TY - JOUR
T1 - Integrating Endocannabinoid Signaling and Cannabinoids into the Biology and Treatment of Posttraumatic Stress Disorder
AU - Hill, Matthew N.
AU - Campolongo, Patrizia
AU - Yehuda, Rachel
AU - Patel, Sachin
N1 - Funding Information:
The writers of this work were supported by NIH grants MH100096 and MH107435 (SP) and operating funds from the Canadian Institutes of Health Research (CIHR). MNH is the recipient of salary support from a Tier II Canada Research Chair from CIHR. SP has an active research contract with Lundbeck A/S pharmaceuticals. MNH receives consulting fees from both Pfizer International and GW Pharmaceuticals and has unrestricted operating funds from GW that is for a project unrelated to anything discussed in this review. The remaining authors declare no conflict of interest.
Publisher Copyright:
© 2018 American College of Neuropsychopharmacology.
PY - 2018/1/1
Y1 - 2018/1/1
N2 - Exposure to stress is an undeniable, but in most cases surmountable, part of life. However, in certain individuals, exposure to severe or cumulative stressors can lead to an array of pathological conditions including posttraumatic stress disorder (PTSD), characterized by debilitating trauma-related intrusive thoughts, avoidance behaviors, hyperarousal, as well as depressed mood and anxiety. In the context of the rapidly changing political and legal landscape surrounding use of cannabis products in the USA, there has been a surge of public and research interest in the role of cannabinoids in the regulation of stress-related biological processes and in their potential therapeutic application for stress-related psychopathology. Here we review the current state of knowledge regarding the effects of cannabis and cannabinoids in PTSD and the preclinical and clinical literature on the effects of cannabinoids and endogenous cannabinoid signaling systems in the regulation of biological processes related to the pathogenesis of PTSD. Potential therapeutic implications of the reviewed literature are also discussed. Finally, we propose that a state of endocannabinoid deficiency could represent a stress susceptibility endophenotype predisposing to the development of trauma-related psychopathology and provide biologically plausible support for the self-medication hypotheses used to explain high rates of cannabis use in patients with trauma-related disorders.
AB - Exposure to stress is an undeniable, but in most cases surmountable, part of life. However, in certain individuals, exposure to severe or cumulative stressors can lead to an array of pathological conditions including posttraumatic stress disorder (PTSD), characterized by debilitating trauma-related intrusive thoughts, avoidance behaviors, hyperarousal, as well as depressed mood and anxiety. In the context of the rapidly changing political and legal landscape surrounding use of cannabis products in the USA, there has been a surge of public and research interest in the role of cannabinoids in the regulation of stress-related biological processes and in their potential therapeutic application for stress-related psychopathology. Here we review the current state of knowledge regarding the effects of cannabis and cannabinoids in PTSD and the preclinical and clinical literature on the effects of cannabinoids and endogenous cannabinoid signaling systems in the regulation of biological processes related to the pathogenesis of PTSD. Potential therapeutic implications of the reviewed literature are also discussed. Finally, we propose that a state of endocannabinoid deficiency could represent a stress susceptibility endophenotype predisposing to the development of trauma-related psychopathology and provide biologically plausible support for the self-medication hypotheses used to explain high rates of cannabis use in patients with trauma-related disorders.
UR - http://www.scopus.com/inward/record.url?scp=85036608733&partnerID=8YFLogxK
U2 - 10.1038/npp.2017.162
DO - 10.1038/npp.2017.162
M3 - Review article
C2 - 28745306
AN - SCOPUS:85036608733
SN - 0893-133X
VL - 43
SP - 80
EP - 102
JO - Neuropsychopharmacology
JF - Neuropsychopharmacology
IS - 1
ER -