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TSRI Researchers Win $3.9 Million in Grants to Study Brain Regions that Suppress Cocaine and Alcohol Cravings

LA JOLLA, CA ­– April 21, 2015 – Scientists at The Scripps Research Institute (TSRI) have been awarded two grants to study brain mechanisms that actively suppress relapse associated with cocaine and alcohol addiction.

The studies will be funded by grants worth more than $2.1 million from the National Institute of Health’s (NIH) National Institute on Alcohol Abuse and Alcoholism (NIAAA) and $1.7 million from the agency’s National Institute on Drug Abuse (NIDA).

Nobuyoshi Suto, a newly appointed assistant professor of molecular and cellular neuroscience at TSRI, will be the principal investigator for the two five-year studies.

“The risk of chronic relapse, even after long periods of abstinence, is a major issue in treating addiction,” Suto explained.

Previous studies have shown that external stimuli or cues signaling the availability of drugs or alcohol (“availability cues”)—such as drug paraphernalia or the smell of beer—can activate certain types of neurons, neurochemicals and circuits in the brain and trigger relapse.

Suto and his colleagues, however, are looking at the opposite phenomenon. In preliminary studies, they have demonstrated that cues signaling the unavailability of drugs or alcohol (“omission cues”) can actually suppress relapse in well-established animal models of drug addiction.

Using the omission cue-induced suppression as the animal model of relapse suppression, the researchers want to know which brain mechanisms mediate the relapse-suppressing action of omission cues. This research could not only uncover fundamental workings of the brain in behavioral inhibition, but could also point to new methods for helping people resist relapse.

Suto’s preliminary data with rat models suggest that omission cues activate neurons in the medial prefrontal cortex, the area of the brain associated with decision making. This is consistent with results from human studies showing activity in the medial prefrontal cortex when addicts are shown images of drug use and told to suppress their cravings.

“If we can better understand these brain mechanisms that actively suppress—as opposed to promote—relapse, we may be able to develop a drug to enhance these mechanisms and maybe mimic those relapse-suppressing cues,” said Suto.

Suto will be collaborating with TSRI Professors Friedbert Weiss, Larry Parsons and Mark Mayford, along with Bruce Hope, investigator with the NIH’s Intramural Research Program.

“The great thing about doing this study at TSRI are the world-class scientists here,” said Suto.

These new projects extend the studies funded by an earlier grant (NIDA - R21DA033533, worth $536,250) awarded to Suto in 2013 when he was a research associate in the Weiss lab.

The number of the new grant from the NIH’s National Institute on Alcohol Abuse and Alcoholism is R01AA023183. The number of the new grant from the NIH’s National Institute on Drug Abuse is R01DA037294.

About The Scripps Research Institute

The Scripps Research Institute (TSRI) is one of the world's largest independent, not-for-profit organizations focusing on research in the biomedical sciences. TSRI is internationally recognized for its contributions to science and health, including its role in laying the foundation for new treatments for cancer, rheumatoid arthritis, hemophilia, and other diseases. An institution that evolved from the Scripps Metabolic Clinic founded by philanthropist Ellen Browning Scripps in 1924, the institute now employs more than 2,500 people on its campuses in La Jolla, CA, and Jupiter, FL, where its renowned scientists—including two Nobel laureates and 20 members of the National Academy of Science, Engineering or Medicine—work toward their next discoveries. The institute's graduate program, which awards PhD degrees in biology and chemistry, ranks among the top ten of its kind in the nation. For more information, see

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Scripps Research Institute Assistant Professor Nobuyoshi Suto will lead the two five-year projects. (High-res image)