Carbohydrate and glucose management Flashcards

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1
Q

Where in the body does degredation of carbohydrates start and which enzyme is responsible?

A

In the mouth: amylase

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2
Q

What carbohydrate polymer cannot be degraded and what are these polymers called?

A

Cellulose for instance, this is a fiber

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3
Q

How can fiber still be degraded?

A

By certain bacteria in the gut

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4
Q

Is glucose transport and uptake active or passive?

A

Glucose in the gut is transported from a high to low concentration so this is active uptake and it costs ATP

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5
Q

What is the problem in lactose intolerance?

A

You lack the enzyme lactasa, so you cannot break the bond between glucose and galactose.

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6
Q

What causes bloating in lactose intolerant people

A

Bacteria in the intestinal lumen will break down the lactose, releasing gas and lactic acid

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7
Q

What causes diarrhea in lactose intolerance

A

The increase in lactic acid increases the osmotic level, causing water to transport into the gut

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8
Q

What is the difference between galactosemia and lactose intolerance?

A

Individuals with lactose intolerance cannot breakdown lactose into galacase and glucose but galactosemia is involved in further metabolizm of lactose: breaking down of galactose

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9
Q

What is galactosemia?

A

A condition where galactose cannot be further metabolized leading to toxic levels of galactose 1-phosphate can cause serious damage

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10
Q

What is fructosemia and when is not serious?

A

Lack of enzymes that can degrade fructose.
- if fructokinase is missing, the fructose cannot be converted but this can just end up in the urine
- if aldolase B is missing, fructose 1-P will build up inhibiting gluconeogenesis and glycogen degredation

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11
Q

What 2 main organs store glycogen?

A

Muscle and liver

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12
Q

What is the difference between glycogen storage in muscle and liver?

A

The liver can regulate blood glucose level with its glycogen stores: homeostasis. But the muscle uses the glycogen stores as energy for the muscle

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13
Q

What enzyme is used for glycogen synthesis and which one for mobilization?

A

Glycogen synthase and glycogen phosphorylase

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14
Q

Explain the glucose –> glycogen pathway using the main enzyme

A

Glucose –> glucose-6-P –> glucose 1-P –> UDP’s are formed by UDP-glucose-pyrophosphorylase by turing UTP into UDP –> glycogen synthase connects these UDP’s into glycogen

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15
Q

Explain the glycogen –> glucose pathway using the main enzyme

A

Glycogen debranched –> Phasphates are added by Glycogen phosphorylase into glucose-1-P

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16
Q

Why is glycogen branched?

A

So that glycogen phosphorylase can act on multiple sites at a time: Speed

17
Q

How is the uptake of glycogen regulated in muscle and liver

A

by insulin

18
Q

How is the release of glycogen regulated in muscle and liver

A
  • liver: only needs to be released when body needs it, so responses to glucagon and epinephrine (during fight or flight)
  • muscle: only responses to excercise, so also epinephrine or activity of muscle so Calcium release. but not glucagon
19
Q

What is protein kinase A

A

enzyme that phosphorylates other enzymes/molecules

20
Q

What is the effect of insulin on glycogen phosphorylase and glycogen synthase

A

Insulin present when glucose high, so insulin dephosphorylates glycogen phosphorylase (making it inactive) and dephosphorylates glycogen synthase (making it active)

21
Q

What do glucagon and epinephrine both activate and what is the result?

A

activation PKA –> phosphorylation of glycogen synthase (making it inactive) and glycogen phosphorylase (making it active)

22
Q

Is phosphorylated Glycogen synthase active?

A

no

23
Q

Is phosphorylated glycogen phosphorylase active?

A

yes

24
Q

What are the glucose regulations in muscle

A
  • external: nerve impulses –> higher calcium –> activates “phosporylase kinase” –> phosphorylates “glucagon phosphorylase” (active) –> breakdown glucogan into glucose for muscle fuel
  • internal: during muscle contraction ATP used generating AMP –> AMP binds to “glycogen phosphorylase” (active due to confirmational change)