Calcium-sensing receptor: A new target for therapy of diarrhea

World J Gastroenterol. 2016 Mar 7;22(9):2711-24. doi: 10.3748/wjg.v22.i9.2711.

Abstract

Management of acute diarrhea remains a global challenge, particularly in resource-limiting countries. Oral rehydration solution (ORS), a passive rehydrating therapy developed approximately 40 years ago, remains the mainstay treatment. Although ORS is effective for hydration, since it does not inhibit enterotoxin-mediated excessive secretion, reduced absorption and compromised barrier function - the primary mechanisms of diarrhea, ORS does not offer a rapid relief of diarrhea symptom. There are a few alternative therapies available, yet the use of these drugs is limited by their expense, lack of availability and/or safety concerns. Novel anti-diarrheal therapeutic approaches, particularly those simple affordable therapies, are needed. This article explores intestinal calcium-sensing receptor (CaSR), a newly uncovered target for therapy of diarrhea. Unlike others, targeting this host antidiarrheal receptor system appears "all-inclusive": it is anti-secretory, pro-absorptive, anti-motility, and anti-inflammatory. Thus, activating CaSR reverses changes of both secretory and inflammatory diarrheas. Considering its unique property of using simple nutrients such as calcium, polyamines, and certain amino acids/oligopeptides as activators, it is possible that through targeting of CaSR with a combination of specific nutrients, novel oral rehydrating solutions that are inexpensive and practical to use in all countries may be developed.

Keywords: Anti-secretory; Cholera toxin; Enteric nervous system; Escherichia coli heat stable toxin; Inflammatory diarrhea; Intestinal barrier function; Intestinal permeability; Oral rehydration solution; Pro-absorptive; Secretory diarrhea.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antidiarrheals / economics
  • Antidiarrheals / therapeutic use*
  • Cost-Benefit Analysis
  • Diarrhea / drug therapy*
  • Diarrhea / economics
  • Diarrhea / metabolism
  • Diarrhea / physiopathology
  • Disease Models, Animal
  • Drug Costs
  • Drug Design
  • Gastrointestinal Motility / drug effects
  • Genotype
  • Humans
  • Intestinal Mucosa / metabolism
  • Intestines / drug effects*
  • Intestines / physiopathology
  • Mice, Knockout
  • Molecular Targeted Therapy
  • Permeability
  • Receptors, Calcium-Sensing / agonists*
  • Receptors, Calcium-Sensing / metabolism
  • Receptors, G-Protein-Coupled / deficiency
  • Receptors, G-Protein-Coupled / genetics
  • Signal Transduction / drug effects

Substances

  • Antidiarrheals
  • CASR protein, human
  • CASR protein, mouse
  • Receptors, Calcium-Sensing
  • Receptors, G-Protein-Coupled