<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(21)</volume><submitter>Zheng J</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4> Obesity, which results from a caloric intake and energy expenditure imbalance, is highly prevalent worldwide. Cathepsin S (CTSS), which is a cysteine protease, is elevated in obesity and may regulate a variety of physiological processes. This study sought to investigate the functional role of CTSS in obesity. &lt;h4>Methods&lt;/h4> Mice were administrated 60 mg/kg of RO5444101 in vivo and fed a high-fat diet (HFD) to induce obesity. The weights of the mice fed a normal-chow diet and a HFD were measured. The expression levels of total triglycerides (TG), total cholesterol (TC), aspartate aminotransferase (AST), alanine aminotransferase (ALT), and monocyte chemoattractant protein-1 (MCP-1) were assessed using appropriate corresponding assay kits. Reverse transcription-quantitat</pubmed_abstract><journal>Annals of Translational Medicine</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9708477</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cathepsin S inhibitor reduces high-fat-induced adipogenesis, inflammatory infiltration, and hepatic lipid accumulation in obese mice</pubmed_title><pmcid>PMC9708477</pmcid><pubmed_authors>Duan J</pubmed_authors><pubmed_authors>Zheng J</pubmed_authors><pubmed_authors>Ran T</pubmed_authors><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Han N</pubmed_authors><pubmed_authors>Zhuang H</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cathepsin S inhibitor reduces high-fat-induced adipogenesis, inflammatory infiltration, and hepatic lipid accumulation in obese mice</name><description>&lt;h4>Background&lt;/h4> Obesity, which results from a caloric intake and energy expenditure imbalance, is highly prevalent worldwide. Cathepsin S (CTSS), which is a cysteine protease, is elevated in obesity and may regulate a variety of physiological processes. This study sought to investigate the functional role of CTSS in obesity. &lt;h4>Methods&lt;/h4> Mice were administrated 60 mg/kg of RO5444101 in vivo and fed a high-fat diet (HFD) to induce obesity. The weights of the mice fed a normal-chow diet and a HFD were measured. The expression levels of total triglycerides (TG), total cholesterol (TC), aspartate aminotransferase (AST), alanine aminotransferase (ALT), and monocyte chemoattractant protein-1 (MCP-1) were assessed using appropriate corresponding assay kits. Reverse transcription-quantitat</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-05T09:42:56.572Z</modification><creation>2025-04-05T09:42:56.572Z</creation></dates><accession>S-EPMC9708477</accession><cross_references/></HashMap>