Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2007-9-20
pubmed:abstractText
In our previous studies that examined in vivo activities of oncostatin M (OM) in upregulation of hepatic LDL receptor (LDLR) expression, we observed reductions of LDL-cholesterol and triglyceride (TG) levels in OM-treated hyperlipidemic hamsters. Interestingly, the OM effect of lowering plasma TG was more pronounced than LDL-cholesterol reduction, suggesting additional LDLR-independent actions. Here, we investigated mechanisms underlying the direct TG-lowering effect of OM.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/ACSL5 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol, Dietary, http://linkedlifedata.com/resource/pubmed/chemical/Coenzyme A Ligases, http://linkedlifedata.com/resource/pubmed/chemical/Extracellular Signal-Regulated MAP..., http://linkedlifedata.com/resource/pubmed/chemical/Fatty Acids, http://linkedlifedata.com/resource/pubmed/chemical/OSM protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Oncostatin M, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides, http://linkedlifedata.com/resource/pubmed/chemical/long-chain-fatty-acid-CoA ligase
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1524-4636
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
27
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2198-205
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17761945-Animals, pubmed-meshheading:17761945-Cell Line, Tumor, pubmed-meshheading:17761945-Cholesterol, Dietary, pubmed-meshheading:17761945-Coenzyme A Ligases, pubmed-meshheading:17761945-Cricetinae, pubmed-meshheading:17761945-Disease Models, Animal, pubmed-meshheading:17761945-Extracellular Signal-Regulated MAP Kinases, pubmed-meshheading:17761945-Fatty Acids, pubmed-meshheading:17761945-Gene Expression Regulation, Enzymologic, pubmed-meshheading:17761945-Humans, pubmed-meshheading:17761945-Hypertriglyceridemia, pubmed-meshheading:17761945-Lipid Metabolism, pubmed-meshheading:17761945-Liver, pubmed-meshheading:17761945-Oncostatin M, pubmed-meshheading:17761945-Oxidation-Reduction, pubmed-meshheading:17761945-RNA, Messenger, pubmed-meshheading:17761945-RNA, Small Interfering, pubmed-meshheading:17761945-RNA Interference, pubmed-meshheading:17761945-Recombinant Proteins, pubmed-meshheading:17761945-Signal Transduction, pubmed-meshheading:17761945-Time Factors, pubmed-meshheading:17761945-Transcriptional Activation, pubmed-meshheading:17761945-Transfection, pubmed-meshheading:17761945-Triglycerides
pubmed:year
2007
pubmed:articleTitle
Transcriptional activation of hepatic ACSL3 and ACSL5 by oncostatin m reduces hypertriglyceridemia through enhanced beta-oxidation.
pubmed:affiliation
VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, CA 94304, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, N.I.H., Extramural