In vivo pharmacology and antidiarrheal efficacy of a thiazolidone CFTR inhibitor in rodents

• Published in: Journal of pharmaceutical sciences Vol. 94; no. 1; pp. 134 - 143
• Main Authors: Sonawane, ND, Muanprasat, C, Nagatani, R, Song, YL, Verkman, AS
• Format: Journal Article
• Language: English
• Published: NEW YORK Elsevier 01.01.2005
• Subjects: Chemistry; Chemistry, Medicinal; Chemistry, Multidisciplinary; Life Sciences & Biomedicine; Pharmacology & Pharmacy; Physical Sciences; Science & Technology; cholera toxin; MECHANISM; diarrhea; TRANSPORT; FLUID SECRETION; METABOLISM; CHANNEL; chloride channel; cystic fibrosis; pharmacology; drug metabolism; DISEASE; ENTEROTOXIN; mass spectrometry; CYSTIC-FIBROSIS; HPLC; CHOLERA-TOXIN
• ISSN: 0022-3549; 1520-6017
• DOI: 10.1002/jps.20228

A small-molecule inhibitor of the cystic fibrosis transmembrane conductance regulator (CFTR), 3-[(3-trifluoromethyl)phenyl]-5-[(4-carboxyphenyl)methylene]-2-thioxo-4-thiazolidinone (CFTRinh-172), reduces enterotoxin-induced intestinal fluid secretion in rodents. Here, we study CFTRinh-172 pharmacology and antidiarrheal efficacy in rodents using C-14-labeled CFTRinh-172, liquid chromatography/mass spectrometry, and a closed intestinal loop model of fluid secretion. CFTRinh-172 was cleared primarily by renal glomerular filtration without chemical modification. CFTRinh-172 accumulated in liver within 5 min after intravenous infusion in mice, and was concentrated fivefold in bile over blood. At 30-240 min, CFTRinh-172 was found mainly in liver, intestine, and kidney, with little detectable in the brain, heart, skeletal muscle, or lung. Pharmacokinetic analysis in rats following intravenous bolus infusion showed a distribution volume of 770 mL with redistribution and elimination half-times of 0.14 h and 10.3 h, respectively. CFTRinh-172 was stable in hepatic microsomes. Closed-loop studies in mice indicated that a single intraperitoneal injection of 20 mug CFTRinh-172 inhibited fluid accumulation at 6 h after cholera toxin by >90% in duodenum and jejunum, similar to60% in ileum and <10% in colon. No toxicity was seen after high-dose CFTRinh-172 administration (3 mg/kg/day in two daily doses) in mice over the first 6 weeks of life. The metabolic stability, enterohepatic recirculation, slow renal elimination, and intestinal accumulation of CFTRinh-172 account for its efficacy as an antidiarrheal. (C) 2004 Wiley-Liss, Inc.