Asthma is a chronic inflammatory disease of the respiratory airways and is becoming epidemic in the United States. Oxidative stress plays an important role in exacerbation of airway inflammation and overall disease symptom. Although it has been shown that the levels of vitamin E and ascorbate were decreased in asthmatics, the potential to use antioxidants in the therapy of asthma has not been well explored. The proposed studies in project 3 is part of the synergistic effort for investigating the utility of natural antioxidants as complementary and alternative medicines (CAMs) in the treatment of asthma. During inflammation, several pro-inflammatory mediators including prostaglandin E2 (PGE2) and leukotriene B4 (LTB4), cytokines and chmokines, play central roles in regulating inflammatory response and asthma. We propose to use various forms of vitamin E and polyphenols as the starting candidates based on the recent studies by us and the others. We have discovered that gamma-tocopherol, the major form of vitamin E in diets, has anti-inflammatory activity by inhibiting PGE2 and LTB4 as well as TNF-a. It has been shown that polyphenols like genistein and resveratrol potentiate the cytokine expression in certain cellular system through NF-kappaB regulated gene expression. In addition, ascorbate, genistein and reseveratrol exhibit beneficial effects on regulating airway epithelial fluid secretion. These observations lead to the current hypothesis that these natural antioxidants, and their combinations may be useful as CAMs in the treatment of asthma. Project 3 aims to discover candidate CAM therapies on a molecular, cellular and mechanistic basis to assess the ability of potential CAMs to inhibit oxidative damage from myeloperoxidase and eosinophil peroxidase, generation of eicosanoids by cyclooxygenase and lipoxygenase, NF-kappaB and MAP kinase mediated gene regulation and cytokine formation, and to modulate Na+ and CI- ion channels, transepithelial barrier function and H+ conductive pathways of the airway epithelium. Our studies will provide the scientific basis for our collaborators, Drs Wagner & Harkema at MSU to test CAMs in rodent models and Drs Peden, Alexis, Bromberg & Patel at UNC in Phase I Clinical Screening of CAMs therapy.

Agency
National Institute of Health (NIH)
Institute
National Center for Complementary & Alternative Medicine (NCCAM)
Type
Research Program Projects (P01)
Project #
5P01AT002620-04
Application #
7455179
Study Section
Special Emphasis Panel (ZAT1)
Project Start
Project End
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
4
Fiscal Year
2007
Total Cost
$182,985
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Wagner, James G; Birmingham, Neil P; Jackson-Humbles, Daven et al. (2014) Supplementation with ?-tocopherol attenuates endotoxin-induced airway neutrophil and mucous cell responses in rats. Free Radic Biol Med 68:101-9
Mills, K; Lay, J; Wu, W et al. (2014) Vitamin E, ?-tocopherol, diminishes ex vivo basophil response to dust mite allergen. Allergy 69:541-4
Fry, Rebecca C; Rager, Julia E; Bauer, Rebecca et al. (2014) Air toxics and epigenetic effects: ozone altered microRNAs in the sputum of human subjects. Am J Physiol Lung Cell Mol Physiol 306:L1129-37
Geiser, Marianne; Lay, John C; Bennett, William D et al. (2013) Effects of ex vivo ?-tocopherol on airway macrophage function in healthy and mild allergic asthmatics. J Innate Immun 5:613-24
Hernandez, Michelle L; Wagner, James G; Kala, Aline et al. (2013) Vitamin E, ?-tocopherol, reduces airway neutrophil recruitment after inhaled endotoxin challenge in rats and in healthy volunteers. Free Radic Biol Med 60:56-62
Fry, Rebecca C; Rager, Julia E; Zhou, Haibo et al. (2012) Individuals with increased inflammatory response to ozone demonstrate muted signaling of immune cell trafficking pathways. Respir Res 13:89
Wang, Yun; Moreland, Michelle; Wagner, James G et al. (2012) Vitamin E forms inhibit IL-13/STAT6-induced eotaxin-3 secretion by up-regulation of PAR4, an endogenous inhibitor of atypical PKC in human lung epithelial cells. J Nutr Biochem 23:602-8
Lay, John C; Peden, David B; Alexis, Neil E (2011) Flow cytometry of sputum: assessing inflammation and immune response elements in the bronchial airways. Inhal Toxicol 23:392-406
Esther Jr, Charles R; Peden, David B; Alexis, Neil E et al. (2011) Airway purinergic responses in healthy, atopic nonasthmatic, and atopic asthmatic subjects exposed to ozone. Inhal Toxicol 23:324-30
Dillon, Madeline A; Harris, Bradford; Hernandez, Michelle L et al. (2011) Enhancement of systemic and sputum granulocyte response to inhaled endotoxin in people with the GSTM1 null genotype. Occup Environ Med 68:783-5

Showing the most recent 10 out of 34 publications