<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>26(34)</volume><submitter>Fernandez-Ramos D</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Arachidyl amido cholanoic acid (Aramchol) is a potent downregulator of hepatic stearoyl-CoA desaturase 1 (SCD1) protein expression that reduces liver triglycerides and fibrosis in animal models of steatohepatitis. In a phase IIb clinical trial in patients with nonalcoholic steatohepatitis (NASH), 52 wk of treatment with Aramchol reduced blood levels of glycated hemoglobin A1c, an indicator of glycemic control.&lt;h4>Aim&lt;/h4>To assess lipid and glucose metabolism in mouse hepatocytes and in a NASH mouse model [induced with a 0.1% methionine and choline deficient diet (0.1MCD)] after treatment with Aramchol.&lt;h4>Methods&lt;/h4>Isolated primary mouse hepatocytes were incubated with 20 μmol/L Aramchol or vehicle for 48 h. Subsequently, analyses were performed including Western blot</pubmed_abstract><journal>World journal of gastroenterology</journal><pagination>5101-5117</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7495035</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Arachidyl amido cholanoic acid improves liver glucose and lipid homeostasis in nonalcoholic steatohepatitis &lt;i>via&lt;/i> AMPK and mTOR regulation.</pubmed_title><pmcid>PMC7495035</pmcid><pubmed_authors>Lu SC</pubmed_authors><pubmed_authors>van Liempd SM</pubmed_authors><pubmed_authors>Goni FM</pubmed_authors><pubmed_authors>Azkargorta M</pubmed_authors><pubmed_authors>Sot J</pubmed_authors><pubmed_authors>Delacruz-Villar L</pubmed_authors><pubmed_authors>Bilbao J</pubmed_authors><pubmed_authors>Serrano-Macia M</pubmed_authors><pubmed_authors>Mato JM</pubmed_authors><pubmed_authors>Pagano M</pubmed_authors><pubmed_authors>Bizkarguenaga M</pubmed_authors><pubmed_authors>Alonso C</pubmed_authors><pubmed_authors>Lopitz-Otsoa F</pubmed_authors><pubmed_authors>Martinez-Chantar ML</pubmed_authors><pubmed_authors>Mosca L</pubmed_authors><pubmed_authors>Hayardeny L</pubmed_authors><pubmed_authors>Iruarrizaga-Lejarreta M</pubmed_authors><pubmed_authors>Tsvirkun D</pubmed_authors><pubmed_authors>Fernandez-Ramos D</pubmed_authors><pubmed_authors>Elortza F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Arachidyl amido cholanoic acid improves liver glucose and lipid homeostasis in nonalcoholic steatohepatitis &lt;i>via&lt;/i> AMPK and mTOR regulation.</name><description>&lt;h4>Background&lt;/h4>Arachidyl amido cholanoic acid (Aramchol) is a potent downregulator of hepatic stearoyl-CoA desaturase 1 (SCD1) protein expression that reduces liver triglycerides and fibrosis in animal models of steatohepatitis. In a phase IIb clinical trial in patients with nonalcoholic steatohepatitis (NASH), 52 wk of treatment with Aramchol reduced blood levels of glycated hemoglobin A1c, an indicator of glycemic control.&lt;h4>Aim&lt;/h4>To assess lipid and glucose metabolism in mouse hepatocytes and in a NASH mouse model [induced with a 0.1% methionine and choline deficient diet (0.1MCD)] after treatment with Aramchol.&lt;h4>Methods&lt;/h4>Isolated primary mouse hepatocytes were incubated with 20 μmol/L Aramchol or vehicle for 48 h. Subsequently, analyses were performed including Western blot</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2025-05-29T19:38:24.39Z</modification><creation>2020-10-01T07:08:36Z</creation></dates><accession>S-EPMC7495035</accession><cross_references><pubmed>32982112</pubmed><doi>10.3748/wjg.v26.i34.5101</doi></cross_references></HashMap>