<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bijland S</submitter><funding>Dutch Research Council (NWO)</funding><pagination>25168-75</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2919079</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>285(33)</volume><pubmed_abstract>The peroxisome proliferator-activated receptor alpha (PPARalpha) activator fenofibrate efficiently decreases plasma triglycerides (TG), which is generally attributed to enhanced very low density lipoprotein (VLDL)-TG clearance and decreased VLDL-TG production. However, because data on the effect of fenofibrate on VLDL production are controversial, we aimed to investigate in (more) detail the mechanism underlying the TG-lowering effect by studying VLDL-TG production and clearance using APOE*3-Leiden.CETP mice, a unique mouse model for human-like lipoprotein metabolism. Male mice were fed a Western-type diet for 4 weeks, followed by the same diet without or with fenofibrate (30 mg/kg bodyweight/day) for 4 weeks. Fenofibrate strongly lowered plasma cholesterol (-38%) and TG (-60%) caused by reduction of VLDL. Fenofibrate markedly accelerated VLDL-TG clearance, as judged from a reduced plasma half-life of glycerol tri[(3)H]oleate-labeled VLDL-like emulsion particles (-68%). This was associated with an increased post-heparin lipoprotein lipase (LPL) activity (+110%) and an increased uptake of VLDL-derived fatty acids by skeletal muscle, white adipose tissue, and liver. Concomitantly, fenofibrate markedly increased the VLDL-TG production rate (+73%) but not the VLDL-apolipoprotein B (apoB) production rate. Kinetic studies using [(3)H]palmitic acid showed that fenofibrate increased VLDL-TG production by equally increasing incorporation of re-esterified plasma fatty acids and liver TG into VLDL, which was supported by hepatic gene expression profiling data. We conclude that fenofibrate decreases plasma TG by enhancing LPL-mediated VLDL-TG clearance, which results in a compensatory increase in VLDL-TG production by the liver.</pubmed_abstract><journal>The Journal of biological chemistry</journal><pubmed_title>Fenofibrate increases very low density lipoprotein triglyceride production despite reducing plasma triglyceride levels in APOE*3-Leiden.CETP mice.</pubmed_title><pmcid>PMC2919079</pmcid><funding_grant_id>917.36.351</funding_grant_id><pubmed_authors>Havekes LM</pubmed_authors><pubmed_authors>Pieterman EJ</pubmed_authors><pubmed_authors>Princen HM</pubmed_authors><pubmed_authors>van Klinken JB</pubmed_authors><pubmed_authors>van Erk MJ</pubmed_authors><pubmed_authors>Bijland S</pubmed_authors><pubmed_authors>van der Hoorn JW</pubmed_authors><pubmed_authors>Rensen PC</pubmed_authors><pubmed_authors>Maas AC</pubmed_authors><pubmed_authors>van Dijk KW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fenofibrate increases very low density lipoprotein triglyceride production despite reducing plasma triglyceride levels in APOE*3-Leiden.CETP mice.</name><description>The peroxisome proliferator-activated receptor alpha (PPARalpha) activator fenofibrate efficiently decreases plasma triglycerides (TG), which is generally attributed to enhanced very low density lipoprotein (VLDL)-TG clearance and decreased VLDL-TG production. However, because data on the effect of fenofibrate on VLDL production are controversial, we aimed to investigate in (more) detail the mechanism underlying the TG-lowering effect by studying VLDL-TG production and clearance using APOE*3-Leiden.CETP mice, a unique mouse model for human-like lipoprotein metabolism. Male mice were fed a Western-type diet for 4 weeks, followed by the same diet without or with fenofibrate (30 mg/kg bodyweight/day) for 4 weeks. Fenofibrate strongly lowered plasma cholesterol (-38%) and TG (-60%) caused by reduction of VLDL. Fenofibrate markedly accelerated VLDL-TG clearance, as judged from a reduced plasma half-life of glycerol tri[(3)H]oleate-labeled VLDL-like emulsion particles (-68%). This was associated with an increased post-heparin lipoprotein lipase (LPL) activity (+110%) and an increased uptake of VLDL-derived fatty acids by skeletal muscle, white adipose tissue, and liver. Concomitantly, fenofibrate markedly increased the VLDL-TG production rate (+73%) but not the VLDL-apolipoprotein B (apoB) production rate. Kinetic studies using [(3)H]palmitic acid showed that fenofibrate increased VLDL-TG production by equally increasing incorporation of re-esterified plasma fatty acids and liver TG into VLDL, which was supported by hepatic gene expression profiling data. We conclude that fenofibrate decreases plasma TG by enhancing LPL-mediated VLDL-TG clearance, which results in a compensatory increase in VLDL-TG production by the liver.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Aug</publication><modification>2026-05-03T13:43:05.518Z</modification><creation>2026-04-07T19:14:32.347Z</creation></dates><accession>S-EPMC2919079</accession><cross_references><pubmed>20501652</pubmed><doi>10.1074/jbc.m110.123992</doi><doi>10.1074/jbc.M110.123992</doi></cross_references></HashMap>