Bioavailability and Pharmacokinetic Parameters of Watermelon (Rind, Flesh and Seeds) Polyphenols

The proposed trial will be a randomized, 4 arm, placebo controlled, within-subject crossover,
study design. It is a pilot trial to establish methods and collect the preliminary data
(N=6). Subjects meeting eligibility criteria (see eligibility criteria) will participate in 4
study visits where they will receive one serving (equivalent to 100 kcal) of 1 of 4
treatments: watermelon rind, watermelon flesh, watermelon seeds or placebo.

Qualified subjects from the screening visit will be randomized into the study and provided
with a standard breakfast consisting of a high carbohydrate and moderate fat western-type
meal 3 hours after the treatment. Each subject will be asked to come for one screening visit,
a pre-study visit, and four dinner pick-ups on the day before each of the four test visits.
The study day visit will last for approximately 9 h with a follow up visit the next day (24
h) for blood collection to allow for the characterization of target watermelon polyphenols
and metabolites in plasma. Subjects will be instructed not to alter their usual diet or fluid
intake during the study periods. Seven days prior to each study day visit, subjects will be
advised not to consume fruits and vegetables rich in polyphenols and carotenoids or other
high phytochemical foods (watermelon and products, arugula, spinach, tea, berries, grapes,
carrots, tomatoes, sweet potatoes etc.).

Each study visit will involve with blood samples collection at time points 0 (fasting), 0.5,
1, 2, 3, 4, 5, 6, 7, 8 h and 24 hour (h). An assigned test treatment will be provided
immediately after the 0 h blood collection, a breakfast meal will be provided immediately
after the 2 h blood collection, and lunch after 6 h blood collection. FMD will be measured at
0 (fasting), 1, 3, 5, and 7h.

Inclusion Criteria:

- • Men or women, 20-45 years of age with body mass index (BMI) in range from 27.5-32
kg/m2

- Nonsmokers (Past smokers can be allowed if they have abstinence for minimum of 2
years)

- No clinical evidence of cardiovascular, metabolic, respiratory, renal,
gastrointestinal or hepatic disease

- Not taking any medications that would interfere with outcomes of the study, i.e.
lipid lowering medications, anti-inflammatory drugs, dietary supplements
especially arginine and L-citrulline, etc.

- Able to provide informed consent

- Able to comply and perform the procedures requested by the protocol (including
dietary restrictions, consumption of study treatments, records of food diary and
questionnaire, and study visit schedule)

Exclusion Criteria:

- • Men and women who smoke

- Men and women with known or suspected intolerance, allergies or hypersensitivity
to study foods or treatments

- Men and women who consume > 2 servings of watermelons per day

- Men and women known to have/diagnosed with diabetes mellitus

- Men and women who have fasting blood glucose concentrations > 125 mg/dL

- Men and women who have uncontrolled blood pressure >140 mmHg (systolic)/90 mmHg
(diastolic)

- Men and women with documented vascular disease, e.g., heart failure, myocardial
infarction, stroke, angina, related surgeries, etc. that, in the opinion of the
investigator, could interfere with the interpretation of the study results

- Men and women with cancer other than non-melanoma skin cancer in previous 5 years

- Men and women diagnosed with chronic constipation, diarrhea or other chronic
gastrointestinal complaint (e.g. irritable bowel syndrome)

- Women who are known to be pregnant or who are intending to become pregnant over
the course of the study

- Women who are lactating

- Taking medication or dietary supplements that may interfere with the outcomes of
the study; e.g., antioxidant supplement, anti-inflammation, lipid lowering
medication, blood pressure lowering medication, etc... Subjects may choose to go
off dietary supplements (requires 30 days washout); e.g., fish oil, probiotics,
etc...

- Men and women who have donated blood within 3 months of the Screening Visit and
blood donors/participants for whom participation in this study will result in
having donated more than 1500 milliliters of blood in the previous 12 months.

- Men and women who are vegans or vegetarian

- History of an eating disorder (e.g., anorexia nervosa, bulimia nervosa, or binge
eating) diagnosed by a health professional

- Substance (alcohol or drug) abuse within the last 2 years

- Excessive coffee and tea consumers (> 5 cups/d)

- Men and women who do excessive exercise regularly or an athlete

- Unstable weight: gained or lost weight +/- 5 kg (11 lbs) in previous 2 months

- Women who are taking unstable dose of hormonal contraceptives and/or stable dose
for less than 6 months

- Unusual working hours i.e., working overnight (e.g. 3rd shift)