lipid metabolism and ketones Flashcards
what does increased fat intake without appropriate energy expenditure lead to
> increase in number of adipocytes
more fat in adipocytes
ie obesity
what does energy balance depend on
genetically linked factors ie protein messengers regulating appetite
environmental factors ie food abundance, fashionable foods
why is fat required
> an energy source
for essential fatty acids
fat soluble vitamins ie A D E and K
what are lipids
they are collections of different compounds
>they are predominantly hydrocarbon
>usually contain long chain fatty acids
>insoluble in water
>important for their biological functions
simple lipids
fatty acids, triglycerides, waxes
compound lipids
phospho- ,glyco-lipids , lipoproteins
steroids
cholesterol and steroid hormones
triglycerides
the same as triglycerols >main energy source form in adipose tissue >compact >hydrophobic >high energy yield per gram >consist of glycerol and 3 fatty acids
fatty acids
> mainly straight chains
aliphatic
usually contain an even number of carbons
branched chains and odd numbers of carbons are rare
they can be saturated, unsaturated and polyunsaturated
double bonds usually cis
the three main natural fatty acids
palmitic acid
stearic acid
oleic acid
polyunsaturated fatty acids
occur only in small amounts
>cannot be synthesised in the body
fatty acid nomenclature
pls just look at the slides i can’t explain this
fatty acid - melting point variation
> fatty acids with up to 8 carbons are liquid at room temp.
double bonds lower the melting point
plant fats contain large proportions of unsaturated fatty acids ie liquids
animal fats contain mostly palmitic and stearic ie solid
what are the main products of fat digestion
glycerol
fatty acids
monoglycerides
how is fat absorbed into mucosal cells of intestine
> short and medium length fatty acids enter portal blood
>longer chain FAs and monoglycerides are re-synthesised to triglycerides
what are chylomicrons
fat that is coated with a layer of protein, phospholipid and cholesterol
chylomicrons
enter the lymph and then the blood stream
>at muscle and adipose tissue, chylomicrons are attacked and cleaved by lipoprotein lipases
**there, free fatty acids are
resynthesised into triacylglycerols, oxidised to provide energy, and this all depends on amount available
lipolysis of stored fat
= the breakdown of lipids >fat is stored in adipose tissue >initial cleavage by hormone sensitive lipases (eg adrenaline sensitive) -releases free fatty acids and glycerol -occurs when energy is needed
fatty acid oxidation - activation
> before fatty acids can be oxidised to generate energy, they have to be converted to CoA derivatives
occurs in the cytoplasm
requires energy ie 2ATP
further oxidation of fatty acids occurs in the mitochondrial matrix
need to be transported into mitochondria by special carrier mechanism
function of the carnitine shuffle
**in the cytoplasm, fatty acids are transferred from acyl-CoA to carnitine
>Acyl-carnitine transport in inner membrane - facilitates antiprotons of acyl-carnitine into the mitochondrion and carnitine out
>ie acyl-CoA located is the mitochondrial matrix
beta oxidation (fatty acids)
cycle of reactions occurs in the mitochondrial matrix
>four steps in each cycle
>products of each cycle = acetyl-CoA
=FADH2
=NADH + H
=fatty acyl-CoA shortened by 2 carbon atoms
beta oxidation and unsaturated fatty acids…
???
requires two additional enzymes:
enoyl-CoA Isomerase
2,4 Dienoyl CoA reductase
yield of beta oxidation
cycle is repeated 8 times creates: >>8 FADH + 8NADH + 8H >used for ATP generation in oxidative phosphorylation >>9 acetyl-CoA >oxidised in citrate cycle to CO2, yield 9 FADH, 27NADH + 27 H , 9 GTP >>P/O ratio: FADH NADH + H total yield = 120 ATP
additional pathways include …
unsaturated fatty acids
odd chain fatty acids
branched chain fatty acids
»requires several enzymes
breakdown of glycerol
> > activated to glycerol-3-phosphate by glycerol kinase
present in liver and kidney but absent from adipose tissue, skeletal and heart muscle
dehydrogenated to dihydroxyacetone phosphate
normal intermediate of carbohydrate metabolism
ketone bodies
> they are formed in the liver mitochondria (from acetyl-CoA from B oxidation)
diffuse into the blood stream and to peripheral tissues
important molecules of energy metabolism for heart muscle and renal cortex (converted back to acetyl-CoA which enters the TCA cycle)
ketosis in starvation and diabetes
> oxaloacetate is consumed for gluconeogenesis
fatty acids are oxidised to provide energy
acetyl-CoA is converted to ketone bodies
high levels in blood
too much for extrahepatic tissue (i.e. heart, brain, etc.)
ketone bodies are moderate acids
accumulation leads to severe acidosis (blood can’t buffer any more)
impairs tissue function, particularly central nervous system
smell of acetone can be detected in breath
**normally
fatty acid oxidation yields acetyl-CoA, it enters citrate cycle if fat and carbohydrate degradation are balanced
>depends on oxaloacetate for formation of citrate
>oxaloacetate can be provided as a side-product of glycolysis
lipid catabolism
!! idk bro study