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Dive into the research topics where Katherine K. Stephenson is active.

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Featured researches published by Katherine K. Stephenson.


Biochemical and Biophysical Research Communications | 2013

Urease from Helicobacter pylori is inactivated by sulforaphane and other isothiocyanates.

Jed W. Fahey; Katherine K. Stephenson; Kristina L. Wade; Paul Talalay

Infections by Helicobacter pylori are very common, causing gastroduodenal inflammation including peptic ulcers, and increasing the risk of gastric neoplasia. The isothiocyanate (ITC) sulforaphane [SF; 1-isothiocyanato-4-(methylsulfinyl)butane] derived from edible crucifers such as broccoli is potently bactericidal against Helicobacter, including antibiotic-resistant strains, suggesting a possible dietary therapy. Gastric H. pylori infections express high urease activity which generates ammonia, neutralizes gastric acidity, and promotes inflammation. The finding that SF inhibits (inactivates) urease (jack bean and Helicobacter) raised the issue of whether these properties might be functionally related. The rates of inactivation of urease activity depend on enzyme and SF concentrations and show first order kinetics. Treatment with SF results in time-dependent increases in the ultraviolet absorption of partially purified Helicobacter urease in the 260-320 nm region. This provides direct spectroscopic evidence for the formation of dithiocarbamates between the ITC group of SF and cysteine thiols of urease. The potencies of inactivation of Helicobacter urease by isothiocyanates structurally related to SF were surprisingly variable. Natural isothiocyanates closely related to SF, previously shown to be bactericidal (berteroin, hirsutin, phenethyl isothiocyanate, alyssin, and erucin), did not inactivate urease activity. Furthermore, SF is bactericidal against both urease positive and negative H. pylori strains. In contrast, some isothiocyanates such as benzoyl-ITC, are very potent urease inactivators, but are not bactericidal. The bactericidal effects of SF and other ITC against Helicobacter are therefore not obligatorily linked to urease inactivation, but may reduce the inflammatory component of Helicobacter infections.


PLOS ONE | 2015

Sulforaphane Bioavailability from Glucoraphanin-Rich Broccoli: Control by Active Endogenous Myrosinase.

Jed W. Fahey; W.David Holtzclaw; Scott L. Wehage; Kristina L. Wade; Katherine K. Stephenson; Paul Talalay

Glucoraphanin from broccoli and its sprouts and seeds is a water soluble and relatively inert precursor of sulforaphane, the reactive isothiocyanate that potently inhibits neoplastic cellular processes and prevents a number of disease states. Sulforaphane is difficult to deliver in an enriched and stable form for purposes of direct human consumption. We have focused upon evaluating the bioavailability of sulforaphane, either by direct administration of glucoraphanin (a glucosinolate, or β-thioglucoside-N-hydroxysulfate), or by co-administering glucoraphanin and the enzyme myrosinase to catalyze its conversion to sulforaphane at economic, reproducible and sustainable yields. We show that following administration of glucoraphanin in a commercially prepared dietary supplement to a small number of human volunteers, the volunteers had equivalent output of sulforaphane metabolites in their urine to that which they produced when given an equimolar dose of glucoraphanin in a simple boiled and lyophilized extract of broccoli sprouts. Furthermore, when either broccoli sprouts or seeds are administered directly to subjects without prior extraction and consequent inactivation of endogenous myrosinase, regardless of the delivery matrix or dose, the sulforaphane in those preparations is 3- to 4-fold more bioavailable than sulforaphane from glucoraphanin delivered without active plant myrosinase. These data expand upon earlier reports of inter- and intra-individual variability, when glucoraphanin was delivered in either teas, juices, or gelatin capsules, and they confirm that a variety of delivery matrices may be equally suitable for glucoraphanin supplementation (e.g. fruit juices, water, or various types of capsules and tablets).


Public Health Nutrition | 2001

Using isothiocyanate excretion as a biological marker of Brassica vegetable consumption in epidemiological studies: Evaluating the sources of variability

Jay H. Fowke; Jed W. Fahey; Katherine K. Stephenson; James R. Hébert

OBJECTIVE Brassica vegetable consumption (e.g. broccoli) leads to excretion of isothiocyanates (ITC) in urine. We evaluated the consistency of ITC as a biomarker for dietary Brassica vegetable consumption across the types of vegetables and methods of preparation used in Western societies, and across consumption levels. DESIGN A single-armed behavioural intervention with duplicate baseline assessment and post-intervention assessment. Urinary ITC excretion and estrogen metabolites were measured from 24-hour urine samples. Dietary intake was measured by a 24-hour recall. SETTING The behavioural intervention facilitated daily Brassica intake among participants by providing peer support, food preparation instruction, guided practice in a teaching kitchen, and other information. SUBJECTS Thirty-four healthy free-living postmenopausal women who recently had a negative screening mammogram at the University of Massachusetts Medical Center. RESULTS Urinary ITC excretion and total Brassica intake followed the same pattern over the intervention. The ITC biomarker significantly predicted Brassica intake when Brassica consumption averaged about 100 g day-1, but not when Brassica consumption averaged about 200 g day-1. Urinary ITC levels were somewhat higher when more raw vegetables were consumed as compared to lightly cooked vegetables, while the types of Brassica consumed appeared to have only a small, non-significant effect on urinary ITC levels. CONCLUSION Urinary ITC excretion would be a good exposure biomarker among populations regularly consuming a vegetable serving/day, but may be less accurate among populations with greater intake levels or a wide range of cooking practices.


Nutrition and Cancer | 2013

Structure-Activity Analysis of Flavonoids: Direct and Indirect Antioxidant, and Antiinflammatory Potencies and Toxicities

Petra A. Tsuji; Katherine K. Stephenson; Kristina L. Wade; Hua Liu; Jed W. Fahey

Flavonoids are secondary plant products that are well represented in healthy diets because of ingestion of fruit, vegetables, herbs, and teas. Increased consumption is correlated with decreased risks of cardiovascular disease, cancer, and other chronic diseases. Certain flavonoids confer direct antioxidant protection to cells, others induce enzymes that protect cells against oxidative and other insults (“indirect antioxidants”), and others appear to be protective by both mechanisms. Hydroxylated flavones manifest substantial direct antioxidant activity but do not effectively induce cytoprotective enzymes. Methoxylated flavones that potently induce cytoprotective enzymes were evaluated to elucidate the structural prerequisites for effective chemoprotective agents: protecting healthy cells with minimal collateral toxicity. Flavones and flavanones methoxylated at the 5-position of the A-ring were among the most potent inducers of the cytoprotective NAD(P)H:quinone-oxidoreductase 1 (NQO1) in 3 different cell lines. Other flavones were equally potent inducers, but more toxic. Flavanones contain no Michael reaction center, yet some are potent inducers of NQO1, have low cytotoxicity, and inhibit LPS-stimulated iNOS activity, which suggests a redox mechanism of action rather than the Keap1/Nrf2/ARE mechanism by which so many of the classic inducers operate. Evaluation in vivo will reveal whether differential protective advantages support their possible evaluation in a cancer prevention setting.


Economic Botany | 2004

Development of Tissue Culture Methods for the Rescue and Propagation of Endangered Moringa Spp. Germplasm

Katherine K. Stephenson; Jed W. Fahey

Moringa is an Old-World dry tropical plant genus with great food, horticultural, industrial, and pharmaceutical potential. Although many of the thirteen known Moringa species are in danger of extinction, one species, M. oleifera Lam., is now widely cultivated. M. oleifera was therefore utilized to develop micropropagation techniques that may be applicable to the more endangered members of this genus. Immature seeds were the most responsive tissue source, and greatest success was achieved using membrane rafts and a liquid growth medium. The success rate was 73%, but the multiplication rate averaged only 4.7 shoots per culture. Most vigorous plantlet development through the transplant stage was achieved using a commercial plant preservative formulation of isothiazolones following shoot proliferation. Although there was no evidence of contamination, treatment with this microbiocide prevented early tissue senescence and it increased culture survivability.


Journal of Agricultural and Food Chemistry | 2002

Influence of Temperature and Ontogeny on the Levels of Glucosinolates in Broccoli (Brassica oleracea Var. italica) Sprouts and Their Effect on the Induction of Mammalian Phase 2 Enzymes

Fernanda Maria Valente Pereira; Eduardo Rosa; Jed W. Fahey; Katherine K. Stephenson; Rosa Carvalho; Alfredo Aires


Journal of Agricultural and Food Chemistry | 2002

Pinostrobin from Honey and Thai Ginger (Boesenbergia pandurata): A Potent Flavonoid Inducer of Mammalian Phase 2 Chemoprotective and Antioxidant Enzymes

Jed W. Fahey; Katherine K. Stephenson


Cancer Epidemiology and Prevention Biomarkers | 2001

Chemoprotective Glucosinolates and Isothiocyanates of Broccoli Sprouts

Theresa A. Shapiro; Jed W. Fahey; Kristina L. Wade; Katherine K. Stephenson; Paul Talalay


Cancer Research | 2004

In vivo and in vitro antitumor effects of ILX651, a pentapeptide with anovel mechanism of action.

Stephanie Roth; Roy Krumbholz; Larry Arthaud; Steve Weitman; Katherine K. Stephenson


Molecular Cancer Therapeutics | 2007

A novel synthetic tricyclic compound with an acetylene group at C-8a and cyano enones in rings A and C is a potent multifunctional agent in vitro and suppresses the formation of aflatoxin-DNA adducts in vivo

Karen Liby; Tadashi Honda; Mark Yore; Chitra Sundararajan; Hidenori Yoshizawa; Renee Risingsong; Charlotte Williams; Darlene Royce; Albena T. Dinkova-Kostova; Katherine K. Stephenson; Patricia G. Egner; Melinda Yates; John Groopman; Thomas W. Kensler; B Roebuck; Gordon Gribble; Michael Sporn

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Jed W. Fahey

Johns Hopkins University

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Kristina L. Wade

Johns Hopkins University School of Medicine

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Paul Talalay

Johns Hopkins University

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B Roebuck

Johns Hopkins University School of Medicine

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Charlotte Williams

Johns Hopkins University School of Medicine

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Chitra Sundararajan

Johns Hopkins University School of Medicine

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Christine M. Munday

Johns Hopkins University School of Medicine

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Darlene Royce

Johns Hopkins University School of Medicine

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Gordon Gribble

Johns Hopkins University School of Medicine

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Hidenori Yoshizawa

Johns Hopkins University School of Medicine

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