<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>33(12)</volume><submitter>Graves JP</submitter><pubmed_abstract>Inflammatory stimuli, such as bacterial LPS, alter the expression of many cytochromes P450. CYP2C and CYP2J subfamily members actively metabolize fatty acids to bioactive eicosanoids, which exhibit potent anti-inflammatory effects. Herein, we examined mRNA levels of the 15 mouse &lt;i>Cyp2c&lt;/i> and 7 mouse &lt;i>Cyp2j&lt;/i> isoforms in liver, kidney, duodenum, and brain over a 96-h time course of LPS-induced inflammation and resolution. Plasma and liver eicosanoid levels were also measured by liquid chromatography with tandem mass spectrometry. Expression changes in &lt;i>Cyp2c&lt;/i> and &lt;i>Cyp2j&lt;/i> isoforms were both isoform and tissue specific. Total liver &lt;i>Cyp2c&lt;/i> and &lt;i>Cyp2j&lt;/i> mRNA content was reduced by 80% 24 h after LPS but recovered to baseline levels by 96 h. Total &lt;i>Cyp2c&lt;/i> and &lt;i></pubmed_abstract><journal>FASEB journal : official publication of the Federation of American Societies for Experimental Biology</journal><pagination>14784-14797</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6894073</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Expression of &lt;i>Cyp2c&lt;/i>/&lt;i>Cyp2j&lt;/i> subfamily members and oxylipin levels during LPS-induced inflammation and resolution in mice.</pubmed_title><pmcid>PMC6894073</pmcid><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Zeldin DC</pubmed_authors><pubmed_authors>Graves JP</pubmed_authors><pubmed_authors>Lih FB</pubmed_authors><pubmed_authors>Edin ML</pubmed_authors><pubmed_authors>Duval C</pubmed_authors><pubmed_authors>Bradbury JA</pubmed_authors><pubmed_authors>Gruzdev A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Expression of &lt;i>Cyp2c&lt;/i>/&lt;i>Cyp2j&lt;/i> subfamily members and oxylipin levels during LPS-induced inflammation and resolution in mice.</name><description>Inflammatory stimuli, such as bacterial LPS, alter the expression of many cytochromes P450. CYP2C and CYP2J subfamily members actively metabolize fatty acids to bioactive eicosanoids, which exhibit potent anti-inflammatory effects. Herein, we examined mRNA levels of the 15 mouse &lt;i>Cyp2c&lt;/i> and 7 mouse &lt;i>Cyp2j&lt;/i> isoforms in liver, kidney, duodenum, and brain over a 96-h time course of LPS-induced inflammation and resolution. Plasma and liver eicosanoid levels were also measured by liquid chromatography with tandem mass spectrometry. Expression changes in &lt;i>Cyp2c&lt;/i> and &lt;i>Cyp2j&lt;/i> isoforms were both isoform and tissue specific. Total liver &lt;i>Cyp2c&lt;/i> and &lt;i>Cyp2j&lt;/i> mRNA content was reduced by 80% 24 h after LPS but recovered to baseline levels by 96 h. Total &lt;i>Cyp2c&lt;/i> and &lt;i></description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Dec</publication><modification>2025-05-18T11:51:10.958Z</modification><creation>2025-05-18T11:51:10.958Z</creation></dates><accession>S-EPMC6894073</accession><cross_references><pubmed>31690125</pubmed><doi>10.1096/fj.201901872R</doi><doi>10.1096/fj.201901872r</doi></cross_references></HashMap>