<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(15)</volume><submitter>Huang L</submitter><pubmed_abstract>The small intestine is main site of exogenous lipid digestion and absorption, and it is important for lipid metabolic homeostasis. Cell death-inducing DNA fragmentation-factor like effector C (CIDEC) is active in lipid metabolism in tissues other than those in the intestine. We developed small intestine-specific CIDEC (SI-CIDEC&lt;sup>-/-&lt;/sup>) knockout C57BL/6J mice by Cre/LoxP recombination to investigate the &lt;i>in vivo&lt;/i> effects of intestinal CIDEC on lipid metabolism. Eight-week-old SI-CIDEC&lt;sup>-/-&lt;/sup> mice fed a high-fat diet for 14 weeks had 15% lower body weight, 30% less body fat mass, and 79% lower liver triglycerides (TG) than wild-type (WT) mice. In addition, hepatic steatosis and fatty liver inflammation were less severe in knockout mice fed a high-fat diet (HFD) compared wi</pubmed_abstract><journal>International journal of biological sciences</journal><pagination>5740-5752</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9576510</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Small Intestine-specific Knockout of CIDEC Improves Obesity and Hepatic Steatosis by Inhibiting Synthesis of Phosphatidic Acid.</pubmed_title><pmcid>PMC9576510</pmcid><pubmed_authors>Zhou L</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Yang Y</pubmed_authors><pubmed_authors>Pan T</pubmed_authors><pubmed_authors>Xiao L</pubmed_authors><pubmed_authors>Xiao Y</pubmed_authors><pubmed_authors>Liao Q</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Aluo Z</pubmed_authors><pubmed_authors>Yu J</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Small Intestine-specific Knockout of CIDEC Improves Obesity and Hepatic Steatosis by Inhibiting Synthesis of Phosphatidic Acid.</name><description>The small intestine is main site of exogenous lipid digestion and absorption, and it is important for lipid metabolic homeostasis. Cell death-inducing DNA fragmentation-factor like effector C (CIDEC) is active in lipid metabolism in tissues other than those in the intestine. We developed small intestine-specific CIDEC (SI-CIDEC&lt;sup>-/-&lt;/sup>) knockout C57BL/6J mice by Cre/LoxP recombination to investigate the &lt;i>in vivo&lt;/i> effects of intestinal CIDEC on lipid metabolism. Eight-week-old SI-CIDEC&lt;sup>-/-&lt;/sup> mice fed a high-fat diet for 14 weeks had 15% lower body weight, 30% less body fat mass, and 79% lower liver triglycerides (TG) than wild-type (WT) mice. In addition, hepatic steatosis and fatty liver inflammation were less severe in knockout mice fed a high-fat diet (HFD) compared wi</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-29T22:25:29.709Z</modification><creation>2025-02-19T03:02:09.607Z</creation></dates><accession>S-EPMC9576510</accession><cross_references><pubmed>36263170</pubmed><doi>10.7150/ijbs.74348</doi></cross_references></HashMap>