic Ketoacidosis
In uncontrolled DM type I, no insulin is produced (autoimmune disease, destroys insulin producing cells). This results in up regulation of lipolysis, and up regulation of ketone body production. Too many ketone bodies in the blood causes acidosis, or acidic blood.
Ketogenesis vs Cholesterol Synthesis
Both produce HMG CoA, but Ketogenesis is located in the mitochondria, while CH synthesis is located in the ER. They also vary based on conditions of the cell _____
Can the liver use ketone bodies?
No, it lacks the thiolase enzyme (it uses thiophorase)