Ethanol Flashcards

1
Q
  1. Is alcohol potent?
  2. What is a “single dose”?
    What is the liquid beverage equivalent?
A
  1. No it is not potent
  2. “Single dose” is 14 grams.
    12 ounces of beer, 5 ounces of wine, 1.5 oz of 80 proof
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2
Q

What is the blood alcohol effect of 14g ETOH on 70kg person?

A

0.03 % w/v = 30mg/dL

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3
Q
  1. What determines distribution of ETOH?
  2. Why does a breathalizer work?
  3. What determines indivual organ distribution of ETOH?
A
  1. Total body water
  2. ETOH crosses membranes freely, including alveoli.
  3. Dependent on amount of blood flow
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4
Q
  1. What is ETOH primarily metabolized into?
  2. What role do gastric and liver alcohol dehydrogenases have?
A
  1. Acetaldehyde
  2. They create a first pass effect
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5
Q
  1. What are the two major enzymes that metabolize ETOH into acetaldehyde?
  2. What type of kinetics are involved with ETOH? Why?
  3. How is Acetaldehyde metabolized for elimination?
A
  1. Alcohol dehydrogenase and CYP2E1
  2. Zero order kinetics. ADH is rapidly saturated.
  3. Aldehyde dehydrogenase
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6
Q
  1. How much alcohol is required to saturate ADH and begin accumulating alcohol?
  2. How long does one 14g drink take to be metabolized?
A
  1. 10g/hr in 70kg person
  2. 1.5 hours
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7
Q
  1. How does Disulfiram (Antabuse) work?
  2. Why do those of Asian decent have impaired ETOH metabolism?
A
  1. It inhibits Aldehyde dehydrogenase and causes an increase acetaldehyde and nausea/vomiting symptoms.
  2. Genetic polymorphism that impairs activity of aldehyde dehydrogenase
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8
Q

Why do alcoholics become hypoglycemic?

A
  1. Increased NADH impairs TCA cycle and reduces gluconeogenesis.
  2. There is also reduced fatty acid oxidation.
  3. Ethanol promotes insulin secretion
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9
Q

What does the metabolite of ETOH, acetaldehyde, cause?

A
  1. Protein adduct formation which results in inflammation.
  2. Inhibition of microtubules
  3. Depletion of glutathione.
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10
Q
  1. What is the most important receptor for ETOH?
  2. Why does ETOH promote inhibition?
A
  1. GABAA receptor-ligand gated Cl-
  2. It disturbs the balance between excitatory and inhibitory neurotransmission
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11
Q

Why is ETOH withdrawal dangerous?

A

Removal of chronic CNS depression can result in over-excitation/seizures. These are significantly worse in the presence of metabolic derangement.

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12
Q

Chronic alcohol use can result in Thiamine deficiency. What three significant clinical effects result from this?

A
  1. Cerebral/cerebellar atrophy
  2. Wernicke’s encephalopathy
  3. Korsakoff’s psychosis
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13
Q

What amount of alcohol generally causes “acute intoxication”?

A

400mg/dl = 12 drinks

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14
Q
  1. What is a Mu Opiate Receptor antagonist that is used to treat alcoholism?
  2. What is Acamprosate?
A
  1. Naltrexone
  2. GABAA agonist that can decrease drinking frequency and relapse. It is thought to normalize dysregulated neurotransmission.
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