Effect of acute hyperinsulinaemia with and without angiotensin II type 1 receptor blockade on resistin and adiponectin concentrations and expressions in healthy subjects
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, randomizované kontrolované studie, práce podpořená grantem
PubMed
17893258
DOI
10.1530/eje-07-0034
PII: 157/4/443
Knihovny.cz E-zdroje
- MeSH
- adiponektin krev genetika metabolismus MeSH
- blokátory receptorů AT1 pro angiotensin II aplikace a dávkování MeSH
- dospělí MeSH
- exprese genu účinky léků MeSH
- fixní kombinace léků MeSH
- glykemický clamp MeSH
- hyperinzulinismus chemicky indukované MeSH
- inzulin aplikace a dávkování MeSH
- lidé MeSH
- losartan aplikace a dávkování MeSH
- nitrobřišní tuk účinky léků metabolismus MeSH
- receptor angiotensinu typ 1 fyziologie MeSH
- resistin krev genetika metabolismus MeSH
- zdraví MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- randomizované kontrolované studie MeSH
- Názvy látek
- adiponektin MeSH
- ADIPOQ protein, human MeSH Prohlížeč
- blokátory receptorů AT1 pro angiotensin II MeSH
- fixní kombinace léků MeSH
- inzulin MeSH
- losartan MeSH
- receptor angiotensinu typ 1 MeSH
- resistin MeSH
- RETN protein, human MeSH Prohlížeč
OBJECTIVE: The potential insulin-sensitizing function of angiotensin II type 1 receptor blockade (ARB) with regard to selected adipokines is not fully explained so far. Our study aimed to explore the influence of acute hyperinsulinaemia and acutely induced ARB on resistin and adiponectin concentrations and expressions in healthy subjects. DESIGN AND METHODS: Plasma adipokines were measured: 1) at 0, 30 and 240 min of hyperinsulinaemic (1 mU/kg per min) euglycaemic (5 mmol/l) clamp (HEC), and 2) during HEC after acute ARB (losartan 200 mg; AT-HEC) using the same protocol, in eight healthy subjects. Needle biopsy of abdominal s.c. fat was performed at 0, 30 and 240 min of both clamps to assess the adipokines' expressions. RESULTS: Comparing the glucose disposals of HEC and AT-HEC, no difference in insulin sensitivity was found. Plasma resistin increased equally during HEC and AT-HEC (P < 0.05). The expression of resistin in s.c. fat increased during HEC (P < 0.05), while no significant changes in expression were observed during AT-HEC. Plasma levels of adiponectin did not change during both clamps. Adiponectin expression increased during HEC (P < 0.05), while it did not change during AT-HEC. CONCLUSIONS: In healthy subjects, acute hyperinsulinaemia is associated with an increase in plasma resistin independently of ARB, while plasma adiponectin is not influenced by insulin or ARB. The expressions of both resistin and adiponectin in s.c. adipose tissue are stimulated by acute hyperinsulinaemia, whereas losartan attenuates their insulin-stimulated expressions. This suggests a potential effect of losartanon adipokines' expression.
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