<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kondev V</submitter><funding>NIMH</funding><funding>NIMH NIH HHS</funding><funding>National Institutes of Health</funding><pagination>739-749</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9827751</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>92(9)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Stress-related disorders are among the most prevalent psychiatric disorders, characterized by excess fear and enhanced avoidance of trauma triggers. Elucidating the mechanisms regulating temporally distinct aspects of innate and conditioned fear responses could facilitate novel therapeutic development for stress-related disorders. One potential target that has recently emerged is the endocannabinoid system, which has been reported to mediate the physiological response to stress and represents an important substrate underlying individual differences in stress susceptibility.&lt;h4>Methods&lt;/h4>Here, we exposed male and female CD-1 mice to an innate predator stressor, 2MT (2-methyl-2-thiazoline), to investigate the ability of endocannabinoid signaling to modulate temporally di</pubmed_abstract><journal>Biological psychiatry</journal><pubmed_title>The Endocannabinoid 2-Arachidonoylglycerol Bidirectionally Modulates Acute and Protracted Effects of Predator Odor Exposure.</pubmed_title><pmcid>PMC9827751</pmcid><funding_grant_id>F31 MH126460</funding_grant_id><funding_grant_id>MH119817</funding_grant_id><funding_grant_id>R01 MH119817</funding_grant_id><funding_grant_id>R01 MH107435</funding_grant_id><funding_grant_id>MH107435</funding_grant_id><pubmed_authors>Kondev V</pubmed_authors><pubmed_authors>Najeed M</pubmed_authors><pubmed_authors>Winters ND</pubmed_authors><pubmed_authors>Patel S</pubmed_authors><pubmed_authors>Kingsley PJ</pubmed_authors><pubmed_authors>Marnett L</pubmed_authors><pubmed_authors>Morgan A</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Endocannabinoid 2-Arachidonoylglycerol Bidirectionally Modulates Acute and Protracted Effects of Predator Odor Exposure.</name><description>&lt;h4>Background&lt;/h4>Stress-related disorders are among the most prevalent psychiatric disorders, characterized by excess fear and enhanced avoidance of trauma triggers. Elucidating the mechanisms regulating temporally distinct aspects of innate and conditioned fear responses could facilitate novel therapeutic development for stress-related disorders. One potential target that has recently emerged is the endocannabinoid system, which has been reported to mediate the physiological response to stress and represents an important substrate underlying individual differences in stress susceptibility.&lt;h4>Methods&lt;/h4>Here, we exposed male and female CD-1 mice to an innate predator stressor, 2MT (2-methyl-2-thiazoline), to investigate the ability of endocannabinoid signaling to modulate temporally di</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-21T14:00:41.311Z</modification><creation>2025-04-21T14:00:41.311Z</creation></dates><accession>S-EPMC9827751</accession><cross_references><pubmed>35961791</pubmed><doi>10.1016/j.biopsych.2022.05.012</doi></cross_references></HashMap>