Effect of cocoa on the brain and gut in healthy subjects: a randomised controlled trial.


Journal

The British journal of nutrition
ISSN: 1475-2662
Titre abrégé: Br J Nutr
Pays: England
ID NLM: 0372547

Informations de publication

Date de publication:
03 2019
Historique:
entrez: 27 3 2019
pubmed: 27 3 2019
medline: 15 2 2020
Statut: ppublish

Résumé

Dark chocolate is claimed to have effects on gastrointestinal function and to improve well-being. This randomised controlled study tested the hypothesis that cocoa slows gastric emptying and intestinal transit. Functional brain imaging identified central effects of cocoa on cortical activity. Healthy volunteers (HV) ingested 100 g dark (72 % cocoa) or white (0 % cocoa) chocolate for 5 d, in randomised order. Participants recorded abdominal symptoms and stool consistency by the Bristol Stool Score (BSS). Gastric emptying (GE) and intestinal and colonic transit time were assessed by scintigraphy and marker studies, respectively. Combined positron emission tomography-computed tomography (PET-CT) imaging assessed regional brain activity. A total of sixteen HV (seven females and nine males) completed the studies (mean age 34 (21-58) years, BMI 22·8 (18·5-26·0) kg/m2). Dark chocolate had no effect on upper gastrointestinal function (GE half-time 82 (75-120) v. 83 (60-120) min; P=0·937); however, stool consistency was increased (BSS 3 (3-5) v. 4 (4-6); P=0·011) and there was a trend to slower colonic transit (17 (13-26) v. 21 (15-47) h; P=0·075). PET-CT imaging showed increased [18F]fluorodeoxyglucose (FDG) in the visual cortex, with increased FDG uptake also in somatosensory, motor and pre-frontal cortices (P<0·001). In conclusion, dark chocolate with a high cocoa content has effects on colonic and cerebral function in HV. Future research will assess its effects in patients with functional gastrointestinal diseases with disturbed bowel function and psychological complaints.

Identifiants

pubmed: 30912735
pii: S0007114518003689
doi: 10.1017/S0007114518003689
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

654-661

Auteurs

Mark Fox (M)

Abdominal Center: Gastroenterology, St. Claraspital, CH-4058 Basel, Switzerland.
Department of Gastroenterology and Hepatology, University Hospital Zürich, CH-8091 Zürich, Switzerland.

Anne Christin Meyer-Gerspach (AC)

St. Clara Research Ltd, St. Claraspital, CH-4058 Basel, Switzerland.

Maria Janina Wendebourg (MJ)

Abdominal Center: Gastroenterology, St. Claraspital, CH-4058 Basel, Switzerland.
Department of Neurology, University Hospital Basel, CH-4058 Basel, Switzerland.

Maja Gruber (M)

Abdominal Center: Gastroenterology, St. Claraspital, CH-4058 Basel, Switzerland.

Henriette Heinrich (H)

Abdominal Center: Gastroenterology, St. Claraspital, CH-4058 Basel, Switzerland.
Department of Gastroenterology and Hepatology, University Hospital Zürich, CH-8091 Zürich, Switzerland.

Matthias Sauter (M)

Abdominal Center: Gastroenterology, St. Claraspital, CH-4058 Basel, Switzerland.
Department of Gastroenterology and Hepatology, University Hospital Zürich, CH-8091 Zürich, Switzerland.

Bettina Woelnerhanssen (B)

St. Clara Research Ltd, St. Claraspital, CH-4058 Basel, Switzerland.

Dieter Koeberle (D)

Department of Nuclear Medicine and PET/CT-Center North-West Switzerland, St. Claraspital, CH-4058 Basel, Switzerland.

Freimut Juengling (F)

Department of Nuclear Medicine and PET/CT-Center North-West Switzerland, St. Claraspital, CH-4058 Basel, Switzerland.

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Classifications MeSH