Alcohol and Xenobiotic Metabolism of the Liver Flashcards

1
Q

phases of drug metabolism in the liver

A

phase I: hydroxylation by microsomal CYP450

phase II: conjugation using UDP glucuronic acid, PAPs (sulfate), Glutathione, AA

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2
Q

where do the phases of drug metabolism occur

A

phase I is in the ER and phase II in they cytosol

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3
Q

reason why we detoxify alcohol/xenobiotics

A

to increase their water solubility (for excretion) in the two phases

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4
Q

do all drugs go through both phases

A

No some skip phase I hence not using CYP450

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5
Q

what does CYP450 do to drugs

A

can inactivate it, make it more polar to be excreted, activate it, convert it to a toxic metabolite

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6
Q

what does CYP3A4 rep/do

A

1/3 of CYP450 and acts on more than half of the therapeutic drugs like statin and tamoxifen

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7
Q

what does CYP2E1 do

A

ethanol metabolism

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8
Q

what does CYP450 contain

A

heme containing enzyme —-induced by drugs and ethanol

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9
Q

provides CYP450 the NADPH it needs to catalyze its reaction

A

CYP450 reductase

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10
Q

what induces CYP450

A

increase transcription of mRNA of CYP450, drugs like phenobarbitol, ethanol consumption (specifically activates the CYP2E1 –part of microsomal ethanol oxidizing system MEOS)

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11
Q

what patients do you avoid giving phenobarbitol to

A

those with acute intermittent porphyria —if you stimulate heme synthesis in them leads to higher ALA (similar to GABA hence cell death)

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12
Q

grapefruit juice can inactive which cytochrome

A

CYP3A4

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13
Q

what happens then when CYP3A4 has been inactivated

A

drugs like statin and tamoxifen would be less inactive

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14
Q

why must one increase the amount of warfarin intake if drug is taken together with phenobarbital

A

phenobarbital degrades warfarin so more must be taken to overcome

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15
Q

what happens if taken high warfarin with phenobaribital then one stops taken phenobarbital but continues high dose of warfarin

A

warfarin level too high hence dangerous bleeding can occur

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16
Q

what happens with acetaminophen (tylenol) in the body of chronic alcoholics

A

it is more processed by CYP2E1 and leads to toxic compound NAPQI

17
Q

fate of NAPQI

A

can be detoxified by glutathione then excreted in urine or can lead to cell death (REAL BAD!!!)

usually leads to cell death if just too much NAPQI and empty stomach in comparison to the glutathione present

18
Q

how do you treat acetaminophen poisoning

A

with drug acetadote – has N acetyl cysteine that binds directly to NAPQI and provides cysteine for glutathione synthesis

19
Q

main cells to metabolizes most of blood ethanol to acetaldehyde

A

hepatocytes

20
Q

enzymes that form acetaldehyde from ethanol

A

alcohol DH (low Km) and MEOS CYP2E1 (high Km)

21
Q

why do asians tend get drunk a lot quicker than most

A

they only have ALDH-1 (acetylaldehyde DH-1) and a less active ALDH-2 so acetaldehyde builds in cytosol –> eventually turned to acetate using ALDH-1 before being released into blood

22
Q

fate of acetaldehyde in blood

A

can be taken up into mito and using ALDH-2 turned into acetate or in the cytosol, using ALDH-1 can be turned into acetate then released into the blood

23
Q

difference between alcohol DH and MEOS CYP2E1

A

ADH has a low Km for ethanol so ethanol is its main substrate but MEOS CYP2E1 has a higher Km so it is induced when excess ethanol

24
Q

which has a higher Km – mitochondrial ALDH-2 or cytosolic ALDH-1

A

cytosolic ALDH-1 has a higher Km which is why acetaldehyde is used as its substrate only if high amounts of ethanol —> higher amounts of acetaldehyde

25
Q

what happens if drug is given that inhibits ALDH

A

build up of acetaldehyde in the cytosol —> flushing and elevated heart rate after small amounts of ethanol

26
Q

where do you form NADH in ethanol breakdown

A

steps that use enzyme ADH and ALDH

27
Q

ratio of NADH/NAD+ when high ethanol

A

high NADH/NAD+

28
Q

what happens as a result of high NADH/NAD+ due to high ethanol levels

A

gluconeogenesis impaired, lactate build up so pyruvate lost, oxaloacetate can’t be formed from malate, glycerol 3-P cant form DHAP

29
Q

conditions that arise from high NADH/NAD+ level

A

hypoglycemia, lactic acidemia, gout, hyperlipidemia, ketoacidosis, acetate (in blood), inhibition of drug metabolism

30
Q

what happens to acetate released by liver into blood

A

acetate it taken up by muscle and forms acetyl CoA using acetyl synthetase —>TCA cycle

31
Q

what happens to the acetylaldehyde released by liver in ethanol abuse

A
inhibits VLDL release--> fatty liver
binds to SH
inhibits release of proteins including clotting factors
toxic to brain
alcohol induced hepatitis
32
Q

drug used as treatment for alcoholism

A

disulfiram

33
Q

how does disulfiram treat alcoholism and what happens if large intake of alcohol with drug

A

prevents alcohol consumption because of flushing and nausea that comes with amount of alcohol

if large intake of alcohol with drug, amount of acetyaldehyde increases 5-10 times

34
Q

how do you treat methanol or ethylene glycol poisoning

A

inhibit alcohol dehydrogenase by ethanol or a competitive drug (Fomepizole), bicarbonate to reverse severe acidosis, and hemodialysis

35
Q

what does inhibiting alcohol dehydrogenase do in methanol poisoning

A

it stops methanol from reacting with alcohol dehydrogenase to form formaldehyde which can lead to blindness or mental problems

36
Q

how does using ethanol treat methanol poisoning

A

ethanol has a higher affinity for alcohol dehydrogenase than methanol so it will react with it rather than methanol

37
Q

what happens when ethylene glycol is ingested

A

it reacts with alcohol dehydrogenase to form glcoaldehyde —> kidney failure and death because of formation of calcium oxalate