Millard Fillmore Gates Hospital
Buffalo, New York, 14209, United States
NCT Number: NCT01151605
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.
Looking for future studies?
Notify Me20 year–65 year
All sexes
Interventional
Not applicable
Buffalo, New York, 14209, United States
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Lean Group:
Obese Group:
DM Group:
Exclusion criteria
insulin to be infused at 3.5 units/hour along with Dextrose 12.5% at a rate to achieve blood glucose levels between 80-120mg/dl
Other names: Intravenous regular insulin infusion
Dextrose 12.5% will be infused at a rate to maintain blood glucose level 80-120mg/dl
Other names: Intravenous dextrose solution infusion
Saline will be infused at 100ml/hr
Other names: normal saline infusion
Time frame: 24 hours
percent change from baseline (0hrs) in TLR2 mRNA in mononuclear cells (MNC) following up to 24 hrs of 3.5U/hr insulin infusion (II) adjusted to the similar average change following up to 24hr infusion of dextrose (DI) and saline (SI) control groups. The correction is calculated as follows: Corrected percent change from baseline following II= change from baseline following II - (average change from baseline following DI and SI)*100. Changes from baseline are calculated as: (expression at 24hrs-expression at 0hr)/expression at 0hr.
Time frame: 24 hours
percent change from baseline (0hrs) in TLR4 mRNA in mononuclear cells (MNC) following up to 24 hrs of 3.5U/hr insulin infusion (II) adjusted to the same change following up to 24hr infusion of dextrose (DI) and saline (SI) control groups in this order. The correction is conducted as follows: Corrected percent change from baseline following II= change from baseline following II - (average change from baseline following DI and SI)*100. Changes from baseline are calculated as: (expression at 24hrs-expression at 0hr)/expression at 0hr.
2- For each PCR measurement of specific target gene, relative expression of 3 housekeeping genes (beta-actin, ubiquitin C and cyclophilin A) from the same cDNA is assessed, and normalization factor (based on the 3 genes) is calculated and entered into PCR software to automatically adjust/normalize target gene expression
Time frame: 24hrs
percent change from baseline (0hrs) in CD14 mRNA in mononuclear cells (MNC) following up to 24 hrs of 3.5U/hr insulin infusion (II) adjusted to the similar average change following up to 24hr infusion of dextrose (DI) and saline (SI) control groups in this specific order. The correction is conducted as follows: Corrected percent change from baseline following II= change from baseline following II - (average change from baseline following DI and SI)*100. Changes from baseline are calculated as: (expression at 24hrs-expression at 0hr)/expression at 0hr. For each PCR measurement of specific target gene, relative expression of 3 housekeeping genes (beta-actin, ubiquitin C and cyclophilin A) from the same cDNA is assessed, and normalization factor (based on the 3 genes) is calculated and entered into PCR software to automatically adjust/normalize target gene expression.
Time frame: baseline/fasting
Comparison of TLR2 mRNA expression in MNC in fasting condition. Fasting TLR2 mRNA expression is measured using real-time PCR at baselines of the 3 visits (II, DI, SI visits) is averaged and reported as arbitrary units. For each PCR measurement of specific target gene, relative expression of 3 housekeeping genes (beta-actin, ubiquitin C and cyclophilin A) from the same cDNA is assessed, and normalization factor (based on the 3 genes) is calculated and entered into PCR software to automatically adjust/normalize target gene expression.
University at Buffalo
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05835999
Aging, Glucose Metabolism Disorders
Madison, Wisconsin, United States
View Trial DetailsNCT04992299
Adolescent Development, Behavior
Aurora, Colorado, United States
View Trial DetailsNCT01809288
Behavior, Body Weight
Bethesda, Maryland, United States
View Trial DetailsNCT00340132
Body Weight, Body Weight Changes
Phoenix, Arizona, United States
View Trial Details