Investigating the Bioavailability of Broccoli Extract Supplements
Purpose
The goal of this clinical trial is to compare how much glucoraphanin and sulforaphane from 3 different versions of broccoli extract supplements is absorbed into the body and excreted in urine. This study involves generally healthy adults age 18-60 years. The supplements contain glucoraphanin and myrosinase enzyme, both naturally occurring in cruciferous vegetables. Once ingested, glucoraphanin is converted to the bioactive compound sulforaphane, which is thought to have numerous health benefits, including cancer prevention. Participants will: - consume 3 different versions of broccoli extract supplements (glucoraphanin will range from 35-70 mg) - complete 3 separate 24 hour study cycles - submit blood and urine samples for 24 hours - follow diet restrictions (no cruciferous vegetables or condiments or phytochemical/herbal supplements for 1 week prior to and during each study cycle)
Condition
- Diet, Healthy
Eligibility
- Eligible Ages
- Between 18 Years and 60 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- Healthy adults, 18-60 years of age - Willing to stop taking herbal and phytochemical (plant-based extract or phytochemical) supplements for 1 week prior to and during each study cycle - Willing to stop cruciferous vegetable intake 1 week prior to and during each study cycle - Must be able to give written informed consent
Exclusion Criteria
- Body Mass Index (BMI) <18.5 or >30.0 kg/m2 - Tobacco use, including e-cigarettes, or smoking of any substance (e.g. cannabis) in the past three months - Pregnancy, breastfeeding, or planning to become pregnant before completing the study - Engaging in vigorous exercise more than 7 hours per week - Have a significant acute or chronic illness such as cardiovascular disease, kidney or liver disease, diabetes, thyroid disorder, or radiation or chemotherapy treatment for cancer within the past five years - Use of medications to control cholesterol (e.g. statins, cholestyramine) or fat absorption (e.g. orlistat) - Have had bariatric surgery (e.g. gastric bypass, gastric banding, sleeve gastrectomy, etc.), other gastrointestinal procedure (e.g. cholecystectomy) or disorders (e.g. Crohn's disease, celiac disease, ulcerative colitis) - Allergic to broccoli, moringa, mustard, or maitake mushrooms - Weighs less than 110 pounds - Diagnosis of sickle cell disease
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Crossover Assignment
- Primary Purpose
- Basic Science
- Masking
- Double (Participant, Outcomes Assessor)
- Masking Description
- Participants will be blinded to the dose of glucoraphanin in each arm. Study staff analyzing samples will be blinded to treatment group.
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Active Comparator 35 mg glucoraphanin |
Participants will swallow by mouth 1 tablet of Avmacol Extra Strength with coating. |
|
|
Active Comparator 60 mg glucoraphanin |
Participants will chew and swallow by mouth 2 tablets of Avmacol chewable wafers (30 mg glucoraphanin each) |
|
|
Active Comparator 70 mg glucoraphanin |
Participants will swallow by mouth 2 tablets of Avmacol Extra Strength with coating (35 mg glucoraphanin each) |
|
Recruiting Locations
Corvallis, Oregon 97331
More Details
- Status
- Recruiting
- Sponsor
- Oregon State University
Detailed Description
This study aims to compare the bioavailability of 3 different versions of a broccoli extract supplement in generally healthy adults age 18-60 years who do not smoke or are not pregnant/lactating. The supplements contain glucoraphanin and myrosinase enzyme, both naturally occurring in cruciferous vegetables. Once ingested, glucoraphanin is converted to the bioactive compound sulforaphane, which is thought to have numerous health benefits, including cancer prevention. The amount of glucoraphanin that subjects will take will range from 35-70 mg. Glucoraphanin, sulforaphane, and sulforaphane metabolites will be measured in plasma and urine for 24 hours (plasma: 0, 0.5, 1, 2, 4, 8, and 24 hours after supplement consumption; urine: 0-2, 2-4, 4-8, and 8-24 hour after supplement consumption).