<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cienfuegos-Pecina E</submitter><funding>Liver Unit and the Department of Analytical Chemistry</funding><funding>National Council of Science and Technology</funding><pagination>e9438</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7357568</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Ischemia-reperfusion (IR) injury is the main cause of delayed graft function in solid organ transplantation. Hypoxia-inducible factors (HIFs) control the expression of genes related to preconditioning against IR injury. During normoxia, HIF-α subunits are marked for degradation by the egg-laying defective nine homolog (EGLN) family of prolyl-4-hydroxylases. The inhibition of EGLN stabilizes HIFs and protects against IR injury. The aim of this study was to determine whether the EGLN inhibitors sodium (&lt;i>S&lt;/i>)-2-hydroxyglutarate [(&lt;i>S&lt;/i>)-2HG] and succinic acid (SA) have a nephroprotective effect against renal IR injury in Wistar rats.&lt;h4>Methods&lt;/h4>(&lt;i>S&lt;/i>)-2HG was synthesized in a 22.96% yield from commercially available L-glutamic acid in a two-step methodology (</pubmed_abstract><journal>PeerJ</journal><pubmed_title>Effect of sodium (&lt;i>S&lt;/i>)-2-hydroxyglutarate in male, and succinic acid in female Wistar rats against renal ischemia-reperfusion injury, suggesting a role of the HIF-1 pathway.</pubmed_title><pmcid>PMC7357568</pmcid><funding_grant_id>2017-01-5652</funding_grant_id><pubmed_authors>Munoz-Espinosa LE</pubmed_authors><pubmed_authors>Perez-Rodriguez E</pubmed_authors><pubmed_authors>Dominguez-Vazquez I</pubmed_authors><pubmed_authors>Alarcon-Galvan G</pubmed_authors><pubmed_authors>Saucedo AL</pubmed_authors><pubmed_authors>Esquivel-Figueroa D</pubmed_authors><pubmed_authors>Ibarra-Rivera TR</pubmed_authors><pubmed_authors>Rodriguez-Rodriguez DR</pubmed_authors><pubmed_authors>Alcantara-Solano KJ</pubmed_authors><pubmed_authors>Torres-Gonzalez L</pubmed_authors><pubmed_authors>Ramirez-Martinez LA</pubmed_authors><pubmed_authors>Cienfuegos-Pecina E</pubmed_authors><pubmed_authors>Moreno-Pena DP</pubmed_authors><pubmed_authors>Cordero-Perez P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of sodium (&lt;i>S&lt;/i>)-2-hydroxyglutarate in male, and succinic acid in female Wistar rats against renal ischemia-reperfusion injury, suggesting a role of the HIF-1 pathway.</name><description>&lt;h4>Background&lt;/h4>Ischemia-reperfusion (IR) injury is the main cause of delayed graft function in solid organ transplantation. Hypoxia-inducible factors (HIFs) control the expression of genes related to preconditioning against IR injury. During normoxia, HIF-α subunits are marked for degradation by the egg-laying defective nine homolog (EGLN) family of prolyl-4-hydroxylases. The inhibition of EGLN stabilizes HIFs and protects against IR injury. The aim of this study was to determine whether the EGLN inhibitors sodium (&lt;i>S&lt;/i>)-2-hydroxyglutarate [(&lt;i>S&lt;/i>)-2HG] and succinic acid (SA) have a nephroprotective effect against renal IR injury in Wistar rats.&lt;h4>Methods&lt;/h4>(&lt;i>S&lt;/i>)-2HG was synthesized in a 22.96% yield from commercially available L-glutamic acid in a two-step methodology (</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2025-04-19T18:01:37.166Z</modification><creation>2025-04-19T18:01:37.166Z</creation></dates><accession>S-EPMC7357568</accession><cross_references><pubmed>32728491</pubmed><doi>10.7717/peerj.9438</doi></cross_references></HashMap>