Glycogen Flashcards
1
Q
General facts about glycogen
A
- Glycogen is a highly branched polymer (dendrimer) of glucose, containing many thousands of such monomers; the presence of the branches provides more opportunities for rapid degradation and synthesis
- Amount of glycogen in healthy man, weighting 70 kg, after carbohydrate meal:
- Liver (1.5 kg) glycogen… 100 grams = 400 kcal
- Muscle (35 kg) glycogen… 400 grams = 1600 kcal
- Compare to blood glucose amounts… 7 grams = 28 kcal; adipose reserves… 14 kg = 126,000 kcal
- Amount of liver glycogen (0.1% of wet weight after 24 hour fast to 10% if on a special diet) fluctuates much more than amount of muscle glycogen (0.7% of wet weight to rarely more than 2 %)
2
Q
Function of glycogenesis and glycogenolysis
A
- The function of glycogenesis and glycogenolysis in the liver is the amintenance of blood glucose levels during early portions of fast, and during exercise
- The function of muscle glycogenesis and glycogenolysis is the provision of a fuel to be used by the muscle during exercise (selfish)
3
Q
Glycogen
A
- Every 8 to 10 glucosyl residues, there is a branch which contains alpha (1→6) linkage
- Glycogen is sotred in both muscle and liver in granules; the enzymes associated with its synthesis and degradation are localized inside these granules
- Note: glycogenolysis stands in contrast to the fate of extra-cellular (dietary) glycogen, which is degraded by amylase into maltose and dextrins.
- Muscle and liver serve different purposes in terms of glycogenlysis; one is blood glucose modulation and the other is energy source.
4
Q
Glycogenesis
A
- Glucose 6-phosphate is “activated” by phosphoglucomutase and become Glucose 1-phosphate. It involves Glucose 1,6-P as a transient intermediate. This reaction takes place in cytosol.
- Uracil Triphosphate (UTP) combines with G 1-P to becomes UDP-glucose, which is an active form of glucosyl molecule, carried out by UDP-glucose pyrophosphorylase.
- The hydrolysis of pyrophosphate (PPi) ensures that UDP-glucose pyrophosphorylase reaction proceeds in the direction of UDP-glucose production.
- Glycogenin, with its tyrosine residue, serves as a primer and become the starting molecule where active form of glucose can bind to. This is because UDP-glucose can only elongate already existing chains of glucose. Since the reaction is catalyzed by glycogenin itself, it is considered both a protein and an enzyme. Glycogenin stays associated.
- Elongation of linear chain involves addition UDP-glucose molecules and glycogen synthase to form alpha (1→4) bonds.
- In every 8-10 glucosyl residues, branching enzyme called 4:6 transferase breaks alpha (1→4) bond and transfers a portion of the chain and create new alpha (1→6) bond thusly making branches in glycogen.
- The elongation and branching repeats via glycogen synthase and 4:6 transferase (branching enzyme).
5
Q
Glycogenolysis
A
- Glycogen chain is broken down via phophorolysis carried out by Glycogen phosphorylase, yielding Glucose 1-P.
- This is the rate-limiting step for digestion/glycogenolysis where some hormones may promote the process.
- Epinephrine will induce glycogenolysis; “adrenalin rush” = energy rush; spurt of energy
- Insulin and epinephrine are antagonistic to each other
- Glycogen phosphorylase requires as a coenzyme pyridoxal phosphate, which is a forom of vitamin B6
- The rate-limiting step in glycogenolysis is the reaction catalyzed by glycogen phosphorylase.
7.
6
Q
Glycogen metabolism
A
- Epinephrine and norepinephrine stimulate the synthesis of cAMP and the elevation of intracellular calcium levels by binding to alpha- and beta- adrenergic receptors. The cAMP functions in a synergistic manner with the calcium to regulate glycogen metabolism.
- The binding of hormones, such as glucagon or epinephrine, to plasma membrane G protein-coupled receptors (GPCR) signals the need for glycogen to be degraded - either to elevate blood glucose levels or to provide energy for exercising muscle.
- Binding of glucagon or epinephrine to GPCR results in G protein-mediate activation of adenylyl cyclase.
- cAMP is synthesized activating protein kinase A, where its catalytic subunit (C) phosphorylates several enzymes of glycogen metabolism
- Phosphorylase kinase is activated which subsequently activates glycogen phosphorylase, ultimately leading to glycogen degradation resulting in G 6-P.
- During muscle contraction, Ca2+ is released from the sarcoplasmic reticulum. Ca2+ binds to the calmodulin subunit of phosphorylase kinase, activiating it without phosphorylation. Phosphorylase kinase can then activate glycogen phosphorylase, causing glycogen degradation.
- Epinephrine is catabolic (involved in break down of glycogen)
- Thus Glucagon and Epinephrine have parallel agenda
- Ca+ is an activator –> glycogen in muscle is broken down for energy use as a result
- Insulin can inactivate glycogen phosphorylase and thus inhibit glycogen degradation
- Glucose 6-phosphate is more useful since it can be either diverted to be used for glycolysis to generate energy OR dephosphorylated by glucose 6-phosphatase.
7
Q
Effect of AMP levels
A
- High AMP → inhibit gluconeogenesis since there is not enough ATP in the system; AMP is inversely related to gluconeogenesis.
- Low AMP → more glycogen in the liver and more glycogenesis since there is already enough ATP in the system.
- Low AMP (muscle) → maximum capacity of glycogen stored in reserve; low glycolysis/hiatus.
8
Q
Inactivation of glycogen synthase
A
- Binding of glucagon or epinephrine further ensures glycogenolysis to proceed by inactivating glycogen synthase, thusly preventing the process from becoming what is called a “futile” reaction.
- Insulin, on the other hand, can activate the glycogen synthase and reverse the process, which with its presence inhibited glycogen phosphorylase and prevent glycogenolysis from taking place.
9
Q
Summary of Inhibition and Activation of glycogen metabolism
A
10
Q
Calmodulin
A
- Calmodulin is involved in many functions indcluding: nerve growth, muscle contraction, inflammation, apoptosis, intracellular movement, and immune processes. It functions inside of different organelles, including the plasma membrane.
- Ca2+ is a critical messenger; generally at a low level so any small change will bring about dramatic change.
- Calcium modulating (CalModulin) protein is not limited to just one place or one function.
- Phosphorylase kinase, which is usually activated by PKA can be activated by the Ca2+-calmodulin complex without the help of the kinase.
11
Q
Good summary
A