? The use of natural products, particularly in the form of dietary supplements, has dramatically increased in the United States. However, biomedical research in this area has been limited and relatively unfocused Many constituents of natural products are bioactive and purported to possess health promoting effects. However, sound scientific data are often lacking, calling into question the safety and efficacy of these products. With the rising use of natural products, there is an increasing need for high quality basic and mechanistic research in this area. To address this need, the University of Mississippi proposes to establish a Center of Research Excellence in Natural Products Neuroscience (CORE-NPN). The center will bring together the existing strength at this university in natural products research with a rapidly developing neuroscience community. The primary goal of this proposal is to develop and sustain a multidisciplinary research center that focuses on the psychoactive properties of natural products. To achieve this goal, the specific aims of this proposal are to: 1) develop the careers of junior faculty with research interests in natural products neuroscience, 2) provide a research infrastructure that increases the ability of all investigators associated with the center to compete for extramural funding, and 3) sponsor educational and outreach activities that enhance and promote the research environment of the center. It is anticipated that the establishment of a Center of Research Excellence in Natural Products Neuroscience will allow investigators at the University of Mississippi to conduct vital research on the health-related consequences on natural product use, while enhancing the career development and research competitiveness of center investigators. ? ?

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR021929-02
Application #
7284169
Study Section
Special Emphasis Panel (ZRR1-RI-8 (02))
Program Officer
Liu, Yanping
Project Start
2006-09-04
Project End
2011-06-30
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
2
Fiscal Year
2007
Total Cost
$2,008,518
Indirect Cost
Name
University of Mississippi
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
067713560
City
University
State
MS
Country
United States
Zip Code
38677
Mohamed, Shaymaa M M; Elokely, Khaled M; Bachkeet, Enaam Y et al. (2015) New Glycosides and Trypanocidal Metabolites from Vangueria edulis. Nat Prod Commun 10:1897-900
Radwan, Mohamed M; ElSohly, Mahmoud A; El-Alfy, Abir T et al. (2015) Isolation and Pharmacological Evaluation of Minor Cannabinoids from High-Potency Cannabis sativa. J Nat Prod 78:1271-6
Tabrizian, Tahmineh; Hataway, Felicia; Murray, David et al. (2015) Prolylcarboxypeptidase gene expression in the heart and kidney: Effects of obesity and diabetes. Cardiovasc Hematol Agents Med Chem 13:113-23
Ahmed, Safwat A; Ross, Samir A; Slade, Desmond et al. (2015) Minor oxygenated cannabinoids from high potency Cannabis sativa L. Phytochemistry 117:194-9
Gómez-Betancur, Isabel; Cortés, Natalie; Benjumea, Dora et al. (2015) Antinociceptive activity of extracts and secondary metabolites from wild growing and micropropagated plants of Renealmia alpinia. J Ethnopharmacol 165:191-7
Maddineni, Sindhuri; Battu, Sunil Kumar; Morott, Joe et al. (2015) Influence of process and formulation parameters on dissolution and stability characteristics of Kollidon® VA 64 hot-melt extrudates. AAPS PharmSciTech 16:444-54
Morgan, J Brian; Liu, Yang; Coothankandaswamy, Veena et al. (2015) Kalkitoxin inhibits angiogenesis, disrupts cellular hypoxic signaling, and blocks mitochondrial electron transport in tumor cells. Mar Drugs 13:1552-68
Malak, Lourin G; Ibrahim, Mohamed Ali; Bishay, Daoud W et al. (2014) Antileishmanial metabolites from Geosmithia langdonii. J Nat Prod 77:1987-91
Tarawneh, Amer H; León, Francisco; Ibrahim, Mohammed A et al. (2014) Flavanones from Miconia prasina. Phytochem Lett 7:130-132
Chatterjee, Arindam; Cutler, Stephen J; Doerksen, Robert J et al. (2014) Discovery of thienoquinolone derivatives as selective and ATP non-competitive CDK5/p25 inhibitors by structure-based virtual screening. Bioorg Med Chem 22:6409-21

Showing the most recent 10 out of 134 publications