Biological Activity |
BMS 299897 is a sulfonamide gamma-secretase inhibitor with an IC50 of 7 nM for Abeta production inhibition in HEK293 cells stably overexpressing amyloid precursor protein (APP). IC50 & Target: IC50: 7 nM (Abeta, in HEK293 cells)[1] In Vitro: BMS-299897 reduces the levels of each of the Abeta peptides. At 1 uM, BMS-299897 decreases these peptides to levels ranging from 20 to 50% of the vehicle control. BMS-299897 treatment reduces the portion of QD-BDNF signals moving in the retrograde direction (p=0.0198) with a concomitant increase in the portion of signals moving in the anterograde direction (p=0.0147)[2]. In Vivo: BMS-299897 shows dose- and time-dependent reductions of amyloid beta-peptide (Abeta) in brain, cerebrospinal fluid (CSF), and plasma in young transgenic mice, with a correlation between brain and CSF Abeta levels. BMS-299897 reduces both brain and plasma Abeta1-40 in APP-YAC mice and increases brain concentrations of APPcarboxy-terminal fragments, consistent with gamma-secretase inhibition. BMS-299897, attenuates this Abeta25-35-induced Abeta1-42 seeding and toxicity. BMS-299897 is administered at 0.1-1 nmol/mouse, concomittantly with Abeta25-35 (9 nmol) in male Swiss mice. After one week, the contents in Abeta1-42 and Abeta1-40, and the levels in lipid peroxidation are analyzed in the mouse hippocampus. Mice are submitted to spontaneous alternation, passive avoidance and object recognition to analyze their short- and long-term memory abilities. Abeta25-35 increases Abeta1-42 content (+240%) but fails to affect Abeta1-40. BMS-299897 blocks the increase in Abeta1-42 content and decreased Abeta1-40 levels significantly. The compound does not affect Abeta25-35-induced increase in hippocampal lipid peroxidation. Behaviorally, BMS-299897 blocks the Abeta25-35-induced deficits in spontaneous alternation or novel object recognition, using a 1 h intertrial time interval. The co-administration of the gamma-secretase inhibitor BMS-299897, in the 0.1-1 umol/mouse dose-range, completely blocks the Abeta25-35-induced increase in Abeta1-42 content[1]. |