{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Chou CL"],"funding":["Taipei Medical University Hospital","Taipei Medical University"],"pagination":["3759"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9502698"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["14(18)"],"pubmed_abstract":["High fructose intake has been implicated in obesity and metabolic syndrome, which are related to increased cardiovascular mortality. However, few studies have experimentally examined the role of renin-angiotensin system blockers and calcium channel blockers (CCB) in obesity. We investigated the effects of valsartan (an angiotensin II receptor blocker) and amlodipine (a CCB) on lipolysis through the potential mechanism of PU.1 inhibition. We observed that high fructose concentrations significantly increased adipose size and triglyceride, monoacylglycerol lipase, adipose triglyceride lipase, and stearoyl-CoA desaturase-1 (SCD1), activating transcription factor 3 and PU.1 levels in adipocytes in vitro. Subsequently, PU.1 inhibitor treatment was able to reduce triglyceride, SCD1, and PU.1 leve"],"journal":["Nutrients"],"pubmed_title":["Benefits of Valsartan and Amlodipine in Lipolysis through PU.1 Inhibition in Fructose-Induced Adiposity."],"pmcid":["PMC9502698"],"funding_grant_id":["110TMU-TMUH-17","DP2-111-21121-01-O-07-02"],"pubmed_authors":["Chou CL","Li CH","Fang TC"],"additional_accession":[]},"is_claimable":false,"name":"Benefits of Valsartan and Amlodipine in Lipolysis through PU.1 Inhibition in Fructose-Induced Adiposity.","description":"High fructose intake has been implicated in obesity and metabolic syndrome, which are related to increased cardiovascular mortality. However, few studies have experimentally examined the role of renin-angiotensin system blockers and calcium channel blockers (CCB) in obesity. We investigated the effects of valsartan (an angiotensin II receptor blocker) and amlodipine (a CCB) on lipolysis through the potential mechanism of PU.1 inhibition. We observed that high fructose concentrations significantly increased adipose size and triglyceride, monoacylglycerol lipase, adipose triglyceride lipase, and stearoyl-CoA desaturase-1 (SCD1), activating transcription factor 3 and PU.1 levels in adipocytes in vitro. Subsequently, PU.1 inhibitor treatment was able to reduce triglyceride, SCD1, and PU.1 leve","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Sep","modification":"2025-04-04T09:02:37.666Z","creation":"2024-11-08T16:57:54.302Z"},"accession":"S-EPMC9502698","cross_references":{"pubmed":["36145135"],"doi":["10.3390/nu14183759"]}}