We face a global health crisis sparked by an epidemic in obesity and metabolic syndrome. Over 34% of US adults suffer from metabolic syndrome and therefore experience increased risk for cardiovascular disease, type 2 diabetes, inflammation and infection. Direct health care costs arising from obesity and/or related disorders account for 7-10% of all US health care expenditures annually. Mounting evidence has implicated the gut microbiota in obesity and metabolic syndrome. Our long-term goal is to discover natural compounds that can modulate immune function and capitalize on that knowledge to develop cost-effective complementary treatments to improve human health. Our objectives in this project are to determine mechanisms by which vitamin D and xanthohumol from the hops plant mediate regulation of innate immunity, improve gut barrier function, alter microbiota composition and reduce manifestations of obesity and metabolic syndrome. Our central hypothesis is that xanthohumol and vitamin D each induce expression of cathelicidin antimicrobial peptide (CAMP) in mucosal epithelia and improve gut epithelial barrier function, reduce inflammation, modify the structure and function of the gut microbiota, and ultimately reduce overweight/obesity and MetS. Our rationale is that, once we establish that we can reproducibly manipulate the composition and function of the microbiota with these two agents, development of new and innovative approaches to prevent and/or treat obesity and related disorders would be possible. We propose three Specific Aims: 1) determine the contribution of gut microbiota to efficacy of oral xanthohumol and/or vitamin D treatment of diet-induced obesity; 2) determine the mechanism by which vitamin D and/or xanthohumol alter the gut microbiota composition/function and reduce diet induced obesity and 3) determine efficacy of vitamin D and/or xanthohumol to improve gut barrier defense and reduce susceptibility of obese mice to infection. We expect this study to elucidate how interactions between bioactive compounds, host factors, and the gut microbiome will integrate to impact the effect of complementary treatment for inflammatory and metabolic disorders that impact millions of lives and add billions of dollars to healthcare costs worldwide.

Public Health Relevance

Elucidating the molecular mechanisms by which the natural compounds vitamin D and xanthohumol (the principal prenylflavonoid of hops) reduce obesity, metabolic syndrome and inflammation of the gut will lay the foundation for well-informed translational and clinical studies to potentially improve the health of millions of individuals, improve overall public health and save billions of dollars in healthcare costs worldwide.

Agency
National Institute of Health (NIH)
Institute
National Center for Complementary & Alternative Medicine (NCCAM)
Type
Research Project (R01)
Project #
5R01AT009168-04
Application #
9547271
Study Section
Special Emphasis Panel (ZAT1)
Program Officer
Duffy, Linda C
Project Start
2015-09-30
Project End
2020-08-31
Budget Start
2018-09-01
Budget End
2019-08-31
Support Year
4
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Oregon State University
Department
Miscellaneous
Type
Organized Research Units
DUNS #
053599908
City
Corvallis
State
OR
Country
United States
Zip Code
97331
Miranda, Cristobal L; Johnson, Lance A; de Montgolfier, Oriane et al. (2018) Non-estrogenic Xanthohumol Derivatives Mitigate Insulin Resistance and Cognitive Impairment in High-Fat Diet-induced Obese Mice. Sci Rep 8:613
Stevens, Jan F; Revel, Johana S; Maier, Claudia S (2018) Mitochondria-Centric Review of Polyphenol Bioactivity in Cancer Models. Antioxid Redox Signal 29:1589-1611
Ellinwood, Duncan C; El-Mansy, Mohamed F; Plagmann, Layhna S et al. (2017) Total synthesis of [13 C]2 -, [13 C]3 -, and [13 C]5 -isotopomers of xanthohumol, the principal prenylflavonoid from hops. J Labelled Comp Radiopharm 60:639-648
Miranda, Cristobal L; Elias, Valerie D; Hay, Joshua J et al. (2016) Xanthohumol improves dysfunctional glucose and lipid metabolism in diet-induced obese C57BL/6J mice. Arch Biochem Biophys 599:22-30
Yang, Liping; Broderick, David; Campbell, Yan et al. (2016) Conformational modulation of the farnesoid X receptor by prenylflavonoids: Insights from hydrogen deuterium exchange mass spectrometry (HDX-MS), fluorescence titration and molecular docking studies. Biochim Biophys Acta 1864:1667-1677
Stevens, Jan F; Maier, Claudia S (2016) The Chemistry of Gut Microbial Metabolism of Polyphenols. Phytochem Rev 15:425-444