meds2003 Flashcards

1
Q

when you lose weight, where does the fat go?

A

mostly, energy/heat

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2
Q

What is the point of the Krebs cycle

A

ripping out hydrogens and complete oxidation of carbon atoms to carbon dioxide.
No oxygen is involved. It just rips out hydrogens.

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3
Q

What does NAD like to oxidise

A

CH2CHOH

becomes NADH

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4
Q

What does FAD like to oxidise

A

CH2CH2 to CHCH

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5
Q

Some massive concepts for how fuel is used to make ATP

A

The hydrogen and electron carriers are in short supply
ADP is in short supply and ATP is really stable

The inner mitochondrial membrane is impermeable to protons
Protons only flow into the matrix if the ATP is being made

The proton pumps don’t work if the proton gradient is very high

No proton pumping would result in no electron movement down the ET chain

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6
Q

Beta oxidation

A

Fatty acids trapped in cytoplasm as fatty AcylCoA

fatty Acyl CoA is transported into matrix by carnitine.
Acetyl CoA somehow released by beta oxidation.

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7
Q

How is fatty acid transported in the blood

A

They are transported as being bound by albumin.

They could passively diffuse from the blood into the cytoplasm

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8
Q

How is fatty acyl CoA moved into the matrix

A

So carnitine acyl transferases turn FA-CoA to just FA

FA basically combines with carnitine and this helps move it into the cytoplasm

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9
Q

Outline beta oxidation

A

basically there are 2 main phases,
first the FAD hydrogen stripping phase

Then the second NAD hydrogen stripping phase

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10
Q

Outline the first hydrogen stripping phase

A

1) with acyl CoA dehydrogenase, and FAD,
a double bond is formed between the alpha and beta carbons
This forms trans enoyl CoA

trans enoyl CoA is hydrated along with enoyl CoA hydratase.
The double bond is hydrated

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11
Q

Outline the second hydrogen stripping phase

A

The hydroxy group is turned into a ketone group by beta hydroxyacyl CoA dehydrogenase

Then acylCoA transferase reacts with beta ketoacyl CoA, and this is what forms acetyl CoA

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12
Q

What are 2 sources of G6P in glycolysis?

A

Glycogen and glucose

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13
Q

How is glucose moved into the cytoplasm

A

Glucose is taken into the cytoplasm from blood using GLUT proteins. Hexokinase transforms glucose into glucose 6 phosphate preventing glucose from exiting the cell

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14
Q

What is the point of glucose preparation

A

to basically produce 2 symmetrical items and
glucose 6 phosphate goes to fructose 6 phosphate
Then it goes to fructose 1,6 bisphosphate
Then fructose 1,6 bisphosphate gets split into 2

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15
Q

outline how G3p goes to pyruvate (the return phase)

A

g3p
gets phosphorylated by inorganic phosphates and NAD to form 1-3 bisphosphoglycerate

Then 1,3-Bisphosphoglycerate gets forms atp this is called substrate level phosphorylation

you eventually get to pyruvate

a second substrate level phosphorylation happens along here

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16
Q

What is the overall point of the kreb cycle

A

completely oxidise acetate carbons to CO2
produce lots of NADH and FADH2
performs the reactions on a carrier molecule and regenerate the carrier

17
Q

How do we measure the rate at which ATP is used?

A

We measure the rate of oxygen and or carbon dioxide, as the rate of fuel oxidation is matched to the rate at which the ATP is used.

18
Q

What happens when there is no proton gradient

A

There is no driving force for ATP synthesis:

1) No back-pressure to stop H+ pumping
2) No restriction on H/e- movement down the transport chain

Instant regeneration of NAD from NADH
massive fuel oxidation rate
massive oxygen consumption

No ATP synthesis

19
Q

DNP

A

hydrophobic when protonated
can move freely across membrane

weak acid

When hydrogen comes off negative charge can be delocalised
still hydrophobic

20
Q

How does uncoupling protein mechanism work?

A

Noradrenaline binds to beta 3 receptors on cell surface, stimulates fatty acid release then opens proton channel so targeted and controllable

21
Q

NAD structure

A

basically a dinucleotide with a nicotanamide group (niacin)

changes absorption spectrum

22
Q

fad structure

A

adenine recerptor with a ring structure called fmn

23
Q

Glycerol 3 phosphate shuttle

A

essentially bypasses complex 1

NADH from the cytoplasm basically just reacts with cytoplasmic glycerol 3 phosphate dehydrogenase to produce glycerol 3 phosphate, and glycerol 3 phosphate donates hydrogen to FAD on a mitochondrial glycerol 3 phosphate dehydrogenase

24
Q

Malate aspartate shuttle

A

reacting cytoplasmic NADH with oxaloacetate to give malate,
and malate delivers hydrogen into the mitochondria
move cytoplasmic NADH into the cytoplasm

With no loss of proton pumping potential

25
Q

What are the 4 routes to Q

A

from complex 1
from complex 2 (which is really succinate dehydrogenase in the krebs cycle

from the first step of beta oxidation

from the glycerol 3 P shuttle

26
Q

what are other ways of uncoupling other than thermogenin

A

apparently you could send the hydrogen from NADH directly to oxygen via alternative oxidase

27
Q

where does free radicals come from?

A

oxygen can react with the complexes prematurely or hydrogens could sneak out of the chain

You get oxygen free radicals that could mutate DNA