| Literature DB >> 27230993 |
Philippe Bissel1, Katie Boes1, Jonathan Hinckley1, Bernard S Jortner1, Geraldine Magnin-Bissel1, Stephen R Werre1, Marion Ehrich2, Adria Carbo3, Casandra Philipson3, Raquel Hontecillas3, Noah Philipson3, Richard D Gandour3, Josep Bassaganya-Riera3.
Abstract
Lanthionine synthetase cyclase-like receptor 2 (LANCL2) is a novel therapeutic target for Crohn's disease (CD). BT-11 is a small molecule that binds LANCL2, is orally active, and has demonstrated therapeutic efficacy in 3 validated mouse models of colitis at doses as low as 8 mg/kg/d. Exploratory experiments evaluated BT-11 in male Harlan Sprague Dawley rats with a single oral dose of 500 mg/kg and 80 mg/kg/d for 14 days (n = 10 rats dosed/group). Treated and control rats were observed for behavioral detriments, and blood and tissues were collected for clinical pathology and histopathological examination. A functional observational battery demonstrated no differences between treated and control groups over multiple times of observation for quantal, categorical, and continuous end points, including posture, in cage activity, approach, response to touch, weight, grip strength, body temperature, and time on a rotarod. Histopathological examination of the brain, kidney, liver, adrenal gland, testes, stomach, small and large intestines, duodenum, pancreas, heart, lungs, spleen, thymus, and rib found no significant differences between the groups. Plasma enzymes associated with liver function were transiently elevated 2 to 4 days after the 500 mg/kg single dose but returned to normal values by 8 days and were not observed at any time in rats given 80 mg/kg/d for 14 days. One hour after oral administration of a single dose of 80 mg/kg, BT-11 had a maximal concentration of 21 ng/mL; the half-life was 3 hours. These experimental results demonstrated that BT-11 is well tolerated in rats, and, with further testing, may hold promise as an orally active therapeutic for CD.Entities:
Keywords: BT-11; LANCL2; rats; safety; toxicology
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Year: 2016 PMID: 27230993 PMCID: PMC5033715 DOI: 10.1177/1091581816646356
Source DB: PubMed Journal: Int J Toxicol ISSN: 1091-5818 Impact factor: 2.032