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Calcium/calcimimetic via calcium-sensing receptor ameliorates cholera toxin-induced secretory diarrhea in mice.
Tang, Lie-Qi; Fraebel, Johnathan; Jin, Shi; Winesett, Steven P; Harrell, Jane; Chang, Wen-Han; Cheng, Sam Xianjun.
Affiliation
  • Tang LQ; Department of Pediatrics, University of Florida, Gainesville, FL 32610, United States.
  • Fraebel J; Department of Pediatrics, University of Florida, Gainesville, FL 32610, United States.
  • Jin S; College of Medicine, University of Florida, Gainesville, FL 32610, United States.
  • Winesett SP; Department of Pediatrics, University of Florida, Gainesville, FL 32610, United States.
  • Harrell J; Applied Physiology and Kinesiology, University of Florida, Gainesville, FL 32610, United States.
  • Chang WH; Brain Rehabilitation Research Center, Malcom Randall VA Medical Center, Gainesville, FL 32610, United States.
  • Cheng SX; Department of Pediatrics, University of Florida, Gainesville, FL 32610, United States.
World J Gastroenterol ; 30(3): 268-279, 2024 Jan 21.
Article in En | MEDLINE | ID: mdl-38314127
ABSTRACT

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 in vitro but not in vivo. The hypothesis to be tested was that activating CaSR inhibits diarrhea in vivo.

AIM:

To determine whether CaSR agonists ameliorate secretory diarrhea evoked by cholera toxin (CTX) in mice.

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 via oral rehydration solution (ORS), whereas R568 was applied serosally using an intraperitoneal route. To verify that their actions resulted from the intestine, effects were also examined on Cre-lox intestine-specific CaSR knockouts. Diarrhea outcome was measured biochemically by monitoring changes in fecal Cl- or clinically by assessing stool consistency and weight loss.

RESULTS:

CTX induced secretory diarrhea, as evidenced by increases in fecal Cl-, stool consistency, and weight loss following CTX exposure, but did not alter CaSR, neither in content nor in function. Accordingly, calcium and R568 were each able to ameliorate diarrhea when applied to diseased intestines. Intestinal CaSR involvement is suggested by gene knockout experiments where the anti-diarrheal actions of R568 were lost in intestinal epithelial CaSR knockouts (villinCre/Casrflox/flox) and neuronal CaSR knockouts (nestinCre/Casrflox/flox).

CONCLUSION:

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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcium / Receptors, Calcium-Sensing / Diarrhea Limits: Animals Language: En Journal: World J Gastroenterol / World j. gastroenterol / World journal of gastroenterology Journal subject: GASTROENTEROLOGIA Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calcium / Receptors, Calcium-Sensing / Diarrhea Limits: Animals Language: En Journal: World J Gastroenterol / World j. gastroenterol / World journal of gastroenterology Journal subject: GASTROENTEROLOGIA Year: 2024 Document type: Article Affiliation country: Estados Unidos Country of publication: Estados Unidos