Retinol-binding protein 4 expression in visceral and subcutaneous fat in human obesity
Language English Country Czech Republic Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
18052678
DOI
10.33549/physiolres.931379
PII: 1379
Knihovny.cz E-resources
- MeSH
- Adiposity MeSH
- Adult MeSH
- Insulin blood MeSH
- Insulin Resistance MeSH
- Blood Glucose analysis MeSH
- Leptin analysis MeSH
- Middle Aged MeSH
- Humans MeSH
- RNA, Messenger analysis MeSH
- Metabolic Syndrome diagnostic imaging metabolism physiopathology MeSH
- Young Adult MeSH
- Intra-Abdominal Fat chemistry diagnostic imaging physiopathology MeSH
- Obesity diagnostic imaging metabolism physiopathology MeSH
- Retinol-Binding Proteins, Plasma analysis genetics MeSH
- Tomography, X-Ray Computed MeSH
- Subcutaneous Fat chemistry diagnostic imaging physiopathology MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Glucose Transporter Type 4 analysis MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Insulin MeSH
- Blood Glucose MeSH
- Leptin MeSH
- RNA, Messenger MeSH
- Retinol-Binding Proteins, Plasma MeSH
- Glucose Transporter Type 4 MeSH
- RBP4 protein, human MeSH Browser
- SLC2A4 protein, human MeSH Browser
Retinol binding protein 4 (RBP4) is a novel adipokine which might be involved in the development of insulin resistance. The aim of the study was to investigate the expression of RBP4 mRNA in subcutaneous and visceral fat depots and the relationship between RBP4 plasma and mRNA levels relative to indices of adiposity and insulin resistance. In 59 Caucasian women (BMI 20 to 49 kg/m(2)) paired samples of subcutaneous and visceral fat were obtained for RBP4, leptin and GLUT 4 mRNA analysis using reverse transcription-quantitative PCR. Euglycemic hyperinsulinemic clamp and computed tomography scans were performed. RBP4 mRNA levels as well as GLUT 4 mRNA and leptin mRNA levels were lower (P<0.001, P<0.01 and P<0.001, respectively) in visceral compared to subcutaneous fat. No differences were found in RBP4 mRNA expression in the two fat depots or in RBP4 plasma levels between subgroups of non-obese subjects (n=26), obese subjects without metabolic syndrome (n=17) and with metabolic syndrome (n=16). No correlations between RBP4 mRNA or plasma levels relative to adiposity, glucose disposal rate and GLUT 4 mRNA expression in adipose tissue were found. There was a weak positive correlation between plasma RBP4 and plasma triglycerides (r = 0.30, p<0.05) and between plasma RBP4 and blood glucose (r = 0.26, p<0.05). Regardless of the state of adiposity or insulin resistance, RBP4 expression in humans was lower in visceral than in subcutaneous fat. We found no direct relationship between either RBP4 mRNA or its plasma levels and the adiposity or insulin resistance.
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