YM758

Transporter-expressing or vector-transfected HEK293 cells are grown in DMEM supplemented with 10% FBS and 1% penicillin-streptomycin (v/v) and 100 μg/mL Zeocin at 37°C in an atmosphere of 5% CO₂ and 95% humidity. The cells are subcultured in a medium containing 0.05% trypsin-EDTA solution. Cells are then seeded in poly-D-lysine-coated 12-well plates at a density of 1.2×10⁵ cells/well. For the transport study, the cell culture medium is replaced with culture medium supplemented with 5 mM sodium-butyrate for 24 h before the transport assay to induce the expression level of hOCT1, rOct1, OATP1B1, and OATP1B3. The transport study is performed. Uptake is initiated by adding Krebs-Henseleit buffer containing radiolabeled substrates (0.6 nM [³H]MPP, 10 μM[¹⁴C]Metformin, 20 nM [³H]E₂17βG, or 10 μM [¹⁴C]YM758) after the cells have been washed twice and preincubated with Krebs-Henseleit buffer at 37°C for 15 min. In the concentration-dependent uptake and/or inhibition studies, the cells are incubated further in the presence of YM758 (1-1000 μM). The Krebs-Henseleit buffer consists of 2.0 mg/mL D-glucose, 0.141 mg/mL Magnesium sulfate, 0.16 mg/mL Potassium phosphate monobasic, 0.35 mg/mL Potassium chloride, 6.9 mg/mL Sodium chloride, 0.373 mg/mL Calcium chloride dihydrate, 1.5 mg/mL HEPES, and 2.1 mg/mL Sodium bicarbonate. The pH of this solution is adjusted to 7.4 with Sodium hydroxide. The uptake is terminated at the designated time by adding ice-cold Krebs-Henseleit buffer after removing the incubation buffer. The cells then are washed twice with 1 mL of ice-cold Krebs-Henseleit buffer, solubilized in 0.5 mL of 1.0 M Sodium hydroxide, and kept overnight at 4°C. Aliquots (0.5 mL) are transferred to scintillation vials after adding 0.25 mL of 2.0 M hydrochloric acid. The radioactivity associated with the cells and incubation buffer is measured in a liquid scintillation counter after adding 5 mL of scintillation fluid to the scintillation vials. The remaining cell lysate is used to determine the protein concentration by the method of Lowry, with bovine serum albumin as the standard^[1].

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

Beagle^[2]
Four male beagles (11.0-15.0 kg) are used for the intravenous administration study. Heart rate (HR) (beats/min) is determined by doubling the number of the QRS complexes on the ECG recorded for 30 s. First, HR is measured at rest and just after initiation of tachycardia induced by intravenous Isoproterenol (0.1 μg/kg) administration, and then YM758, which is dissolved in saline, is intravenously administered at doses of 0.03, 0.1, and 0.3 mg/kg. At 0.1, 0.25, 0.5, 1, 2, 3, 4, 5, 6, 7, 8, and 24 h after the YM758 administration, HR is measured just after intravenous isoproterenol (0.1 μg/kg) to induce tachycardia, following the measurement of resting HR at each designated point. This is followed by a minimum 1-week washout period between each study period. Blood samples (approximately 3.0 mL) are withdrawn from the vein using a heparin-treated syringe, and the electrocardiogram (ECG) is recorded at the times designated (0.1, 0.25, 0.5, 1, 2, 3, 4, 5, 6, 7, 8, and 24 h after administration). Plasma is obtained by centrifugation of the blood samples at 1870g for 15 min at 4°C and then stored at -20°C until determination of the YM758 concentrations^[2].
Rats^[3]
Male Long-Evans rats (7 weeks) and Sprague-Dawley rats (9 weeks) are used. 3 mg/2.57 MBq/10 mL/kg is given to rats orally by gavage using a syringe with a gastric tube.The nonalbino rats are sacrificed by ether overdose 4 and 24 h after a single oral administration of 3 mg/kg ¹⁴C-YM758. The fur is then rapidly clipped off, and the nasal cavity and anus are filled with 4% carboxymethylcellulose-Na. The carcass is frozen in a dry ice-acetone mixture, and the forelimbs, hind limbs, and tail are surgically removed^[3].

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