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Ceramide metabolism is affected by obesity and diabetes in human adipose tissue
- Source :
- Journal of Cellular Physiology. 227:550-557
- Publication Year :
- 2011
- Publisher :
- Wiley, 2011.
-
Abstract
- Ceramide is involved in development of insulin resistance. However, there are no data on ceramide metabolism in human adipose tissue. The aim of our study was to examine sphingolipid metabolism in fat tissue from obese nondiabetic (n = 11), obese diabetic (n = 11), and lean nondiabetic (n = 8) subjects. The content of ceramide (Cer), dihydroceramide (dhCer), sphingosine (SPH), sphinganine (SPA), sphingosine-1-phosphate (S1P; pmol/mg of protein), the expression (mRNA) and activity of key enzymes responsible for Cer metabolism: serine palmitoyltransferase (SPT), neutral and acidic sphingomyelinase (nSMase and aSMase, respectively), and neutral and acidic ceramidase (nCDase and aCDase, respectively) were examined in human adipose tissue. The contents of SPA and Cer were significantly lower whereas the content of dhCer was higher in both obese groups than the respective values in the lean subjects. The expression of examined enzymes was elevated in both obese groups. The SPT and CDases activity increased whereas aSMase activity deceased in both obese groups. We have found correlation between adipose tissue Cer content and plasma adiponectin concentration (r = 0.69, P
- Subjects :
- Adult
Male
medicine.medical_specialty
Ceramide
Physiology
Clinical Biochemistry
Adipose tissue
Biology
Ceramides
Gene Expression Regulation, Enzymologic
chemistry.chemical_compound
Insulin resistance
Diabetes mellitus
Internal medicine
Ceramidases
Diabetes Mellitus
medicine
Humans
Obesity
Sphingolipids
Molecular Structure
Sphingosine
Serine C-palmitoyltransferase
Cell Biology
Middle Aged
medicine.disease
Ceramidase
Sphingomyelin Phosphodiesterase
Endocrinology
Adipose Tissue
chemistry
Female
lipids (amino acids, peptides, and proteins)
Homeostasis
Subjects
Details
- ISSN :
- 00219541
- Volume :
- 227
- Database :
- OpenAIRE
- Journal :
- Journal of Cellular Physiology
- Accession number :
- edsair.doi.dedup.....af07d89398ac3cdc41b60cdc6c14fa99