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Elevated brain cannabinoid CB1 receptor availability in post-traumatic stress disorder: a positron emission
A Neumeister1, M D Normandin, R H Pietrzak
1Molecular Imaging Program, Department of Psychiatry and Radiology, New York University School of Medicine, New York, NY 10016, USA. alexander.neumeister@nyumc.org
Molecular Psychiatry
|May 15, 2013
Summary
Post-traumatic stress disorder (PTSD) involves altered endocannabinoid signaling. This study found higher CB1 receptor availability and lower anandamide levels in PTSD patients, suggesting a new therapeutic target.
Area of Science:
- Neuroscience
- Psychiatry
- Pharmacology
Background:
- Endocannabinoids and cannabinoid type 1 (CB1) receptors are implicated in animal models of PTSD.
- The specific role of these systems in human PTSD remains understudied.
Purpose of the Study:
- To investigate in vivo CB1 receptor availability and endocannabinoid levels in individuals with PTSD.
- To explore the relationship between these biomarkers and PTSD diagnosis.
Main Methods:
- Positron emission tomography (PET) with [(11)C]OMAR (a CB1 radioligand) was used to measure CB1 receptor availability (VT).
- Participants included individuals with PTSD (N=25), trauma-exposed controls (TC, N=12), and healthy controls (HC, N=23).
- Peripheral levels of anandamide, other endocannabinoids, and cortisol were assessed.
Main Results:
- Elevated brain-wide [(11)C]OMAR VT values were observed in the PTSD group compared to HC and TC groups (P=0.001).
- Anandamide concentrations were significantly reduced in the PTSD group relative to both control groups (P<0.001).
- A combination of OMAR VT, anandamide, and cortisol levels achieved nearly 85% accuracy in classifying PTSD cases.
Conclusions:
- Abnormal CB1 receptor-mediated anandamide signaling is implicated in the etiology of PTSD.
- These findings suggest a promising neurobiological model for developing novel pharmacotherapies for PTSD.
