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glycogen storage sites
LIVER
10 percent of liver is glycogen
broken down into glucose during exercise and overnight fast for use by other tissues
liver glycogen used to buffer blood glucose
SKELETAL MUSKE
2 percent of mass of skeletal muscle is glycogen
is an energy store only for muscle
msiing key enzyme is g6p
used to provide energy during strenuous exercise
short term energy storage
large polymer of glucose molecules
linear backbones of ⍺-1,4 linkages with branchpoints at every 12 – 15 glucose molecules formed by secondary ⍺-1,6 linkages
has a central protein core- glycogenin
is branched so easy access for glycogen degrading enzymes
glycogen symthesis
white adipose tissue
energy storage
cushioning/mechanical fucntions
large uniocular lipid droplet
low mithcondrial content
undetectable ucp1 expression
no theromogenic capacity
beige adipose tissue
adaptive thermogenesis
endocrine functions
small multiocular lipid roplets
medium mitochondrial content
inducible UCP1 expression
medium thermogenic capacity
brown adipose tissue
thermogenesis and energy expenditure
endocrine functions
small multiocular lipid droplets
high mitochndrial content
high UCP1 expression
high thermogenic capacity
fatty acid structure
carbon backbone terminated by a COOH at one and and a CH3 at the other
triacylglycerols
main constiutent of body fat
energy storage
esters of glycerol, a 3 carbon alochol backbone and 3 fatty acids
can be saturated or unsaturated
lipolysis
TAG to fatty acids and glycerol
fatty acids undergo beta oxidation to generate acetyl coA for TCA cycle for ATP production
glycerol component can be utilised in gluconeogenesis
albumin
bind fatty acids in hydrophobic pockets enabling transport in the blood
solubilised fatty acids and prevemts formation of harmful aggregates
enhances transcytossi across capillary endothelia enabling tissue delivery
binding is transient enabling exchange at tissue sites
lipoprotein
transport lipids in blood
core of hydrophobic lipids surrounded by an outer shell of aphiphatic proteins, hosphoipids and cholesterol
4types
Chylomicrons: carry dietary triglycerides from the intestine to other tissues • Very-low density lipoproteins (VLDL): transport triglycerides synthesised in the liver to the adipose tissue for storage • Low-density lipoproteins (LDL): transport cholesterol from the liver to peripheral tissues • High-density lipoproteins (HDL): transport cholesterol from the peripheral tissues to the liver
pancreatic lipase
secreted into small intestine
digestion of lipids in food
lipoprotein lipase
endothelial cells
hydroysis of TAG in lipoproteins toaid uptake into tissues
apidose triglyceride lipase
apidocytes and other lipid storage cells
hydrolysis of stored TAG to yield diaceylglyerol and fatty acid. first and rate limiting step of lipolysis
Adipose hormonesensitive lipase (HSL
Adipocytes and other lipid-storing cells
Hydrolysis of DAG to yield monoacylglycerol (MAG) + FA. Activated by: glucagon, adrenaline, ACTH. Inhibited by: Insulin
Adipose monoacylglycerol lipase (MAGL/MGL)
Adipocytes and other lipid-storing cells
Hydrolysis of MAG to yield FA and glycerol
lipogenesis
process of synthesin and storing lipids as TAGs from diestar fags and de novo fatty acid synthesis
occurs especially in liver, adipose, muscl
TAG synthesised from fatty acyl CoA and a glyerol precursosr glycerol 3 phospate
adipose specialised tissies for synthesis stprage and relase of TAGs
muscle TAG turnover for local use
liver uses TAGs primarily to generate lipoproteins
metabolic derangement leads to excess TAG accumulation in muscle and liver—> ectopic fat
release of fatty acids from stored TAGs
hormone sensitive lipase catalyses the main rate controlling step
this is activated by glucagon signalling and inhibited by insulin signalling
glycerol is transported to liver where it can be used in gluconeogenesis to form glucpse
fatty acids are transported in circulation bound to albumin and transported inot cells where they undergo beta oxidation in mitochondria
chylomicrons
carry dietary triglycerides from the intestine to other tissues
very low density lipoproteins
transport triglycerides synthesised in the liver to the apidose tissues for stoage
low density lipoproteins
transport cholesterol from the liver to peripheral tissues
high density lipoprotein
transport cholesterol from the peripheral tissues to the liver
mitochondrial beta oxidation of fatty acids
activation: fatty acids activated to fatty acyl coa by coA and ATP in the cytoplasm
oxidation: acyl coa dehydrogenase removed 2x H forming a double bond and FADH
hydration
oxidation: hydroxyl group is oxidised and NADH formed too
thiolysis: beta ketothiolase cleaves the molecule forming one molecule acetyl CoA and a shorter fatty acyl coA which re enters the cycle
each cycle produces 1 FADH2, 1 NADH, and 1 Acetyl-CoA
cycle continues, shortening the fatty acids by 2 carbons until it is completely broken down