Skip to main content
Top
Published in: CNS Drugs 5/2014

01-05-2014 | Review Article

Adenosine A2A Receptor Antagonists in Parkinson’s Disease: Progress in Clinical Trials from the Newly Approved Istradefylline to Drugs in Early Development and Those Already Discontinued

Author: Annalisa Pinna

Published in: CNS Drugs | Issue 5/2014

Login to get access

Abstract

Neurotransmitters other than dopamine, such as norepinephrine, 5-hydroxytryptamine, glutamate, adenosine and acetylcholine, are involved in Parkinson’s disease (PD) and contribute to its symptomatology. Thus, the progress of non-dopaminergic therapies for PD has attracted much interest in recent years. Among new classes of drugs, adenosine A2A antagonists have emerged as promising candidates. The development of new highly selective adenosine A2A receptor antagonists, and their encouraging anti-parkinsonian responses in animal models of PD, has provided a rationale for clinical trials to evaluate the therapeutic potential and the safety of these agents in patients with PD. To date, the clinical research regarding A2A antagonists and their potential utilization in PD therapy continues to evolve between drugs just or previously discontinued (preladenant and vipadenant), new derivatives in development (tozadenant, PBF-509, ST1535, ST4206 and V81444) and the relatively old drug istradefylline, which has finally been licensed as an anti-parkinsonian drug in Japan. All these compounds have been shown to have a good safety profile and be well tolerated. Moreover, results from phase II and III trials also demonstrate that A2A antagonists are effective in reducing off-time, without worsening troublesome dyskinesia, and in increasing on-time with a mild increase of non-troublesome dyskinesia, in patients at an advanced stage of PD treated with l-DOPA. In addition, early findings suggest that A2A antagonists might also be efficacious as monotherapy in patients at an early stage of PD. This review summarizes pharmacological and clinical data available on istradefylline, tozadenant, PBF-509, ST1535, ST4206, V81444, preladenant and vipadenant.
Literature
1.
go back to reference Obeso JA, Rodriguez-Oroz MC, Rodriguez M, et al. Pathophysiology of the basal ganglia in Parkinson’s disease. Trends Neurosci. 2000;23:S8–19.PubMedCrossRef Obeso JA, Rodriguez-Oroz MC, Rodriguez M, et al. Pathophysiology of the basal ganglia in Parkinson’s disease. Trends Neurosci. 2000;23:S8–19.PubMedCrossRef
2.
go back to reference Chaudhuri KR, Healy DG, Schapira AH. National Institute for Clinical Excellence. Non-motor symptoms of Parkinson’s disease: diagnosis and management. Lancet Neurol. 2006;5(3):235–45.PubMedCrossRef Chaudhuri KR, Healy DG, Schapira AH. National Institute for Clinical Excellence. Non-motor symptoms of Parkinson’s disease: diagnosis and management. Lancet Neurol. 2006;5(3):235–45.PubMedCrossRef
3.
go back to reference Braak H, Del Tredici K, Rüb U, de Vos RA, Jansen Steur EN, Braak E. Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging. 2003;24:197–211.PubMedCrossRef Braak H, Del Tredici K, Rüb U, de Vos RA, Jansen Steur EN, Braak E. Staging of brain pathology related to sporadic Parkinson’s disease. Neurobiol Aging. 2003;24:197–211.PubMedCrossRef
4.
go back to reference Jellinger KA. Recent developments in the pathology of Parkinson’s disease. J Neural Transm. 2002;62:347–76.CrossRef Jellinger KA. Recent developments in the pathology of Parkinson’s disease. J Neural Transm. 2002;62:347–76.CrossRef
5.
go back to reference Alves G, Forsaa EB, Pedersen KF, et al. Epidemiology of Parkinson’s disease. J Neurol. 2008;255:18–32.PubMedCrossRef Alves G, Forsaa EB, Pedersen KF, et al. Epidemiology of Parkinson’s disease. J Neurol. 2008;255:18–32.PubMedCrossRef
7.
go back to reference Olanow CW, Agid Y, Mizuno Y, et al. Levodopa in the treatment of Parkinson’s disease: current controversies. Mov Disord. 2004;19:997–1005.PubMedCrossRef Olanow CW, Agid Y, Mizuno Y, et al. Levodopa in the treatment of Parkinson’s disease: current controversies. Mov Disord. 2004;19:997–1005.PubMedCrossRef
8.
go back to reference Horstink M, Tolosa E, Bonuccelli U, et al. Review of the therapeutic management of Parkinson’s disease. Report of a joint task force of the European Federation of Neurological Societies (EFNS) and the Movement Disorder Society-European Section (MDS-ES). Part II: late (complicated) Parkinson’s disease. Eur J Neurol. 2006;13(11):1186–202.PubMedCrossRef Horstink M, Tolosa E, Bonuccelli U, et al. Review of the therapeutic management of Parkinson’s disease. Report of a joint task force of the European Federation of Neurological Societies (EFNS) and the Movement Disorder Society-European Section (MDS-ES). Part II: late (complicated) Parkinson’s disease. Eur J Neurol. 2006;13(11):1186–202.PubMedCrossRef
9.
go back to reference Goetz CG, Poewe W, Rascol O, Sampaio C. Evidence-based medical review update: pharmacological and surgical treatments of Parkinson’s disease: 2001 to 2004. Mov Disord. 2005;20:523–39.PubMedCrossRef Goetz CG, Poewe W, Rascol O, Sampaio C. Evidence-based medical review update: pharmacological and surgical treatments of Parkinson’s disease: 2001 to 2004. Mov Disord. 2005;20:523–39.PubMedCrossRef
10.
go back to reference Ferré S, Fredholm BB, Morelli M, Popoli P, Fuxe K. Adenosine-dopamine receptor-receptor interactions as an integrative mechanism in the basal ganglia. Trends Neurosci. 1997;20:482–7.PubMedCrossRef Ferré S, Fredholm BB, Morelli M, Popoli P, Fuxe K. Adenosine-dopamine receptor-receptor interactions as an integrative mechanism in the basal ganglia. Trends Neurosci. 1997;20:482–7.PubMedCrossRef
11.
go back to reference Hettinger BD, Lee A, Linden J, Rosin DL. Ultrastructural localization of adenosine A2A receptors suggests multiple cellular sites for modulation of GABAergic neurons in rat striatum. J Comp Neurol. 2001;431:331–46.PubMedCrossRef Hettinger BD, Lee A, Linden J, Rosin DL. Ultrastructural localization of adenosine A2A receptors suggests multiple cellular sites for modulation of GABAergic neurons in rat striatum. J Comp Neurol. 2001;431:331–46.PubMedCrossRef
12.
go back to reference Schiffmann SN, Vanderhaeghen JJ. Adenosine A2 receptors regulate the gene expression of striatopallidal and striatonigral neurons. J Neurosci. 1993;13:1080–7.PubMed Schiffmann SN, Vanderhaeghen JJ. Adenosine A2 receptors regulate the gene expression of striatopallidal and striatonigral neurons. J Neurosci. 1993;13:1080–7.PubMed
13.
go back to reference Kurokawa M, Koga K, Kase H, Nakamura J, Kuwana Y. Adenosine A2a receptor-mediated modulation of striatal acetylcholine release in vivo. J Neurochem. 1996;66:1882–8.PubMedCrossRef Kurokawa M, Koga K, Kase H, Nakamura J, Kuwana Y. Adenosine A2a receptor-mediated modulation of striatal acetylcholine release in vivo. J Neurochem. 1996;66:1882–8.PubMedCrossRef
14.
go back to reference Gerevich Z, Wirkner K, Illes P. Adenosine A2A receptors inhibit the N-methyl-d-aspartate component of excitatory synaptic currents in rat striatal neurons. Eur J Pharmacol. 2002;451:161–4.PubMedCrossRef Gerevich Z, Wirkner K, Illes P. Adenosine A2A receptors inhibit the N-methyl-d-aspartate component of excitatory synaptic currents in rat striatal neurons. Eur J Pharmacol. 2002;451:161–4.PubMedCrossRef
15.
go back to reference Łukasiewicz S, Błasiak E, Faron-Górecka A, Polit A, Tworzydło M, Górecki A, Wasylewski Z, Dziedzicka-Wasylewska M. Fluorescence studies of homooligomerization of adenosine A2A and serotonin 5-HT1A receptors reveal the specificity of receptor interactions in the plasma membrane. Pharmacol Rep. 2007;59:379–92.PubMed Łukasiewicz S, Błasiak E, Faron-Górecka A, Polit A, Tworzydło M, Górecki A, Wasylewski Z, Dziedzicka-Wasylewska M. Fluorescence studies of homooligomerization of adenosine A2A and serotonin 5-HT1A receptors reveal the specificity of receptor interactions in the plasma membrane. Pharmacol Rep. 2007;59:379–92.PubMed
16.
go back to reference Armentero MT, Pinna A, Ferré S, Lanciego JL, Müller CE, Franco R. Past, present and future of A(2A) adenosine receptor antagonists in the therapy of Parkinson’s disease. Pharmacol Ther. 2011;132:280–99.PubMedCentralPubMedCrossRef Armentero MT, Pinna A, Ferré S, Lanciego JL, Müller CE, Franco R. Past, present and future of A(2A) adenosine receptor antagonists in the therapy of Parkinson’s disease. Pharmacol Ther. 2011;132:280–99.PubMedCentralPubMedCrossRef
17.
go back to reference Bogenpohl JW, Ritter SL, Hall RA, Smith Y. Adenosine A2A receptor in the monkey basal ganglia: Ultrastructural localization and colocalization with the metabotropic glutamate receptor 5 in the striatum. J Comp Neurol. 2012;520:570–89.PubMedCentralPubMedCrossRef Bogenpohl JW, Ritter SL, Hall RA, Smith Y. Adenosine A2A receptor in the monkey basal ganglia: Ultrastructural localization and colocalization with the metabotropic glutamate receptor 5 in the striatum. J Comp Neurol. 2012;520:570–89.PubMedCentralPubMedCrossRef
18.
go back to reference Jones CK, Bubser M, Thompson AD, Dickerson JW, Turle-Lorenzo N, Amalric M, et al. The metabotropic glutamate receptor 4-positive allosteric modulator VU0364770 produces efficacy alone and in combination with l-DOPA or an adenosine 2A antagonist in preclinical rodent models of Parkinson’s disease. J Pharmacol Exp Ther. 2012;340:404–21.PubMedCentralPubMedCrossRef Jones CK, Bubser M, Thompson AD, Dickerson JW, Turle-Lorenzo N, Amalric M, et al. The metabotropic glutamate receptor 4-positive allosteric modulator VU0364770 produces efficacy alone and in combination with l-DOPA or an adenosine 2A antagonist in preclinical rodent models of Parkinson’s disease. J Pharmacol Exp Ther. 2012;340:404–21.PubMedCentralPubMedCrossRef
19.
go back to reference Jenner P. Istradefylline, a novel adenosine A2A receptor antagonist, for the treatment of Parkinson’s disease. Expert Opin Investig Drugs. 2005;14:729–38.PubMedCrossRef Jenner P. Istradefylline, a novel adenosine A2A receptor antagonist, for the treatment of Parkinson’s disease. Expert Opin Investig Drugs. 2005;14:729–38.PubMedCrossRef
20.
go back to reference Pinna A. Novel investigational adenosine A2A receptor antagonists for Parkinson’s disease. Expert Opin Investig Drugs. 2009;18:1619–31.PubMedCrossRef Pinna A. Novel investigational adenosine A2A receptor antagonists for Parkinson’s disease. Expert Opin Investig Drugs. 2009;18:1619–31.PubMedCrossRef
22.
go back to reference Hickey P, Stacy M. Adenosine A2A antagonists in Parkinson’s disease: what’s next? Curr Neurol Neurosci Rep. 2012;12:376–85.PubMedCrossRef Hickey P, Stacy M. Adenosine A2A antagonists in Parkinson’s disease: what’s next? Curr Neurol Neurosci Rep. 2012;12:376–85.PubMedCrossRef
24.
go back to reference Xu K, Bastia E, Schwarzschild M. Therapeutic potential of adenosine A(2A) receptor antagonists in Parkinson’s disease. Pharmacol Ther. 2005;105:267–310.PubMedCrossRef Xu K, Bastia E, Schwarzschild M. Therapeutic potential of adenosine A(2A) receptor antagonists in Parkinson’s disease. Pharmacol Ther. 2005;105:267–310.PubMedCrossRef
25.
go back to reference Simola N, Morelli M, Pinna A. Adenosine A2A receptor antagonists and Parkinson’s disease: state of the art and future directions. Curr Pharm Des. 2008;14(15):1475–89.PubMedCrossRef Simola N, Morelli M, Pinna A. Adenosine A2A receptor antagonists and Parkinson’s disease: state of the art and future directions. Curr Pharm Des. 2008;14(15):1475–89.PubMedCrossRef
27.
go back to reference Salamone JD. Preladenant, a novel adenosine A(2A) receptor antagonist for the potential treatment of parkinsonism and other disorders. IDrugs. 2010;13:723–31.PubMed Salamone JD. Preladenant, a novel adenosine A(2A) receptor antagonist for the potential treatment of parkinsonism and other disorders. IDrugs. 2010;13:723–31.PubMed
28.
go back to reference Shiozaki S, Ichikawa S, Nakamura J, Kitamura S, Yamada K, Kuwana Y. Actions of adenosine A2A receptor antagonist KW-6002 on drug-induced catalepsy and hypokinesia caused by reserpine or MPTP. Psychopharmacology. 1999;147:90–5.PubMedCrossRef Shiozaki S, Ichikawa S, Nakamura J, Kitamura S, Yamada K, Kuwana Y. Actions of adenosine A2A receptor antagonist KW-6002 on drug-induced catalepsy and hypokinesia caused by reserpine or MPTP. Psychopharmacology. 1999;147:90–5.PubMedCrossRef
29.
go back to reference Stasi MA, Borsini F, Varani K, Vincenzi F, Di Cesare MA, Minetti P, et al. ST 1535: a preferential A2A adenosine receptor antagonist. Int J Neuropsychopharmacol. 2006;9:575–84.PubMedCrossRef Stasi MA, Borsini F, Varani K, Vincenzi F, Di Cesare MA, Minetti P, et al. ST 1535: a preferential A2A adenosine receptor antagonist. Int J Neuropsychopharmacol. 2006;9:575–84.PubMedCrossRef
30.
go back to reference Gillespie RJ, Bamford SJ, Botting R, et al. Antagonists of the human A2A adenosine receptor. 4. Design, synthesis, and preclinical evaluation of 7-aryltriazolo[4,5-d]pyrimidines. J Med Chem. 2009;52:33–47.PubMedCrossRef Gillespie RJ, Bamford SJ, Botting R, et al. Antagonists of the human A2A adenosine receptor. 4. Design, synthesis, and preclinical evaluation of 7-aryltriazolo[4,5-d]pyrimidines. J Med Chem. 2009;52:33–47.PubMedCrossRef
31.
go back to reference Hodgson RA, Bertorelli R, Varty GB, Lachowicz JE, Forlani A, Fredduzzi S, et al. Characterization of the potent and highly selective A2A receptor antagonists preladenant and SCH 412348 in rodent models of movement disorders and depression. J Pharmacol Exp Ther. 2009;330:294–303.PubMedCrossRef Hodgson RA, Bertorelli R, Varty GB, Lachowicz JE, Forlani A, Fredduzzi S, et al. Characterization of the potent and highly selective A2A receptor antagonists preladenant and SCH 412348 in rodent models of movement disorders and depression. J Pharmacol Exp Ther. 2009;330:294–303.PubMedCrossRef
32.
go back to reference Salamone JD, Betz AJ, Ishiwari K, Felsted J, Madson L, Mirante B, et al. Tremorolytic effects of adenosine A2A antagonists: implications for parkinsonism. Front Biosci. 2008;13:3594–605.PubMedCrossRef Salamone JD, Betz AJ, Ishiwari K, Felsted J, Madson L, Mirante B, et al. Tremorolytic effects of adenosine A2A antagonists: implications for parkinsonism. Front Biosci. 2008;13:3594–605.PubMedCrossRef
33.
go back to reference Tronci E, Simola N, Borsini F, Schintu N, Frau L, Carminati P, et al. Characterization of the antiparkinsonian effects of the new adenosine A2A receptor antagonist ST1535: acute and subchronic studies in rats. Eur J Pharmacol. 2007;566:94–102.PubMedCrossRef Tronci E, Simola N, Borsini F, Schintu N, Frau L, Carminati P, et al. Characterization of the antiparkinsonian effects of the new adenosine A2A receptor antagonist ST1535: acute and subchronic studies in rats. Eur J Pharmacol. 2007;566:94–102.PubMedCrossRef
34.
go back to reference Fenu S, Pinna A, Ongini E, Morelli M. Adenosine A2A receptor antagonism potentiates l-DOPA-induced turning behaviour and c-fos expression in 6-hydroxydopamine-lesioned rats. Eur J Pharmacol. 1997;321:143–7.PubMedCrossRef Fenu S, Pinna A, Ongini E, Morelli M. Adenosine A2A receptor antagonism potentiates l-DOPA-induced turning behaviour and c-fos expression in 6-hydroxydopamine-lesioned rats. Eur J Pharmacol. 1997;321:143–7.PubMedCrossRef
35.
go back to reference Koga K, Kurokawa M, Ochi M, Nakamura J, Kuwana Y. Adenosine A(2A) receptor antagonists KF17837 and KW-6002 potentiate rotation induced by dopaminergic drugs in hemi-Parkinsonian rats. Eur J Pharmacol. 2000;408:249–55.PubMedCrossRef Koga K, Kurokawa M, Ochi M, Nakamura J, Kuwana Y. Adenosine A(2A) receptor antagonists KF17837 and KW-6002 potentiate rotation induced by dopaminergic drugs in hemi-Parkinsonian rats. Eur J Pharmacol. 2000;408:249–55.PubMedCrossRef
36.
go back to reference Rose S, Ramsay Croft N, Jenner P. The novel adenosine A2a antagonist ST1535 potentiates the effects of a threshold dose of l-DOPA in unilaterally 6-OHDA-lesioned rats. Brain Res. 2007;1133:110–4.PubMedCrossRef Rose S, Ramsay Croft N, Jenner P. The novel adenosine A2a antagonist ST1535 potentiates the effects of a threshold dose of l-DOPA in unilaterally 6-OHDA-lesioned rats. Brain Res. 2007;1133:110–4.PubMedCrossRef
37.
go back to reference Bibbiani F, Oh JD, Petzer JP, Castagnoli N Jr, Chen JF, Schwarzschild MA, et al. A2A antagonist prevents dopamine agonist-induced motor complications in animal models of Parkinson’s disease. Exp Neurol. 2003;184:285–94.PubMedCrossRef Bibbiani F, Oh JD, Petzer JP, Castagnoli N Jr, Chen JF, Schwarzschild MA, et al. A2A antagonist prevents dopamine agonist-induced motor complications in animal models of Parkinson’s disease. Exp Neurol. 2003;184:285–94.PubMedCrossRef
38.
go back to reference Pinna A, Pontis S, Borsini F, Morelli M. Adenosine A2A receptor antagonists improve deficits in initiation of movement and sensory motor integration in the unilateral 6-hydroxydopamine rat model of Parkinson’s disease. Synapse. 2007;61:606–14.PubMedCrossRef Pinna A, Pontis S, Borsini F, Morelli M. Adenosine A2A receptor antagonists improve deficits in initiation of movement and sensory motor integration in the unilateral 6-hydroxydopamine rat model of Parkinson’s disease. Synapse. 2007;61:606–14.PubMedCrossRef
39.
go back to reference Lundblad M, Vaudano E, Cenci MA. Cellular and behavioural effects of the adenosine A2a receptor antagonist KW-6002 in a rat model of l-DOPA-induced dyskinesia. J Neurochem. 2003;84:1398–410.PubMedCrossRef Lundblad M, Vaudano E, Cenci MA. Cellular and behavioural effects of the adenosine A2a receptor antagonist KW-6002 in a rat model of l-DOPA-induced dyskinesia. J Neurochem. 2003;84:1398–410.PubMedCrossRef
40.
go back to reference Kanda T, Jackson MJ, Smith LA, Pearce RK, Nakamura J, Kase H, et al. Adenosine A2A antagonist: a novel antiparkinsonian agent that does not provoke dyskinesia in parkinsonian monkeys. Ann Neurol. 1998;43:507–13.PubMedCrossRef Kanda T, Jackson MJ, Smith LA, Pearce RK, Nakamura J, Kase H, et al. Adenosine A2A antagonist: a novel antiparkinsonian agent that does not provoke dyskinesia in parkinsonian monkeys. Ann Neurol. 1998;43:507–13.PubMedCrossRef
41.
go back to reference Kanda T, Jackson MJ, Smith LA, Pearce RK, Nakamura J, Kase H, et al. Combined use of the adenosine A(2A) antagonist KW-6002 with l-DOPA or with selective D1 or D2 dopamine agonists increases antiparkinsonian activity but not dyskinesia in MPTP-treated monkeys. Exp Neurol. 2000;162:321–7.PubMedCrossRef Kanda T, Jackson MJ, Smith LA, Pearce RK, Nakamura J, Kase H, et al. Combined use of the adenosine A(2A) antagonist KW-6002 with l-DOPA or with selective D1 or D2 dopamine agonists increases antiparkinsonian activity but not dyskinesia in MPTP-treated monkeys. Exp Neurol. 2000;162:321–7.PubMedCrossRef
42.
go back to reference Rose S, Jackson MJ, Smith LA, Stockwell K, Johnson L, Carminati P, et al. The novel adenosine A2a receptor antagonist ST1535 potentiates the effects of a threshold dose of l-DOPA in MPTP treated common marmosets. Eur J Pharmacol. 2006;546:82–7.PubMedCrossRef Rose S, Jackson MJ, Smith LA, Stockwell K, Johnson L, Carminati P, et al. The novel adenosine A2a receptor antagonist ST1535 potentiates the effects of a threshold dose of l-DOPA in MPTP treated common marmosets. Eur J Pharmacol. 2006;546:82–7.PubMedCrossRef
43.
go back to reference Hodgson RA, Bedard PJ, Varty GB, Kazdoba TM, Di Paolo T, Grzelak ME, et al. Preladenant, a selective A(2A) receptor antagonist, is active in primate models of movement disorders. Exp Neurol. 2010;225:384–90.PubMedCrossRef Hodgson RA, Bedard PJ, Varty GB, Kazdoba TM, Di Paolo T, Grzelak ME, et al. Preladenant, a selective A(2A) receptor antagonist, is active in primate models of movement disorders. Exp Neurol. 2010;225:384–90.PubMedCrossRef
44.
go back to reference Grondin R, Bedard PJ, Hadj Tahar A, Gregoire L, Mori A, Kase H. Antiparkinsonian effect of a new selective adenosine A2A receptor antagonist in MPTP-treated monkeys. Neurology. 1999;52:1673–7.PubMedCrossRef Grondin R, Bedard PJ, Hadj Tahar A, Gregoire L, Mori A, Kase H. Antiparkinsonian effect of a new selective adenosine A2A receptor antagonist in MPTP-treated monkeys. Neurology. 1999;52:1673–7.PubMedCrossRef
45.
go back to reference Costa J, Lunet N, Santos C, Santos J, Vaz-Carneiro A. Caffeine exposure and the risk of Parkinson’s disease: a systematic review and meta-analysis of observational studies. J Alzheimers Dis. 2010;20:S221–38.PubMed Costa J, Lunet N, Santos C, Santos J, Vaz-Carneiro A. Caffeine exposure and the risk of Parkinson’s disease: a systematic review and meta-analysis of observational studies. J Alzheimers Dis. 2010;20:S221–38.PubMed
46.
go back to reference Kalda A, Yu L, Oztas E, Chen JF. Novel neuroprotection by caffeine and adenosine A(2A) receptor antagonists in animal models of Parkinson’s disease. J Neurol Sci. 2006;248(1–2):9–15.PubMedCrossRef Kalda A, Yu L, Oztas E, Chen JF. Novel neuroprotection by caffeine and adenosine A(2A) receptor antagonists in animal models of Parkinson’s disease. J Neurol Sci. 2006;248(1–2):9–15.PubMedCrossRef
47.
go back to reference Prediger RD. Effects of caffeine in Parkinson’s disease: from neuroprotection to the management of motor and non-motor symptoms. J Alzheimers Dis. 2010;20(Suppl 1):S205–20.PubMed Prediger RD. Effects of caffeine in Parkinson’s disease: from neuroprotection to the management of motor and non-motor symptoms. J Alzheimers Dis. 2010;20(Suppl 1):S205–20.PubMed
48.
go back to reference Pinna A, Simola N, Frau F, Morelli M. Symptomatic and neuroprotective effects of A2A receptor antagonists in Parkinson’s disease. In: Masino S, Boison D, editors. Adenosine—a key link between metabolism and brain activity. Berlin: Springer; 2013. p. 361–84. Pinna A, Simola N, Frau F, Morelli M. Symptomatic and neuroprotective effects of A2A receptor antagonists in Parkinson’s disease. In: Masino S, Boison D, editors. Adenosine—a key link between metabolism and brain activity. Berlin: Springer; 2013. p. 361–84.
49.
go back to reference Takahashi RN, Pamplona FA, Prediger RD. Adenosine receptor antagonists for cognitive dysfunction: a review of animal studies. Front Biosci. 2008;13:2614–32.PubMedCrossRef Takahashi RN, Pamplona FA, Prediger RD. Adenosine receptor antagonists for cognitive dysfunction: a review of animal studies. Front Biosci. 2008;13:2614–32.PubMedCrossRef
50.
go back to reference Salamone JD, Correa M, Randall PA, Nunes EJ, Pardo M, Lopez-Cruz L. The role of adenosine in the ventral stiatal circuits regulating behavioural activation and effort-related decision making: importance of normal and pathological aspect of motivation. In: Masino S, Boison D, editors. Adenosine—a key link between metabolism and brain activity. Berlin: Springer; 2013. p. 493–512. Salamone JD, Correa M, Randall PA, Nunes EJ, Pardo M, Lopez-Cruz L. The role of adenosine in the ventral stiatal circuits regulating behavioural activation and effort-related decision making: importance of normal and pathological aspect of motivation. In: Masino S, Boison D, editors. Adenosine—a key link between metabolism and brain activity. Berlin: Springer; 2013. p. 493–512.
51.
go back to reference Ritchie K, Carrière I, de Mendonca A, Portet F, Dartigues JF, Rouaud O, Barberger-Gateau P, Ancelin ML. The neuroprotective effects of caffeine: a prospective population study (the Three City Study). Neurology. 2007;69:536–45.PubMedCrossRef Ritchie K, Carrière I, de Mendonca A, Portet F, Dartigues JF, Rouaud O, Barberger-Gateau P, Ancelin ML. The neuroprotective effects of caffeine: a prospective population study (the Three City Study). Neurology. 2007;69:536–45.PubMedCrossRef
54.
go back to reference Knebel W, Rao N, Uchimura T, Mori A, Fisher J, Gastonguay MR, Chaikin P. Population pharmacokinetic analysis of istradefylline in healthy subjects and in patients with Parkinson’s disease. J Clin Pharmacol. 2011;51:40–52.PubMedCrossRef Knebel W, Rao N, Uchimura T, Mori A, Fisher J, Gastonguay MR, Chaikin P. Population pharmacokinetic analysis of istradefylline in healthy subjects and in patients with Parkinson’s disease. J Clin Pharmacol. 2011;51:40–52.PubMedCrossRef
55.
go back to reference Brooks DJ, Doder M, Osman S, Luthra SK, Hirani E, Hume S, Kase H, Kilborn J, Martindill S, Mori A. Positron emission tomography analysis of [11C]KW-6002 binding to human and rat adenosine A2A receptors in the brain. Synapse. 2008;62:671–81.PubMedCrossRef Brooks DJ, Doder M, Osman S, Luthra SK, Hirani E, Hume S, Kase H, Kilborn J, Martindill S, Mori A. Positron emission tomography analysis of [11C]KW-6002 binding to human and rat adenosine A2A receptors in the brain. Synapse. 2008;62:671–81.PubMedCrossRef
56.
go back to reference Bara-Jimenez W, Sherzai A, Dimitrova T, Favit A, Bibbiani F, Gillespie M, et al. Adenosine A(2A) receptor antagonist treatment of Parkinson’s disease. Neurology. 2003;61:293–6.PubMedCrossRef Bara-Jimenez W, Sherzai A, Dimitrova T, Favit A, Bibbiani F, Gillespie M, et al. Adenosine A(2A) receptor antagonist treatment of Parkinson’s disease. Neurology. 2003;61:293–6.PubMedCrossRef
57.
go back to reference Hauser RA, Hubble JP, Truong DD. Randomized trial of the adenosine A(2A) receptor antagonist istradefylline in advanced PD. Neurology. 2003;61:297–303.PubMedCrossRef Hauser RA, Hubble JP, Truong DD. Randomized trial of the adenosine A(2A) receptor antagonist istradefylline in advanced PD. Neurology. 2003;61:297–303.PubMedCrossRef
60.
go back to reference LeWitt PA, Guttman M, Tetrud JW, Tuite PJ, Mori A, Chaikin P, et al. Adenosine A2A receptor antagonist istradefylline (KW-6002) reduces OFF time in Parkinson’s disease: a double-blind, randomized, multicenter clinical trial (6002-US-005). Ann Neurol. 2008;63:295–302.PubMedCrossRef LeWitt PA, Guttman M, Tetrud JW, Tuite PJ, Mori A, Chaikin P, et al. Adenosine A2A receptor antagonist istradefylline (KW-6002) reduces OFF time in Parkinson’s disease: a double-blind, randomized, multicenter clinical trial (6002-US-005). Ann Neurol. 2008;63:295–302.PubMedCrossRef
61.
go back to reference Stacy M, Silver D, Mendis T, Sutton J, Mori A, Chaikin P, et al. A 12-week, placebo-controlled study (6002-US-006) of istradefylline in Parkinson disease. Neurology. 2008;70:2233–40.PubMedCrossRef Stacy M, Silver D, Mendis T, Sutton J, Mori A, Chaikin P, et al. A 12-week, placebo-controlled study (6002-US-006) of istradefylline in Parkinson disease. Neurology. 2008;70:2233–40.PubMedCrossRef
63.
go back to reference Hauser RA, Shulman LM, Trugman JM, Roberts J, Mori A, Ballerini R, et al. Study of istradefylline in patients with Parkinson’s disease on levodopa with motor fluctuations. Mov Disord. 2008;23:2177–85.PubMedCrossRef Hauser RA, Shulman LM, Trugman JM, Roberts J, Mori A, Ballerini R, et al. Study of istradefylline in patients with Parkinson’s disease on levodopa with motor fluctuations. Mov Disord. 2008;23:2177–85.PubMedCrossRef
65.
go back to reference Factor S, Mark MH, Watts R, Struck L, Mori A, Ballerini R, et al. A long-term study of istradefylline in subjects with fluctuating Parkinson’s disease. Parkinsonism Relat Disord. 2010;16:423–6.PubMedCrossRef Factor S, Mark MH, Watts R, Struck L, Mori A, Ballerini R, et al. A long-term study of istradefylline in subjects with fluctuating Parkinson’s disease. Parkinsonism Relat Disord. 2010;16:423–6.PubMedCrossRef
68.
go back to reference Mizuno Y, Hasegawa K, Kondo T, Kuno S, Yamamoto M. Clinical efficacy of istradefylline (KW-6002) in Parkinson’s disease: a randomized, controlled study. Mov Disord. 2010;25:1437–43.PubMedCrossRef Mizuno Y, Hasegawa K, Kondo T, Kuno S, Yamamoto M. Clinical efficacy of istradefylline (KW-6002) in Parkinson’s disease: a randomized, controlled study. Mov Disord. 2010;25:1437–43.PubMedCrossRef
69.
go back to reference Mizuno Y, Kondo T. Japanese Istradefylline Study Group. Adenosine A2A receptor antagonist istradefylline reduces daily OFF time in Parkinson’s disease. Mov Disord. 2013;28:1138–41.PubMedCentralPubMedCrossRef Mizuno Y, Kondo T. Japanese Istradefylline Study Group. Adenosine A2A receptor antagonist istradefylline reduces daily OFF time in Parkinson’s disease. Mov Disord. 2013;28:1138–41.PubMedCentralPubMedCrossRef
70.
go back to reference Chen W, Wang H, Wei H, Gu S, Wei H. Istradefylline, an adenosine A2A receptor antagonist, for patients with Parkinson’s disease: a meta-analysis. J Neurol Sci. 2013;324:21–8.PubMedCrossRef Chen W, Wang H, Wei H, Gu S, Wei H. Istradefylline, an adenosine A2A receptor antagonist, for patients with Parkinson’s disease: a meta-analysis. J Neurol Sci. 2013;324:21–8.PubMedCrossRef
72.
go back to reference Pourcher E, Fernandez HH, Stacy M, Mori A, Ballerini R, Chaikin P. Istradefylline for Parkinson’s disease patients experiencing motor fluctuations: results of the KW-6002-US-018 study. Parkinsonism Relat Disord. 2012;18:178–84.PubMedCrossRef Pourcher E, Fernandez HH, Stacy M, Mori A, Ballerini R, Chaikin P. Istradefylline for Parkinson’s disease patients experiencing motor fluctuations: results of the KW-6002-US-018 study. Parkinsonism Relat Disord. 2012;18:178–84.PubMedCrossRef
77.
go back to reference Fernandez HH, Greeley DR, Zweig RM, Wojcieszek J, Mori A, Sussman NM. Istradefylline as monotherapy for Parkinson disease: results of the 6002-US-051 trial. Parkinsonism Relat Disord. 2010;16:16–20.PubMedCrossRef Fernandez HH, Greeley DR, Zweig RM, Wojcieszek J, Mori A, Sussman NM. Istradefylline as monotherapy for Parkinson disease: results of the 6002-US-051 trial. Parkinsonism Relat Disord. 2010;16:16–20.PubMedCrossRef
78.
go back to reference Ferré S, Diamond I, Goldberg SR, Yao L, Hourani SM, Huang ZL, Urade Y, Kitchen I. Adenosine A2A receptors in ventral striatum, hypothalamus and nociceptive circuitry implications for drug addiction, sleep and pain. Prog Neurobiol. 2007;83(5):332–47.PubMedCentralPubMedCrossRef Ferré S, Diamond I, Goldberg SR, Yao L, Hourani SM, Huang ZL, Urade Y, Kitchen I. Adenosine A2A receptors in ventral striatum, hypothalamus and nociceptive circuitry implications for drug addiction, sleep and pain. Prog Neurobiol. 2007;83(5):332–47.PubMedCentralPubMedCrossRef
81.
go back to reference Minetti P, Tinti MA, Carminati P, Castorina M, Di Cesare MA, Di Serio S, et al. 2-n-Butyl-9-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine and analogues as A2A adenosine receptor antagonists. Design, synthesis, and pharmacological characterization. J Med Chem. 2005;48:6887–96.PubMedCrossRef Minetti P, Tinti MA, Carminati P, Castorina M, Di Cesare MA, Di Serio S, et al. 2-n-Butyl-9-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine and analogues as A2A adenosine receptor antagonists. Design, synthesis, and pharmacological characterization. J Med Chem. 2005;48:6887–96.PubMedCrossRef
82.
go back to reference Di Serio S, Danese V, Guaraldi D, et al. The novel adenosine A2A receptor antagonist 2-butyl-9-methyl-8-(2H-1,2,3-triazol-2-yl)-9H-purin-6-ylamine (ST1535) ameliorates memory disruption mediated by adenosine A1 receptor stimulation. Behav Pharmacol. 2009;20:S92. Di Serio S, Danese V, Guaraldi D, et al. The novel adenosine A2A receptor antagonist 2-butyl-9-methyl-8-(2H-1,2,3-triazol-2-yl)-9H-purin-6-ylamine (ST1535) ameliorates memory disruption mediated by adenosine A1 receptor stimulation. Behav Pharmacol. 2009;20:S92.
85.
go back to reference Piersanti G, Bartoccini F, Lucarini S, Cabri W, Stasi MA, Riccioni T, Borsini F, Tarzia G, Minetti P. Synthesis and biological evaluation of metabolites of 2-n-butyl-9-methyl-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine (ST1535), a potent antagonist of the A(2A) adenosine receptor for the treatment of Parkinson’s disease. J Med Chem. 2013;56:5456–63.PubMedCrossRef Piersanti G, Bartoccini F, Lucarini S, Cabri W, Stasi MA, Riccioni T, Borsini F, Tarzia G, Minetti P. Synthesis and biological evaluation of metabolites of 2-n-butyl-9-methyl-8-[1,2,3]triazol-2-yl-9H-purin-6-ylamine (ST1535), a potent antagonist of the A(2A) adenosine receptor for the treatment of Parkinson’s disease. J Med Chem. 2013;56:5456–63.PubMedCrossRef
89.
go back to reference Black KJ, Campbell MC, Dickerson W, Creech ML, Koller JM, Chung S, et al. A randomized, double-blind, placebo-controlled cross-over trial of the adenosine 2a antagonist SYN115 in Parkinson disease. Presented at the annual meetings of the American Academy of Neurology, Toronto (Canada). Neurology. Vol. 74; 2010. p. A317. Black KJ, Campbell MC, Dickerson W, Creech ML, Koller JM, Chung S, et al. A randomized, double-blind, placebo-controlled cross-over trial of the adenosine 2a antagonist SYN115 in Parkinson disease. Presented at the annual meetings of the American Academy of Neurology, Toronto (Canada). Neurology. Vol. 74; 2010. p. A317.
90.
go back to reference Black KJ, Koller JM, Campbell MC, Bandak SI. Quantification of indirect pathway inhibition by the adenosine A2a antagonist SYN115 in Parkinson’s disease. J Neurosci. 2010;30:16284–92.PubMedCentralPubMedCrossRef Black KJ, Koller JM, Campbell MC, Bandak SI. Quantification of indirect pathway inhibition by the adenosine A2a antagonist SYN115 in Parkinson’s disease. J Neurosci. 2010;30:16284–92.PubMedCentralPubMedCrossRef
92.
go back to reference Hauser RA, Olanow CW, Kieburtz, Neale A, Resburg C, Maya U, Bandak S. A phase 2, placebo-controlled, randomized, double-blind trial of tozadenant (SYN-115) in patients with Parkinson’s disease with wearing-off fluctuations on levodopa. Mov Disord. 2013;28:S158. Hauser RA, Olanow CW, Kieburtz, Neale A, Resburg C, Maya U, Bandak S. A phase 2, placebo-controlled, randomized, double-blind trial of tozadenant (SYN-115) in patients with Parkinson’s disease with wearing-off fluctuations on levodopa. Mov Disord. 2013;28:S158.
98.
go back to reference Neustadt BR, Hao J, Lindo N, Greenlee WJ, Stamford AW, Tulshian D, et al. Potent, selective, and orally active adenosine A2A receptor antagonists: arylpiperazine derivatives of pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines. Bioorg Med Chem Lett. 2007;17:1376–80.PubMedCrossRef Neustadt BR, Hao J, Lindo N, Greenlee WJ, Stamford AW, Tulshian D, et al. Potent, selective, and orally active adenosine A2A receptor antagonists: arylpiperazine derivatives of pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines. Bioorg Med Chem Lett. 2007;17:1376–80.PubMedCrossRef
99.
go back to reference Cutler DL, Tendolkar A, Grachev ID. Safety, tolerability and pharmacokinetics after single and multiple doses of preladenant (SCH420814) administered in healthy subjects. J Clin Pharm Ther. 2012;37:578–87.PubMedCrossRef Cutler DL, Tendolkar A, Grachev ID. Safety, tolerability and pharmacokinetics after single and multiple doses of preladenant (SCH420814) administered in healthy subjects. J Clin Pharm Ther. 2012;37:578–87.PubMedCrossRef
100.
go back to reference Brooks DJ, Warrington S, Tendolkar A, Cutler DL, Hunter J. Positron emission tomography (PET) study of preladenant in healthy male subjects. Mov Disord. 2009;24:S257.CrossRef Brooks DJ, Warrington S, Tendolkar A, Cutler DL, Hunter J. Positron emission tomography (PET) study of preladenant in healthy male subjects. Mov Disord. 2009;24:S257.CrossRef
101.
go back to reference Hunter J. SCH 420814: a novel adenosine A2a antagonist. Exploring Parkinson’s disease and beyond. Presented at International research conference “Targeting adenosine A2A receptors in PD and other CNS Disorders”, Boston, USA. 2006. http://handle.dtic.mil/100.2/ADA452764. Accessed 15 Oct 2013. Hunter J. SCH 420814: a novel adenosine A2a antagonist. Exploring Parkinson’s disease and beyond. Presented at International research conference “Targeting adenosine A2A receptors in PD and other CNS Disorders”, Boston, USA. 2006. http://​handle.​dtic.​mil/​100.​2/​ADA452764. Accessed 15 Oct 2013.
103.
go back to reference Hauser RA, Cantillon M, Pourcher E, Micheli F, Mok V, Onofrj M, et al. Preladenant in patients with Parkinson’s disease and motor fluctuations: a phase 2, double-blind, randomised trial. Lancet Neurol. 2011;10:221–9.PubMedCrossRef Hauser RA, Cantillon M, Pourcher E, Micheli F, Mok V, Onofrj M, et al. Preladenant in patients with Parkinson’s disease and motor fluctuations: a phase 2, double-blind, randomised trial. Lancet Neurol. 2011;10:221–9.PubMedCrossRef
107.
go back to reference Factor SA, Wolski K, Togasaki DM, Huyck S, Cantillon M, Ho TW, Hauser RA, Pourcher E. Long-term safety and efficacy of preladenant in subjects with fluctuating Parkinson’s disease. Mov Disord. 2013;28:817–20.PubMedCrossRef Factor SA, Wolski K, Togasaki DM, Huyck S, Cantillon M, Ho TW, Hauser RA, Pourcher E. Long-term safety and efficacy of preladenant in subjects with fluctuating Parkinson’s disease. Mov Disord. 2013;28:817–20.PubMedCrossRef
112.
go back to reference Wang Z, Xuan F, Lin WH, Troyer MD, Tendolkar A, Cutler DL. Preladenant, a selective adenosine A2A receptor antagonist, is not associated with QT/QTc prolongation. Eur J Clin Pharmacol. 2013;69(10):1761–7.PubMedCrossRef Wang Z, Xuan F, Lin WH, Troyer MD, Tendolkar A, Cutler DL. Preladenant, a selective adenosine A2A receptor antagonist, is not associated with QT/QTc prolongation. Eur J Clin Pharmacol. 2013;69(10):1761–7.PubMedCrossRef
117.
go back to reference He P, Papapetropoulos S, O’Neill GN, Wade A, Kwiatkowski K, Donaldson K. Pharmacokinetic profile of the adenosine A2A receptor antagonist BIIB014 in healthy volunteers. Mov Disord. 2010;2010(25):S298. He P, Papapetropoulos S, O’Neill GN, Wade A, Kwiatkowski K, Donaldson K. Pharmacokinetic profile of the adenosine A2A receptor antagonist BIIB014 in healthy volunteers. Mov Disord. 2010;2010(25):S298.
118.
go back to reference Brooks DJ, Papapetropoulos S, Vandenhende F, Tomic D, He P, Coppell A, et al. An open-label, positron emission tomography study to assess adenosine A2A brain receptor occupancy of vipadenant (BIIB014) at steady-state levels in healthy male volunteers. Clin Neuropharmacol. 2010;33:55–60.PubMedCrossRef Brooks DJ, Papapetropoulos S, Vandenhende F, Tomic D, He P, Coppell A, et al. An open-label, positron emission tomography study to assess adenosine A2A brain receptor occupancy of vipadenant (BIIB014) at steady-state levels in healthy male volunteers. Clin Neuropharmacol. 2010;33:55–60.PubMedCrossRef
120.
go back to reference Papapetropoulos S, Borgohain R, Kellet M, Giladi N, Tomic D, Coppell A, et al. The adenosine A2A receptor antagonist BIIB014 is effective in improving ON-time in Parkinson’s disease (PD) patients with motor fluctuations. Mov Disord. 2010;25:S305. Papapetropoulos S, Borgohain R, Kellet M, Giladi N, Tomic D, Coppell A, et al. The adenosine A2A receptor antagonist BIIB014 is effective in improving ON-time in Parkinson’s disease (PD) patients with motor fluctuations. Mov Disord. 2010;25:S305.
121.
go back to reference Papapetropoulos S, Borgohain R, Kellet M, Giladi N, Tomic D, Coppell A, et al. Safety and tolerability profile of the adenosine A2A receptor antagonist BIIB014 in Parkinson’s disease: pooled analysis of two placebo-controlled 8-week studies. Mov Disord. 2010;25:S304. Papapetropoulos S, Borgohain R, Kellet M, Giladi N, Tomic D, Coppell A, et al. Safety and tolerability profile of the adenosine A2A receptor antagonist BIIB014 in Parkinson’s disease: pooled analysis of two placebo-controlled 8-week studies. Mov Disord. 2010;25:S304.
125.
go back to reference Rascol O, Brooks DJ, Melamed E, et al., for the LARGO study group. Rasagiline as an adjunct to levodopa in patients with Parkinson’s disease and motor fluctuations (LARGO, Lasting eff ect in Adjunct therapy with Rasagiline Given Once daily, study): a randomised, double-blind, parallel-group trial. Lancet. 2005;365:947–54. Rascol O, Brooks DJ, Melamed E, et al., for the LARGO study group. Rasagiline as an adjunct to levodopa in patients with Parkinson’s disease and motor fluctuations (LARGO, Lasting eff ect in Adjunct therapy with Rasagiline Given Once daily, study): a randomised, double-blind, parallel-group trial. Lancet. 2005;365:947–54.
126.
go back to reference Lees AJ. Evidence-based efficacy comparison of tolcapone and entacapone as adjunctive therapy in Parkinson’s disease. CNS Neurosci Ther. 2008;14:83–93.PubMedCrossRef Lees AJ. Evidence-based efficacy comparison of tolcapone and entacapone as adjunctive therapy in Parkinson’s disease. CNS Neurosci Ther. 2008;14:83–93.PubMedCrossRef
127.
go back to reference Rascol O, Lozano A, Stern M, Poewe W. Milestones in Parkinson’s disease therapeutics. Mov Disord. 2011;26(6):1072–82.PubMedCrossRef Rascol O, Lozano A, Stern M, Poewe W. Milestones in Parkinson’s disease therapeutics. Mov Disord. 2011;26(6):1072–82.PubMedCrossRef
128.
go back to reference El Yacoubi M, Ledent C, Parmentier M, Ongini E, Costentin J, Vaugeois JM. In vivo labelling of the adenosine A2A receptor in mouse brain using the selective antagonist [3H]SCH 58261. Eur J Neurosci. 2001;14(9):1567–70.PubMedCrossRef El Yacoubi M, Ledent C, Parmentier M, Ongini E, Costentin J, Vaugeois JM. In vivo labelling of the adenosine A2A receptor in mouse brain using the selective antagonist [3H]SCH 58261. Eur J Neurosci. 2001;14(9):1567–70.PubMedCrossRef
Metadata
Title
Adenosine A2A Receptor Antagonists in Parkinson’s Disease: Progress in Clinical Trials from the Newly Approved Istradefylline to Drugs in Early Development and Those Already Discontinued
Author
Annalisa Pinna
Publication date
01-05-2014
Publisher
Springer International Publishing
Published in
CNS Drugs / Issue 5/2014
Print ISSN: 1172-7047
Electronic ISSN: 1179-1934
DOI
https://doi.org/10.1007/s40263-014-0161-7

Other articles of this Issue 5/2014

CNS Drugs 5/2014 Go to the issue