Energy Storage Flashcards
Describe the mechanism of glycogenolysis.
Glycogen (n) + Pi —————> Glucose-1-P + Glycogen (n-1)
a-1,4-bonds hydrolysed by glycogen phosphorylase
a-1,6-bonds hydrolysed by de-branching enzyme
Glucose-1-P converted to Glucose-6-P by phosphoglucomutase.
Describe the mechanism of glycogen synthesis (glycogenesis)
Glycogen (n) + UDP-glucose ——-> Glycogen (n+1) + UDP
a-1,4-bonds catalysed by glycogen synthase
a-1,6-bonds catalysed by branching enzymes
Glycogen stored in liver and skeletal muscle.
How does glycogenolysis differ in the muscle and the liver?
Glycogen ——–> Glucose-1-P ———-> Glucose-6-P
Muscle:
Glucose-6-P ——-> GLYCOLYSIS
Liver:
Glucose-6-P ——–> Glucose ———–> BLOOD
(glucose-6-phospahatase)
How is glycogen metabolism regulated?
Glucagon/adrenaline (fasting hormone) activates phosphorylating enzymes (glycogenolysis)
Insulin (storage hormone) inhibits phosphorylating enzymes (glycogenesis)
Explain the glycogen storage diseases and what effects they cause.
Excess glycogen storage ——-> tissue damage
Diminished glycogen storage ——–> hypoglycaemia, poor exercise tolerance
e.g. von Gierke’s disease = deficiency of glucose-6-phosphatase
What substrates can be used for gluconeogensis?
Lactate Galactose Fructose Glycerol Glucogenic amino acids
What enzymes are important for gluconeogenesis? How are they regulated?
Fructose-1,6-bisphosphatase
PEPCK catalyses conversion of oxaloacetate to phosphoeneolpyruvate.
Glucagon & cortisol stimulates, and insulin inhibits