Drug abuse 3: Alcohol Flashcards

1
Q

What is the formulae for absolute amount of alcohol?

A

% ABV x 0.78 = g alcohol/100ml

ABV = alcohol by volume

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2
Q

How do you calculate the number of units?

A

[%ABV x volume (ml)]/ 1000 = units

1 unit = 10ml or 8g of absolute alcohol

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3
Q

What are the safe levels of alcohol?

A

Men and Women; =< 14 units/week LOW RISK

Binge drinking i.e. > 8 units in one sitting; 18% of 16-24 yrs (> 30%) ↓

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4
Q

How does drinking on a full stomach influence your blood alcohol level?

A

Oral administrated

Speed of onset is directly proportional to gastric emptying.

When you eat the stomach will remained closed off for a while while it digests the food. This means the alcohol remains in the stomach when you drink on a full stomach = slower release of alcohol into the blood stream.

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5
Q

Where is alcohol absorbed?

A

Alcohol is absorbed from the stomach but better in the small intestine.
20% - stomach
80% - small intestine

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6
Q

Describe the metabolism of alcohol?

A

90% of the alcohol is metabolised, 10% is secreted unchanged.

85% is metabolised in the liver:

  • Alcohol dehydrogenase (metabolises 75% of the alcohol)
  • Mixed function oxidase (cytochrome p450) (metabolises 25% of the alcohol)

The metabolite is acetaldehyde

15% is metabolised in the GIT:

  • Absorbs through the stomach the lining - it can break down alcohol with alcohol dehydrogenase
  • Women have 50% less Alcohol dehydrogenase int he stomach wall compared to men.
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7
Q

Which enzyme increases with chronic use?

A

Cytochrome p450 increases with chronic use –> you become tolerant.

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8
Q

What happens when you drink alcohol very quickly

A

If you flood the liver with alcohol the enzymes in the liver can become saturated.
When it is saturated it can get into the systemic circulation.

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9
Q

Why can alcohol be absorbed through the stomach?

A

Alcohol is very water soluble - so you don’t expect it to diffuse through membranes very well.

However it is very small –> It can diffuse across lipid membranes because its so small.

Broken down by alcohol dehydrogenase

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10
Q

A man and a woman of similar height and weight share a bottle of wine. Explain why the blood alcohol levels in the woman are likely to be higher.

A

Less body water

Less ADH

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11
Q

How is acetaldehyde broken down?

A

Aldehyde dehydrogenase: breaks acetaldehyde (has negative effects) to acetic acid.

(Genetic polymorphism - asian people aldehyde dehydrogenase doesn’t work as effectively)

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12
Q

What drug can be effective as alcohol aversion therapy.

A

Aldehyde dehydrogenase inhibitor = build up of acetalydehyde which has negative effects

Disulfiram

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13
Q

Describe the pharmacodynamics of alcohol

A

Alcohol is a depressant (primary effect)

CNS agitation may occur and it is dependent on various factors.
See diagram

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14
Q

Can you identify a pharmacological target for alcohol? What would you predict regarding the affinity and efficacy for this target?

A

Not really - very simple molecule.
It can bind to a lot of receptors but not really have any effects. Low affinity and efficacy.

The idea is to take a high dose so that the overall effect is higher.

High enough dose literally everything becomes a depressant.

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15
Q

How does alcohol have a depressant effect?

A

Enhance GABA receptor activation - positively modualtes.
Increases presynaptic effects. Allopregnenole is a neuro active steroid. Alcohol increases its production which has a positive effect on the GABA receptor

NMDA receptors - binds and decreases its activity. Decreases an excitatory receptor

Ca2+ channels - decreases calcium channel opening

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16
Q

What are the acute effects of alcohol? CNS

A

1) CNS is functionally complex - alcohol binds to lots of receptors

  • Corpus Collosum - Passes info from the left brain (rules, logic)
    to the right brain (impulse, feelings) and vice versa.
  • Hypothalamus - Controls appetite, emotions, temperature,
    and pain sensation.
  • Reticular Activating System – Consciousness
  • Hippocampus - Memory
  • Cerebellum - Movement
    and coordination
  • Basal Ganglia –
    Perception of time

2) Ethanol has low potency = low selectivity

17
Q

How might alcohol cause euphoria?

A

Alcohol at a high dose can behave like heroin/morphine. It will bind to the opiate receptors on GABA

18
Q

What are the acute effects of alcohol? CVS?

A

Cutaneous vasodilation - Asian flush

  • Decrease Ca2+ entry
  • Increase prostaglandins

We think it is acetaldehyde - link back to the genetic polymorphism

Acute tachycardia - a depressant effect on the baroreceptor. It decreases the sensitivity of the baroreceptor = less parasympathetic innervation and less inhibition of the sympathetic –> tachycardia

19
Q

What are the acute effects of the alcohol? Endocrine system

A

Diuresis (polyuria)

Probably due to inhibiting ADH - maybe acetaldehyde.

20
Q

What are the chronic effect of alcohol in the brain?

A

Thiamine deficiency. Thiamine is cofactor for several enzymes that are involved in energy metabolism –> cerebral energy utilisation

If you have a deficiency it diminishes brain activity.

Brain regions with high metabolic demand are the most affected – impaired metabolism, NMDA excitotoxicity, Reactive Oxygen Species.

Dementia – Cortical atrophy/decrease in volume cerebral white matter confusion (encephalopathy), oculomotor symptoms
Ataxia – Cerebellar cortex degeneration - gait

Wernicke-Korsakoff syndrome (due to thiamine deficiency)

  • Wernicke’s encephalopathy – (hypothalamus/thalamus) Reversible
  • Korsakoff’s psychosis – (deep brain e.g. hippocampus) Irreversible, essentially regions of the brain are dying

SEE THIS SLIDE LOOK AT THE BLACK HIGHLIGHTS - associated with Wernicke’s

21
Q

Chronic effects in the liver?

A

Alcohol is using NAD+ in the liver.

beta oxidation of fats needs NAD+ –> build up of fat in the liver if the alcohol is using it all up. The glycerol and fatty acids are converted to triacylglycerol leading to a fatty liver

TCA cycle needs NAD+ means pyruvate and acetyl CoA can’t be recycled. This leads to ketones and lactic acid build up.

22
Q

How do you develop hepatitis?

A

Oxygen free radicals.
Chronic drinking means you get a constant depletion of NAD+ and exposure to acetaldehyde.
- Lack of NAD+ means oxygen free radicals are released. These can damage tissue and cause inflammation
- Acetaldehyde is also proinflammatory and causes tissue damage.
- Deranged metabolism; pyruvate and acetyl CoA can’t be recycled. Ketone and lactic acid build up

Together you get hepatitis.

23
Q

How does cirrhosis develop?

A

For the same reasons which causes hepatitis. If it continues for a long time you get fibroblast infiltration.

These fibroblasts will then lay down connective tissue and replace active hepatocytes.

They are essentially replacing the metabolic tissue.

24
Q

What is the order of liver disease?

A

Fatty liver - very reversible
Hepatitis - reversible
Cirrhosis - irreversible

25
Q

What are the beneficial effects of chronic alcohol?

A

Decreased mortality from coronary artery disease (Men 2-4 units/day);

Increased HDLs (improves lipid profile)
Increased tPA levels/ decreased platelet aggregation
26
Q

What are the chronic effects on the GIT?

A

Damage to gastric mucosa (proportional to dose)

Ulceration is common in alcoholics

We are not sure if it is directly carcinogenic

27
Q

What are the chronic effects on the endocrine system?

A

Increased ACTH

Decreased Testosterone secretion

28
Q

What are the effects of hangover?

A

Symptoms - peak as rebound excitation

Nausea: Irritant –>Vagus
–>Vomiting center

Headache: Vasodilation

Fatigue:

1) Sleep deprivation,
2) ‘Rebound’

Restlessness and muscle tremors: ‘Rebound’

Polyuria and polydipsia:
↓ ADH secretion

Best thing to do is to sleep