Glycolitic Metabolites, Lactate And The Metabolism Of Sugars and pentose phosphate pathway Flashcards

1
Q

What is 2,3 bisphosphoglycerate

A

Produced in RBC

Regulator of haemoglobin o2 affinity promotors release of o2

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2
Q

Glycerol phosphate

A

Important to triglycerides and phospholipid biosynthesis

Produced from DHAP

Lipid synthesis required glycolysis

Liver can phosphorylate glycerol directly

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3
Q

Why do RBC need to regenerate NAD+ in a another way

A

They have no stage 3 pr 4 of metabolism

Stage 4 needs 02 and the supply of 02 to muscles and gut is often reduced

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4
Q

Lactate dehydrogenase reaction

A

NADH + H + PYRUVATE = NAD and lactate

Using lactat dehydrogenase

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5
Q

What is hyperlactaemia?

A

2-5mM - plasma lactate
Below renal threshold
No change in blood pH

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6
Q

What is lactic acidosis?

A

Above 5mM plasma lactate

Above renal threshold
Blood pH lowered

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7
Q

How can fructose be used in glycolysis

A

Fructose can be converted to G3P which can under glycolysis to form pyruvate

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8
Q

What is essential fructosuria?

A

Fructokinase missing

-fructose in urine

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9
Q

Fructose intolerance

A

Adolase B missing

-fructose 1-P accumulates in liver leads to liver damage

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10
Q

How is galactose metabolised

A

Galactokinase converted it to galactose 1-P

Uridyl transferase converts galactose 1-P to gluose 1-P then gluose 6P which can enter glycolysis

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11
Q

What causes galactosaemia?

A

Deficiency in
UDP-Galactose epimerase
Uridyl transferase
Galactokinase

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12
Q

What does UDP-galactose epimerase do

A

Converts galactose 1-p to UDP- galactose which tunes into UDP-glucose which can form glycogen

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13
Q

What is galactosaemia ?

A

Milk rich diet in infancy

Unable to utilise galactose 
Galactokinase deficiency (rare)- galactose accumulates 

Trasnferase deficicy (common) - galactose and galactose 1-P accumulate

Galactose enters other pathways to form galacticol
Which depletes levels of NADH as it i used to form galacticol

NADH is important is preventing the formation of inappropriate disulphide bonds therefore when NADH levels are reduced they form which causes cross linking- cataracts

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14
Q

What is the pentose phosphate pathway

A

Two stage pathway - cytoplasmic

Glucose -6-P to c5 sugar and CO2 using NADP
NADP is reduced to NADPH

Using glucose 6P dehydrogenase

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15
Q

What is the function of the pentose phosphate pathway?

A

Produce NADH in cytoplasm

Bio synthetic reducing power- lipid synthesis

Maintain free SH cysteine groups on certain proteins
Prevent oxidation to disulphide bonds

Produce C5 sugar for nucleotides needed for nucleic acid synthesis

High activity in dividing tissues

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16
Q

What occurs when there is a Deficiency of glucose 6-phosphate dehydrogenase deficiency

A

Leads to an inability to produce NADPH from NADP so NADPH will drop

In RBC this needs to disulphide bonds forming which cause appreciated proteins- Heinz bodies whic leads to haemlysis

17
Q

What is the important source of NADH required for

A

Reducing power for biosynthesis
Maintenance of reduced glutathionine (GSH) levels
Detoxification reaction

18
Q

What are C5 sugar-ribose required for

A

Synthesis of
-nucleotide
DNA
RNA

19
Q

what converts galactose to galacticol

A

aldose reductase using NADPH- galactosaemia

decreased NADPH levels leads to galactosaemia

20
Q

What is the rate limiting enzyme in the pentose phosphate pathway?

A

Glucose 6-phosphate dehydrogenase