News Coverage
The Wilbrecht Lab’s recent paper appearing in Neuropharmacology, Brief cognitive training interventions in young adulthood promote long-term resilience to drug-seeking behavior, has attracted some news attention:
- Addiction Isn’t Hardwired: Intellectual Pursuits May Buffer Brain Against Addiction, Science 2.0, July 23, 2015.
- Kayla Kettmann, UC Berkeley researchers find connection between lack of mental stimulation, addiction, The Daily Californian, July 22, 2015.
- KCBS covered the paper. Here is the audio in OGG and MP3.
- New study finds that intellectual pursuits can buffer the brain’s reward system against drug dependence, News Medical, July 15, 2015.
- Anastasia Subervi, Estudio: Actividades intelectuales pueden desviar las adicciones, UPI Espanol, July 15, 2015.
- Matthieu Delacharlery, Stimuler le cerveau permet de réduire la tentation aux drogues, MetroNews, July 15, 2015.
- Ali Venosa, Addiction Solitaire: Increasing Cognitive Stimulation May Reduce Drug-Seeking Behavior, Medical Daily, July 15, 2015.
- Un entorno estimulante ayuda a abandonar las adicciones,Tendencias De La Salud, July 15, 2015.
- Intellectual pursuits may buffer the brain against addiction, ScienceBlog, July 14, 2015.
- Yasmin Anwar, Intellectual pursuits may buffer the brain against addiction, UC Berkeley News, July 13, 2015 (press release, also pasted below).
Intellectual pursuits may buffer the brain against addiction
Challenging the idea that addiction is hardwired in the brain, a new UC Berkeley study of mice suggests that even a short time spent in a stimulating learning environment can rewire the brain’s reward system and buffer it against drug dependence.
Scientists tracked cocaine cravings in more than 70 adult male mice and found that those rodents whose daily drill included exploration, learning and finding hidden tasty morsels were less likely than their enrichment-deprived counterparts to seek solace in a chamber where they had been given cocaine.
“We have compelling behavioral evidence that self-directed exploration and learning altered their reward systems so that when cocaine was experienced it made less of an impact on their brain,” said Linda Wilbrecht, assistant professor of psychology and neuroscience at UC Berkeley and senior author of the paper just published in the journal, Neuropharmacology.
By contrast, mice who were not intellectually challenged and/or whose activities and diets were restricted, were eager to return to the quarters where they had been injected with cocaine for weeks on end.
“We know that mice living in deprived conditions show higher levels of drug-seeking behavior than those living in stimulating environments, and we sought to develop a brief intervention that would promote resilience in the deprived animals,” said study lead author Josiah Boivin, a Ph.D. student in neuroscience at UC San Francisco who conducted the research at UC Berkeley as part of his thesis work.
Drug abuse and addiction rank among the world’s more costly, destructive and seemingly insurmountable problems. Previous studies have found that poverty, trauma, mental illness and other environmental and physiological stressors can alter the brain’s reward circuitry and make us more susceptible to substance abuse.
The good news about this latest study is that it offers scalable interventions against drug-seeking behaviors, albeit through evidence based on animal behavior.
“Our data are exciting because they suggest that positive learning experiences, through education or play in a structured environment, could sculpt and develop brain circuits to build resilience in at-risk individuals, and that even brief cognitive interventions may be somewhat protective and last a relatively long time,” Wilbrecht said.
Intellectually challenged mice vs. deprived mice
Researchers compared the lure of drugs, specifically cocaine, in three sets of mice: The test or “trained” mice were put through a nine-day cognitive training program based on exploration, incentives and rewards while their “yoked-to-trained” counterparts received rewards but no challenges. The “standard-housed” mice stayed in their home cages with restricted diets and activities.
For a few hours each day, the trained mice and yoked-to-trained mice were set loose in adjacent chambers. The trained mice were free to explore and engage in enrichment activities, which included digging up Honey Nut Cheerios in a pot of scented wood shavings. The exercise kept them on their toes because the rules for how to find the treats would change on a regular basis.
Meanwhile, their yoked-to-trained counterparts received a Honey Nut Cheerio each time their trained partner hit the jackpot, but did not have to work for it. As for the standard-housed mice, they remained in their cages without enrichment opportunities or Honey Nut Cheerios. After the cognitive training phase of the experiment, all three sets of mice remained in their cages for a month.
Cocaine conditioning tests desire for drugs
Next, the mice were set loose, one by one, to explore two adjoining chambers in a plexiglass box, which differed from one another in smell, texture and pattern. The researchers recorded which chamber each mouse preferred and then set about changing their preference by giving them cocaine in the chamber that they had repeatedly not favored.
For the drug seeking test, the mice received mock injections, and were freed to explore both chambers for 20 minutes, using the open doorway to scamper back and forth. At first, all the mice overwhelmingly returned to the chamber where they had presumably enjoyed the cocaine. But in subsequent weekly drug seeking tests, the mice who had received cognitive training showed less preference for the chamber where they had been high on cocaine. And that pattern continued.
“Overall, the data suggest that deprivation may confer vulnerability to drug seeking behavior and that brief interventions may promote long-term resilience,” Wilbrecht said.
Denise Piscopo, an assistant professor at the University of Oregon and former member of Wilbrecht’s lab, is the third co-author on the paper.