Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
11
pubmed:dateCreated
2007-10-29
pubmed:abstractText
Recent observations indicate that the delivery of nitric oxide by endothelial nitric oxide synthase (eNOS) is not only critical for metabolic homeostasis, but could also be important for mitochondrial biogenesis, a key organelle for free fatty acid (FFA) oxidation and energy production. Because mice deficient for the gene of eNOS (eNOS(-/-)) have increased triglycerides and FFA levels, in addition to hypertension and insulin resistance, we hypothesized that these knockout mice may have decreased energy expenditure and defective beta-oxidation.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1939-327X
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
56
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2690-6
pubmed:meshHeading
pubmed-meshheading:17682093-Animals, pubmed-meshheading:17682093-Body Size, pubmed-meshheading:17682093-Calorimetry, Indirect, pubmed-meshheading:17682093-DNA, Mitochondrial, pubmed-meshheading:17682093-Energy Metabolism, pubmed-meshheading:17682093-Epididymis, pubmed-meshheading:17682093-Fatty Acids, Nonesterified, pubmed-meshheading:17682093-Lipolysis, pubmed-meshheading:17682093-Male, pubmed-meshheading:17682093-Mice, pubmed-meshheading:17682093-Mice, Knockout, pubmed-meshheading:17682093-Mitochondria, pubmed-meshheading:17682093-Mitochondria, Muscle, pubmed-meshheading:17682093-Muscle, Skeletal, pubmed-meshheading:17682093-Nitric Oxide Synthase, pubmed-meshheading:17682093-Nitric Oxide Synthase Type I, pubmed-meshheading:17682093-Nitric Oxide Synthase Type III, pubmed-meshheading:17682093-Oxidation-Reduction, pubmed-meshheading:17682093-Oxygen Consumption, pubmed-meshheading:17682093-Polymerase Chain Reaction, pubmed-meshheading:17682093-Triglycerides
pubmed:year
2007
pubmed:articleTitle
Endothelial nitric oxide synthase (eNOS) knockout mice have defective mitochondrial beta-oxidation.
pubmed:affiliation
Department of Cellular Biology and Morphology, University of Lausanne, Lausanne, Switzerland.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't