The Suppression of Toll Like Receptors by Insulin
- Conditions
- Insulin Resistance
- Interventions
- Drug: insulin infusionDrug: Dextrose infusionDrug: Saline Infusion
- Registration Number
- NCT01151605
- Lead Sponsor
- University at Buffalo
- Brief Summary
This study will help us understand the possible beneficial effects of insulin in inflammation. Inflamamtion is considered to be the cause of atherosclerosis and heart disease.
- Detailed Description
Obesity and type 2 diabetes are major health problems in the United States and the world. Both conditions are characterized by increased inflammation and oxidative stress and are associated with increased risk of cardiovascular disease.
Our previous work shows that insulin exerts a prompt and powerful anti-inflammatory effect, on circulating blood cells and in plasma in healthy subjects and in critically ill patients.
Toll like receptors (TLRs) recognize bacterial and viral products like endotoxin and viruses and are major determinants of the inflammatory response against foreign pathogens. In view of the recent data showing that TLRs recognize a range of molecules and proteins that are not of pathogenic source like saturated lipids and that TLRs are involved in the pathogenesis of atherosclerosis which leads to cardiovascular disease and insulin resistance which leads to type 2 diabetes (DM) we hypothesized that insulin infusion suppresses TLRs expression.
Our preliminary data show that insulin infusion for 4 hours reduces the levels of many TLRs and thus might protect from inflammation induced conditions We therefore propose to investigate, in more detail, the effect of infusing different doses of insulin on TLRs mRNA and protein levels and its activity in obese and DM subjects over a longer infusion period and a larger number of subjects in circulating white blood cells and in fat tissue. Also we will be comparing the baseline levels of TLRs and TLRs related proteins as well as their modulation by insulin between normal, obese and DM subjects.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description obese subjects Dextrose infusion obese (BMI \>30Kg/m2) subjects infused with insulin dextrose or saline 1 week apart. Each infusion will continue for up to 14 hr Normal weight subjects Dextrose infusion Normal weight subjects infused with insulin dextrose or saline 1 week apart. Each infusion will continue for up to 14 hr obese type 2 diabetes subjects Saline Infusion obese (BMI \>30Kg/m2) subjects with type 2 diabetes infused with insulin dextrose or saline 1 week apart. Each infusion will continue for up to 14 hr obese type 2 diabetes subjects insulin infusion obese (BMI \>30Kg/m2) subjects with type 2 diabetes infused with insulin dextrose or saline 1 week apart. Each infusion will continue for up to 14 hr obese subjects insulin infusion obese (BMI \>30Kg/m2) subjects infused with insulin dextrose or saline 1 week apart. Each infusion will continue for up to 14 hr obese subjects Saline Infusion obese (BMI \>30Kg/m2) subjects infused with insulin dextrose or saline 1 week apart. Each infusion will continue for up to 14 hr Normal weight subjects insulin infusion Normal weight subjects infused with insulin dextrose or saline 1 week apart. Each infusion will continue for up to 14 hr Normal weight subjects Saline Infusion Normal weight subjects infused with insulin dextrose or saline 1 week apart. Each infusion will continue for up to 14 hr obese type 2 diabetes subjects Dextrose infusion obese (BMI \>30Kg/m2) subjects with type 2 diabetes infused with insulin dextrose or saline 1 week apart. Each infusion will continue for up to 14 hr
- Primary Outcome Measures
Name Time Method The Suppression of Toll Like receptors by Insulin 24 hours Expression of TLR2, TLR4, TLR7 and TLR9 mRNA in mononuclear cells and adipose tissue
- Secondary Outcome Measures
Name Time Method TLR expression 0 hours Basal TLR expression in obese and type 2 diabetic subjects as compared to lean subjects
Trial Locations
- Locations (1)
Millard Fillmore Gates Hospital
🇺🇸Buffalo, New York, United States