Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2009-8-24
pubmed:abstractText
Fibroblast growth factor 21 (FGF21) is a novel metabolic regulator shown to improve glycemic control. However, the molecular and functional mechanisms underlying FGF21-mediated improvements in glycemic control are not completely understood. We examined FGF21 effects on insulin sensitivity and glucose fluxes upon chronic (daily injection for 8 d) and acute (6 h infusion) administration in ob/+ and ob/ob mice. Results show that chronic FGF21 ameliorated fasting hyperglycemia in ob/ob mice via increased glucose disposal and improved hepatic insulin sensitivity. Acute FGF21 suppressed hepatic glucose production, increased liver glycogen, lowered glucagon, and improved glucose clearance in ob/+ mice. These effects were blunted in ob/ob mice. Neither chronic nor acute FGF21 altered skeletal muscle or adipose tissue glucose uptake in either genotype. In conclusion, FGF21 has potent glycemic effects caused by hepatic changes in glucose flux and improved insulin sensitivity. Thus, these studies define mechanisms underlying anti-hyperglycemic actions of FGF21 and support its therapeutic potential.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-10959776, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-12021254, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-1275237, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-13362584, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-14475952, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-15902306, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-16443772, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-16644802, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-16801605, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-16936195, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-17063460, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-17068132, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-17229936, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-17452648, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-17550777, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-17550778, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-17601491, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-17926232, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18064602, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18187602, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18215089, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18252893, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18398139, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18460341, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18467542, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18469201, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18687777, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-18948104, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-19337957, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-7575418, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-8227065, http://linkedlifedata.com/resource/pubmed/commentcorrection/19470704-8692973
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1945-7170
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
150
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
4084-93
pubmed:dateRevised
2011-8-1
pubmed:meshHeading
pubmed:year
2009
pubmed:articleTitle
Fibroblast growth factor 21 controls glycemia via regulation of hepatic glucose flux and insulin sensitivity.
pubmed:affiliation
Department of Molecular Physiology and Biophysics, National Institutes of Health-Vanderbilt University Mouse Metabolic Phenotyping Center, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural