Integration of whole body metabolism Flashcards

1
Q

How much energy does the brain use and what is it used for

A
  • Uses 100-120g of glucose daily
  • Over half of the energy used is for Na+ K+ transport to maintain membrane potential and the synthesis of neurotransmitters
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2
Q

How is glucose transported in the brain

A

GLUT3, which has a low Km therefore is saturated at low glucose concentrations

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3
Q

Why aren’t fatty acids used for energy

A

Since they are used membrane biosynthesis

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4
Q

How does cardiac muscle get its energy

A

It is exclusively aerobic with little or no glycogen stores

Fatty acids are the main source of energy but lactate and ketone bodies can be used

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5
Q

What does cardiac muscle require

A

Requires the TCA cycle and oxidative phosphorylation

Lactate converted to pyruvate which is made into acetyl CoA

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6
Q

What is adipose tissue

A

Reservoir of metabolic energy in the form of triglycerides

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7
Q

How are adipose tissue filled

A

Lipids are not actually synthesised in the tissue apart from post starvation recovery
However fatty acids are made in the liver and come from our diet
Chylomicrons bring them to the tissue

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8
Q

How is fat mobilisation influenced

A

Glucagon and insulin

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9
Q

Kidney role

A

Main role is to produce urine

During starvation the kidney may contribute half of the blood glucose through gluconeogenesis

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10
Q

What does the liver do

A

Provides fuel for the brain, muscles and other peripheral organs
Takes its energy from alpha-keto-ketoacids
Very little of the glucose is used as an energy source, most of its used for synthesis of fats or used as a temporary store in the form of glycogen

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11
Q

Hexokinase vs Glucokinase

A

In non-hepatic tissue, most cells have hexokinase which phosphorylates glucose trapping it in the cell
Hexokinase is saturated at much lower levels of glucose, so its activity plateaus at much lower concentration of glucose
However glucokinase is minimally activate at low concentrations of glucose but maximally active at high concentrations of glucose

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12
Q

How is glucose transported into hepatocytes =

A

GLUT-2, since its not insulin sensitive.

Its instantly phosphorylated by glucokinase

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13
Q

How is glucose transported out of hepatocytes

A

Glucose-6-phosphate is converted to glucose by the action of glucose-6-phosphatase
It is then transported out of the cell and into the blood by GLUT-2 which is concentration dependant

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14
Q

How is glucose taken up by muscle cells and what happens to it

A

Glucose is taken up into muscle by GLUT-4 which is insulin dependant
Its converted into G6P by hexokinase so there is a low free glucose concentration in the cell
Glycolysis of the G6P is a rapid source of ATP

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15
Q

How is a sprint powered

A

ATP stores
Glycolysis
Glycogen
Creatine phosphate

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16
Q

What reaction does creatine kinase facilitate

A

Creatine phosphate + ADP = ATP + creatine kinase

17
Q

What type of respiration is most effective for sprinting but what are the downfalls

A

Anaerobic respiration but produces of lactate and a fall in pH

18
Q

What is the liver Cori cycle

A

Lactate from pyruvate and amino acids from muscle protein breakdown will be converted into alanine
Alanine and lactate will be transported to the liver where it combines to form pyruvate
This pyruvate is converted into glucose through gluconeogenesis and is then transported back to the muscle

19
Q

What is the flow of molecules during the fed state

A

Initially the flow of molecules is to the liver

Then the excess glucose and fatty acids are stored

20
Q

Where is glucose stored and what is it used for

A

Stored as glycogen in the liver and used as a glucose source for the brain. It can store roughly 100g of glucose

21
Q

Where is excess glucose stored and how

A

Initially excess glucose is stored in muscle as glycogen. The muscle can store around 500g of glucose
Any extra glucose is converted to fatty acids and stored in adipocytes

22
Q

What is glucose in the liver used for and why

A

Some of it is used to make NADPH in the pentose phosphate pathway
NADPH is a substrate in fatty acid synthesis
The liver will also be making acetyl CoA for triglyceride formation

23
Q

How are fats delivered to the muscle

A

Through VLDLS, resting muscle will use fatty acids as a source of energy

24
Q

What are amino acids used for

A

Used for protein synthesis and the excess is converted to keto-acids and ultimately urea

25
Q

What processes are active in the fed state

A

Glycolysis, glycogen synthase and fatty acid synthesis are active

26
Q

What processes are inactive in the fed state

A

Glycogenolysis, gluconeogenesis and fatty acid degradation are inactive

27
Q

What molecules are produced in the fed state

A

Glycogen and fatty acids

28
Q

What molecules are not produced in the fed state

A

Glucose and ketone bodies

29
Q

Where does the body gets its energy source in the famine state

A

Glycogen and fatty acid energy stores will be used first

Lastly protein will be used as an energy source

30
Q

What happen in the post absorptive stage

A

Blood glucose will drop after several hours after the last meal
The major energy source will be glycogen

31
Q

What enzymes and hormones will be active and why

A

There will be an increase in phosphorylase a activity so glycogen breakdown will increase
Glucagon will mainly be active so normal blood glucose levels can be maintained so brain function continues

32
Q

What processes are active during the post absorptive stage

A

Glycogenolysis, gluconeogenesis and fatty acid degradation are active

33
Q

What processes are inactive during the post absorptive stage

A

Glycolysis, glycogen synthesis and fatty acid synthesis are inactive

34
Q

What molecules are produced during the post absorptive stage

A

Glucose and ketone bodies

35
Q

What molecules are not produced during the post absorptive stage

A

Glycogen and fatty acids

36
Q

What happens in early starvation

A

Glucose is released from the liver due to gluconeogenesis and glycogenolysis
Fatty acids are mobilised from adipose tissue
Glucose use falls as muscle switches to fatty acid oxidation
Insulin drops causing GLUT4 expression by muscle to fall reducing glucose uptake

37
Q

What happens in intermediate starvation

A

Glycogen stores are depleted
Increased lipolysis and ketogenesis
Increased gluconeogenesis to maintain blood glucose
Increased beta hydroxybuterate production
Further starvation sees the kidney take over gluconeogenesis from the liver

38
Q

What happens in prolonged starvation

A

Beta hydroxybuterate plateaus at 20 days
Brain starts to use ketone bodies as an energy source as well so the need for glucose drops
Lactate and glycerol are required are used as gluconeogenic precursors
Lactate is recycled back by the Cori cycle to produce pyruvate
Glycerol and amino acids are oxidised
Proteins are broken down forming amino acid precursors

39
Q

What happens to molecules produced by the skeletal muscle

A

Alanine formed from the transamination of pyruvate is released into the blood, taken up by the liver and converted into glucose
The muscle cannot form urea so the liver removes nitrogen and releases pyruvate