| Literature DB >> 30253666 |
Karin E Thompson1,2, Ramesh M Ray1,2, Shanta Alli1, Wenbo Ge1, Alyssa Boler1, W Shannon McCool1, Avtar S Meena3, Pradeep K Shukla3, Radakrishna Rao3, Leonard R Johnson1,3, Mark A Miller4, Gabor J Tigyi1,3.
Abstract
IMPACT STATEMENT: A critical barrier in treating diarrheal disease is easy-to-use effective treatments. Rx100 is a first in class, novel small molecule that has shown efficacy after both subcutaneous and oral administration in a mouse cholera-toxin- and Citrobacter rodentium infection-induced diarrhea models. Our findings indicate that Rx100 a metabolically stable analog of the lipid mediator lysophosphatidic acid blocks activation of CFTR-mediated secretion responsible for fluid discharge in secretory diarrhea. Rx100 represents a new treatment modality which does not directly block CFTR but attenuates its activation by bacterial toxins. Our results provide proof-of-principle that Rx100 can be developed for use as an effective oral or injectable easy-to-use drug for secretory diarrhea which could significantly improve care by eliminating the need for severely ill patients to regularly consume large quantities of oral rehydration therapies and offering options for pediatric patients.Entities:
Keywords: Citrobacter rodentium; G-protein-coupled receptors; Rx100; Secretory diarrhea; cholera toxin; cystic fibrosis transmembrane conductance regulator; lysophosphatidic acid; lysophosphatidic acid receptor; oral rehydration therapy
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Year: 2018 PMID: 30253666 PMCID: PMC6434456 DOI: 10.1177/1535370218803349
Source DB: PubMed Journal: Exp Biol Med (Maywood) ISSN: 1535-3699