At Vanderbilt University Medical Center, a study by researchers is offering a glimmer of hope to alcoholics who find it hard to remain sober because their abstinence is hounded by stubborn, difficult-to-treat depression.
Using an anesthetic drug that also has antidepressant properties, and another drug that raises levels of a mood-enhancing natural chemical in the brain, the researchers found that they could alleviate depressive-like symptoms in a mouse model of alcoholism. The findings, published online this month in the journal Neuropsychopharmacology, could set the stage for development of novel treatments for mood and anxiety disorders that are induced by withdrawal from alcohol.
Depression is highly associated with alcohol abuse disorders. Yet before these findings can be applied to humans, "much work remains to be done," said senior author Danny Winder, Ph.D., professor of Molecular Physiology and Biophysics and of Psychiatry. Clinical studies in which both conditions have been treated at the same time are "woefully lacking," he and his colleagues wrote.
When the mice were given ketamine, the depressive symptoms were reversed. The researchers also tested the effect of raising brain levels of an endocannabinoid called 2-AG by blocking the enzyme monoacylglycerol (MAG) lipase. Endocannabinoids are naturally produced chemical messengers that have been implicated in depression and anxiety-like behavior.
A previous Vanderbilt study found that raising 2-AG levels with an MAG lipase inhibitor reduced stress-induced anxiety-like behaviors in mice. In the current study, treatment with a MAG lipase inhibitor had a similar effect to ketamine in reversing depressive symptoms after alcohol withdrawal. "We are excited to pursue the role of the endocannabinoid system further," Winder said. But clinical use of ligands (compounds) that bind endogenous cannabinoid receptors is still in its infancy, he said.
Winder's co-authors included first author Katherine Holleran, a graduate student in the Vanderbilt Neuroscience Graduate Program, and Sachin Patel, M.D., Ph.D., associate professor of Psychiatry and of Molecular Physiology and Biophysics. The study was supported by National Institutes of Health grants AA021623, AA019455 and MH103950, and by the Brain & Behavior Research Foundation, formerly the National Alliance for Research on Schizophrenia and Depression (NARSAD).