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Effect of L. Plantarum Probiotic Supplementation on Broccoli Sulforaphane Bioavailability: Randomised Double-blind Placebo-controlled Crossover Study (PRO-BROC)

U

University of Exeter

Status

Active, not recruiting

Conditions

Nutrition, Healthy

Treatments

Dietary Supplement: Broccoli sprouts extract supplementation

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT06561893
6190780

Details and patient eligibility

About

Broccoli has the precursor of an active compound (sulforaphane) that has shown a wide range of health promoting benefits. Sulforaphane formation depends on the conversion of glucoraphanin (precursor) by myrosinase enzyme. Thus, the bioavailability of sulforaphane is affected by myrosinase activity. Some bacteria, such as L. plantarum (probiotic), have shown they can also convert glucoraphanin to sulforaphane in vitro. This study investigates the effect of short-term L. plantarum supplementation on broccoli sulforaphane bioavailability in humans using a randomised double-blind placebo-controlled crossover trial.

Full description

Brassicas (i.e. broccoli, kale, cabbage) are a group of edible plants that contain a phytochemical called glucoraphanin that upon enzymatic hydrolysis forms the bioactive form sulforaphane. Sulforaphane has shown consistent in vitro and in vivo (animals) anti-cancer activity. The enzyme responsible for this conversion is called myrosinase; however, the enzymatic activity of myrosinase can be affected by several biological factors (e.g. plant variety, growth conditions, etc...) and food processing (e.g. cooking, drying, etc...). Broccoli is one of the richest sources of glucoraphanin, but its myrosinase activity can be easily lost during cooking: 10 minutes at 70 °C reduces the enzyme activity by 95%. This means broccoli prepared this way will contain little to no biologically active sulforaphane. Therefore, is important to find strategies to increase the bioavailability of sulforaphane in broccoli and other brassicas for human consumption.

Certain bacteria have shown myrosinase-like activity and were able to convert glucoraphanin to sulforaphane in vitro, one of these bacteria is Lactiplantibacillus plantarum. This bacterium is present in the human gut, however, there is a large biological variability in the prevalence of this bacteria between individuals. Several human studies have demonstrated that chronic (>1 week) consumption of probiotic supplements containing L. plantarum was able to increase the presence of this bacterium in human gut participants. Thus, the investigators aim to test if supplementing participants with L. plantarum will increase the bioavailability of sulforaphane, compared to placebo.

Enrollment

12 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy adults (male and female)
  • age range of 18-65 years
  • BMI range of 18-30 kg/m2

Exclusion criteria

  • have been on a course of antibiotics within the period of the past 3 months.
  • have allergies or intolerance towards probiotic substances or broccoli used in the study and/or food intolerances associated with gastrointestinal upset.
  • have been taking pre- or probiotics supplements regularly during the last month prior (this does not include foods containing probiotics and/or prebiotics foods)
  • are following any restricting diet (e.g., vegan, FODMAP, etc.).
  • have a gastrointestinal inflammatory condition (e.g., irritable bowel syndrome, inflammatory bowel diseases, coeliac diseases, constipation, etc.).
  • have a medical condition or take medication for any heart, endocrine, or metabolic condition, such as high blood pressure, high cholesterol, insulin resistance, or diabetes, or autoimmune disease.
  • are a pregnant and/or breastfeeding.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

12 participants in 2 patient groups, including a placebo group

Probiotic (L. plantarum) supplementation
Active Comparator group
Description:
Dose: 20 Billion CFU/day for 14 days (total of two pills of 10 Billion CFU)
Treatment:
Dietary Supplement: Broccoli sprouts extract supplementation
Placebo (dextrose) supplementation
Placebo Comparator group
Description:
Dose: 700 mg of dextrose (total of two pills; 2 x 350 mg pills)
Treatment:
Dietary Supplement: Broccoli sprouts extract supplementation

Trial contacts and locations

2

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Central trial contact

Luciana Torquati, PhD; Antony Walsh, PhD

Data sourced from clinicaltrials.gov

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