The Bioavailability Of Sulforaphane From Broccoli Soups Study (BOBS)

This study will be a randomized, double-blinded, three-phase crossover trial which will investigate the bioavailability of SF following consumption of broccoli + stilton soup containing different concentrations of glucoraphanin.

The study population will consist of non-smoking men and women aged between 18 and 65 years old. Participants will undergo three phases separated by a minimum of two weeks (wash-out period). Each phase will consist of a 48 hour pre-intervention diet restriction, a study day involving an 8 hour cannulation at the Human Nutrition Unit (HNU) of the Institute of Food Research (IFR) and collection of a 24 hour urine and blood sample the following morning. Participants will be randomly allocated to one of the three soups in each phase. The following soups will be tested in the three phases: i) 300g standard broccoli + stilton soup, ii) 300g Beneforte® broccoli + stilton soup, iii) 300g Beneforte Extra broccoli + stilton soup.

Beneforte and Beneforte extra broccoli are especially cultivated to deliver high sulforaphane levels after consumption. All the three broccoli varieties have the same appearance and flavour thus enabling a blinded human intervention study to be undertaken. Broccoli soups will be manufactured by a food company that supplies soups to the leading supermarket retailers in the United Kingdom.

Each phase will consist of a 48 hour pre-intervention diet restriction, a study day (study day 1) comprising of approximately a nine hour stay at the HNU which will involve cannulation. The following morning participants will visit the HNU for up to 1 hour for collection of a single blood sample at 24 hour post-dose followed by breakfast. During study day 1, eleven 10ml blood samples will be collected over the course of the day from participants at the following timepoints: 0, 30, 45, 60, 90, 120, 180, 240, 360, 480 mins and a 24 hour blood sample. Six urine samples will be collected at the following timepoints: 0, 0-2, 2-4, 4-6, 6-8, 8-24 hours.

The three phases will be separated by a minimum of a two week washout period. For the duration of the study, participants will be required to follow a glucosinolate-free diet for a total of nine days which will be three days per phase. The three days are split into 48 hours (2 days) prior to the study day, 24 hours (1 day) on the study day as well as the following morning until the 24 hour blood and urine sample have been collected. After the 24 hour urine and blood samples have been collected, participants can resume their normal diet for a minimum of two weeks until 48 hours prior to their next study day. This will reduce the contribution of glucosinolate from other foods having an impact on the results of the study. The involvement of the participants will last approximately 11-12 weeks.

Inclusion criteria

• Men and women
• Aged 18-65 years
• Non-smokers
• Those that live within 40 miles of IFR
• Those who like broccoli + stilton soups

Exclusion criteria

• Those unwilling/unable to provide urine and blood samples
• Results of the clinical screening indicate, or are judged by the HNU medical advisor to be indicative of a health problem which could compromise the well-being of the participants if they participated, or which would affect the study outcome.
• Those whose vein status is assessed by HNU senior research nurse as unsuitable for cannulation
• Known history of fainting when blood samples are taken, feel unwell or faint during any clinical study day procedures at the HNU
• Women who are or have been pregnant within the last 12 months or who are breast feeding.
• Those diagnosed with any long-term medical condition (e.g. diabetes, haemophilia, cardiovascular disease, glaucoma, anaemia) or requiring medication that may affect the study outcome.
• Smokers
• Those taking dietary supplements or herbal remedies which may affect the study outcome - unless the participant is willing to discontinue taking them for 1 month prior to starting study. Please note that some supplements may not affect the study and this will be assessed on an individual basis
• Those allergic to any of the ingredients in broccoli + stilton soups
• Participants allergic to members of the Brassica family, e.g. mustard allergy (often combined with sensitivity to mugwort pollen, cabbage and peach) or to Brassica pollens (mustard or rapeseed).
• Those taking any prescribed or non-prescribed medication (short or long term), which may affect the study data or participant's wellbeing. This will be assessed by the HNU medical advisor on an individual basis.
• Those on an anti-coagulant therapy or have had anti-coagulant therapy in the past 3 months.
• Parallel participation in another research project that involves dietary intervention
• Any person related to or living with any member of the study team
• Participation in another research project, which involves blood sampling within the last four months unless total blood from both studies does not exceed 470mL (unless the participants are willing to wait 4 months and then be re-screened).
• Those unwilling to provide GP's contact details
• Those unable to provide written informed consent
• Those not suitable to take part in this study because of the screening results
• Those who have donated or intend to donate blood within 16 weeks prior to the study or during the study
• Those with a body mass index (BMI, kg/m2) ≤20 or ≥35 kg/m2
• Depressed or elevated blood pressure measurements (<90/50 or 95/55 if symptomatic or >160/100)
• Those that have used antibiotics within the previous one month or on long-term antibiotic therapy.
• Those who are unable to completely finish the 300g portion of broccoli + stilton soup on any of the study days as this will affect study data.