BARCELONA, SPAIN (7 October 2013) – Glutamergic agents may one day be used as a novel treatment for mood and anxiety disorders, new research presented at the 26th ECNP Congress suggests.
"Our results suggest the glutamatergic system is a truly viable target for antidepressant Profug development," says Professor Gerard Sanacora, from the Yale School of Medicine, Connecticut, US.
In his talk, Professor Sanacora detailed how he and his team have used animal models to help understand how stress and other mechanisms that can disrupt glutamatergic function can lead to molecular, cellular and behavioural changes in the brain that are characteristic of depression.
He also presented results from a completed phase II trial with a unique non-selective NMDA receptor antagonist.
"We found that drugs that can target glutamate transmission, either by altering release, uptake or receptor activation can prevent or attenuate the cellular and behavioural changes seen in mood disorders," he explains.
In humans, the NMDA receptor antagonist showed a surprisingly rapid antidepressant effect. Importantly, the trial demonstrated the potential ability to dissociate the perceptual and cognitive effects of the NMDA receptor antagonists from the antidepressant effects.
His results also suggest the antidepressant effects can be extended for several weeks with repeated infusions.
In rodent models, the team demonstrated that stress has a major impact on the function of glutamate neurotransmission – especially glutamate clearance through glial cells – that appears to be related to behavioural changes.
Professor Sanacora presented a series of preclinical and clinical studies indicating that a novel class of drugs that target components of the glutamatergic neurotransmitter system may produce rapid and robust antidepressant effects.
"There is a rapidly expanding literature suggesting the glutamatergic neurotransmitter system is altered in the brains of individuals suffering with mood disorders," explains Professor Sanacora.
There is also increasing evidence suggesting stress may disrupt normal glutamtergic function in the brain and may be a mechanism contributing to the pathogenesis of several stress-related neuropsychiatric disorders," he adds.
Their research, due to be published in the journal Molecular Psychiatry adds to this body of evidence.
"First and foremost, our findings suggest the glutamatergic system is a truly viable target for antidepressant drug development," concludes Professor Sanacora.
Contact:
Professor Gerard Sanacora
Professor of Psychiatry
Director, Yale Depression Research Program
Yale School of Medicine
New Haven, Connecticut
US
Email: gerard.sanacora@yale.edu
ECNP Press Office
For all enquiries, please contact:
Sonja Mak
Update Europe GmbH
Tigergasse 3/5
1080 Vienna, Austria
T: +43 1 405 5734
F: +43 1 405 5734-16
s.mak@update.europe.at
About ECNP
The European College of Neuropsychopharmacology (ECNP) is an independent scientific association dedicated to translating advances in the understanding of brain function and human behaviour into better treatments and enhanced public health. ECNP organises a wide range of scientific and educational activities, programmes and events across Europe, promoting exchange of high-quality experimental and clinical research and fostering young scientists and clinicians in the field. The annual ECNP Congress attracts around 4,000-7,000 scientists and clinicians from across the world to discuss the latest advances in brain research in Europe's largest meeting on brain science.
Disclaimer: Information contained in this press release was provided by the abstracts authors and reflects the content of the studies. It does not necessarily express ECNP's point of view.
Further information
- Depression affects 9.1% of Americans per year and up to 19.2% over the course of their lifetime
- In the United States, it is estimated that people with depression receive 60% less days of education per year and lose 5.6 hours of productive work per week, 50% of which is due to absenteeism and short-term disability.
- Depression costs an estimated $83 billion in lost productivity and increased medical expenses.
- Existing literature indicates that the glutamatergic neurotransmitter system is altered in the brains of individuals suffering with mood disorders.
- Stress may disrupt normal glutamtergic function and contribute to the pathogenesis of stress-related neuropsychiatric disorders.
EMBARGOED FOR RELEASE Sunday 6 October 2013, 12.50 hours (CET)