Preladenant  (Synonyms: SCH-420814)

Receptor binding is performed using membranes prepared from cells with recombinant expression of adenosine receptors as follows: human A_2A and HEK 293, rat A_2A and Chinese hamster ovary, human and rat A1 and Chinese hamster ovary, and human A₃ and HEK 293. Radioligand competition binding assays are performed in 96-well plates in a total assay volume of 200 μL using a final test drug concentration range of between 0.1 and 3 μM. Membranes are diluted in assay buffer, pH 7.4 (A₁ and A_2A, Dulbecco's phosphate-buffered saline with 10 mM MgCl₂; A₃, 50 mM Tris-HCl, 120 mM NaCl, 10 mM MgCl₂). To remove endogenous adenosine from the membrane preparations, 4 U/mL adenosine deaminase is added to the membranes, which are then incubated at room temperature for 15 min. Radioligand is added to a final concentration of 0.5 ([³H]SCH 58261, A_2A), 1 ([³H]DPCPX, A₁), or 0.25 ([¹²⁵I]AB-MECA, A₃) nM. Nonspecific binding is defined by adding 100 nM CGS 15923 (A_2A), 100 nM NECA (A₁), or 100 nM DPCPX (A₃). Plates are incubated at room temperature with agitation for 1.5 h (A_2A and A₁) or 2 h (A₃). Membranes are filtered onto Packard GF-B filter plates and washed in ice-cold assay buffer using a Brandel cell harvester to separate bound and free radioligand. The plates are dried before addition of 45 μL of Microscint 20 to each well. IC₅₀ values are determining by fitting the displacement curves using an iterative curve-fitting program. K_i values are calculated using the Cheng-Prusoff equation^[1].

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

HEK 293 cells stably expressing either human A_2A or A_2B receptors are grown to confluence, harvested using enzyme-free cell dissociation buffer and pelleted by centrifugation (1000g; 5 min). The cells are washed and diluted to a final density of 4×10⁶ cells/mL in Hanks' balanced salt solution supplemented with 10 nM HPS, pH 7.4,, 5 mM MgCl₂, and 0.2% bovine serum albumin. Preladenant is diluted in the above buffer with inclusion of the following components to achieve the respective final assay concentrations: 0.25% DMSO, 2 U/mL adenosine deaminase, and 100 μM Ro 201724. Cell suspensions (20 μL) are preincubated for 15 min at room temperature in 96-well plates containing 25 μL of vehicle or Preladenant. CGS-21680 (A_2A) or 5-N-cyclopropylcarboxamidoadenosine (A_2B) at 10-fold the desired concentration is then added, and the reactions are incubated for 15 min at 37°C. The reactions are terminated by the addition of 50 μL of assay/lysis buffer. The concentration response curves for CGS-21680 in the presence and absence of Preladenant are plotted, and the EC₅₀ values are determined by fitting the curves using GraphPad Prism software^[1].

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

Mice and Rats^[1]
Male CD rats and male CD1 mice are used. Preladenant is administered orally in 50% polyethylene glycol 400 at a dose volume of 3 to 5 mL/kg. In the forced swim test (FST), mice are placed individually into glass cylinders filled to a depth of 10 cm with water (25°C) and left for 6 min. A mouse is judged to be immobile when it floats in an upright position and made only small movements to keep its head above water. The duration of immobility is recorded during the last 4 min of the 6-min testing period by an observer blind to the treatment of the animals. Animals are dosed with vehicle, Preladenant, or SCH 412348 1 h before behavioral testing. Each rat is placed individually in a cylinder of water (25°C) and left to swim for 15 min before being removed and dried in a heated enclosure and returned its home cage. Twenty-four hours later (test day), the animal is re-exposed to the conditions, and the total immobility time during a 5-min period is recorded. In addition, the duration of time that the rats spent climbing the sides of the cylinder is recorded. On test day, each animal is dosed with Preladenant, SCH 412348, or vehicle 1 h before behavioral testing.
Monkeys^[2]
Six female cynomolgus (Macaca fascicularis) monkeys (weighing 3.5-4.2 kg) are used. The animals are rendered parkinsonian by subcutaneous (sc) administrations of MPTP (2-3 mg/kg) once per week until a stable parkinsonian syndrome (unchanged disability score of 8 or greater for at least a month) developed as measured by a parkinsonian disability scale. At least 2 months after the final administration of MPTP, the monkeys are treated chronically with Prolopa (L-Dopa/benserazide, 100/25 mg) until clear and reproducible dyskinesias developed. The present experiment with L-Dopa and Preladenant (1 mg/kg and 3 mg/kg, p.o.) is performed in these monkeys.

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

• [1]. Hodgson RA, et al. Characterization of the potent and highly selective A2A receptor antagonists preladenant and SCH 412348 [7-[2-[4-2,4-difluorophenyl]-1-piperazinyl]ethyl]-2-(2-furanyl)-7H-pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine] in rodent  [Content Brief]

  [2]. Hodgson RA, et al. Preladenant, a selective A(2A) receptor antagonist, is active in primate models of movement disorders. Exp Neurol. 2010 Oct;225(2):384-90.  [Content Brief]