Metabolic Pathways Flashcards

1
Q

Glycogenesis

A

Glucose->glycogen

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2
Q

Glycogenolysis

A

breakdown of glycogen to form glucose

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3
Q

Gluconeogenesis

A

de novo synthesis of glucose from metabolic precursors (lactate amino acids, glycerol)

Essentialy the reverse of glycolysis

ie synthesis of glucose within the body from precursor substrates

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4
Q

Role of glycogen

A

main storage form of glucose in liver and muscle cells

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5
Q

When is liver glycogen broken down?

A

Between meals

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6
Q

Why is liver glycogen released?

A

To maintain blood glucose levels for RBC and the brain

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7
Q

Role of muscle glycogen cells?

A

not for maintenance of blood glucose levels

provide energy via glycolysis and TCA during bursts of physical activity

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8
Q

What is the primary source of glucose overnight when hepatic glycogen is depleted?

A

gluconeogenesis

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9
Q

Structure of glycogen

A

polymer consisting of glucose molecules joined by alpha 1-4 glycosidic links

Branches introduced by alpha 1-6 glycosidic links

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10
Q

Primer for adding glucose residue to a glycogen chain

A

glycogenin

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11
Q

What causes glycogenolysis to fluctuate?

A

It fluctuates depending on meal times

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12
Q

What can UDP-glucose be thought of as?

A

An active intermediate of glucose

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13
Q

What happens to the phosphate ester linkage in a nucleotide sugar during hydrolysis?

A

It releases free energy

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14
Q

Role of glycogen synthase

A

Rate limiting enzyme of glycogenesis

Makes glycogen from UDP-glucose

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15
Q

Glycogen breakdown summary

A

Glycogen-> glucose-1-phosphate-> glucose-6-phosphate

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16
Q

Role of glycogen phosphorylase

A

Rate limiting enzyme for glycogenolysis

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17
Q

Enzyme involved in lysis of glucose-1-phosphate to form glucose-6-phosphate

A

Phosphoglucomutase

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18
Q

Precursor substrates involved in gluconeogenesis

A

Lactate, amino acids, glycerol

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19
Q

synthesis of lactate

A

made by skeletal muscle under anaerobic condtions

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20
Q

Where are amino acids derived from?

A

muscle protein by proteolysis

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21
Q

Where is glycerol derived from?

A

triglycerides by lipolysis in adipose tissue

22
Q

Where is energy for gluconeogenesis from?

A

oxidation of fatty acids released from adipose tissue

23
Q

where does gluconeogenesis occur?

A

Mainly in the liver, but small amounts in the kidneys

24
Q

Gluconeogenesis proceeds via the synthesis of _____ in the _____

A

Oxaloacetate

Mitochondria

25
Oxaloacetate
TCA cycle intermediate which is important for accepting acetyl groups from fat break down
26
Cori cycle
Lactate produced in muscle Blood transfers lactate to liver Liver converts lactate back to glucose Glucose released to bloodstream
27
Why is fat required in the body?
energy source, essential polyunsaturated fatty acids (those needed but cannot be made by body) and absorption of fat soluble vitamins
28
Different types of lipids
Simple lipids Compound lipids Steroids
29
Features of lipids
- usually hydrocarbons - contain long chain fatty acids - insoluble in water
30
Examples of simple lipids
fatty acids triglycerides waxes
31
examples of compound lipids
phospholipids, glycolipids, lipoproteins
32
examples of steroids
cholesterol, steroid hormones eg adrogens
33
What is the main energy storage form in adipose tissue?
Triglycerides (triacylglycerols)
34
Structure of triglycerides
Glycerol and 3 fatty acids
35
Fatty acids are aliphatic. T/F?
True, they have no rings
36
Double bonds of fatty acids are usually in trans configuration. T/F
False | Cis
37
All fatty acids are liquid at room temperature. T/F?
False Liquid up to 8 C atoms, longer ones are solid
38
Impact of presence of double bonds on melting point
Lowers melting point
39
Why are plant acids liquid?
they contain large proportions of unsaturated fatty acids | animal fats are solid as they mostly contain palmitic and stearic acid
40
Main products of fat digestion
Glycerol, fatty acids and monoglycerides
41
Which cells absorb fat in the intestine?
Mucosal cells
42
Chylomicrons
Lipoproteins coated with a layer of protein, phospholipid and cholesterol
43
Enzyme involved in llipolysis
Hormone sensitive lipase, which release free fatty acids and glycerol
44
What must happen before fatty acids can be oxidised to generate energy?
They must be converted to CoA derivatives
45
Where does initiation of fatty acid oxidation occur?
in the cytoplasm | further oxidation occurs in the mitochondrial matrix
46
The carnitine shuttle
Fatty acids in cytoplasm are transferred from Acyl-CoA to carnitine (a transporter in inner membrane) and moves acyl-CoA to mitochondrial matrix
47
Beta oxidation
Cycle of reactions which occurs in the mitochondrial matrix Consists of four steps per cycle
48
Products of each cycle of beta oxidation
- 1 acetyl-CoA - 1 FADH2 - 1 NADH + H+ - 1 fatty acyl-CoA, shortened by 2 C atoms
49
Breakdown of glycerol
glycerol kinase causes activation to glycerol-3-phosphate it is then dehydrogenated to dihydroxyacterone phosphate
50
Where are ketone bodies formed?
In liver mitochondria from acetyl-CoA from B oxidation
51
Role of ketone bodies
molecules of energy metabolism for heart muscle and renal cortex It is converted back to acetyl-CoA which enters TCA cycle
52
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