Metabolic Stores Flashcards

1
Q

how are carbohydrates stored in the liver and muscle

A

glycogen (a branched glucose polymer)

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2
Q

when glucose is broken down what is it directly converted to

A

glucose-6-P and this is without consuming ATP
CAN ONLY OCCUR IN THE CELL IT IS FORMED
as it cannot easily pass through the cell membrane

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3
Q

what happens when glucose is required somewhere else in the body

A

the glucose-6-P is only phosphorylated when it has been transported to its destination as once phosphorylated it is not easily removed
THIS USES ATP
in the liver there is an enzyme known as glucose-6-phosphotase which can cleaves the phosphates it can escape

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4
Q

how may horse worth of glycogen in the body

A

3-5 hours

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5
Q

what is the major form in which fuel is stored

A

lipids

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6
Q

triglycerides/triacylglycerols

A

produce about 6 times s much energy as glycogen

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7
Q

what is fat mainly stored as

A

triglycerides (triacylglycerols) these are esters of glycerol and fatty acids
as esterification occurs at carbon 123

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8
Q

what is an ester

A

formed by reaction of an alcohol with an organic acid

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9
Q

tell me about the oxidisation of fatty acids

A

they are linked to coenzyme A before they are oxidised and 2-carbon fragments cleaved off (as acetyl-Co-A)

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10
Q

What happens during the oxidisation of fatty acids

A

no ATP is directly generated however hydrogen and electrons are removed and are passed along the respiratory chain so are indirectly producing ATP

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11
Q

where are fatty acids and glycerol released from

A

adipose tissue and are mainly metabolised in the liver

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12
Q

when there are no other fuels available, the breakdown of fatty acids leads to what

A

the formation of chemicals known as ketone bodies

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13
Q

what ketone bodies are mainly present post breakdown of fatty acids

A

acetoacetate
3-hydroxybutyrate
acetone

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14
Q

how are ketone bodies produced

A

acetyl-CoA formed in the breakdown of fatty acids cannot enter the citric acid cycle since oxaloacetate becomes depleted because the liver converts it to pyruvate to produce glucose by glycogenesis
so acetyl-CoA = ketone bodies

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15
Q

omega-3 fatty acids

double bond at three position

A

not metabolised
has to be acquired in the diet
vital fatty acid

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16
Q

What is the appearance of ketone bodies

A

fruity smell (often smelled on breath when fasting.)

17
Q

what happens to amino acids not needed for making new proteins as they cannot be stored

A

they are used as metabolic fuel
some can be deaminated, yielding nh4 + a ketone acid that are intermediates of the glycolytic pathway or of the citric acid cycle

18
Q

what happens to the products of transamination

A

the resulting ketone acids can be fed into glycolysis or the citric acid cycle (as pyruvate , acetylene-Co-A, oxalocetate

19
Q

what happens to the NH4+ formed from transamination

A

rapidly converted to urea as it is very toxic

20
Q

gluconeogenesis

A

formation of glucose from non-carbohydrate sources )glycerol and the carbon backbone of amino acids can be fed into this pathway)

21
Q

where does the bulk of gluconeogenesis take place

A

the liver

22
Q

where are the bulk triglycerides stored

A

adipose tissue

23
Q

why do athletes load up on carbs before an event

A

fats are not used as effectively as fuel carbohydrate so energy production cannot be as high when using lipids rather than carbs
(when fasting, burns fat so produces more keto bodies hence fruity breath)

24
Q

tell me about fuel in the brain

A

glucose is normally only source
can’t store glucose glycogen so needs constant supply in the blood
60% of all glucose used by the body
in times of starvation can use ketone bodies)acetoacetate and 3-hydroxybutyrate) formed in other tissues
CANT USED FATTY ACIDS due to BBB that protects the brain from other potentially dangerous chemicals

25
Q

what stores can muscle (large glycogen stores) use

A

glucose, fatty acids and ketone bodies

26
Q

resting muscle uses

A

fatty acids

27
Q

tell me about the actions in muscle

A

glucose-6-P is formed from glycogen
Like brain, muscle cannot convert this to glucose, so
neither tissue can export glucose
When muscle is active the rate of glycolysis far outpaces the
citric acid cycle
pyruvate must be converted to lactate
The lactate passes into the blood and to the liver, where it is converted back to glucose

28
Q

under conditions where muscle protein is being broken down

A

amino acids pass their amino group pyruvate (through transamination) to form alanine

29
Q

role of alanine

A

enters the blood and in the liver can be converted back to pyruvate which is used to synthesise glucose

30
Q

main function of adipose tissue

A

to synthesize and store triglycerides (=triacylglycerols) and release fatty acids and glycerol in times of need

31
Q

what is the role of lipase

A

hydrolyses triglycerides and is HORMONE SENSITIVE

32
Q

What determines the rate at which fatty acids are esterified

A

the availability of glucose

33
Q

tell me about the role of the liver

A

the hepatic portal system ensures that the liver has ready access to nutrients absorbed by the gut.
readily store, release glucose and make new glucose from lactate, alanine and glycerol in the diet or released by other tissues.

34
Q

what is the formation of glucose known as

A

gluconeogenesis

35
Q

When fuel supplies are available what does the liver do

A

synthesizes fatty acids, esterifies them and then secretes them into the blood as very low density lipoprotein (VLDL)