BMS-564929 

The human cancer epithelial breast cell lines MDA MB-453 and T47D, which endogenously express AR and progesterone receptor (PR), respectively, are used for radioligand competition binding assays. Binding assays are conducted by incubating BMS-564929 at various concentrations with either [³H]DHT or [³H]progesterone with the cells for 2 h at room temperature. For ERα and ERβ, fusion proteins expressed in Escherichia coli, consisting of maltose binding protein, a specific biotinylation sequence, an enterokinase cleavage site, and either the ERα or ERβ LBD is used. Binding reactions are conducted by incubating ERα and ERβ LBD with BMS-564929 and [³H]E2 for 2 h at room temperature. Specific binding activity to the mineralocorticoid receptor (MR) by BMS-564929 is evaluated by competition binding assay using kidney cytosolic preparations and [³H]aldosterone. The kidneys are obtained from adrenalectomized rats to remove the endogenous source of aldosterone and to increase the MR concentration in the cytosol of kidney cells. Binding reactions are incubated for 2 h on ice in the presence of excess mifepristone (RU486) to block nonspecific glucocorticoid receptor (GR) binding. A fluorescence polarization based assay is used for GR binding, as per manufacturer recommendations. Inhibitory constants (K_i, app) defining apparent binding affinity of test compounds to intracellular receptors are calculated from the observed inhibition of natural ligand binding at multiple concentrations of test compound. SHBG binding is performed using a standard charcoal assay. Reagents: 1 mg lyophilized SHGB powder (Tris), [³H]DHT, 3% charcoal, and 0.4% Dextran in PBS; binding buffer: 50 mM Tris, pH 7.6, 100 mM NaCl, 1 mM EDTA, 1 mM DTT, and mock lysate (3.5 μg/100 μL buffer); stock solutions: stock SHBG protein: 1 mg/mL in water=20 μM; stock [³H]DHT ligand: 9 μM; DHT: 10 mM in DMSO; BMS 564929: 10 mM in DMSO. Compounds diluted in binding buffer are added to 40 nM [³H]DHT and 20 nM SHBG protein in 200 μL volume and incubated for 1 h at room temperature. Total binding: 40 nM [³H]DHT and 20 nM SHBG protein in 200 μL volume; nonspecific binding: 40 nM [³H]DHT and 20 nM SHBG protein and 1 mM cold DHT in 200 μL volume. At the end of the incubation period, 200 μL of the charcoal solution (3% containing 0.04% dextran) is added to 200 μL of the reactions and shaken for 15 min before centrifugation. Supernatant (200 μL) is then transferred to the wells of a 24-well white Optiplate; 200 μL of scintillant are added with mixing. Radioactivity counts are read in Topcount^[1].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Rats^[1]
Matched sets of castrated, sexually mature Harlan Sprague Dawley rats (42-56 d old, 200-250 g) are dosed once daily by oral gavage with BMS-564929 (0.00001-10 mg/kg) in solution/suspension of 80% PEG 400 and 20% Tween 20 for 14 d. Two control groups, one sham operated intact and one castrated, are dosed orally with the PEG/TW vehicle only, beginning on d 15 after surgery. Animals are dosed (vol/wt) at 1 mL/kg body weight. T propionate (TP) is dosed once daily sc in a 10% ethanol/90% peanut oil vehicle as a reference compound (0.03-10 mg/kg). After 14 d of treatment, the animals are killed by carbon dioxide asphyxiation, the levator ani and the ventral prostate are surgically removed and weighed, and serum is collected for LH measurements.

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

• [1]. Ostrowski J, et al. Pharmacological and x-ray structural characterization of a novel selective androgen receptor modulator: potent hyperanabolic stimulation of skeletal muscle with hypostimulation of prostate in rats. Endocrinology. 2007 Jan;148(1):4-12.  [Content Brief]