Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
2005-7-12
pubmed:abstractText
To examine the involvement of ghrelin in obesity, we investigated the effects of treatment with peripherally administered ghrelin on food intake, adiposity, and expression of uncoupling protein (UCP) mRNA in brown (BAT) and white (WAT) adipose tissue in mice. Acute bolus administration of ghrelin at a dose of 120 nmol/kg increased cumulative food intake over 4 and 24 h as compared to controls (p<0.05 for each), whereas 12 nmol/kg/day ghrelin showed no remarkable effect (p>0.1). Chronic repeated treatment with 12 nmol/kg/day ghrelin for 7 days increased body weight and adiposity assessed by the weight of adipose tissue, triglyceride content in WAT (p<0.05 for each versus control). In addition, the same treatment decreased and increased mRNA expression of BAT UCP1 and WAT UCP2, respectively (p<0.05 for each). In conclusion, ghrelin can regulate body weight, adiposity and UCPs mRNA expression in mice. The present results provide evidence for a new regulatory loop involving ghrelin and UCP, and add novel insights into the regulatory mechanisms of obesity.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Fatty Acids, Nonesterified, http://linkedlifedata.com/resource/pubmed/chemical/Ghrelin, http://linkedlifedata.com/resource/pubmed/chemical/Glucose, http://linkedlifedata.com/resource/pubmed/chemical/Insulin, http://linkedlifedata.com/resource/pubmed/chemical/Ion Channels, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Mitochondrial Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Peptide Hormones, http://linkedlifedata.com/resource/pubmed/chemical/Protein Isoforms, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides, http://linkedlifedata.com/resource/pubmed/chemical/mitochondrial uncoupling protein, http://linkedlifedata.com/resource/pubmed/chemical/mitochondrial uncoupling protein 2
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0167-0115
pubmed:author
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
130
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
97-103
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:15946750-Adipose Tissue, pubmed-meshheading:15946750-Adipose Tissue, Brown, pubmed-meshheading:15946750-Animals, pubmed-meshheading:15946750-Body Composition, pubmed-meshheading:15946750-Body Weight, pubmed-meshheading:15946750-Carrier Proteins, pubmed-meshheading:15946750-Eating, pubmed-meshheading:15946750-Fatty Acids, Nonesterified, pubmed-meshheading:15946750-Food, pubmed-meshheading:15946750-Gene Expression Regulation, pubmed-meshheading:15946750-Ghrelin, pubmed-meshheading:15946750-Glucose, pubmed-meshheading:15946750-Insulin, pubmed-meshheading:15946750-Ion Channels, pubmed-meshheading:15946750-Male, pubmed-meshheading:15946750-Membrane Proteins, pubmed-meshheading:15946750-Membrane Transport Proteins, pubmed-meshheading:15946750-Mice, pubmed-meshheading:15946750-Mice, Inbred C57BL, pubmed-meshheading:15946750-Mitochondrial Proteins, pubmed-meshheading:15946750-Obesity, pubmed-meshheading:15946750-Peptide Hormones, pubmed-meshheading:15946750-Protein Isoforms, pubmed-meshheading:15946750-RNA, Messenger, pubmed-meshheading:15946750-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:15946750-Time Factors, pubmed-meshheading:15946750-Triglycerides
pubmed:year
2005
pubmed:articleTitle
Ghrelin regulates adiposity in white adipose tissue and UCP1 mRNA expression in brown adipose tissue in mice.
pubmed:affiliation
Department of Internal Medicine 1, School of Medicine, Faculty of Medicine, Oita Medical University, 1-1 Idaigaoka, Hasama, Oita 879-5593, Japan.
pubmed:publicationType
Journal Article