<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Stewart MJ</submitter><funding>U.S. Department of Defense (DOD) Chronic Pain Management Research Program (CPMRP) Investigator-Initiated Research Award</funding><funding>NHLBI NIH HHS</funding><funding>National Institutes of Health</funding><pagination>3326</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9971260</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>The growing opioid use and overdose crisis in the US is closely related to the abuse of pain medications. Particularly for postoperative pain (POP), ~ 310 million major surgeries are performed globally per year. Most patients undergoing surgical procedures experience acute POP, and ~ 75% of those with POP report the severity as moderate, severe, or extreme. Opioid analgesics are the mainstay for POP management. It is highly desirable to develop a truly effective and safe non-opioid analgesic to treat POP and other forms of pain. Notably, microsomal prostaglandin E2 (PGE&lt;sub>2&lt;/sub>) synthase-1 (mPGES-1) was once proposed as a potentially promising target for a next generation of anti-inflammatory drugs based on studies in mPGES-1 knockouts. However, to the best of our knowledge, no studies</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Analgesic effects of a highly selective mPGES-1 inhibitor.</pubmed_title><pmcid>PMC9971260</pmcid><funding_grant_id>W81XWH2211000</funding_grant_id><funding_grant_id>U01 HL152392</funding_grant_id><pubmed_authors>Loftin CD</pubmed_authors><pubmed_authors>Weaver LM</pubmed_authors><pubmed_authors>Kyomuhangi A</pubmed_authors><pubmed_authors>Zhan CG</pubmed_authors><pubmed_authors>Stewart MJ</pubmed_authors><pubmed_authors>Ding K</pubmed_authors><pubmed_authors>Zheng F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analgesic effects of a highly selective mPGES-1 inhibitor.</name><description>The growing opioid use and overdose crisis in the US is closely related to the abuse of pain medications. Particularly for postoperative pain (POP), ~ 310 million major surgeries are performed globally per year. Most patients undergoing surgical procedures experience acute POP, and ~ 75% of those with POP report the severity as moderate, severe, or extreme. Opioid analgesics are the mainstay for POP management. It is highly desirable to develop a truly effective and safe non-opioid analgesic to treat POP and other forms of pain. Notably, microsomal prostaglandin E2 (PGE&lt;sub>2&lt;/sub>) synthase-1 (mPGES-1) was once proposed as a potentially promising target for a next generation of anti-inflammatory drugs based on studies in mPGES-1 knockouts. However, to the best of our knowledge, no studies</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-26T10:18:01.365Z</modification><creation>2025-04-06T13:19:29.154Z</creation></dates><accession>S-EPMC9971260</accession><cross_references><pubmed>36849491</pubmed><doi>10.1038/s41598-023-30164-3</doi></cross_references></HashMap>