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. The goal of this investigation is to determine the influences of treatment with fluticasone and salmeterol on smooth muscle alterations in asthma at the biochemical level, and to relate these findings to genotype at selected gene loci. The overall hypothesis is that treatment with these agents quantitatively and/or qualitatively alters asthmatic smooth muscle, in the amounts and types of protein and/or RNA species present, and that such responses to treatment may relate to genetic variations at selected gene loci.
Our specific aims are to: (i) obtain endobronchial biopsies from subjects with mild, persistent asthma for laser capture microdissection prior to and immediately following 4 weeks of treatment with inhaled fluticasone and salmeterol or neither in a placebo-controlled, double-blind fashion; (ii) analyze the smooth muscle compartment, or other airway compartments, for protein and/or RNA species contents, using western analysis, gene profiling, real-time PCR, and other methods as they become available; (iii) compare these biochemical profiles between pre-treatment and post-treatment samples, and determine whether treatment type influences any pre- to post-treatment differences found; and (iv) relate biochemical findings to genotypes at selected gene loci, using a venous blood sample to provide DNA for genetic analysis

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR000055-45
Application #
7378611
Study Section
National Center for Research Resources Initial Review Group (RIRG)
Project Start
2006-05-18
Project End
2007-02-28
Budget Start
2006-05-18
Budget End
2007-02-28
Support Year
45
Fiscal Year
2006
Total Cost
$2,104
Indirect Cost
Name
University of Chicago
Department
Pathology
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Rosenfield, Robert L; Ehrmann, David A (2016) The Pathogenesis of Polycystic Ovary Syndrome (PCOS): The Hypothesis of PCOS as Functional Ovarian Hyperandrogenism Revisited. Endocr Rev 37:467-520
Garyu, Justin W; Meffre, Eric; Cotsapas, Chris et al. (2016) Progress and challenges for treating Type 1 diabetes. J Autoimmun 71:1-9
Fleming, Gini F; Schumm, Philip; Friberg, Greg et al. (2015) Circadian variation in plasma 5-fluorouracil concentrations during a 24 hour constant-rate infusion. BMC Cancer 15:69
Rosenfield, Robert L (2015) The Polycystic Ovary Morphology-Polycystic Ovary Syndrome Spectrum. J Pediatr Adolesc Gynecol 28:412-9
Maitland, Michael L; Xu, Chun-Fang; Cheng, Yu-Ching et al. (2015) Identification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of Pazopanib. Clin Cancer Res 21:365-72
Bershad, Anya K; Jaffe, Jerome H; Childs, Emma et al. (2015) Opioid partial agonist buprenorphine dampens responses to psychosocial stress in humans. Psychoneuroendocrinology 52:281-8
Refetoff, Samuel; Bassett, J H Duncan; Beck-Peccoz, Paolo et al. (2014) Classification and proposed nomenclature for inherited defects of thyroid hormone action, cell transport, and metabolism. J Clin Endocrinol Metab 99:768-70
Kirkpatrick, Matthew G; Francis, Sunday M; Lee, Royce et al. (2014) Plasma oxytocin concentrations following MDMA or intranasal oxytocin in humans. Psychoneuroendocrinology 46:23-31
Copinschi, Georges; Leproult, Rachel; Spiegel, Karine (2014) The important role of sleep in metabolism. Front Horm Res 42:59-72
Müller, Peter; Quintana, Fernando A; Rosner, Gary L et al. (2014) Bayesian inference for longitudinal data with non-parametric treatment effects. Biostatistics 15:341-52

Showing the most recent 10 out of 244 publications