ADENOSINE RECEPTOR AGONISTS
20220152077 · 2022-05-19
Inventors
Cpc classification
A61P25/28
HUMAN NECESSITIES
A61P25/18
HUMAN NECESSITIES
A61K31/7076
HUMAN NECESSITIES
International classification
A61K31/7076
HUMAN NECESSITIES
A61P25/18
HUMAN NECESSITIES
A61P25/28
HUMAN NECESSITIES
Abstract
The present invention relates to compounds of Formula (I) for use in the treatment of nervous system disorders and pain, wherein Formula (I) is:
##STR00001##
or a pharmaceutically acceptable salt or isomer thereof, wherein R is defined herein. The compounds are selective A.sub.1 adenosine receptor agonists with preferential action in the nervous system, with spared cardiovascular system and respiratory effects. The invention also relates to pharmaceutical compositions comprising the compounds.
Claims
1-15. (canceled)
16. A compound of Formula (I) for use in the treatment of a nervous system disorder or pain, wherein Formula (I) is: ##STR00013## or a pharmaceutically acceptable salt or isomer thereof, wherein: R is independently hydrogen or R.sup.1R.sup.2R.sup.3, wherein: R.sup.1 is independently C.sub.1-10 alkyl; R.sup.2 is independently aryl; and R.sup.3 is independently hydrogen, OH, C(O)NH.sub.2, linear or branched C.sub.1-C.sub.10 alkyl, or C.sub.3-C.sub.8 cycloalkyl.
17. The compound for use according to claim 16, wherein: (i) R.sup.1 is CH.sub.2; and/or (ii) R.sup.2 is phenyl; and/or (iii) R.sup.3 is hydrogen, OH, C(O)NH.sub.2, linear or branched C.sub.4-C.sub.10 alkyl, or C.sub.3-C.sub.8 cycloalkyl.
18. The compound for use according to claim 16, wherein the compound is selected from the group consisting of: ##STR00014## or a pharmaceutically acceptable salt thereof.
19. The compound for use according to claim 16, wherein the nervous system disorder is selected from the group consisting of: epilepsy, ischemia, stroke, traumatic brain injury (TBI), hypoxia, Parkinson's disease, Alzheimer's disease, Huntington's disease, multiple sclerosis, cerebral palsy, encephalitis, meningitis, adrenoleukodystrophy, amyotrophic lateral sclerosis, phenylketonuria, spinal cord injury, dementia, schizophrenia and sleep disorders including insomnia.
20. The compound for use according to claim 16, wherein the compound does not activate the Gα protein subunit Gob.
21. The compound for use according to claim 16, wherein the compound acts as an antagonist of post-synaptic A.sub.1Rs.
22. The compound for use according to claim 16, wherein the compound is not capable of inducing membrane hyperpolarisation.
23. The compound for use according to claim 16, wherein said use does not cause at least one of bradycardia, hypotension and dyspnea.
24. The compound for use according to claim 16, wherein said use comprises administering the compound to a subject who is suffering from, at risk of or in need of treatment for a cardiovascular or respiratory disease.
25. The compound for use according to claim 16, wherein the pain is selected from the group consisting of: neuropathic, nociceptive, peripheral acute and chronic, somatic, visceral, neuroma, diabetic neuropathy, surgical pain, chemotherapy-induced pain, bone pain, inflammatory, phantom limb, myalgia, and multiple sclerosis-related pain; optionally wherein the bone pain is fracture pain or cancer pain.
26. A compound of Formula (I), ##STR00015## or a pharmaceutically acceptable salt or isomer thereof and wherein R is R.sup.1R.sup.2R.sup.3, and wherein: i. R.sup.1 is CH.sub.2; ii. R.sup.2 is aryl; and iii. R.sup.3 is independently hydrogen, OH, C(O)NH.sub.2, linear or branched C.sub.1-C.sub.10 alkyl, or C.sub.3-C.sub.8 cycloalkyl.
27. A compound according to claim 26, wherein the compound is not: ##STR00016##
28. A compound according to claim 26, wherein the compound is selected from the group consisting of: ##STR00017## or a pharmaceutically acceptable salt or isomer thereof.
29. A compound according to claim 26, for use as a medicament.
30. A pharmaceutical composition comprising a compound of Formula (I), according to claim 16, and a pharmaceutically or therapeutically acceptable excipient or carrier.
31. A pharmaceutical composition comprising a compound of Formula (I), according to claim 26, and a pharmaceutically or therapeutically acceptable excipient or carrier.
32. A method of treating a disease or condition, comprising the step of administering a therapeutically effective amount of the compound I of claim 16 to a patient.
33. A method according to claim 32, wherein the disease or condition is selected from nervous system disorders, cardiovascular disease, respiratory disease and pain.
Description
[0094] Particular non-limiting examples of the present invention will now be described with reference to the following drawings, in which:
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EXPERIMENTAL
[0105] Experiments were performed in accordance with the European Commission Directive 2010/63/EU (European Convention for the Protection of Vertebrate Animals used for Experimental and Other Scientific Purposes) and the United Kingdom Home Office (Scientific Procedures) Act (1986) with project approval from the institutional animal welfare and ethical review body (AWERB).
[0106] Preparation of hippocampal slices: Sagittal slices of hippocampus (300-400 μm) were prepared from male Sprague Dawley rats, at postnatal days 12 to 20. Rats were kept on a 12-hour light-dark cycle with slices made 90 minutes after entering the light cycle. In accordance with the U.K. Animals (Scientific Procedures) Act (1986), male rats were killed by cervical dislocation and decapitated. The brain was removed, cut down the mid line and the two sides of the brain stuck down to a metal base plate. Slices were cut around the midline with a Microm HM 650V microslicer in cold (2 to 4° C.) high Mg.sup.2+, low Ca2+ aCSF, composed of (mM): 127 NaCl, 1.9 KCl, 8 MgCl.sub.2, 0.5 CaCl.sub.2, 1.2 KH.sub.2PO.sub.4, 26 NaHCO.sub.3, 10 D-glucose (pH 7.4 when bubbled with 95% O.sub.2 and 5% CO.sub.2, 300 mOSM). Slices were stored at 34° C. for 1 to 6 hours in aCSF (1 mM MgCl.sub.2, 2 mM CaCl.sub.2) before use.
[0107] Extracellular recording: A slice was transferred to the recording chamber, submerged in aCSF and perfused at 4 to 6 mL/min (32° C.). The slice was placed on a grid allowing perfusion above and below the tissue and all tubing was gas tight (to prevent loss of oxygen). For extracellular recording, an aCSF filled microelectrode was placed on the surface of stratum radiatum in CA1. Extracellular recordings were made using either a differential model 3000 amplifier (AM systems, WA USA) or a DP-301 differential amplifier (Warner Instruments, Hampden, Conn. USA) with field excitatory postsynaptic potentials (fEPSPs) evoked with either an isolated pulse stimulator model 2100 (AM Systems, WA) or ISO-Flex (AMPI, Jerusalem, Israel). For fEPSPs a 10 to 20 minute baseline was recorded at a stimulus intensity that gave 40 to 50% of the maximal response. Signals were filtered at 3 kHz and digitised on line (10 kHz) with a Micro CED (Mark 2) interface controlled by Spike software (Vs 6.1, Cambridge Electronic Design, Cambridge UK) or with WinLTP (W. W. Anderson et al., J. Neurosci Methods, 2007, 162, 346-356). For fEPSP slope, a 1 ms linear region after the fibre volley was measured. Extracellular recordings were made independently on two electrophysiology rigs. As the data obtained from each rig was comparable both sets of data have been pooled.
[0108] Seizure model: Seizure activity was induced in hippocampal slices using aCSF which contained no added Mg.sup.2+ and with the total K.sup.+ concentration increased to 6 mM with KCl. Removal of extracellular Mg.sup.2+ facilitates NMDA receptor activation producing long lasting EPSPS, which can sum together to produce tonic activation. Increasing the extracellular concentration of K.sup.+ depolarises neurons leading to firing and release of glutamate to sustain activity. Both the increase in K.sup.+ concentration and removal of Mg.sup.2+ are required to produce spontaneous activity in hippocampal slices. Spontaneous activity was measured with an aCSF-filled microelectrode placed within stratum radiatum in CA1.
[0109] Whole cell patch clamp recording from hippocampal pyramidal cells: A slice was transferred to the recording chamber and perfused at 3 mL/min with aCSF at 32±0.5° C. Slices were visualised using IR-DIC optics with an Olympus BX151W microscope (Scientifica) and a CCD camera (Hitachi). Whole-cell current clamp recordings were made from pyramidal cells in area CA1 of the hippocampus using patch pipettes (5 to 10 MΩ) manufactured from thick walled glass (Harvard Apparatus, Edenbridge UK) and containing (mM): potassium gluconate 135, NaCl 7, HEPES 10, EGTA 0.5, phosphocreatine 10, MgATP 2, NaGTP 0.3 and biocytin 1 mg/mL (290 mOSM, pH 7.2). Voltage and current recordings were obtained using an Axon Multiclamp 700B amplifier (Molecular Devices, USA) and digitised at 20 KHz. Data acquisition and analysis was performed using Pclamp 10 (Molecular Devices). For voltage clamp experiments, CA1 pyramidal cells were held at −60 mV. Peptides to interfere with G protein signalling were introduced via the patch pipette into the recorded cell. The cell was held for at least 10 minutes before adenosine (10 μM) was added to induce an outward current.
[0110] Frog heart preparation: Xenopus leavis frogs (young adult males) were supplied from Portsmouth Xenopus Resource Centre. Frogs were euthanized with MS222 (0.2% at a pH of 7), decapitated and pithed. The animals were dissected to reveal the heart and the pericardium carefully removed. Heart contractions were measured with a force transducer (AD instruments). Heart rate was acquired via a PowerLab 26T (AD instruments) controlled by LabChart 7 (AD instruments). The heart was regularly washed with ringer and drugs were applied directly to the heart.
[0111] In vivo anaesthetised rat preparation for cardiorespiratory recordings: Anaesthesia was induced in adult male Sprague Dawley rats (230-330 g) with isofluorane (2-4%; Piramal Healthcare). The femoral vein was catheterised for drug delivery. Anaesthesia was maintained with urethane (1.2-1.7 g/kg; Sigma) in sterile saline delivered via the femoral catheter. The femoral artery was catheterised and connected to a pressure transducer (Digitimer) to record arterial blood pressure. Body temperature was maintained at 36.7° C. via a thermocouple heating pad (TCAT 2-LV; Physitemp). The rats were then allowed to stabilise before the experiments began. Blood pressure signals were amplified using the NeuroLog system (Digitimer) connected to a 1401 interface and acquired on a computer using Spike2 software (Cambridge Electronic Design). Arterial blood pressure recordings were used to derive heart rate (HR: beats.Math.minute.sup.−1; BPM), and to calculate mean arterial blood pressure (MAP: Diastolic pressure+⅓*[Systolic Pressure−Diastolic pressure]). Airflow measurements were used to calculate: tidal volume (V.sub.T; mL; pressure sensors were calibrated with a 3 mL syringe), and respiratory frequency (f; breaths.Math.min-1; BrPM). Minute ventilation (V.sub.E; mL.Math.min-1) was calculated as f×V.sub.T.
[0112] After allowing the animal to stabilise following surgery, A.sub.1R agonists were administered by intravenous (IV) injection and the changes in HR, MAP, f, V.sub.T, and V.sub.E were measured. In pilot studies, the optimal dose of adenosine was determined by increasing the dose until robust and reliable changes in HR and MAP were produced (1 mg.Math.kg.sup.−1). The dose of CPA was adjusted until equivalent effects to adenosine were produced on HR and MAP (6.3 μg.Math.kg.sup.−1). For BnOCPA we initially used 5 μg.Math.kg.sup.−1, but saw no agonist effect on HR and MAP. To ensure this was not a false negative we increased the dose of BnOCPA (8.3 μg.Math.kg.sup.−1), which still gave no agonist effect on HR and MAP. However, as BnOCPA produced an antagonistic effect when co-administered with adenosine (
[0113] In the experimental study, rats received an injection of adenosine. After cardiorespiratory parameters returned to baseline (5-10 minutes) rats were given BnOCPA. After allowing sufficient time for any effect of BnOCPA to be observed, rats received adenosine with BnOCPA co-administered in a single injection. After cardiorespiratory parameters returned to baseline, rats were injected with CPA.
[0114] To check that the volume of solution injected with each drug did not itself induce a baroreflex response leading to spurious changes in cardiorespiratory responses, equivalent volumes of saline (0.9%) were injected. These had no effect on either heart rate or MAP. To confirm that repeated doses of adenosine produced the same response and that the responses did not run-down, rats were given two injections of adenosine (1 mg.Math.kg.sup.−1). There was no significant difference in the changes in cardiovascular parameters produced by each adenosine injection.
[0115] An additional series of experiments (n=4) were undertaken to directly compare BnOCPA and CPA on respiration. Adult male Sprague Dawley rats (400-500 g) were anaesthetised with urethane and instrumented as described above, with the exception that the arterial cannulation was not performed.
[0116] After allowing the animal to stabilise following surgery, BnOCPA (8.3 μg.Math.kg.sup.−1) was administered. After a 20 minutes recovery period CPA (6.3 μg.Math.kg.sup.−1) was administered. All injections were administered IV as a 350 μl.Math.kg.sup.−1 bolus. Changes in f, V.sub.T, and V.sub.E were measured. If the dosing occurred close to a respiratory event such as a sigh a second IV dose was administered, with 20 minute recovery periods either side of the injection. Measurements for the effect of BnOCPA were time-matched to when CPA induced a change in respiration in the same preparation. As no difference was observed between the respiratory responses to BnOCPA in these rats (n=4) and those instrumented for both cardiovascular and respiratory recordings (n=4), the data were pooled (n=8;
[0117] Spinal cord slice preparation: Adult male Sprague-Dawley rats, aged 8-12 weeks (260-280 g), were housed in an air-conditioned room on a 12 hour light/dark cycle with food and water available ad libitum. Rats were terminally anaesthetized using isofluorane and decapitated. The vertebral column, rib cage and surrounding tissues was rapidly removed and pinned under ice-cold (<4° C.), high sucrose-containing aCSF of the following composition (mM): Sucrose 127, KCl 1.9, KH.sub.2PO.sub.4 1.2, CaCl.sub.2 0.24, MgCl.sub.2 3.9, NaHCO.sub.3 26, D-glucose 10, ascorbic acid 0.5. A laminectomy was performed and the spinal cord and associated roots gently dissected and teased out of the spinal column and surrounding tissues. Dura and pia mater and ventral roots were subsequently removed with fine forceps and the spinal cord hemisected. Care was taken to ensure dorsal root inputs to the spinal cord were maintained. The hemisected spinal cord-dorsal root preparations were secured to a tissue slicer and spinal cord slices (400-450 μm thick) with dorsal roots attached cut in chilled (<4° C.) high sucrose aCSF using a Leica VT1000s microtome. Slices were transferred to a small beaker containing ice-cold standard aCSF (see below) and rapidly warmed to 35±1° C. in a temperature-controlled water bath over a 20 minute period, then subsequently removed and maintained at room temperature (22±2° C.) prior to electrophysiological recording. Slice incubation and electrophysiological recording aCSF was of the following composition (mM): NaCl 127, KCl 1.9, KH.sub.2PO.sub.4 1.2, MgCl.sub.2 1.3, CaCl.sub.2 2.4, NaHCO.sub.3 26 and D-glucose 10. Similar procedures were adopted to make recordings from the macaque spinal cord following euthanasia by anaesthetic overdose.
[0118] Spinal cord electrophysiological recording: For electrophysiological recording, a spinal cord slice was transferred to a custom-built chamber. Connected slice and dorsal roots were continuously perfused with aCSF, at 35±1° C. at a flow rate of 5-10 mL.Math.min.sup.−1) to the slice and roots were maintained constant and consistent throughout recording. Whole-cell patch-clamp recordings were obtained from dorsal horn neurones of the spinal cord using Axopatch 1 D or 700 A amplifiers employing the “blind” version of the patch-clamp technique. Patch pipettes were pulled from thin-walled borosilicate glass with resistances of between 3 and 8 MΩ when filled with intracellular solution of the following composition (mM): K.sup.+gluconate, 140; KCl, 10; EGTA-Na, 1; HEPES, 10; Na.sub.2ATP, 4, Na.sub.2GTP, 0.3. Recordings were performed in the ‘current-clamp’ mode of the whole-cell patch clamp technique on slices continuously perfused with aCSF (rate: 4-10 mL/min; 35±1° C.). Drugs were administered to the slice by bath perfusion.
[0119] Electrical Stimulation of Dorsal Roots: Excitatory post-synaptic potentials (EPSPs) were evoked by electrical stimulation of the dorsal roots using a concentric bipolar stimulating electrode positioned on the roots. Control EPSPs were evoked at 0.1 Hz.
[0120] Drugs: Drugs were made up as stock solutions (1 to 10 mM) and then diluted in aCSF on the day of use. Compounds were dissolved in dimethyl-sulphoxide (DMSO, 0.01% final concentration of DMSO). Adenosine, 8-CPT (8-cyclopentyltheophylline), NECA (5′-(N-Ethylcarboxamido) adenosine) and CPA (N-Cyclopentyladenosine) were purchased from Sigma-Aldrich (Poole, Dorset, UK). BnOCPA was synthesised as previously published (Knight et al., J. Med. Chem., 2016, 59, 947-964). 1,3-[.sup.3H]-dipropyl-8-cyclopentylxanthine ([.sup.3H]-DPCPX) was purchased from PerkinElmer (Life and Analytical Sciences, Waltham, Mass.). Peptides for interfering with G protein signalling were obtained from Hello Bio (Bristol, UK) and were based on published sequences (Varani et al., Adv Exp Med Biol 1051, 193-232 (2017)). For G.sub.oa the peptide had a sequence of MGIANNLRGCGLY. The scrambled version was LNRGNAYLCIGMG. For G.sub.ob the peptide had a sequence of MGIQNNLKYIGIC. Peptides were made up as stock solutions (2 mM) and stored at −20° C. The stock solutions were dissolved in filtered intracellular solution just before use.
[0121] Analysis: Concentration-response curves were constructed in OriginPro 2016 (OriginLab; Northampton, Mass., USA) and fitted with a logistic curve using the Levenberg Marquadt iteration algorithm. Statistical significance was tested using the unpaired t-test and one-way and two-way ANOVAs with Bonferroni correction for multiple comparisons.
[0122] Spinal nerve ligation (Chung model): Adult male Sprague-Dawley rats, 7-8 weeks old, weighing around 250 g at the time of Chung model surgery, were purchased from Charles River UK Ltd. The animals were housed in groups of 4 in an air-conditioned room on a 12-hour light/dark cycle. Food and water were available ad libitum. They were allowed to acclimatise to the experimental environment for three days by leaving them on a raised metal mesh for at least 40 min. The baseline paw withdrawal threshold (PWT) was examined using a series of graduated von Frey hairs (see below) for 3 consecutive days before surgery and re-assessed on the 6.sup.th to 8.sup.th day after surgery and on the 13.sup.th to 17.sup.th day after surgery before drug dosing.
[0123] Prior to surgery each rat was anaesthetized with 3% isoflurane mixed with oxygen (2 L.Math.min.sup.−1) followed by an i.m. injection of ketamine (60 mg.Math.kg.sup.−1) plus xylazine (10 mg.Math.kg.sup.−1). The back was shaved and sterilized with povidone-iodine. The animal was placed in a prone position and a para-medial incision was made on the skin covering the L4-6 level. The L5 spinal nerve was carefully isolated and tightly ligated with 6/0 silk suture. The wound was then closed in layers after a complete hemostasis. A single dose of antibiotics (Amoxipen, 15 mg/rat, i.p.) was routinely given for prevention of infection after surgery. The animals were placed in a temperature-controlled recovery chamber until fully awake before being returned to their home cages. The vehicle (normal saline) was administered via the intravenous (IV) route at 1 ml.Math.kg.sup.−1 and via the intrathecal (IT) route at 10 μl for each injection. The rats with validated neuropathic pain state were randomly divided into 8 groups: vehicle IV, BnOCPA at 1, 3, 10 μg.Math.kg.sup.−1 g IV; vehicle IT, BnOCPA at 0.3, 1, and 3 nmol IT groups.
[0124] To test for mechanical allodynia the animals were placed in individual Perspex boxes on a raised metal mesh for at least 40 minutes before the test. Starting from the filament of lower force, each filament was applied perpendicularly to the centre of the ventral surface of the paw until slightly bent for 6 seconds. If the animal withdrew or lifted the paw upon stimulation, then a hair with force immediately lower than that tested was used. If no response was observed, then a hair with force immediately higher was tested. The highest value was set at 15 g. The lowest amount of force required to induce reliable responses (positive in 3 out of 5 trials) was recorded as the value of PWT. On the testing day, PWT were assessed before and 1, 2 and 4 hours following BnOCPA or vehicle administration. The animals were returned to their home cages to rest (about 30 min) between two neighbouring testing time points. At the end of each experiment, the animals were deeply anaesthetised with isoflurane and killed by decapitation.
[0125] Rotarod test for motor function. A rotarod test was used to assess motor coordination following intravenous and intraperitoneal administration of BnOCPA. An accelerating rotarod (Ugo Basile) was set so speed increased from 6 to 80 rpm over 170 seconds. Male Sprague Dawley rats (n=24), 7 weeks of age (212-258 g) were trained on the rotarod twice daily for two days (≥2 trials per session) until performance times were stable. On the day of the experiment, three baseline trials were recorded. The compound was administered IP or intravenously via tail vein injection (10 μg/kg, n=6 per group). The control group received subcutaneous saline and the positive control group received subcutaneous morphine (15 mg/kg). Latency to fall (seconds) was measured in triplicate at 1, 2, 3 and 5 hours post drug administration.
[0126] Cell signaling assays. CHO-K1-hA.sub.1R cells were routinely cultured in Hams F12 nutrient mix supplemented with 10% Foetal bovine serum (FBS), at 37° C. with 5% CO.sub.2, in a humidified atmosphere. For cAMP inhibition experiments, cells were seeded at a density of 2000 cells per well of a white 384-well optiplate and co-stimulated, for 30 minutes, with 1 μM forskolin and a range of agonist concentrations (1 μM-1 pM). cAMP levels were then determined using a LANCE® cAMP kit.
[0127] For determination of individual Gα.sub.i/o/z couplings, CHO-K1-hA.sub.1R cells were transfected with pcDNA3.1-GNAZ or, pcDNA3.1 containing pertussis toxin (PTX) insensitive Gα.sub.i/o protein mutants (C351I, C352I, C351I, C351I, C351I, for G.sub.i1, G.sub.i2, G.sub.i3, G.sub.oa, G.sub.ob, respectively, obtained from cDNA Resource Center; www.cdna.org), using 500 ng plasmid and Fugene HD at a 3:1 (Fugene:Plasmid) ratio. Cells were then incubated for 24 hours before addition of 100 ng/ml PTX, to inhibit activity of endogenous Gα.sub.i/o, and then incubated for a further 16-18 hours. Transfected cells were then assayed as per cAMP inhibition experiments, but co-stimulated with agonist and 100 nM forskolin.
[0128] β-arrestin recruitment assays. HEK 293 cells were routinely grown in DMEM/F-12 GlutaMAX™ (Thermo Fisher Scientific) supplemented with 10% foetal bovine serum (FBS) (F9665, Sigma-Aldrich) and 1× antibiotic-antimycotic (Thermo Fisher Scientific) (DMEM complete). For analysis of β-arrestin2 recruitment following ligand stimulation at the human A.sub.1R or A.sub.3R, HEK 293 cells in a single well of 6-well plate (confluency≥80%) were transiently co-transfected with either A.sub.1R-Nluc or A.sub.3R-Nluc and β-arrestin2-YFP (total 2 μg, at a 1:6 ratio) using polyethyleneimine (PEI, 1 mg/ml, MW=25,000 g/mol) (Polysciences Inc) at a DNA:PEI ratio of 1:6 (w/v). Briefly, in sterile tubes containing 150 mM sodium chloride (NaCl), DNA or PEI was added (final volume 50 μl), allowed to incubate at room temperature for 5 minutes, mixing together and incubating for a further 10 minutes prior to adding the combined mix dropwise to the cells. 24 hours post-transfection, HEK 293 cell were harvested, resuspended in reduced serum media (MEM, NEAA (Thermo Fisher Scientific) supplemented with 1% L-glutamine (2 mM final) (Thermo Fisher Scientific), 2% FBS and 1× antibiotic-antimycotic) and seeded (50,000 cells/well) in a poly-L-lysine-coated (MW 150,000-300,000, Sigma-Aldrich) white 96-well plate (PerkinElmer Life Sciences). 24 hours post seeding, media was removed, cells gently washed in PBS and 90 μl of furimazine (4 μM) containing solution added (PBS supplemented with 0.49 mM MgCl.sub.2, 0.9 mM CaCl.sub.2 and 0.1% BSA) to each well before incubating in the dark for 10 minutes. After incubation, 10 μl of ligand (NECA/CPA, adenosine, BnOCPA) was added in the range of 10 μM to 0.01 μM and filtered light emission measured at 450 nm and 530 nm every minute for 1 hour using a Mithras LB 940 (Berthold technology). Here, Nluc on the C-terminus of A.sub.1R or A.sub.3R acted as the BRET donor (luciferase oxidizing its substrate) and YFP acted as the fluorescent acceptor. Vehicle control (DMSO) was added to determine background emission.
[0129] Radioligand binding. Radioligand displacement assays were conducted using crude membrane preparations (100 μg protein per tube) acquired from homogenisation of CHO-K1-hA.sub.1R cells in ice-cold buffer (2 mM MgCl.sub.2, 20 mM HEPES, pH 7.4). The ability to displace binding of the A.sub.1R selective antagonist radioligand, 1,3-[.sup.3H]-dipropyl-8-cyclopentylxanthine ([.sup.3H]-DPCPX) at a concentration (1 nM) around the Kd value (1.23 nM, as determined by saturation binding experiments) by increasing concentrations of NECA, adenosine, CPA, BnOCPA or HOCPA (10 μM-0.1 nM) allowed the binding affinities (Ki) to be determined. Non-specific binding was determined in the presence of 10 μM DPCPX. Membrane incubations were conducted in Sterilin™ scintillation vials (Thermo Fisher Scientific; Wilmington, Mass., USA) for 60 minutes at room temperature. Free radioligand was separated from bound radioligand by filtration through Whatman® glass microfiber GF/B 25 mm filters (Sigma-Aldrich). Each filter was then placed in a Sterilin™ scintillation vial and radioactivity determined by: addition of 4 mL of Ultima Gold XR liquid scintillant (PerkinElmer), overnight incubation at room temperature and the retained radioactivity determined using a Beckman Coulter LS 6500 Multi-purpose scintillation counter (Beckman Coulter Inc.; Indiana, USA).
[0130] Data Analysis. Concentration-response curves for the effects of A.sub.1R agonists on synaptic transmission were constructed in OriginPro 2018 (OriginLab; Northampton, Mass., USA) and fitted with a logistic curve using the Levenberg Marquadt iteration algorithm. OriginPro 2018 was also used for statistical analysis. Statistical significance was tested as indicated in the text using paired or unpaired t-tests or one-way or two-way ANOVAs with repeated measures (RM) as appropriate. Bonferroni corrections for multiple comparisons were performed. All in vitro cell signalling assay data was analysed using Prism 7.0e (Graphpad software, San Diego, Calif.), with all concentration-response curves being fitted using a 3 parameter logistic equation to calculate response range and IC.sub.50. All cAMP data was normalised to a forskolin concentration-response curve ran in parallel to each assay. Statistical significance to adenosine was calculated using a one-way ANOVA with a Dunnett's post-test for multiple comparisons. Radioligand displacement curves were fitted to the one-site competition binding equation yielding log Ki values. One-way ANOVA (Dunnett's post-test) was used to determine significance by comparing the log Ki value for each compound when compared to adenosine. To determine the extent of ligand-induced recruitment of β-arrestin2-YFP to either the A.sub.1R or A.sub.3R, the BRET signal was calculated by subtracting the 530 nm/450 nm emission for vehicle-treated cells from ligand-treated cells (ligand-induced ΔBRET). ΔBRET for each concentration at 5 minutes (maximum response) was used to produce concentration-response curves.
[0131] All in vivo cardiovascular and respiratory data were analysed using OriginPro 2018. One-way ANOVAs, with repeated measures as appropriate, and with Bonferroni correction for multiple comparisons were used. Statistical significance for the effects of IV saline was tested using paired t-tests. Data are reported throughout as mean±SEM and n values are reported for each experiment. For the neuropathic pain studies, one-way ANOVAs with Fisher's Least Significant Difference (LSD) post-hoc test was used to compare drug treatment groups to the vehicle group (OriginPro 2018). The significance level was set at P<0.05, with actual P values reported in the figure legends and summaries, by way of abbreviations and asterisks, on the graphs: ns, not significant; * P<0.05; **, P<0.02; ***, P<0.001; ****, P<0.0001.
[0132] Molecular Dynamics Simulations
[0133] Ligand parameterization. The CHARMM36 (10, 11)/CGenFF (12-14) force field combination was employed in all the molecular dynamic (MD) simulations performed. Initial topology and parameter files of BnOCPA, HOCPA, and PSB36 were obtained from the Paramchem webserver. Higher penalties were associated with a few BnOCPA dihedral terms, which were therefore optimized at the HF/6-31G* level of theory using both the high throughput molecular dynamics (HTMD) parameterize functionality and the Visual Molecular Dynamics (VMD) Force Field Toolkit (ffTK) (17), after fragmentation of the molecule. Short MD simulations of BnOCPA in water were performed to visually inspect the behavior of the optimized rotatable bonds.
[0134] Systems preparation for fully dynamic docking of BnOCPA and HOCPA. Coordinates of the A.sub.1R in the active, adenosine- and G protein-bound state were retrieved from the Protein Data Bank database (PDB ID 6D9H). Intracellular loop 3 (ICL3) which is missing from PDB ID 6D9H was rebuilt using Modeller 9.19. The G protein, with the exception of the C-terminal helix (helix 5) of the G protein alpha subunit (the key region responsible for the receptor TM6 active-like conformation) was removed from the system. BnOCPA and HOCPA were placed in the extracellular bulk, in two different systems, at least 20 Å from the receptor vestibule. The resulting systems were prepared for simulations using in-house scripts able to exploit both python HTMD and Tool Command Language (TCL) scripts. Briefly, this multistep procedure performs the preliminary hydrogen atoms addition by means of the pdb2pqr and propka software, considering a simulated pH of 7.0 (the proposed protonation of titratable side chains was checked by visual inspection). Receptors were then embedded in a square 80 Å×80 Å 1-palmitoyl-2-oleyl-sn-glycerol-3-phosphocholine (POPC) bilayer (previously built by using the VMD Membrane Builder plugin 1.1, Membrane Plugin, Version 1.1.; http://www.ks.uiuc.edu/Research/vmd/plugins/membrane/) through an insertion method, considering the A.sub.1R coordinates retrieved from the OPM database to gain the correct orientation within the membrane. Lipids overlapping the receptor transmembrane bundle were removed and TIP3P water molecules were added to the simulation box (final dimensions 80 Å×80 Å×125 Å) using the VMD Solvate plugin 1.5 (Solvate Plugin, Version 1.5; http://www.ks.uiuc.edu/Research/vmd/plugins/solvate/). Finally, overall charge neutrality was achieved by adding Na.sup.+/Cl.sup.− counter ions (concentration of 0.150 M) using the VMD Autoionize plugin 1.3 (Autoionize Plugin, Version 1.3; http://www.ks.uiuc.edu/Research/vmd/plugins/autoionize/). All histidine side chains were considered in the delta tautomeric state, with the exception of H251 (epsilon tautomer) and H278 (protonated).
[0135] The MD engine ACEMD was employed for both the equilibration and productive simulations. Systems were equilibrated in isothermal-isobaric conditions (NPT) using the Berendsen barostat (31) (target pressure 1 atm), the Langevin thermostat (target temperature 300 K) with a low damping factor of 1 ps.sup.−1 and with an integration time step of 2 fs. Clashes between protein and lipid atoms were reduced through 2000 conjugate-gradient minimization steps before a 2 ns long MD simulation was run with a positional constraint of 1 kcal mol.sup.−1 Å.sup.−2 on protein and lipid phosphorus atoms. Twenty nanoseconds of MD simulation were then performed constraining only the protein atoms. Lastly, positional constraints were applied only to the protein backbone alpha carbons for a further 5 ns.
[0136] Dynamic docking of BnOCPA and HOCPA. The supervised MD (SuMD) approach is an adaptive sampling method for simulating binding events in a timescale one or two orders of magnitudes faster than the corresponding classical (unsupervised) MD simulations. In the present work, the distances between the centers of mass of the adenine scaffold of the A.sub.1R agonist and N254.sup.6.55, F171.sup.ECL2, T277.sup.7.42 and H278.sup.7.43 of the receptor were considered for the supervision during the MD simulations. The dynamic docking of BnOCPA was hindered by the ionic bridge formed between the E172.sup.ECL2 and K265.sup.ECL3 side chains. A metadynamics energetic bias was therefore introduced in order to facilitate the rupture of this ionic interaction, thus favouring the formation of a bound complex. More precisely, Gaussian terms (height=0.01 kcal mol-1 and widths=0.1 Å) were deposited every 1 ps along the distance between the E172.sup.ECL2 carboxyl carbon and the positively charged K265.sup.ECL3 nitrogen atom using PLUMED 2.3. For each replica, when the ligands reached a bound pose (i.e. a distance between the adenine and the receptor residues centers of mass <3 Å), a classic (unsupervised and without energetic bias) MD simulation was performed for at least a further 100 ns.
[0137] BnOCPA bound state metadynamics. We decided to perform a detailed analysis of the role played by the E172.sup.ECL2-K265.sup.ECL3 ionic interaction in the dynamic docking of BnOCPA. Three 250 ns long well-tempered metadynamics simulations were performed using the bound state obtained from a previous dynamic docking simulation, which resulted in binding mode A, as a starting point. The collective variables (CVs) considered were: i) the distance between the E172.sup.ECL2 carboxyl carbon and the positively charged K265.sup.ECL3 nitrogen atom and ii) the dihedral angle formed by the 4 atoms linking the cyclopentyl ring to the phenyl moiety (which was the most flexible ligand torsion during the previous SuMD simulations). Gaussian widths were set at 0.1 Å and 0.01 radians respectively, heights at 0.01 kcal/mol.sup.−1, and the deposition was performed every 1 ps (bias-factor=5). Three replicas allowed sampling of three main energetic minima on the energy surface.
[0138] Classic MD simulations of BnOCPA binding modes A, B, C and D. To test the hypothesis that BnOCPA and HOCPA may differently affect TM6 and/or TM7 mobility when bound to A.sub.1R (and to further sample the stability of each BnOCPA binding mode), putative binding conformations A, B and C were superposed to the experimental A.sub.1R active state coordinates with the modelled ICL3. This should have removed any A.sub.1R structural artefacts, possibly introduced by metadynamics. As reference and control, two further systems were considered: i) the pseudo-apo A.sub.1R and ii) the selective A.sub.1R antagonist PSB36 superposed in the same receptor active conformation. The BnOCPA binding mode D was modelled from mode B by rotating the dihedral angle connecting the cyclopentyl ring and the N6 nitrogen atom in order to point the benzyl of the agonist toward the hydrophobic pocket underneath ECL3 delimited by L253.sup.6.56, T257.sup.6.52, K265.sup.ECL3, T270.sup.7.35, and L269.sup.7.34. The G protein atoms were removed, and the resulting systems prepared for MD as reported above.
[0139] Dynamic docking of the Goa, Gob and Gi2 GαCT helix. A randomly extracted frame from the classic MD performed on the BnOCPA:A1R complex was prepared for three sets of simulations placing the GαCT helix 5 (last 27 residues) of the Gα proteins Goa, Gob and Gi2 in the intracellular solvent bulk side of the simulation boxes. As a further control, a frame from the classic MD performed on the unbiased ligand HOCPA:A.sub.1R complex was randomly extracted and prepared along with the Gob GαCT. The resulting four systems were embedded in a POPC membrane and prepared as reported above.
[0140] The different structural effects putatively triggered by BnOCPA and HOCPA on the recognition mechanism of Goa, Gob and Gi2 GαCT were studied by performing 10 SuMD replicas. During each replica, the distance between the centroid of the GαCT residues 348-352 and the centroid of the A1R residues D42.sup.2.37, I232.sup.6.33, and Q293.sup.8.48 was supervised until it reached a value lower than 8 Å. A classic MD simulation was then run for a further 300 ns.
[0141] Classic MD simulations on the A.sub.1R:Goa and Gob complexes. The A.sub.1R cryo-EM structure (PDB ID 6D9H) was used as template for all the five systems simulated. The endogenous agonist adenosine was removed and HOCPA and BnOCPA (modes B and D) were inserted in the orthosteric site superimposing 6D9H to the systems prepared for the classic MD simulations in the absence of G protein. ICL3 was not modelled, nor were the missing part of the G protein a subunit. As subunits β and γ were removed, the Gα NT helix was truncated to residue 27 to avoid unnatural movements (NT is constrained by Gβ in 6D9H). The Gα subunit was mutated according to the Goa and Gob primary sequences using in-house scripts. The resulting five systems were embedded in a POPC membrane and prepared as reported above.
[0142] Analysis of the classic MD simulations. During the classic MD simulations that started from Modes A-C, BnOCPA had the tendency to explore the three conformations by rapidly interchanging between the three binding modes. In order to determine the effect exerted on the TM domain by each conformation, 21 μs of MD simulations (BnOCPA mode A, BnOCPA mode B, BnOCPA mode C) were subjected to a geometric clustering. More precisely, a simulation frame was considered in pose A if the distance between the phenyl ring of BnOCPA and the I175.sup.ECL2 alpha carbon was less than 5 Å; in pose B if the distance between the phenyl ring of BnOCPA and the L258.sup.6.59 alpha carbon was less than 6 Å, and in pose C if the distance between the phenyl ring of BnOCPA and the Y271.sup.7.36 alpha carbon was less than 6 Å. During the MD simulations started from mode D, a frame was still considered in mode D if the root mean square deviation (RMSD) of the benzyl ring to the starting equilibrated conformation was less than 3 Å. For each of the resulting four clusters, the RMSD of the GPCR conserved motif NPXXY (N.sup.7.49 PIV Y.sup.7.53 in the A.sub.1R) was computed using Plumed 2.3 considering the inactive receptor state as reference, plotting the obtained values as frequency distributions (
[0143] Hydrogen bonds and atomic contacts were computed using the GetContacts analysis tool (https://github.com/getcontacts/getcontacts) and expressed in terms of occupancy (the percentage of MD frames in which the interaction occurred).
[0144] Analysis of the Goa, Gob and Gi2 GαCT classic MD simulations after SuMD. For each system, only the classic MD simulations performed after the GαCT reached the A1R intracellular binding site were considered for the analysis.
[0145] The RMSD values to the last 15 residues of the Gi2 GαCT reported in the A.sub.1R cryo-EM PDB structure 6D9H were computed using VMD. The MD frames associated with the peaks in the RMSD plots (states CS1, MS1, MS2 and MS3 in
Example 1: Synthesis of Cyclopentyladenosine (CPA) Derivatives—General Procedures
[0146] tBuOCPA was prepared according to the following procedure:
(i) tert-butyl ((1R,2R)-2-hydroxycyclopentyl)carbamate (1)
[0147] ##STR00008##
[0148] (1R,2R)-2-aminocyclopentanol hydrochloride (1 eq, 10.9 mmol) was dissolved in 70 mL dichloromethane and di-tert-butyl decarbonate (1 eq, 10.9 mmol) was added. The suspension was stirred at room temperature. To the suspension, N,N-diisopropylethylamine (1 eq, 10.9 mmol) was added. After 2 hours, the clear solution was concentrated under reduced pressure. After purification by silica gel chromatography (hexane/ethyl acetate gradient) 1 was obtained as a white solid (2.03 g, 10.3731 mmol, 93%). .sup.1H NMR: (300 MHz, DMSO-d.sub.6) δ 6.71 (d, J=7.4 Hz, 1H), 4.60 (d, J=4.3 Hz, 1H), 3.77 (m, 1H), 3.49 (m, 1H), 1.95-1.68 (m, 2H), 1.61 (m, 2H), 1.42-1.24 (m, 1H), 1.38 (s, 9H), 1.37-1.24 (m, 2H). .sup.13C NMR: (75 MHz, DMSO-d.sub.6) δ 155.73, 77.84, 76.49, 59.20, 32.53, 30.08, 28.75, 20.83. HR-MS: (NSI+), ACN, [M+H].sup.+: m/z calculated 224.1250, found 224.1257, Δ: −3.41 ppm.
(ii) tert-butyl ((1R,2R)-2-((4-(tert-butyl)benzyl)oxy)cyclopentyl)carbamate (2)
[0149] ##STR00009##
[0150] Compound 1 (1 eq, 1.242 mmol) and 4-tert-butylbenzyl bromide (1 eq, 1.242 mmol) were dissolved in dry THF. The reaction mixture was cooled to 0° C. and NaH 60% dispersion in mineral oil (2 eq, 2.484 mmol) was added. After 1 hour and 30 minutes at 0° C., methanol (0.1 mL) and NH.sub.4Cl aq. were added and the flask was removed from the ice bath. The reaction mixture was extracted with ethyl acetate, the organic phase was dried over sodium sulfate and concentrated under reduced pressure. After purification by silica gel chromatography (hexane/ethyl acetate gradient), 2 was obtained as an oil (126 mg, 0.363 mmol, 30%). .sup.1H NMR: (300 MHz, DMSO-d.sub.6) δ 7.35 (d, J=8.2 Hz, 2H), 7.22 (d, J=8.2 Hz, 2H), 6.93-6.84 (m, 1H), 4.51-4.40 (m, 2H), 3.75 (s, 1H), 3.69 (m, 1H), 1.94-1.72 (m, 2H), 1.65-1.51 (m, 3H), 1.40 (m, 1 h) 1.40 (s, 9H), 1.27 (s, 9H). .sup.13C NMR: (101 MHz, DMSO) δ 155.44, 150.09, 136.33, 127.77, 125.33, 84.81, 78.01, 70.08, 56.89, 34.66, 31.63, 30.65, 30.55, 28.76, 21.88. HR-MS: (NSI+), ACN, [M+H].sup.+: m/z calculated 348.2533, found 348.2533, Δ: 0.03 ppm.
(iii) (1R,2R)-2-((4-(tert-butyl)benzyl)oxy)cyclopentan-1-aminium chloride (3)
[0151] ##STR00010##
[0152] Compound 2 (1 eq, 0.329 mmol) was dissolved in 1 mL dioxane and HCl in dioxane 4N (5 eq, 1.649 mmol) was added. After 5 hours the solvent was removed under reduced pressure. After co-evaporation with dichloromethane, 3 was obtained as a white solid (93 mg, 0.328 mmol, 99%). .sup.1H NMR: (300 MHz, DMSO-d.sub.6) δ 8.02 (s, 2H), 7.42-7.35 (m, 2H), 7.28 (d, J=8.3 Hz, 2H), 4.54-4.39 (m, 2H), 3.93-3.86 (m, 1H), 3.42 (s, 1H), 2.00 (m, 2H), 1.75-1.48 (m, 5H), 1.28 (s, 9H). .sup.13C NMR: (75 MHz, DMSO-d6) δ 150.35, 135.74, 128.01, 125.38, 82.82, 70.70, 56.29, 34.70, 31.63, 30.27, 28.92, 21.64. HR-MS: (NSI+), ACN, [M+H].sup.+: m/z calculated 248.2005, found 248.2009, Δ: −1.70 ppm.
(iv)(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(((1S,2R)-2-((4-(tert-butyl)benzyl)oxy)cyclopentyl)amino)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate (4)
[0153] ##STR00011##
[0154] (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-chloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate (1 eq, 0.235 mmol) was dissolved in 15 mL isopropanol. NaHCO.sub.3 (3 eq, 0.705 mmol) and 3 (1.5 eq, 0.352 mmol) were added. The reaction mixture was heated at 105° C. under reflux overnight. At reaction completion, the reaction mixture was let to cool down until room temperature and the remaining solid was filtered off and washed with absolute ethanol. The filtrate was evaporated under reduced pressure. After purification by silica gel chromatography (hexane/ethyl acetate gradient), 4 was obtained as a solid (52.7 mg, 0.0845 mmol, 36%). 1H NMR: (300 MHz, Methanol-d.sub.4) δ 8.31 (s, 1H), 8.24 (s, 1H), 7.32 (d, J=8.5 Hz, 2H), 7.23 (d, J=8.4 Hz, 2H), 6.25 (d, J=5.3 Hz, 1H), 6.03 (t, J=5.5 Hz, 1H), 5.73 (dd, J=5.7, 4.5 Hz, 1H), 4.67 (s, 1H), 4.63 (s, 2H), 4.50-4.35 (m, 3H), 4.01 (m, 1H), 2.26 (m, 1H), 2.16 (s, 3H), 2.08 (d, J=1.8 Hz, 6H), 2.05-1.99 (m, 1H), 1.90-1.57 (m, 5H), 1.29 (s, 9H). .sup.13C NMR: (101 MHz, Methanol-d.sub.4) δ 170.80, 169.98, 169.74, 154.33, 152.85, 139.22, 135.53, 127.34, 124.73, 86.39, 84.68, 80.21, 72.99, 70.74, 70.61, 62.83, 33.90, 30.39, 30.26, 30.03, 21.11, 19.24, 19.04, 18.87. HR-MS: (NSI+), ACN, [M+H].sup.+: m/z calculated 624.3012, found 624.3028, Δ: −2.53 ppm.
(v) (2R,3R,4S,5R)-2-(6-(((1S,2R)-2-((4-(tert-butyl)benzyl)oxy)cyclopentyl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol (tBuOCPA)
[0155] ##STR00012##
[0156] Compound 4 (1 eq, 0.0834 mmol) was dissolved in 4 mL methanol and K.sub.2CO.sub.3 (0.6 eq, 0.0500 mmol) was added at room temperature. After 30 minutes the reaction mixture was filtered and concentrated under reduced pressure. After purification by silica gel column chromatography, tBuOCPA was obtained as a white solid (30 mg, 0.0603 mmol, 73%). 1H NMR: 300 MHz, Methanol-d4) δ 8.16 (s, 2H), 7.21 (d, J=8.4 Hz, 2H), 7.11 (d, J=8.3 Hz, 2H), 5.85 (d, J=6.5 Hz, 1H), 4.65 (dd, J=6.5, 5.1 Hz, 1H), 4.57 (s, 1H), 4.40-4.55 (m, 1H), 4.22 (dd, J=5.1, 2.5 Hz, 1H), 4.06-4.09 (m, 1H), 3.87-3.91 (m, 4.0 Hz, 1H), 3.79 (dd, J=12.6, 2.5 Hz, 1H), 3.64 (dd, J=12.5, 2.6 Hz, 1H), 2.09-2.20 (m, 1H), 1.99-1.85 (m, 1H), 1.80-1.45 (m, 4H), 1.18 (s, 9H). .sup.13C NMR: (101 MHz, Methanol-d.sub.4) δ 154.46, 152.15, 150.22, 140.05, 135.50, 127.33, 124.74, 89.95, 86.85, 84.58, 74.06, 71.32, 70.70, 62.13, 33.91, 30.38, 30.19, 29.99, 21.09. UPLC: t.sub.R=3.01 min. (NSI+), ACN, [M+H].sup.+: m/z calculated 498.2690, found 498.2711, Δ: −4.21 ppm.
[0157] It will be appreciated that the synthetic methods above can be adapted by the skilled person to prepare other compounds according to the invention, for example by using alternative electrophiles for the alkylation of the oxygen in step (ii).
Example 2: Effect of Compound BnOCPA on Synaptic Transmission in Rat Hippocampus
[0158] In order to assess the action of the A.sub.1 receptor agonist compound BnOCPA in mammalian brain tissue, firstly its effects on excitatory synaptic transmission, which is strongly inhibited by the activation of adenosine A.sub.1 receptors on presynaptic terminals, was investigated. The effects of the agonist were compared to the effects of established adenosine receptor agonists (adenosine, CPA and NECA). Synaptic transmission was inhibited by the endogenous non-specific agonist adenosine (
[0159] Compound BnOCPA inhibited synaptic transmission, in a manner that was reversed by co-application of the A.sub.1 receptor antagonist 8-CPT (4 μM, n=12;
[0160] To establish if this inhibition of synaptic transmission was presynaptic in nature, paired-pulse facilitation experiments were performed, in which the paired-pulse ratio is inversely proportional to the initial probability of transmitter release. Thus, compounds that inhibit synaptic transmission by reducing transmitter release would be expected to increase paired-pulse facilitation. Compound BnOCPA (100 nM) significantly increased paired-pulse facilitation (for a paired-pulse interval of 50 ms the paired-pulse ratio increased from 1.88±0.08 in control slices to 2.41±0.08; n=6 slices,
Example 3: Effects of Compound BnOCPA on Seizure Activity in Hippocampal Slices
[0161] The actions of the atypical agonist compound BnOCPA on seizure activity induced in hippocampal slices were investigated. During seizure activity, adenosine is released to activate A.sub.1 receptors leading to termination of the burst of activity, and also delaying the occurrence of the next burst. Application of exogenous adenosine and other A.sub.1 receptor ligands would therefore be expected to inhibit activity (see, for example: M. J. Wall et al., 2015). The actions of compound BnOCPA was compared to the actions of prototypical agonists. A nominally Mg.sup.2+-free/increased K.sup.+ (6 mM) aCSF was used to initiate seizure activity in the hippocampus, reflected by the appearance of robust long-lasting epileptiform activity characterised by frequent neuronal spikes (see, for example: J. Lopatář et al., Neuropharmacology, 2011, 61, 25-34). Adenosine (20 to 100 μM, n=5 slices;
[0162] There are two components to the anti-seizure effects of A.sub.1 receptor agonists: presynaptic inhibition of excitatory synaptic transmission, and the postsynaptic hyperpolarisation of the neuronal membrane potential. It is hypothesised that the weak effect of compound BnOCPA against seizure activity arose from an inability to hyperpolarise the postsynaptic membrane potential, unlike other prototypical A.sub.1 receptor agonists.
Example 4: Effects of Compound BnOCPA on Membrane Potential Hyperpolarisation in Pyramidal Cells
[0163] To establish the influence of postsynaptic A.sub.1 receptor activation, the degree of membrane potential hyperpolarisation in CA1 pyramidal cells produced via the activation of K.sup.+ channels was measured. Adenosine (100 μM) and CPA (300 nM) markedly hyperpolarised the membrane potential of pyramidal cells (adenosine: membrane potential changed from −69.4±1.5 to −74.1±1.5 mV, mean change of −4.7±0.5 mV, n=8; CPA: membrane potential changed from to −64±2.1 to −71.3±1.4 mV, mean change of −7.3±0.85 mV, n=7;
[0164] If compound BnOCPA binds to postsynaptic A.sub.1 receptors but does not activate them, then it might be expected to act in a manner analogous to a receptor antagonist, preventing activation by other agonists, a property that has been observed for biased agonists at other receptors. To test this theory, compound BnOCPA (300 nM, 10 minutes) was first applied, followed by CPA (300 nM) in the presence of compound BnOCPA. The effects of CPA on membrane potential were significantly (P=2.89×10.sup.−5) reduced by compound BnOCPA (mean hyperpolarisation reduced from −7.3±0.85 mV to 2.7±2 mV;
[0165] To test whether BnOPCA blocked K+ channels mediating postsynaptic hyperpolarisation, or in some other way non-specifically interfered with G protein signalling, we applied the GABA.sub.b receptor agonist baclofen to CA1 pyramidal cells. BnOCPA had no effect on membrane hyperpolarisation produced by baclofen (
Example 5: BnOCPA Demonstrates Unique Signalling Bias
[0166] To investigate the molecular basis for the unprecedented properties of BnOCPA, we generated a recombinant cell system (CHO-K1 cells) expressing the human A.sub.1R (hA.sub.1R). BnOCPA was a potent (IC.sub.50 0.7 nM; Table 1) full agonist at the hA.sub.1R and bound to the receptor with an affinity equal to that of CPA and NECA, and higher than that of adenosine (
[0167] The data from whole-cell patch-clamp recordings showed that BnOCPA did not influence neuronal membrane potential (
Example 6: The Signalling Bias Displayed by BnOCPA is Reflected in Non-Canonical Binding Modes and a Selective Interaction with Gα Subunits
[0168] To understand better the unusual signalling properties of BnOCPA and the highly specific Gα coupling, we carried out dynamic docking simulations to study the basic orthosteric binding mode of BnOCPA in an explicit, fully flexible environment using the active cryo-EM structure of the A.sub.1R (PDB code 6D9H). We compared BnOCPA to the unbiased agonists adenosine and HOCPA, and an antagonist (PSB36) of the A.sub.1R. BnOCPA engaged the receptor with the same fingerprint as adenosine and HOCPA. Further explorations of the BnOCPA docked state using metadynamics revealed interchangeable variations on this fingerprint (namely modes A, B, and C) that could be distinguished by the orientation of the BnOCPA-unique benzyl (Bn) group. Having established the possible BnOCPA binding modes, we examined the respective contribution of the orthosteric agonists, the G protein a subunit α5 (C-terminal) helix (GαCT), and the Gα protein subunit to the empirically-observed G protein selectivity displayed by BnOCPA (Table 1,
[0169] Simulations in the absence of G protein. Firstly, following Dror et al., (PNAS USA, 108, 18684-18689 (2011)) we compared the dynamics of the BnOCPA-bound A.sub.1R with the corresponding dynamics of the receptor bound to either HOCPA, the A.sub.1R antagonist PSB36, or the apo receptor, our hypothesis being that there may be ligand-dependent differences in the way that the intracellular region of the receptor responds in the absence of the G protein. In these simulations the G protein was omitted so that inactivation was possible and so that the results were not G protein-dependent. The BnOCPA binding modes A-C were interchangeable during MD simulations but were associated with distinctly different dynamics, as monitored by changes in a structural hallmark of GPCR activation, the N.sup.7.49PXXY.sup.7.53 motif. Given the high flexibility shown by the BnOCPA benzyl group during the simulations and its lipophilic character, we hypothesized and simulated a further binding (namely Mode D) not explored during MD. This conformation involves a hydrophobic pocket underneath ECL3 which is responsible for the A.sub.1/A.sub.2A selectivity. Superimposition of the four BnOCPA binding modes (A-D) revealed the highly motile nature of the benzyl group of BnOCPA under the simulated conditions (data not shown).
[0170] Quantification of the N.sup.7.49PXXY.sup.7.53 dynamics revealed that HOCPA, BnOCPA mode A, BnOCPA mode C and the apo receptor show a similar distribution of the RMSD of the conserved N.sup.7.49PXXY.sup.7.53 motif (
[0171] Dynamic Docking of GαCT. To simulate the agonist-driven interaction between the A.sub.1R and the G protein, the α5 (C-terminal) helix (GαCT) of the G protein (Gi2, Goa, Gob) was dynamically docked to the HOCPA and BnOCPA-bound active A.sub.1R structure (again lacking G protein). This allowed us to evaluate the effect of different GαCT on the formation of the complex with A.sub.1R to test the hypothesis that, of Goa, Gob and Gi2, only the GαCT of Gob would fully engage with the BnOCPA-bound active A.sub.1R, in line with the empirical observations of G protein selectivity summarized in Table 1.
[0172] MD simulations on the full G protein. To test the hypothesis that the non-functional BnOCPA:A.sub.1R:Goa complex showed anomalous dynamics, we increased the complexity of the simulations by considering the Gα subunit of the Goa and Gob protein bound to the A.sub.1R:BnOCPA (mode B or D) complex or the Gob protein bound to A.sub.1R:HOCPA (a functional system). The most visible differences between Goa and Gob comprised the formation of transient hydrogen bonds between the α4-β6 and α3-β5 loops of Goa and helix 8 (H8) of the receptor (data not shown). Similar contacts are present in the non-canonical state of the neurotensin receptor:G protein complex. Overall, Goa interacted more with TM3 and ICL2 residues, while TM5 and TM6, along with ICL1, were more engaged by Gob. Interestingly, R291.sup.7.56 and I292.sup.8.47, which are located under the N.sup.7.49PXXY.sup.7.53 motif, showed a different propensity to interact with Goa or Gob. In this scenario, it is plausible that a particular A.sub.1R conformation stabilized by BnOCPA (as suggested by the simulations in the absence of G protein,
Example 7: Effect of Compound BnOCPA on Heart Rate and Mean Arterial Pressure
[0173] One of the major obstacles to the development of clinically useful compounds that target nervous system adenosine A.sub.1 receptors is the strong expression of A.sub.1 receptors in the heart and the subsequent effects on the cardiovascular system when they are activated. Activation of these A.sub.1 receptors is negatively dromotropic (reducing conduction speed in AV node) causing slowing of the sinus rate. There is also depression of atrial (but not ventricular) contractility, and attenuation of the stimulatory effects of catecholamines on the myocardium. The effects of adenosine in the AV node are the consequence of the opening of G.sub.iβy-coupled K.sup.+ channels as well as to a depression of other currents including I.sub.Ca.
[0174] Given BnOCPA's clear differential effects in a native physiological system, strong Gα bias, unique binding characteristics and selective Gα interaction, it was hypothesised that these properties might circumvent a key obstacle to the development of A1R agonists for therapeutic use—their powerful effects in the cardiovascular system (CVS) where their activation markedly reduces both heart rate and blood pressure. As these CVS effects are likely through Goa, which is expressed at high levels in the heart and plays an important role in regulating cardiac function, the lack of effect of BnOCPA on Goa predicted that BnOCPA would have minimal effects on the CVS.
[0175] To test the effects of compound BnOCPA on cardiac physiology, two approaches were taken. Firstly, the effects of adenosine and compound BnOCPA on the rate of contraction of the isolated frog heart were compared. Frogs (Xenopus leavis) were pithed (to remove any central reflexes) and drugs were directly applied to the exposed heart. Application of 30 μM adenosine (about IC.sub.50 for mammalian hippocampal synaptic depression) reversibly reduced the heart rate from 42±1.2 BPM to 35.5±1.2 BPM (mean reduction of 6.25±0.6 BPM, about 15% reduction, n=4 frogs). Following recovery from adenosine, 300 nM (about 5 times the IC.sub.50 for synaptic depression) of compound BnOCPA was applied and had no significant effect on the heart rate (change 0.6±0.2 BPM), but reduced the effects of subsequent adenosine applications (from a reduction of 6.25 BPM in control conditions to 0.27±0.2 BPM following compound BnOCPA). The prototypical A.sub.1 receptor agonist CPA reduced HR by 6.2±0.5 BPM (n=3) (
[0176] To fully investigate the effects of BnOCPA on the mammalian CVS, its effects were measured on heart rate (HR) and mean arterial blood pressure (MAP) in urethane-anaesthetised, spontaneously breathing adult rats (
[0177] The effects on both the isolated frog heart and ventilated rat are consistent and are similar to the effects of compound BnOCPA observed for membrane potential hyperpolarisation in hippocampal neurons. Compound BnOCPA has little or no effect on heart rate and MAP, but blocks the effects of agonists which activate A.sub.1 receptors. The lack of effect on the cardiovascular system increases the usefulness of compound BnOCPA as a lead compound for the development of new A.sub.1 receptor ligands for nervous system disorders.
Example 8: Respiration
[0178] Since adverse effects on respiration (dyspnea) limit the use of systemic A1R agonists, we additionally examined the effects of BnOCPA on respiration. In urethane-anaesthetised, spontaneously breathing adult rats, intravenous injection of the selective A1R agonist CPA caused significant respiratory depression. In stark contrast, BnOCPA had no appreciable effect on respiration (
Example 9: Pain
[0179] The lack of effect of BnOCPA on the CVS and respiration prompted an investigation into a potential application of A.sub.1R agonists that had previously been severely curtailed by adverse cardiorespiratory events: A.sub.1R agonists as analgesics.
[0180]
Example 10: In Vivo Pain Model
[0181] To further test BnOCPA's potential as an analgesic, we used a rat model of chronic neuropathic pain (spinal nerve ligation) a feature of which is mechanical allodynia whereby the affected limb is rendered sensitive to previously innocuous tactile stimuli. Both intravenous (
CONCLUSIONS
[0182] The actions of the atypical A.sub.1 adenosine receptor agonist, compound BnOCPA, were characterised on synaptic transmission, membrane potential hyperpolarisation, seizure activity in the hippocampus and spinal nociceptive afferents. The actions were compared to well-established ligands (adenosine, CPA and NECA). All agonists inhibited synaptic transmission, increased paired-pulse facilitation and these effects were blocked by the A.sub.1 receptor antagonist 8-CPT. Thus, the actions of all of the agonists were consistent with the activation of presynaptic A1 receptors.
[0183] It has been found that compound BnOCPA does not hyperpolarise the membrane potential of pyramidal cells unlike adenosine and CPA. Even at very high concentrations (up to 1 μM, some 15 times the IC.sub.50 against synaptic transmission) it had no effect. Compound BnOCPA does bind to postsynaptic A.sub.1 receptors as it reduces the membrane potential hyperpolarisation produced by CPA and reverses the effects of adenosine. Thus, compound BnOCPA can distinguish between pre- and postsynaptic A.sub.1 receptors being a potent agonist at presynaptic receptors but acts in a manner analogous to an antagonist at postsynaptic A.sub.1 receptors.
[0184] Compound BnOCPA had little effect on a model of seizure activity, unlike other prototypical adenosine receptor agonists (CPA, NECA and adenosine) which abolished activity. There are at least two processes that would be expected to contribute to the seizure suppression produced by an A.sub.1 receptor agonist: the inhibition of synaptic transmission and the hyperpolarisation of the membrane potential leading to a reduction in action potential firing. In the seizure model used, the activity is driven mainly by action potential firing and thus the weak effects of compound BnOCPA are consistent with its inability to hyperpolarise neuronal membrane potential.
[0185] Using both the isolated frog heart and the anaesthetised ventilated rat preparation, the same effects were observed in both preparations: clear depressant effects of adenosine and the prototypical A.sub.1 receptor agonist CPA on heart rate with no significant effects of compound BnOCPA. A marked reduction in the effects of adenosine on heart rate following the application of compound BnOCPA was also observed, which is consistent with the antagonistic effect of compound BnOCPA on membrane hyperpolarisation induced by adenosine and CPA observed in the hippocampus. Thus, BnOCPA does not activate the A.sub.1 receptors on the heart and also reduces the activation of these receptors by other A.sub.1 receptor agonists, including the endogenous agonist, adenosine.
[0186] Thus, native A.sub.1Rs can be induced to signal via distinct signalling pathways and have identified a novel chemotype capable of doing so.
[0187] It will be appreciated by those skilled in the art that several variations to the aforementioned embodiments are envisaged without departing from the scope of the invention.
[0188] It will also be appreciated by those skilled in the art that any number of combinations of the aforementioned features and/or those shown in the appended drawings provide clear advantages over the prior art and are therefore within the scope of the invention described herein.