Duodenal and proximal jejunal motility inhibition associated with bisacodyl-induced colonic high-amplitude propagating contractions.


Journal

American journal of physiology. Gastrointestinal and liver physiology
ISSN: 1522-1547
Titre abrégé: Am J Physiol Gastrointest Liver Physiol
Pays: United States
ID NLM: 100901227

Informations de publication

Date de publication:
01 09 2021
Historique:
pubmed: 8 7 2021
medline: 24 9 2021
entrez: 7 7 2021
Statut: ppublish

Résumé

Bisacodyl is a stimulant laxative often used in manometric studies of pediatric constipation to determine if it can initiate propulsive high-amplitude propagating contractions (HAPCs). Whereas the effects of bisacodyl infusion on colonic motility are well described, the effects of the drug on other regions of the gut after colonic infusion are not known. The aim of the present study was to characterize the effects of bisacodyl on both colonic and small bowel motility. Twenty-seven children (9.3 ± 1.2 yr) undergoing simultaneous high-resolution antroduodenal and colonic manometry were included. Small bowel and colonic motor patterns were assessed before and after colonic infusion of bisacodyl. Patients were divided into two groups: responders and nonresponders based on the presence of high-amplitude propagating contractions (HAPCs) after bisacodyl infusion. Nineteen patients were responders. A total of 188 postbisacodyl HAPCs was identified with a mean count of 10.4 ± 5.5 (range, 3-22), at a frequency of 0.6 ± 0.2/min and mean amplitude of 119.8 ± 23.6 mmHg. No motor patterns were induced in the small bowel. However, in the 19 responders the onset of HAPCs was associated with a significant decrease in small bowel contractile activity. In the nonresponders, there was no detectable change in small bowel motility after bisacodyl infusion. Bisacodyl-induced HAPCs are associated with a significant reduction in small bowel motility probably mediated by extrinsic sympathetic reflex pathways. This inhibition is potentially related to rectal distension, caused by the HAPC anal propulsion of colonic content.

Identifiants

pubmed: 34231391
doi: 10.1152/ajpgi.00209.2021
doi:

Substances chimiques

Laxatives 0
Bisacodyl 10X0709Y6I

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

G325-G334

Auteurs

Phil G Dinning (PG)

College of Medicine & Public Health, Flinders University, Adelaide, Australia.
Department of Surgery and Gastroenterology, Flinders Medical Centre, Adelaide, Australia.

Lukasz Wiklendt (L)

College of Medicine & Public Health, Flinders University, Adelaide, Australia.

Marcello Costa (M)

College of Medicine & Public Health, Flinders University, Adelaide, Australia.

Simon J H Brookes (SJH)

College of Medicine & Public Health, Flinders University, Adelaide, Australia.

Maureen Amicangelo (M)

Center for Motility and Functional Gastrointestinal Disorders, Boston Children's Hospital, Boston, Massachusetts.

Lyneisha Whitter (L)

Center for Motility and Functional Gastrointestinal Disorders, Boston Children's Hospital, Boston, Massachusetts.

Samuel Nurko (S)

Center for Motility and Functional Gastrointestinal Disorders, Boston Children's Hospital, Boston, Massachusetts.

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Classifications MeSH