Metabolic Pathways: Glycogen Flashcards
glycogenesis
synthesis of glycogen from glucose
glycogenolysis
breakdown of glycogen to form glucose
gluconeogenesis
de novo synthesis of glucose from metabolic precursors
lactate, amino acids, glycerol
what is glycogen
main storage form of glucose in liver and muscle cells
liver glycogen
broken down between meals and released to maintain blood glucose levels fro red blood cells and brain
muscle glycogen
not available for maintenance of blood glucose levels
provides energy via glycolysis and the TCA during bursts of physical activity
sources of blood glucose
glyogenolysis fluctuates dependent upon meal times
gluconeogenesis is the primary source of glucose overnight when hepatic glycogen is depleted
glycogenin
glycogen primer containing at least 4 glucose residues is covalently attached to protein
allows glucose residues to be added to existing glycogen chain
glycogen synthesis
ATP required
glycolysis
UDP-glucose
activated intermediate form of glucose
phosphate ester linkage in a nucleotide sugar releases free energy on hydrolysis
glycogen synthase
synthesises glycogen from UDP-glucose
adds one glucose molecule to glycogen at a time
can only extend the chains of glycogen - can’t start new molecules
can not introduce branches
rate limiting enzyme of glycogenesis
branching enzyme, transglycosylase, introduces Alpha 1-6 glycosidic branches
glycogenolysis
catalysed by glycogen phosphorylase
rate limiting step of glycogenolysis
one glucose molecule is cleaved of the ends of glycogen at a time
glucose-1-phosphate — glucose-6-phosphate
glycogenolysis - in liver
glucose-6-phosphate can be de-phosphorylated and the resulting glucose released into the blood stream
glycogenolysis - skeletal muscle
glucose-6-phosphate cannot be de-phosphorylated but instead is used to provide energy via glycolysis and the TCA cycle
glycogenolysis - debranching
requires additional enzymes
gluconeogenesis
synthesis of glucose within the body from precursor substrates
essentially the reverse of glycolysis
requires four unique liver enzymes
proceeds via the synthesis of oxaloacetate in mitochondria
energy consuming - energetically expensive
ATP hydrolysis drives an unfavourable reaction
glycolysis
three irreversible reactions - hexokinase, phosphofructokinase, pyruvate kinase
several special reactions are required to bypass the irreversible reactions
cori cycle
lactate is a precursor of gluconeogenesis - formed in fast-twitch muscle under conditions of heavy exercise
blood transports lactate to liver
liver converts lactate back to glucose
glucose released into bloodstream
buys time and shifts metabolic burden from muscle to other organs
precursors for gluconeogenesis
amino acids
reciprocal regualtion
glycolysis and gluconeogenesis
hormonal regualtion - glucagon and insulin
glycogen storage diseases
groups of diseases with increased glycogen deposits in liver/muscle
+10 different types - defects in different enzymes