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New insights into the metabolic regulation of insulin action and insulin resistance: role of glucose and amino acids
- Source :
- FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 5(15)
- Publication Year :
- 1991
-
Abstract
- In primary cultured adipocytes, metabolic substrates such as glucose and amino acids have profound effects on modulating insulin's stimulatory actions on glucose uptake and protein synthesis. Insights into how substrates modulate insulin action were recently obtained when we discovered that the routing of incoming glucose through the hexosamine biosynthesis pathway leads to a refractory state over a period of several hours in which the ability of insulin to stimulate glucose uptake is severely impaired--a state known as insulin resistance. Glutamine:fructose-6-phosphate amidotransferase was found to play a central role in the development of insulin resistance as this enzyme catalyzes the first and rate-limiting step in the formation of hexosamine products. Collectively, these results are consistent with the idea that the hexosamine biosynthesis pathway serves as a glucose sensor coupled to a negative feedback system that can limit the extent of glucose uptake in response to hyperglycemic and hyperinsulinemic conditions.
- Subjects :
- medicine.medical_specialty
Monosaccharide Transport Proteins
medicine.medical_treatment
Glucose uptake
Biology
Biochemistry
Diabetes Mellitus, Experimental
chemistry.chemical_compound
Insulin resistance
Biosynthesis
Internal medicine
Adipocyte
Genetics
medicine
Animals
Humans
Insulin
Obesity
Amino Acids
Molecular Biology
Cells, Cultured
chemistry.chemical_classification
Metabolism
medicine.disease
Glutamine
Endocrinology
Enzyme
Glucose
chemistry
Adipose Tissue
Insulin Resistance
Biotechnology
Subjects
Details
- ISSN :
- 08926638
- Volume :
- 5
- Issue :
- 15
- Database :
- OpenAIRE
- Journal :
- FASEB journal : official publication of the Federation of American Societies for Experimental Biology
- Accession number :
- edsair.doi.dedup.....1a7ba9ce61fac7572c76ab1caffaa34e