{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Luo A"],"funding":["NIEHS NIH HHS","National Natural Science Foundation of China"],"pagination":["71"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9896784"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["21(1)"],"pubmed_abstract":["<h4>Background</h4>Patients suffering from chronic pain often also exhibit depression symptoms. Soluble epoxide hydrolase (sEH) inhibitors can decrease blood levels of inflammatory cytokines. However, whether inhibiting sEH signaling is beneficial for the comorbidity of pain and depression is unknown.<h4>Methods</h4>According to a sucrose preference test (SPT), spared nerve injury (SNI) mice were classified into pain with or without an anhedonia phenotype. Then, sEH protein expression and inflammatory cytokines were assessed in selected tissues. Furthermore, we used sEH inhibitor TPPU to determine the role of sEH in chronic pain and depression. Importantly, agonists and antagonists of aryl hydrocarbon receptor (AHR) and translocator protein (TSPO) were used to explore the pathogenesis of s"],"journal":["Journal of translational medicine"],"pubmed_title":["The soluble epoxide hydrolase inhibitor TPPU improves comorbidity of chronic pain and depression via the AHR and TSPO signaling."],"pmcid":["PMC9896784"],"funding_grant_id":["81974171","P42 ES004699","R35 ES030443"],"pubmed_authors":["Liu H","Luo A","Huang C","Wang D","Yang C","Hammock BD","McReynolds CB","Wu Z","He T","Li S","Zhang X","Liu C","Wang Y","Hashimoto K"],"additional_accession":[]},"is_claimable":false,"name":"The soluble epoxide hydrolase inhibitor TPPU improves comorbidity of chronic pain and depression via the AHR and TSPO signaling.","description":"<h4>Background</h4>Patients suffering from chronic pain often also exhibit depression symptoms. Soluble epoxide hydrolase (sEH) inhibitors can decrease blood levels of inflammatory cytokines. However, whether inhibiting sEH signaling is beneficial for the comorbidity of pain and depression is unknown.<h4>Methods</h4>According to a sucrose preference test (SPT), spared nerve injury (SNI) mice were classified into pain with or without an anhedonia phenotype. Then, sEH protein expression and inflammatory cytokines were assessed in selected tissues. Furthermore, we used sEH inhibitor TPPU to determine the role of sEH in chronic pain and depression. Importantly, agonists and antagonists of aryl hydrocarbon receptor (AHR) and translocator protein (TSPO) were used to explore the pathogenesis of s","dates":{"release":"2023-01-01T00:00:00Z","publication":"2023 Feb","modification":"2025-05-29T19:45:35.304Z","creation":"2025-05-29T19:45:35.304Z"},"accession":"S-EPMC9896784","cross_references":{"pubmed":["36732752"],"doi":["10.1186/s12967-023-03917-x"]}}