Calcium/calcimimetic

Calcium-sensing receptor Cholera Enteric nervous system Gene knockout Oral rehydration solution Secretory diarrhea

Journal

World journal of gastroenterology
ISSN: 2219-2840
Titre abrégé: World J Gastroenterol
Pays: United States
ID NLM: 100883448

Informations de publication

Date de publication:
21 Jan 2024
Historique:
received: 02 10 2023
revised: 01 12 2023
accepted: 02 01 2024
medline: 5 2 2024
pubmed: 5 2 2024
entrez: 5 2 2024
Statut: ppublish

Résumé

Enterotoxins produce diarrhea through direct epithelial action and indirectly by activating the enteric nervous system. Calcium-sensing receptor (CaSR) inhibits both actions. The latter has been well documented To determine whether CaSR agonists ameliorate secretory diarrhea evoked by cholera toxin (CTX) in mice. CTX was given orally to C57BL/6 mice to induce diarrhea. Calcium and calcimimetic R568 were used to activate CaSR. To maximize their local intestinal actions, calcium was administered luminally CTX induced secretory diarrhea, as evidenced by increases in fecal Cl Treatment of acute secretory diarrheas remains a global challenge. Despite advances in diarrhea research, few have been made in the realm of diarrhea therapeutics. ORS therapy has remained the standard of care, although it does not halt the losses of intestinal fluid and ions caused by pathogens. There is no cost-effective therapeutic for diarrhea. This and other studies suggest that adding calcium to ORS or using calcimimetics to activate intestinal CaSR might represent a novel approach for treating secretory diarrheal diseases.

Sections du résumé

BACKGROUND BACKGROUND
Enterotoxins produce diarrhea through direct epithelial action and indirectly by activating the enteric nervous system. Calcium-sensing receptor (CaSR) inhibits both actions. The latter has been well documented
AIM OBJECTIVE
To determine whether CaSR agonists ameliorate secretory diarrhea evoked by cholera toxin (CTX) in mice.
METHODS METHODS
CTX was given orally to C57BL/6 mice to induce diarrhea. Calcium and calcimimetic R568 were used to activate CaSR. To maximize their local intestinal actions, calcium was administered luminally
RESULTS RESULTS
CTX induced secretory diarrhea, as evidenced by increases in fecal Cl
CONCLUSION CONCLUSIONS
Treatment of acute secretory diarrheas remains a global challenge. Despite advances in diarrhea research, few have been made in the realm of diarrhea therapeutics. ORS therapy has remained the standard of care, although it does not halt the losses of intestinal fluid and ions caused by pathogens. There is no cost-effective therapeutic for diarrhea. This and other studies suggest that adding calcium to ORS or using calcimimetics to activate intestinal CaSR might represent a novel approach for treating secretory diarrheal diseases.

Identifiants

pubmed: 38314127
doi: 10.3748/wjg.v30.i3.268
pmc: PMC10835527
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

268-279

Informations de copyright

©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict-of-interest statement: All the authors report having no relevant conflicts of interest for this article.

Auteurs

Lie-Qi Tang (LQ)

Department of Pediatrics, University of Florida, Gainesville, FL 32610, United States.

Johnathan Fraebel (J)

Department of Pediatrics, University of Florida, Gainesville, FL 32610, United States.
College of Medicine, University of Florida, Gainesville, FL 32610, United States.

Shi Jin (S)

Department of Pediatrics, University of Florida, Gainesville, FL 32610, United States.

Steven P Winesett (SP)

Applied Physiology and Kinesiology, University of Florida, Gainesville, FL 32610, United States.
Brain Rehabilitation Research Center, Malcom Randall VA Medical Center, Gainesville, FL 32610, United States.

Jane Harrell (J)

Department of Pediatrics, University of Florida, Gainesville, FL 32610, United States.

Wen-Han Chang (WH)

Department of Medicine, Endocrine Research Unit, Veterans Affairs Medical Center, University of California, San Francisco, San Francisco, CA 94121, United States.

Sam Xianjun Cheng (SX)

Department of Pediatric Gastroenterology, Hepatology, and Nutrition, University of Florida Shands Children's Hospital, Gainesville, FL 32608, United States. sam.cheng@ufl.edu.

Classifications MeSH