Published bySamantha Pope Modified over 6 years ago
METABOLISM OF CARBOHYDRATES: SYNTHESIS AND DEGRADATION OF GLYCOGEN
Glycogen Metabolism 1. Liver glycogen:
-Forms 8-10% of the wet weight of the liver. -Maintains blood glucose (especially between meals). -Liver glycogen is depleted after hours fasting. 2. Muscle glycogen: -Forms 2% of the wet weight of muscle. -Supplies glucose within muscles during contraction. -Muscle glycogen is only depleted after prolonged exercise.
Glycogen metabolism includes:
Glycogenesis: synthesis of glycogen from glucose. Glycogenolysis: breakdown of glycogen to glucose-1-phosphate. Gluconeogenesis: synthesis of glucose or glycogen from noncarbohydrates precursors.
In the well-fed state the glucose after absorption is taken by liver and deposited as a glycogen
Glycogen is a very large, branched polymer of glucose residues that can be broken down to yields glucose molecules when energy is needed Most glucose residues in glycogen are linked by a-1,4-glyco-sidic bonds, branches are created by a-1,6-glycosidic bonds
Glycogen serves as a buffer to maintain blood-glucose level
Glycogen serves as a buffer to maintain blood-glucose level Stable blood glucose level is especially important for brain where it is the only fuel The glucose from glycogen is readily mobilized and is therefore a good source of energy for sudden, strenuous activity. Liver (10 % of weight) and skeletal muscles (2 %) – two major sites of glycogen storage Glycogen is stored in cytosolic granules in muscle and liver cells of vertebrates
Glucose-6-phosphate is the central metabolite in the synthesis and decomposition of glycogen.
In the well-fed state glucose is converted to glucose-6-phosphate, which is the precursor for the glycogen synthesis. The glucose-6-phosphate derived from the breakdown of glycogen has three fates: (1) glycolysis; (2) pentose-phosphate pathway; (3) convertion to free glucose for transport to another organs.
DEGRADATION OF GLYCOGEN
Glycogenolysis - degradation of glycogen The reaction to release glucose from polysaccharide is not simple hydrolysis as with dietary polysaccharides but cleavage by inorganic phosphate – phosphorolytic cleavage Phosphorolytic cleavage or phosphorolysis is catalyzed by enzyme glycogen phosphorylase There are two ends on the molecules of starch or glycogen: a nonreducing end (the end glucose has free hydroxyl group on C4) and a reducing end (the end glucose has an anomeric carbon center (free hydroxyl group on C1)
Acts only on a-1-4 linkages of glycogen polymer
Glycogen phosphorylase removes glucose residues from the nonreducing ends of glycogen Acts only on a-1-4 linkages of glycogen polymer Product is a-D-glucose 1-phosphate (G1P) Cleavage of a glucose residue from the nonreducing end of glycogen
Structure of glycogen phosphorylase (GP)
GP is a dimer of identical subunits (97kD each) Catalytic sites are in clefts between the two domains of each subunit Binding sites for glycogen, allosteric effectors and a phosphorylation site Two forms of GP Phosphorylase a (phospho- rylated) active form Phosphorylase b (dephospho- rylated) less active
GP catalyzes the sequential removal of glucose residues from the nonreducing ends of glycogen
GP stops 4 residues from an a 1-6 branch point Tranferase shifts a block of three residues from one outer branch to the other A glycogen-debranching enzyme or 1,6-glucosidase hydrolyzes the 1-6-glycosidic bond The products are a free glucose-1-phosphate molecule and an elongated unbranched chain
Metabolism of Glucose 1-Phosphate (G1P)
Phosphoglucomutase catalyzes the conversion of G1P to glucose 6-phosphate (G6P)
Glycogen Synthesis Synthesis and degradation of glycogen require separate enzymatic steps Cellular glucose converted to G6P by hexokinase Three separate enzymatic steps are required to incorporate one G6P into glycogen Glycogen synthase is the major regulatory step
Glucose 1-Phosphate formation
Phosphoglucomutase catalyzes the conversion of glucose 6-phosphate (G6P) to glucose 1-phosphate (G1P).
UDP-glucose is activated form of glucose.
UDP-glucose is synthesized from glucose-1-phosphate and uridine triphosphate (UTP) in a reaction catalized by UDP-glucose pyrophosphorylase
Glycogen synthase adds glucose to the nonreducing end of glycogen
A branching enzyme forms -1,6-linkages
Glycogen synthase catalyzes only -1,4-linkages. The branching enzyme is required to form -1,6-linkages. Branching is important because it increases the solubility of glycogen. Branching creates a large number of terminal residues, the sites of action of glycogen phosphorylase and synthase.
Diagram of Glycogenesis
Regulation of Glycogen Metabolism
Muscle glycogen is fuel for muscle contraction Liver glycogen is mostly converted to glucose for bloodstream transport to other tissues Both mobilization and synthesis of glycogen are regulated by hormones Insulin, glucagon and epinephrine regulate mammalian glycogen metabolism
Insulin Hormones Regulate Glycogen Metabolism
Insulin is produced by b-cells of the pancreas (high levels are associated with the fed state) Insulin increases rate of glucose transport into muscle, adipose tissue via GluT4 transporter Insulin stimulates glycogen synthesis in the liver via the second messenger phosphatidylinositol 3,4,5-triphosphate (PIP3)
Glucagon Secreted by the a cells of the pancreas in response to low blood glucose (elevated glucagon is associated with the fasted state) Stimulates glycogen degradation to restore blood glucose to steady-state levels Only liver cells are rich in glucagon receptors and therefore respond to this hormone
Released from the adrenal glands in response to sudden energy requirement (“fight or flight”) Stimulates the breakdown of glycogen to G1P (which is converted to G6P) Increased G6P levels increase both the rate of glycolysis in muscle and glucose release to the bloodstream from the liver and muscles Both liver and muscle cells have receptors to epinephrine
Effects of hormones on glycogen metabolism
Reciprocal Regulation of Glycogen Phosphorylase and Glycogen Synthase
Glycogen phosphorylase (GP) and glycogen synthase (GS) control glycogen metabolism in liver and muscle cells GP and GS are reciprocally regulated both covalently and allosterically (when one is active the other is inactive) Covalent regulation by phosphorylation (-P) and dephosphorylation (-OH) Allosteric regulation by glucose-6-phosphate (G6P)
Reciprocal Regulation of GP and GS
COVALENT REGULATION Active form “a” Inactive form “b” Glycogen phosphorylase -P OH Glycogen synthase OH -P ALLOSTERIC REGULATION by G6P GP a (active form) - inhibited by G6P GS b (inactive form) - activated by G6P
Activation of GP and inactivation of GS by Epinephrine and Glucagone
Activation of GS and inactivation of GP by Insulin
Muscle glycogen and blood glucose
Muscle glycogen can be converted to glucose via indirect pathways: Cori's cycle: during muscle exercise Glucose- alanine cycle: during starvation
Cori's cycle: Glycogen glycolysis gluconeogenesis
Cori Cycle When anaerobic conditions occur in active muscle, glycolysis produces lactate. The lactate moves through the blood stream to the liver, where it is oxidized back to pyruvate. Gluconeogenesis converts pyruvate to glucose, which is carried back to the muscles. The Cori cycle is the flow of lactate and glucose between the muscles and the liver.
Glucose- alanine cycle:
Glycogen gluconeogenesis transamination
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