Core A of the Iowa Center for Botanical Supplement Research has five long-term objectives in support of theresearch being conducted within the Center to improve our understanding of the human health benefits andpotential risks of the dietary supplements, Echinacea, Hypericum, and Prunella.First, we will expand comprehensive plant germplasm collections of Echinacea and Hypericum, and developcollections of Prunella, in a manner designed to represent a broad range of taxonomic,genetic andbiochemical diversity, and to propagate the plants through control-pollinated seed production and vegetativemeans. In this way, these well-documented and characterized plant collections will be made available forresearch by Center investigators and the broader research community.Second, we will actively curate these medicinal plant germplasm collections at the North Central RegionalPlant Introduction Station (NCRPIS) as part of the US National Plant Germplasm System, along with all dataassociated with their origins, taxonomic identities, and biochemical characteristics, which will be madeavailable via the Internet in the Germplasm Resources Information Network (GRIN) database.Third, we will produce vegetative materials of known-source populations of these plants under controlledconditions at the NCRPIS, through both field and controlled-environment culture, to serve as well-characterized plant materials for the Center's research projects.Fourth, we will conduct fingerprint analyses and chemical identification of the phytochemicals found in theseplants by conducting analytical research at Iowa State University's W.M. Keck Metabolomics ResearchLaboratory.And finally, we will survey the effects of environmental and developmental cues on the phytochemicalfingerprints of germplasm collections of Echinacea, Hypericum, Prunella, focusing on Prunella, where little isknown about the roles of environment and plant development on its chemical profiles.These core activities provide valuable tools that allow researchers, who study the bioactive and toxiccomponents of these botanical supplements, methods for sorting out variation among plant species andpopulations being used as sources for these supplements. This has been a complicating factor in the studyof all botanical supplements. By using known-source materials that are well characterized biochemically,Center researchers can more efficiently identify bioactive components, and make recommendations that leadto better clinical trials to maximize the human health benefits from these supplements while minimizing risksto consumers.

Agency
National Institute of Health (NIH)
Institute
National Center for Complementary & Alternative Medicine (NCCAM)
Type
Specialized Center (P50)
Project #
9P50AT004155-06
Application #
7293904
Study Section
Special Emphasis Panel (ZAT1-SM (05))
Project Start
2007-04-01
Project End
2010-03-31
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
6
Fiscal Year
2007
Total Cost
$247,656
Indirect Cost
Name
Iowa State University
Department
Type
DUNS #
005309844
City
Ames
State
IA
Country
United States
Zip Code
50011
Haarberg, Kelley Mk; Wymore Brand, Meghan J; Overstreet, Anne-Marie C et al. (2015) Orally administered extract from Prunella vulgaris attenuates spontaneous colitis in mdr1a(-/-) mice. World J Gastrointest Pharmacol Ther 6:223-37
Hammer, Kimberly D P; Birt, Diane F (2014) Evidence for contributions of interactions of constituents to the anti-inflammatory activity of Hypericum perforatum. Crit Rev Food Sci Nutr 54:781-9
Kraus, George A; Chaudhary, Divya; Riley, Sean et al. (2013) Synthesis of 3-farnesyl salicylic acid, a novel antimicrobial from Piper multiplinervium. Nat Prod Commun 8:911-3
Qiang, Zhiyi; Hauck, Cathy; McCoy, Joe-Ann et al. (2013) Echinacea sanguinea and Echinacea pallida extracts stimulate glucuronidation and basolateral transfer of Bauer alkamides 8 and 10 and ketone 24 and inhibit P-glycoprotein transporter in Caco-2 cells. Planta Med 79:266-74
Huang, Nan; Singh, Navrozedeep; Yoon, Kyoungjin et al. (2013) The immuno-regulatory impact of orally-administered Hypericum perforatum extract on Balb/C mice inoculated with H1n1 influenza A virus. PLoS One 8:e76491
Feng, Yaping; Hurst, Jonathan; Almeida-De-Macedo, Marcia et al. (2012) Massive human co-expression network and its medical applications. Chem Biodivers 9:868-87
Qu, Luping; Widrlechner, Mark P (2012) Reduction of Seed Dormancy in Echinacea pallida (Nutt.) Nutt. by In-dark Seed Selection and Breeding. Ind Crops Prod 36:88-93
Wurtele, Eve Syrkin; Chappell, Joe; Jones, A Daniel et al. (2012) Medicinal plants: a public resource for metabolomics and hypothesis development. Metabolites 2:1031-59
Zhang, Xiaozhu; Rizshsky, Ludmila; Hauck, Catherine et al. (2012) Bauer ketones 23 and 24 from Echinacea paradoxa var. paradoxa inhibit lipopolysaccharide-induced nitric oxide, prostaglandin E2 and cytokines in RAW264.7 mouse macrophages. Phytochemistry 74:146-58
Huang, Nan; Rizshsky, Ludmila; Hauck, Catherine C et al. (2012) The inhibition of lipopolysaccharide-induced macrophage inflammation by 4 compounds in Hypericum perforatum extract is partially dependent on the activation of SOCS3. Phytochemistry 76:106-16

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