Skip to content

The Effect of Capsaicin and Cinnamaldehyde on Intestinal Permeability

The Effect of Capsaicin and Cinnamaldehyde on Intestinal Permeability, Gallbladder Motility and Satiety

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01667523
Enrollment
13
Registered
2012-08-17
Start date
2011-02-28
Completion date
2011-12-31
Last updated
2012-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

capsaicin, cinnamaldehyde

Brief summary

An altered permeability has been proposed to play an important role in the pathogenesis of several gastrointestinal disorders, such as irritable bowel syndrome and inflammatory bowel disease. Nutrients derived from food are able to influence the permeability of the intestine and can therefore also affect gastrointestinal symptoms. In this study, the investigators will investigate the effects of capsaicine and cinnamaldehyde, which can be found in hot peppers and cinnamon, respectively, on gastrointestinal physiology. Objective: To obtain more information about the effects of capsaicin and cinnamaldehyde on the intestine, these substances will be infused directly in the duodenum. Hereafter, the permeability of the intestine, gallbladder motility and the effects on satiety will be assessed. Hypothesis: Duodenal capsaicin and cinnamaldehyde infusion induces changes in the intestinal epithelial barrier function by selectively acting on TRPV1 and TRPA1 receptors and releasing serotonin from enterochromaffin cells as determined by the multi sugar permeability test

Interventions

DIETARY_SUPPLEMENTPlacebo

Physiological saline

DIETARY_SUPPLEMENTCapsaicin

1.5 mg capsaicin administered intraduodenally

DIETARY_SUPPLEMENTCinnamaldehyde

70 mg per intervention administered intraduodenally

Sponsors

Top Institute Food and Nutrition
CollaboratorOTHER
Maastricht University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Based on medical history and previous examination, no gastrointestinal complaints can be defined. 2. Age between 18 and 65 years. This study will include healthy adult subjects. Subjects over 65 years have an increased risk for comorbidities, therefore, subjects over 65 years will not be included. Furthermore, age has an influence on the homeostasis of the intestinal mucosa \[21\], which can potentially influence outcome parameters of the study. 3. BMI between 20 and 30 kg/m2

Exclusion criteria

1. History of severe cardiovascular, respiratory, urogenital, gastrointestinal/ hepatic, hematological/immunologic, HEENT (head, ears, eyes, nose, throat), dermatological/connective tissue, musculoskeletal, metabolic/nutritional, endocrine, neurological/psychiatric diseases, allergy, major surgery and/or laboratory assessments which might limit participation in or completion of the study protocol. The severity of the disease (major interference with the execution of the experiment or potential influence on the study outcomes) will be decided by the principal investigator. 2. Use of medication, including vitamin supplementation, except oral contraceptives, within 14 days prior to testing 3. Administration of investigational drugs or participation in any scientific intervention study which may interfere with this study (to be decided by the principle investigator), in the 180 days prior to the study 4. Major abdominal surgery interfering with gastrointestinal function (uncomplicated appendectomy, cholecystectomy and hysterectomy allowed, and other surgery upon judgement of the principle investigator) 5. Dieting (medically prescribed, vegetarian, diabetic, macrobiological, biological dynamic), pregnancy, lactation 6. Excessive alcohol consumption (\>20 alcoholic consumptions per week) 7. Smoking 8. Blood donation within 3 months before the study period 9. Self-admitted HIV-positive state

Design outcomes

Primary

MeasureTime frameDescription
To assess the effect of capsaicin and cinnamaldehyde (CA) infusion on intestinal permeabilityMeasured at start and end of infusion (30 min), on each of the 3 test daysMeasurements performed in plasma

Secondary

MeasureTime frameDescription
To assess the effect of capsaicin and CA infusion on the activation of the TRP receptors as defined by the mucosal concentrations of the neuropeptides SP, CGRP and NKA1 dayMeasurements will be performed in mucosal biopsy samples
To assess the effect capsaicin and CA on parameters that are known to be associated with satiety, measured by satiety hormones in blood plasma and mucosal tissue (CCK) as well as satiety scoring on a visual analogue scale1 dayVisual analogue scores will be collected from the start of the infusion until 90 minutes thereafter.
To assess the effect of capsaicin and CA on serotonergic function in duodenal biopsy specimens by measuring serotonin and its metabolites by HPLC1 dayMeasurements will be performed on biopsy specimens
To assess the effect of capsaicin and CA on gallbladder motility by ultrasoundMeasurements will be performed during the testday starting from 08.00 AM to 11.00AM
To assess the effect of capsaicin and CA on the expression of tight junction proteins measured by immunohistochemistry and by quantitative PCR1 dayMeasurements will be performed in biopsy specimens of the duodenal mucosa

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 14, 2026