Nachshon Korem, Anahita Bassir Nia, Ansel T Hillmer, Deepak D'Souza, Nabeel Nabulsi, Jim Ropchan, Yiyun Huang, Kelly Cosgrove, Ifat Levy, Robert H Pietrzak, Ilan Harpaz-Rotem
{"title":"Cannabinoid 1 receptor availability in posttraumatic stress disorder: A positron emission tomography study.","authors":"Nachshon Korem, Anahita Bassir Nia, Ansel T Hillmer, Deepak D'Souza, Nabeel Nabulsi, Jim Ropchan, Yiyun Huang, Kelly Cosgrove, Ifat Levy, Robert H Pietrzak, Ilan Harpaz-Rotem","doi":"10.1038/s41398-025-03519-9","DOIUrl":null,"url":null,"abstract":"<p><p>The endocannabinoid system (ECS) plays a critical role in fear learning and maintenance and may, therefore, be implicated in the pathophysiology of posttraumatic stress disorder (PTSD). The exact role of cannabinoid receptor 1 (CB1R), a key component of the ECS, remains unclear. Although preclinical studies largely suggest CB1R downregulation in PTSD, the only prior study of CB1R availability in individuals with PTSD reported higher levels than in controls. In this study, we investigated the relationship between CB1R availability and PTSD diagnosis and symptoms. Using positron emission tomography (PET) with the CB1R-specific radiotracer [<sup>11</sup>C]OMAR, scans from 62 individuals, including 46 trauma-exposed participants (19 with current PTSD) and 16 healthy controls, were analyzed. Our findings revealed no differences in CB1R availability between groups in either the whole brain or regions of interest. However, emotional numbing symptoms of PTSD were significantly linked to CB1R availability. These results suggest that the ECS role in the maintenance of PTSD is more nuanced than previously suggested. The ECS was linked to specific PTSD symptom expression, highlighting the potential for treatments targeting the ECS in mitigating these specific symptoms of this multi-faceted disorder.</p>","PeriodicalId":23278,"journal":{"name":"Translational Psychiatry","volume":"15 1","pages":"310"},"PeriodicalIF":6.2000,"publicationDate":"2025-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12373994/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41398-025-03519-9","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
引用次数: 0
Abstract
The endocannabinoid system (ECS) plays a critical role in fear learning and maintenance and may, therefore, be implicated in the pathophysiology of posttraumatic stress disorder (PTSD). The exact role of cannabinoid receptor 1 (CB1R), a key component of the ECS, remains unclear. Although preclinical studies largely suggest CB1R downregulation in PTSD, the only prior study of CB1R availability in individuals with PTSD reported higher levels than in controls. In this study, we investigated the relationship between CB1R availability and PTSD diagnosis and symptoms. Using positron emission tomography (PET) with the CB1R-specific radiotracer [11C]OMAR, scans from 62 individuals, including 46 trauma-exposed participants (19 with current PTSD) and 16 healthy controls, were analyzed. Our findings revealed no differences in CB1R availability between groups in either the whole brain or regions of interest. However, emotional numbing symptoms of PTSD were significantly linked to CB1R availability. These results suggest that the ECS role in the maintenance of PTSD is more nuanced than previously suggested. The ECS was linked to specific PTSD symptom expression, highlighting the potential for treatments targeting the ECS in mitigating these specific symptoms of this multi-faceted disorder.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.