A study conducted by Rutgers University found that changes in the brain can lead to a desire for drugs and demonstrated how certain insomnia medications may be able to prevent this behavior.
Researchers at Rutgers University have discovered a potential biological process for drug and alcohol addiction and believe that current treatments for insomnia could potentially be utilized to reduce or eliminate cravings.
An article recently published in the journal Biological Psychiatry discusses the findings of researchers at the Rutgers Brain Health Institute and other institutions on the role of the orexin system in drug addiction. The orexin system, which regulates sleep patterns, reward pathways, and mood, has been found to drive drug-seeking behavior. It has been observed that many drugs of abuse increase orexin production in both human and animal brains, and blocking this system can reverse addiction in animals. In addition, a separate study has shown that one of the three FDA-approved insomnia medications that block orexin can reduce opioid cravings in human subjects.
“There’s still much to discover about how orexin drives drug craving, but we know more than enough to justify testing orexin antagonists in clinical trials as addiction treatments,” said Gary Aston-Jones, coauthor of the review and director of the Brain Health Institute. “We’re applying for funding from the National Institutes of Health and looking to hire a physician-scientist with clinical trial experience to lead these efforts.”
The review, which draws on more than a decade of publications from researchers at Rutgers and peer institutions, suggests that orexin spurs drug craving and, thus, motivation to procure a drug.
Under normal circumstances, many orexin-producing cells in the brain turn orexin production on and off in ways that raise and lower motivation. These cells turn on when, e.g., people face a tight deadline and need to get work done and turn off at night to enable sleep. However, when people become addicted to opioids, cocaine, alcohol and other substances, these cells increase orexin production but no longer turn it off. They stay on constantly, producing high levels of orexin that motivates one behavior: getting another hit.
Controlled studies of mice, rats, zebrafish and other animals have allowed researchers to systematically examine each step in the process. Postmortem analysis of brain tissue from people who used heroin shows the same increase in the human orexin system that researchers have observed in addicted animals. Once triggered, this overactivity may last forever – indeed, the research team observed increased orexin levels in cocaine-addicted rats that stayed sober for more than a quarter of their natural lifespan.
Earlier research into orexin’s sleep-blocking effects spurred the creation of anti-orexin insomnia medications, three of which have been approved by the U.S. Food and Drug Administration (Belsomra, Quviviq and Davigo). As orexin’s role in addiction has emerged, researchers have tested these medications as addiction treatments, mostly in animals. Research at Rutgers has found that low doses of one of these medications can reduce drug-seeking behavior in rats without sedating them or impairing cognitive function. Moreover, a recent study from Johns Hopkins University showed that this medication can reduce cravings in people detoxifying from opioids.
“There’s obviously no guarantee orexin antagonists will effectively treat addiction, but our research gives us good reason for hope,” said Morgan James, coauthor of the review and a professor of psychiatry at Rutgers Robert Wood Johnson Medical School. “And the need for effective treatments is enormous. Overdose deaths have skyrocketed past 100,000 a year and existing treatment options have limited efficacy.”
Reference: “Orexin Reserve: A Mechanistic Framework for the Role of Orexins (Hypocretins) in Addiction” by Morgan H. James and Gary Aston-Jones, 1 July 2022, Biological Psychiatry.