Why do some people only have one drink, whereas others find it difficult to stop? A neuroscientific study sheds light.
According to the most recent estimates, over
Approximately 88,000 people die from alcohol-related problems every year, making alcohol the “third leading preventable cause of death” in the United States.
However, what makes some of us crave alcohol so much, even when it’s bad for us? One answer is dopamine, the so-called
Dopamine helps the brain learn new things, but it may also lead us down the path of addiction.
Dopamine earned its nickname because it is a feel-good chemical that is released as a reward for the brain when we learn new things or during pleasurable activities such as sex. It is also the substance that “tells” us to prolong the pleasure and continue to “chase the high.”
In the case of alcohol dependence, when alcohol reaches the brain, it causes the neurons in a region called the ventral tegmental area (VTA) to release dopamine.
Until now, the precise molecular steps through which this occurred weren’t clear. So, researchers at the Center for Alcohol Research in Epigenetics at the University of Illinois at Chicago (UIC) set out to investigate, and their findings shed new light on binge drinking and alcohol use disorder.
Prof. Brodie and his team started from the hypothesis that alcohol may inhibit a potassium channel called KCNK13. This channel can be found inside the membrane of dopamine neurons in the VTA. So, when this pathway is blocked, neurons release more dopamine than usual.
To verify their hypothesis, the researchers performed a range of experiments. In one of them, the scientists created a mouse model in which KCNK13 was genetically reduced by 15 percent.
The KCNK13-deprived mice drank 20–30 percent more alcohol than their normal counterparts.
Prof. Brodie explains the findings, saying, “We believe that mice with less KCNK13 in the VTA drank more alcohol in order to achieve the same ‘reward’ from alcohol as normal mice, presumably because alcohol was triggering the release of less dopamine in their brains.”
Another experiment focused on the neuronal response to alcohol in the VTA region for mice with less KCNK13.
These neurons were 50 percent less excited in response to ethanol when compared with normal VTA neurons that were exposed to ethanol.
The study’s lead author says that the findings may help explain why some people are more prone to binge drinking than others.
“If someone has naturally lower levels of this channel, then in order to produce the pleasurable effects of alcohol, that person would have to drink much more, and may be at higher risk for binge drinking disorder.”
Prof. Mark Brodie
In the future, Prof. Brodie and team plan to study how tweaking the KCNK13 channel in other brain regions and cells may change alcohol dependence and alcohol-related behavior.
“Without the channel, alcohol can’t stimulate the release of dopamine, and so drinking is likely less rewarding. We think that the KCNK13 channel presents an extremely exciting new target for drugs that could potentially help people with alcohol use disorder to stop drinking.”
“This channel,” Prof. Brodie goes on to say, “seems to be specific to alcohol effects in the VTA, so targeting it with a drug would dampen the effects of alcohol only.” In other words, a drug that targets KCNK13 would not dampen the brain’s response to pleasure in general; only to pleasure derived from alcohol.
“Currently available drugs reduce the impact of alcohol on the brain that is akin to turning down the volume on a stereo,” he says. “A drug that would target KCNK13 would be different in that it would be like an on/off switch. If it’s turned off, alcohol just wouldn’t trigger increased dopamine release.”