How does alcohol make you drunk? - Judy Grisel

Ethanol: this molecule, made of little more than a few carbon atoms,

is responsible for drunkenness.

Often simply referred to as alcohol,

ethanol is the active ingredient in alcoholic beverages.

Its simplicity helps it sneak across membranes

and nestle into a many different nooks,

producing a wide range of effects compared to other, clunkier molecules.

So how exactly does it cause drunkenness,

and why does it have dramatically different effects on different people?

To answer these questions,

we’ll need to follow alcohol on its journey through the body.

Alcohol lands in the stomach and is absorbed into the blood

through the digestive tract, especially the small intestine.

The contents of the stomach impact alcohol’s ability

to get into the blood because after eating, the pyloric sphincter,

which separates the stomach from the small intestine, closes.

So the level of alcohol that reaches the blood after a big meal

might only be a quarter that from the same drink on an empty stomach.

From the blood, alcohol goes to the organs,

especially those that get the most blood flow:

the liver and the brain.

It hits the liver first, and enzymes in the liver

break down the alcohol molecule in two steps.

First, an enzyme called ADH turns alcohol into acetaldehyde, which is toxic.

Then, an enzyme called ALDH converts the toxic acetaldehyde to non-toxic acetate.

As the blood circulates, the liver eliminates alcohol continuously—

but this first pass of elimination determines how much alcohol

reaches the brain and other organs.

Brain sensitivity is responsible for the emotional, cognitive,

and behavioral effects of alcohol— otherwise known as drunkenness.

Alcohol turns up the brain’s primary brake, the neurotransmitter GABA,

and turns down its primary gas, the neurotransmitter glutamate.

This makes neurons much less communicative,

and users feel relaxed at moderate doses, fall asleep at higher doses,

and can impede the brain activity necessary for survival at toxic doses.

Alcohol also stimulates a small group of neurons

that extends from the midbrain to the nucleus accumbens,

a region important for motivation.

Like all addictive drugs,

it prompts a squirt of dopamine in the nucleus accumbens

which gives users a surge of pleasure.

Alcohol also causes some neurons to synthesize and release endorphins.

Endorphins help us to calm down in response to stress or danger.

Elevated levels of endorphins contribute to the euphoria

and relaxation associated with alcohol consumption.

Finally,

as the liver’s breakdown of alcohol outpaces the brain’s absorption,

drunkenness fades away.

Individual differences at any point in this journey

can cause people to act more or less drunk.

For example, a man and a woman who weigh the same and drink the same amount

during an identical meal will still have different blood alcohol concentrations,

or BACs.

This is because women tend to have less blood—

women generally have a higher percentage of fat,

which requires less blood than muscle.

A smaller blood volume, carrying the same amount of alcohol,

means the concentration will be higher for women.

Genetic differences in the liver’s alcohol processing enzymes also influence BAC.

And regular drinking can increase production of these enzymes,

contributing to tolerance.

On the other hand, those who drink excessively for a long time

may develop liver damage, which has the opposite effect.

Meanwhile, genetic differences in dopamine, GABA,

and endorphin transmission may contribute to risk

for developing an alcohol use disorder.

Those with naturally low endorphin or dopamine levels may self-medicate

through drinking.

Some people have a higher risk for excessive drinking

due to a sensitive endorphin response that increases the pleasurable effects

of alcohol.

Others have a variation in GABA transmission

that makes them especially sensitive to the sedative effects of alcohol,

which decreases their risk of developing disordered drinking.

Meanwhile, the brain adapts to chronic alcohol consumption by reducing GABA,

dopamine, and endorphin transmission, and enhancing glutamate activity.

This means regular drinkers tend to be anxious, have trouble sleeping,

and experience less pleasure.

These structural and functional changes can lead to disordered use

when drinking feels normal, but not drinking is uncomfortable,

establishing a vicious cycle.

So both genetics and previous experience impact how a person experiences alcohol—

which means that some people are more prone

to certain patterns of drinking than others,

and a history of consumption leads to neural and behavioral changes.