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Possible Reason for Rimonabant's Side Effects Discovered
Weight-loss drug not approved in U.S. may block brain receptor among some users
By Steven Reinberg
HealthDay Reporter
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WEDNESDAY, March 12 (HealthDay News) -- The weight-loss drug rimonabant has been associated with troubling psychiatric side effects, and now researchers think they have discovered why.
A receptor in the brain called TRPV1, which is central to learning and memory, may be blocked by large doses of rimonabant (Acomplia), resulting in depression, anxiety and suicidal thoughts among some people taking the drug, a new study shows.
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"We think that changes in the strength of connections between neurons in the brain underlie all kinds of important changes in the brain like learning, the development of the nervous system and many other adaptations to the environment, such as responses to pain and responses to drugs," said lead researcher Julie Kauer, an associate professor of molecular pharmacology, physiology and biotechnology at Brown University in Rhode Island.
The report was published in the March 13 issue of Neuron.
In experiments with rat brains, Kauer's group found that TRPV1 controls a brain mechanism called long-term depression, which is thought to be a key component in memory. The team thinks this finding may relate to the psychiatric side effects that have been seen with Acomplia.
"We found that rimonabant blocked TRPV1, and also another receptor CB1. It's possible that when the patient takes the drug, and the dose range is correct, it may not affect TRPV1 at all," Kauer said. "However, in some patients, Acomplia could be hitting TRPV1 and may well have an effect on activating this receptor," she said.
Acomplia is used widely outside the United States. To date, the U.S. Food and Drug Administration has not approved Acomplia because of its psychiatric side effects.
In addition, the researchers found that a new class of painkillers may interfere with learning and memory, because they also block TRPV1.
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Copyright © 2008 ScoutNews, LLC. All rights reserved.
Last updated 3/12/2008
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SOURCES: Julie Kauer, Ph.D., associate professor, molecular pharmacology, physiology and biotechnology, Brown University, Providence, R.I.;
Raj Padwal, M.D., assistant professor, general internal medicine, University of Alberta, Edmonton, Canada; March 13, 2008, Neuron
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