Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Horm Metab Res ; 40(4): 262-8, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18548385

ABSTRACT

A number of human and animal studies using conjugated linoleic acids (CLA) or diacylglycerol (DAG) oil have shown positive physiological effects on abdominal adiposity, plasma triglycerides, plasma glucose, and insulin sensitivity. A novel DAG composition containing CLA called CLA diacylglyceride (CLA-DAG) may offer potential as a therapeutic agent in reducing some of the symptoms associated with the diabetic phenotype and metabolic syndrome. This study was designed to investigate the effect of CLA-DAG oil on the diabetic phenotype in male Zucker diabetic fatty rats. Animals were assigned to one of four groups: control (C), rosiglitazone (ROS), CLA-DAG, or CLA as free fatty acid (CLA-FFA). After 11 weeks, body weight was higher and kidney weight was lower in the CLA-DAG and ROS groups compared with the C group. The ROS treatment increased the percentage of body fat as compared with all other groups. Final fasting blood glucose was lower in the CLA-DAG and ROS groups than in the C group. Plasma cholesterol was lower in the CLA-DAG group, and plasma triglycerides were lower in the ROS group compared with the C group. We also observed changes in transcript abundance of PPAR-gamma, PPAR-alpha, FAS, LPL, UCP2, UCP3, CPT1, RxR, ObRb, ApoAII, ApoD, and IRS1 in liver, muscle, and adipose tissue, suggesting treatment-induced effects on these genes. Collectively, these data suggest the need for further research on the therapeutic relevance of CLA-DAG oil in obesity and diabetes. Future research should also differentiate between CLA alone and DAG alone compared with the combination.


Subject(s)
Diabetes Mellitus/metabolism , Diglycerides/pharmacology , Linoleic Acid/pharmacology , Adipose Tissue/metabolism , Animals , Blood Glucose/metabolism , Body Weight/drug effects , Cholesterol/blood , DNA, Complementary/biosynthesis , DNA, Complementary/genetics , Diabetes Mellitus/genetics , Diglycerides/blood , Eating/drug effects , Gene Expression/drug effects , Hypoglycemic Agents/pharmacology , Insulin/blood , Insulin Resistance , Kidney/metabolism , Linoleic Acid/blood , Liver/metabolism , Muscle, Skeletal/metabolism , Myocardium/metabolism , Phenotype , Rats , Rats, Zucker , Reverse Transcriptase Polymerase Chain Reaction , Rosiglitazone , Thiazolidinediones/pharmacology , Triglycerides/blood
SELECTION OF CITATIONS
SEARCH DETAIL
...