A decreased adipose tissue blood flow results in adipose tissue hypoxia, which in turn may contribute to the development of insulin resistance.
ID
Bron
Verkorte titel
Aandoening
Diabetes Mellitus, Insulin resistance, Adipose tissue blood flow, Adipose tissue hypoxia
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Primary outcoem parameters are adipose tissue blood flow and adipose tissue oxygen tension.
Achtergrond van het onderzoek
Increasing evidence suggests that adipose tissue dysfunction plays a prominent role in the development of insulin resistance and type 2 diabetes mellitus. One aspect of adipose tissue dysfunction is an impaired adipose tissue blood flow (ATBF). We and others have demonstrated that ATBF is decreased in obese and type 2 diabetic subjects. It is tempting to speculate that adipose tissue hypoperfusion may induce hypoxia in this tissue, which in turn may contribute to insulin resistance via induction of adipose tissue inflammation.
Doel van het onderzoek
A decreased adipose tissue blood flow results in adipose tissue hypoxia, which in turn may contribute to the development of insulin resistance.
Onderzoeksopzet
In this cross-section study, blood samples are collected during the clamp (every 5min) and during the oxygen tension measurements (during the OGTT at time-points t0, t10, t20, t30, t60, t90 and t120).
Onderzoeksproduct en/of interventie
Adipose tissue oxygen tension will be measured using an optochemical measurement system for the continuous monitoring of oxygen tension in vivo in humans using microdialysis. Adipose tissue oxygen tension will be mreasured during pharmacological (local angiotensin II and isoprenaline administration) and physiological (a standardized 75g oral glucose tolerance test (OGTT)) manipulation of adipose tissue blood flow. Insulin sensitivity will be assessed during a hyperinsulinemic-euglycemic clamp. An adipose tissue biopsy and blood samples will be taken under fasting (baseline) conditions and at several time-point during the protocol (e.g. during local administration of pharmacological agents and during the OGTT).
Publiek
G.H. Goossens
NUTRIM School for Nutrition, Toxicology and Metabolism
Department of Human Biology
Maastricht University Medical Centre+
Maastricht 6200 MD
The Netherlands
+31 (0)43 3881314
G.Goossens@hb.unimaas.nl
Wetenschappelijk
G.H. Goossens
NUTRIM School for Nutrition, Toxicology and Metabolism
Department of Human Biology
Maastricht University Medical Centre+
Maastricht 6200 MD
The Netherlands
+31 (0)43 3881314
G.Goossens@hb.unimaas.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Male sex;
2. BMI < 25 kg/m2;
3. Age 25-70 yrs;
4. Weigth stable for at least 3 months prior to participation;
5. Normal glucose tolerant (NGT);
6. No family history of type 2 diabetes mellitus (first degree).
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Diabetes mellitus;
2. Cardiovascular disease;
3. Cancer;
4. Asthma or bronchitis;
5. Liver or kidney malfunction;
6. Disease with a life expectancy shorter then 5 years;
7. Abuse of products (alcohol consumption > 15 units/week);
8. Plans to lose weight;
9. Use of high doses of anti-oxidant vitamins;
10. Use of any medication that influences glucose metabolism and/or inflammation.
Opzet
Deelname
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