Evaluation of the involvement of endovanilloid and endocannabinoid systems in behavioral and plastic consequences after trauma exposure in mice

• Grant number: 19/19226-5
• Support Opportunities: Scholarships in Brazil - Master
• Effective date (Start): October 01, 2019
• Effective date (End): November 30, 2021
• Field of knowledge: Biological Sciences - Pharmacology - Neuropsychopharmacology
• Principal Investigator: Sabrina Francesca de Souza Lisboa
• Grantee: Larissa Fernanda Matias Werworn
• Host Institution: Faculdade de Ciências Farmacêuticas de Ribeirão Preto (FCFRP). Universidade de São Paulo (USP). Ribeirão Preto , SP, Brazil
• Associated research grant: 17/19731-6 - Identification of epigenetic mechanisms induced by stress which modulate endocannabinoid signaling and neuroimmunological mechanisms as new therapeutic targets to treat the posttraumatic stress disorder (PTSD), AP.JP

Abstract

Post-traumatic stress disorder (PTSD) is a debilitating psychiatric disorder that can develop after exposure to intensely traumatic situations such as physical or sexual violence, war, traffic accident, and others. Nowadays, the treatments approved for PTSD are ineffective, have a considerable latency period, and have numerous adverse effects. Therefore, it is extremely important to study the pathophysiology and neural mechanisms involved in PTSD, in order that more effective medications can be used. One of the systems that may be involved in the pathophysiology of PTSD is endocannabinoid. The objective of the present project is to test the hypothesis that a stress-induced endocannabinoid signaling dysfunction will be involved in PTSD-related behavioral changes as well as in neuroplastic changes. Also, if such changes will be prevented by treatment with drugs that modulate the endocannabinoid system. The specific objectives of the present project will be: to evaluate if the development of anxious behavior and deficits in the extinction of conditioned memories, as well as cellular and molecular alterations resulting from trauma exposure, involve alterations in endocannabinoid signaling and via TRPV1 receptors; and to verify whether facilitation of endocannabinoid signaling via CB1 and CB2 receptors and inhibition of endovanilloid signaling by TRPV1 is able to reverse the long-term consequences of trauma exposure. For this purpose, endocannabinoid-modulating drugs will be administered to wild-type C57 and TRPV1 receptor knockouts mice prior to the realization of the repeated social defeat stress. To assess behavioral alterations, elevated plus maze and contextual conditioned fear tests will be performed. In addition, ATP and endocannabinoid levels in the brain, phenotypic changes in microglia and neuronal activation, dendritic afforestation and gene expression in microglia will be evaluated. (AU)

Academic Publications

(References retrieved automatically from State of São Paulo Research Institutions)

WERWORN, Larissa Fernanda Matias. Evaluation of the participation of the endocannabinoid system in the extinction of conditioned fear memory of mice. 2022. Master's Dissertation - Universidade de São Paulo (USP). Faculdade de Ciências Farmacêuticas de Ribeirão Preto (PCARP/BC) Ribeirão Preto.