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> Strålfors Peter >
PPAR-gamma response...
PPAR-gamma response element activity in intact primary human adipocytes : effects of fatty acids
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- Sauma, Lilian (författare)
- Linköpings universitet,Internmedicin,Hälsouniversitetet
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- Stenkula, Karin G (författare)
- Linköpings universitet,Cellbiologi,Hälsouniversitetet
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- Kjølhede, Preben (författare)
- Linköpings universitet,Obstetrik och gynekologi,Hälsouniversitetet
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- Strålfors, Peter (författare)
- Linköpings universitet,Cellbiologi,Hälsouniversitetet
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- Söderström, Mats (författare)
- Linköpings universitet,Cellbiologi,Hälsouniversitetet
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- Nyström, Fredrik H (författare)
- Linköpings universitet,Internmedicin,Hälsouniversitetet
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(creator_code:org_t)
- Elsevier BV, 2006
- 2006
- Engelska.
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Ingår i: Nutrition. - : Elsevier BV. - 0899-9007 .- 1873-1244. ; 22:1, s. 60-68
- Relaterad länk:
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http://urn.kb.se/res...
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- OBJECTIVE: We studied the activity and regulation of the peroxisome proliferator-activated receptor-gamma response element (PPRE) in primary human adipocytes.METHODS: We transfected primary human adipocytes with a plasmid-encoding firefly luciferase cDNA under control of a PPRE from the acyl-coenzyme A oxidase gene by using our newly developed electroporation-based method. Several fatty acids were added to the fat cells to study potential activation of peroxisome proliferator-activated receptor-gamma.RESULTS: Cells responded maximally to 5 microM of rosiglitazone at a 5.1 +/- 1.4-fold over basal increase in luciferase activity. There was a positive correlation between body mass index and the response to 5 microM of rosiglitazone (r = 0.36, P = 0.03). Patients with type 2 diabetes had similar basal PPRE activity but responded more strongly to 5 microM of rosiglitazone than did non-diabetic subjects (10.2 +/- 5-fold and 5.4 +/- 1-fold over basal increase, respectively, P < 0.0001). Among saturated fatty acids, lauric acid was without effect, but 10 microM of palmitic or stearic acid increased PPRE activity 20% to 35% above basal levels. Monounsaturated palmitoleic acid at 1 microM induced a PPRE transcriptional activity that corresponded to half the therapeutic levels of rosiglitazone.CONCLUSION: Adipocytes from obese subjects and patients with type 2 diabetes responded particularly strongly to the effect of rosiglitazone on PPRE. Because fatty acids in the diet can affect the transcriptional activity of peroxisome proliferator-activated receptor-gamma over decades, the stimulation induced by stearic and palmitoleic acids can affect insulin sensitivity and, hence, cardiovascular morbidity and mortality in humans.
Nyckelord
- Human
- Fat cells
- Fatty acid
- peroxisome proliferator-activated receptor-γ
- Rosiglitazone
- MEDICINE
- MEDICIN
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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