This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Acute lung injury and its more severe form, the acute respiratory distress syndrome (ARDS), are common reasons for admission to the intensive care unit (ICU). In acute lung injury and ARDS, the tissues of the lungs fill up with white blood cells that are activated to release substances producing intense inflammation in the lungs. It is estimated that about 100,000 to 150,000 people per year in the U.S. have acute lung injury or ARDS. Death rates from this condition remain high, with about a third of patients with acute lung injury dying from this problem. Although there are many reasons for the development of acute lung injury, infection and particularly lung infections, like pneumonia, are among the most common reasons. This study is designed to find out why some people develop acute lung injury while others, with the same medical problems, don't have this problem. There are parts of bacterial organisms that seem to be responsible for tisssue damage and inflammation due to infection. One of these bacterial products is called endotoxin. In this study, we will place small amounts of endotoxin into a part of the lung and then see how much inflammation is produced. To put the endotoxin into the lung and then to collect specimens from the lungs, a procedure called a bronchoscopy is performed. A bronchoscopy is when a pencil-thin flexible tube is passed into the large airways of the lungs. The amounts of endotoxin to be used in this study cause inflammation in a small part of the lungs without affecting the general way the lungs function. Cells from the inflamed part of the lungs should be similar to those in patients with acute lung injury and will give us important information on why acute lung injury develops after pneumonias. These studies should provide us with important information about the reasons that people develop acute lung injury. These experiments also may help us develop treatments that will improve the care of patients with acute lung injury and reduce the number of people who die from this serious medical condition.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
5M01RR000051-45
Application #
7377844
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2006-04-01
Project End
2007-03-31
Budget Start
2006-04-01
Budget End
2007-03-31
Support Year
45
Fiscal Year
2006
Total Cost
$10,211
Indirect Cost
Name
University of Colorado Denver
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Millstein, Richard J; Pyle, Laura L; Bergman, Bryan C et al. (2018) Sex-specific differences in insulin resistance in type 1 diabetes: The CACTI cohort. J Diabetes Complications 32:418-423
Martin, Maureen P; Naranbhai, Vivek; Shea, Patrick R et al. (2018) Killer cell immunoglobulin-like receptor 3DL1 variation modifies HLA-B*57 protection against HIV-1. J Clin Invest 128:1903-1912
Nowak, Kristen L; You, Zhiying; Gitomer, Berenice et al. (2018) Overweight and Obesity Are Predictors of Progression in Early Autosomal Dominant Polycystic Kidney Disease. J Am Soc Nephrol 29:571-578
Haas, David W; Bradford, Yuki; Verma, Anurag et al. (2018) Brain neurotransmitter transporter/receptor genomics and efavirenz central nervous system adverse events. Pharmacogenet Genomics 28:179-187
Venuto, Charles S; Lim, Jihoon; Messing, Susan et al. (2018) Inflammation investigated as a source of pharmacokinetic variability of atazanavir in AIDS Clinical Trials Group protocol A5224s. Antivir Ther 23:345-351
Li, Binglan; Verma, Shefali S; Veturi, Yogasudha C et al. (2018) Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression. Pac Symp Biocomput 23:448-459
Hayden, Kathleen M; Baker, Laura D; Bray, George et al. (2018) Long-term impact of intensive lifestyle intervention on cognitive function assessed with the National Institutes of Health Toolbox: The Look AHEAD study. Alzheimers Dement (Amst) 10:41-48
Shah, V N; Sippl, R; Joshee, P et al. (2018) Trabecular bone quality is lower in adults with type 1 diabetes and is negatively associated with insulin resistance. Osteoporos Int 29:733-739
Jensen, Thomas; Bjornstad, Petter; Johnson, Richard J et al. (2018) Copeptin and Estimated Insulin Sensitivity in Adults With and Without Type 1 Diabetes: The CACTI Study. Can J Diabetes :
Dad, Taimur; Abebe, Kaleab Z; Bae, K Ty et al. (2018) Longitudinal Assessment of Left Ventricular Mass in Autosomal Dominant Polycystic Kidney Disease. Kidney Int Rep 3:619-624

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