Cannabidiol and Sertraline Regulate Behavioral and Brain Gene Expression Alterations in an Animal Model of PTSD

被引:20
作者
Gasparyan, Ani [1 ,2 ,3 ]
Navarrete, Francisco [1 ,2 ,3 ]
Manzanares, Jorge [1 ,2 ,3 ]
机构
[1] Univ Miguel Hernandez CSIC, Inst Neurociencias, Alicante, Spain
[2] Inst Salud Carlos III, Red Temat Invest Cooperat Salud RETICS, Red Trastomos Adict, MICINN, Madrid, Spain
[3] FEDER, Madrid, Spain
关键词
PTSD; mice model; cannabidiol; sertraline; mRNA; POSTTRAUMATIC-STRESS-DISORDER; ANXIETY;
D O I
10.3389/fphar.2021.694510
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This study evaluated the effects of cannabidiol (CBD) and/or sertraline (STR) on behavioral and gene expression alterations induced by a new chronic animal model of post-traumatic stress disorder (PTSD). C57BL/6J male mice were repeatedly exposed to physical and psychogenic alternate stressful stimuli. Fear-related memory and anxiety-like behaviors were evaluated. The effects of the administration of CBD (20 mg/kg, i.p.) and/or STR (10 mg/kg, p.o.) were analyzed on behavioral and gene expression changes induced by the model of PTSD. Gene expression alterations of targets related with stress regulation, endocannabinoid and serotonergic systems were analyzed by real-time PCR. The results revealed an increased and long-lasting fear-related memory and anxiety-like behaviors in mice exposed to the animal model of PTSD. Treatment with CBD improved these behaviors in PTSD animals, effects that were significantly potentiated when combined with STR. Gene expression analyses revealed a long-term increase of corticotropin releasing factor (Crf) that was significantly normalized with the combination CBD plus STR. Cannabinoid receptors (Cnr1 and Cnr2) were up regulated in PTSD mice whereas the serotonin transporter (Slc6a4) was reduced. Interestingly, CBD and STR alone or combined induced a significant and marked increase of Slc6a4 gene expression. These results point out the cooperative action of the combination CBD plus STR to enhance fear extinction and reduce anxiety-like behaviors, normalizing gene expression alterations in this animal model of PTSD and suggesting that the combination of CBD with STR deserves to be further explored for the treatment of patients with PTSD.
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页数:14
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共 50 条
[11]   Translational Investigation of the Therapeutic Potential of Cannabidiol (CBD): Toward a New Age [J].
Crippa, Jose A. ;
Guimaraes, Francisco S. ;
Campos, Alline C. ;
Zuardi, Antonio W. .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[12]   Cannabidiol enhances consolidation of explicit fear extinction in humans [J].
Das, Ravi K. ;
Kamboj, Sunjeev K. ;
Ramadas, Mayurun ;
Yogan, Kishoj ;
Gupta, Vivek ;
Redman, Emily ;
Curran, H. Valerie ;
Morgan, Celia J. A. .
PSYCHOPHARMACOLOGY, 2013, 226 (04) :781-792
[13]   Animal models in translational studies of PTSD [J].
Daskalakis, Nikolaos P. ;
Yehuda, Rachel ;
Diamond, David M. .
PSYCHONEUROENDOCRINOLOGY, 2013, 38 (09) :1895-1911
[14]  
Schier ARD, 2012, REV BRAS PSIQUIATR, V34, pS104
[15]   Plasma and brain pharmacokinetic profile of cannabidiol (CBD), cannabidivarine (CBDV), Δ9-tetrahydrocannabivarin (THCV) and cannabigerol (CBG) in rats and mice following oral and intraperitoneal administration and CBD action on obsessive-compulsive behaviour [J].
Deiana, Serena ;
Watanabe, Akihito ;
Yamasaki, Yuki ;
Amada, Naoki ;
Arthur, Marlene ;
Fleming, Shona ;
Woodcock, Hilary ;
Dorward, Patricia ;
Pigliacampo, Barbara ;
Close, Steve ;
Platt, Bettina ;
Riedel, Gernot .
PSYCHOPHARMACOLOGY, 2012, 219 (03) :859-873
[16]  
Dohl J., 2019, UPDATES PTSD ANIMAL
[17]   Cannabidiol in the Treatment of Post-Traumatic Stress Disorder: A Case Series [J].
Elms, Lucas ;
Shannon, Scott ;
Hughes, Shannon ;
Lewis, Nicole .
JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINE, 2019, 25 (04) :392-397
[18]   The complexity of pharmacology of cannabidiol (CBD) and its implications in the treatment of brain disorders [J].
Elsaid, Sonja ;
Le Foll, Bernard .
NEUROPSYCHOPHARMACOLOGY, 2020, 45 (01) :229-230
[19]   Hair corticosterone measurement in mouse models of type 1 and type 2 diabetes mellitus [J].
Erickson, Rebecca L. ;
Browne, Caroline A. ;
Lucki, Irwin .
PHYSIOLOGY & BEHAVIOR, 2017, 178 :166-171
[20]   Depression-resistant endophenotype in mice overexpressing cannabinoid CB2 receptors [J].
Garcia-Gutierrez, M. S. ;
Perez-Ortiz, J. M. ;
Gutierrez-Adan, A. ;
Manzanares, J. .
BRITISH JOURNAL OF PHARMACOLOGY, 2010, 160 (07) :1773-1784