Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
8
pubmed:dateCreated
2003-9-3
pubmed:abstractText
We studied the effects of a 10-day oral 10 micromol/kg oleoyl-estrone (OE) treatment on streptozotocin-diabetic Wistar, Goto-Kakizaki and control Wistar rats. Streptozotocin rats lost more than half the energy ingested as urine glucose. Oleoyl-estrone induced the loss of body weight (mainly body fat) in all groups. Energy expenditure was similar in the three groups of rats studied. Water turnover was deranged in streptozotocin rats, which spent 14% of energy available heating the water drunk. Body lipids were highest in Goto-Kakizaki; lipid levels in streptozotocin rats were very low. Oleoyl-estrone decreased body lipid content in Wistar and Goto-Kakizaki; oleoyl-estrone decreased triacylglycerols (44% in Wistar and Goto-Kakizaki and 22% in streptozotocin rats) and phospholipids but did not affect body cholesterol. Oleoyl-estrone decreased insulin and leptin, did not affect blood glucose but decreased plasma glucose in all groups. There were no changes in plasma triacylglycerols or fatty acids, but HDL, LDL and cholesterol decreased in all groups. The same effects of OE on insulin, plasma (but not blood) glucose and leptin were observed in both models, but the presence of insulin seems to be needed for OE to normalise glycaemia and to facilitate the uptake and utilisation of glucose by tissues. This different handling of glucose and triacylglycerol energy accounts for the disparate effects of OE on energy balance. The main conclusion of this study is that OE function as a lipid-mobilising hormone is dependent on the mass of reserves available, which in turn is closely related to insulin status. Lack of insulin thus results in limited OE effects, and insulin resistance does not prevent or limit the effects of OE on energy homeostasis or the mobilisation of fat.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Anti-Obesity Agents, http://linkedlifedata.com/resource/pubmed/chemical/Blood Glucose, http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol, HDL, http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol, LDL, http://linkedlifedata.com/resource/pubmed/chemical/Estrone, http://linkedlifedata.com/resource/pubmed/chemical/Glucose, http://linkedlifedata.com/resource/pubmed/chemical/Insulin, http://linkedlifedata.com/resource/pubmed/chemical/Leptin, http://linkedlifedata.com/resource/pubmed/chemical/Lipids, http://linkedlifedata.com/resource/pubmed/chemical/Oleic Acids, http://linkedlifedata.com/resource/pubmed/chemical/Streptozocin, http://linkedlifedata.com/resource/pubmed/chemical/Urea, http://linkedlifedata.com/resource/pubmed/chemical/glucosylurea, http://linkedlifedata.com/resource/pubmed/chemical/oleoyl-estrone
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0018-5043
pubmed:author
pubmed:issnType
Print
pubmed:volume
35
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
471-8
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:12953164-Administration, Oral, pubmed-meshheading:12953164-Animals, pubmed-meshheading:12953164-Anti-Obesity Agents, pubmed-meshheading:12953164-Blood Glucose, pubmed-meshheading:12953164-Body Water, pubmed-meshheading:12953164-Body Weight, pubmed-meshheading:12953164-Cholesterol, HDL, pubmed-meshheading:12953164-Cholesterol, LDL, pubmed-meshheading:12953164-Drinking, pubmed-meshheading:12953164-Energy Metabolism, pubmed-meshheading:12953164-Estrone, pubmed-meshheading:12953164-Glucose, pubmed-meshheading:12953164-Insulin, pubmed-meshheading:12953164-Leptin, pubmed-meshheading:12953164-Lipid Metabolism, pubmed-meshheading:12953164-Lipids, pubmed-meshheading:12953164-Oleic Acids, pubmed-meshheading:12953164-Rats, pubmed-meshheading:12953164-Rats, Inbred Strains, pubmed-meshheading:12953164-Rats, Wistar, pubmed-meshheading:12953164-Streptozocin, pubmed-meshheading:12953164-Urea
pubmed:year
2003
pubmed:articleTitle
Effect of oral oleoyl-estrone on the energy balance of diabetic rats.
pubmed:affiliation
Centre Especial de Recerca en Nutrició i Ciència dels Aliments, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't