Pełna treść
2/2024
vol. 40
Artykuł przeglądowy
Nowe grupy leków neuroleptycznych – inhibitory fosfodiesterazy 10A. Przegląd narracyjny
- Geriatrics Clinic and Polyclinic, National Geriatrics, Rheumatology and Rehabilitation Institute, Poland; Klinika i Poliklinika Geriatrii, Narodowy Instytut Geriatrii, Reumatologii i Rehabilitacji im. prof. dr hab. med. Eleonory Reicher, Warszawa, Polska
- Department Clinical Pharmacology, Medical University of Lodz, Poland; Zakład Farmakologii Klinicznej, Uniwersytet Medyczny w Łodzi, Polska
Farmakoterapia w Psychiatrii i Neurologii 2024, 40 (2), 119–126
Data publikacji online: 2025/03/31
Plik artykułu
- Akinola PS, Tardif I, Leclerc J. Antipsychotic-Induced Metabolic Syndrome: A Review. Metab Syndr Relat Disord. 2023; 21: 294-305.
- Amin HS, Parikh PK, Ghate MD. Medicinal chemistry strategies for the development of phosphodiesterase 10A (PDE10A) inhibitors – An update of recent progress. Eur J Med Chem. 2021; 214: 113155.
- Amsallem E, Kasparian C, Haddour G, Boissel JP, Nony P. Phosphodiesterase III inhibitors for heart failure. Cochrane Database Syst Rev. 2005; 2005 (1): CD002230.
- Arakawa K, Maehara S, Yuge N, Ishikawa M, Miyazaki Y. Pharmacological characterization of a novel potent, selective, and orally active phosphodiesterase 10A inhibitor, PDM-042 [(E)-4-(2-(2-(5,8-dimethyl-[1,2,4]triazolo[1,5-a]pyrazin-2-yl)vinyl)-6-(pyrrolidin-1-yl)pyrimidin-4-yl)morpholine] in rats: potential for the treatment of schizophrenia. Pharmacol Res Perspect. 2016; 4 (4): e00241.
- Beach SR, Celano CM, Noseworthy PA, Januzzi JL, Huffman JC. QTc prolongation, torsades de pointes, and psychotropic medications. Psychosomatics. 2013; 54: 1-13.
- Carli M, Kolachalam S, Longoni B, Pintaudi A, Baldini M et al. Atypical Antipsychotics and Metabolic Syndrome: From Molecular Mechanisms to Clinical Differences. Pharmaceuticals (Basel). 2021; 14: 238.
- Chappie TA, Helal CJ, Hou X. Current landscape of phosphodiesterase 10A (PDE10A) inhibition. J Med Chem. 2012; 55: 7299-331.
- Chappie TA, Humphrey JM, Allen MP, Estep KG, Fox CB, et al. Discovery of a series of 6,7-dimethoxy-4-pyrrolidylquinazoline PDE10A inhibitors. J Med Chem. 2007; 50: 182-5.
- Coskran TM, Morton D, Menniti FS, Adamowicz WO, Kleiman RJ, et al. Immunohistochemical localization of phosphodiesterase 10A in multiple mammalian species. J Histochem Cytochem. 2006 ;54: 1205-13.
- Charych EI, Jiang L-X, Lo F, Sullivan K, Brandon NJ. Interplay of Palmitoylation and Phosphorylation in the Trafficking and Localization of Phosphodiesterase 10A: Implications for the Treatment of Schizophrenia. J Neurosci 2010; 30: 9027–37.
- Dias MF, Nogueira YJA, Romano-Silva MA, Marques de Miranda D. Effects of antipsychotics on the gastrointestinal microbiota: A systematic review. Psychiatry Res. 2024; 336: 115914.
- Francis SH, Sekhar KR, Ke H, Corbin JD. Inhibition of cyclic nucleotide phosphodiesterases by methylxanthines and related compounds. Handb Exp Pharmacol. 2011; (200): 93-133.
- Fujishige K, Kotera J, Michibata H, Yuasa K, Takebayashi SI, et al. (1999). Cloning and characterization of a novel human phosphodiesterase that hydrolyzes both cAMP and cGMP (PDE10A). J Biol Chem 1999; 274: 18438-45.
- García AM, Redondo M, Martinez A, Gil C. Phosphodiesterase 10 inhibitors: new disease modifying drugs for Parkinson’s disease? Curr Med Chem. 2014; 21(10): 1171-87.
- Gomes DA, Joubert AM, Visagie MH. The Biological Relevance of Papaverine in Cancer Cells. Cells. 2022; 11: 3385.
- Grauer SM, Pulito VL, Navarra RL, Kelly MP, Kelley C, et al. Phosphodiesterase 10A inhibitor activity in preclinical models of the positive, cognitive, and negative symptoms of schizophrenia. J Pharmacol Exp Ther. 2009; 331: 574-90.
- Harada A, Suzuki K, Kamiguchi N, Miyamoto M, Tohyama K. Characterization of binding and inhibitory properties of TAK-063, a novel phosphodiesterase 10A inhibitor. PLoS One. 2015; 10: e0122197.
- Hjorthøj C, Stürup AE, McGrath JJ, Nordentoft M. Years of potential life lost and life expectancy in schizophrenia: a systematic review and meta-analysis. Lancet Psychiatry. 2017; 4: 295-301.
- Kaczor AA, Silva AG, Loza MI, Kolb P, Castro M, et al. Structure-Based Virtual Screening for Dopamine D2 Receptor Ligands as Potential Antipsychotics. ChemMedChem. 2016; 11: 718-29.
- Kantrowitz JT. Trace Amine-Associated Receptor 1 as a Target for the Development of New Antipsychotics: Current Status of Research and Future Directions. CNS Drugs. 2021; 35 (11): 1153-61.
- Kotera J, Sasaki T, Kobayashi T, Fujishige K, Yamashita Y, Omori K. Subcellular localization of cyclic nucleotide phosphodiesterase type 10A variants, and alteration of the localization by cAMP-dependent protein kinase-dependent phosphorylation. J Biol Chem. 2004; 279: 4366-75.
- Lakics V, Karran EH, Boess FG. Quantitative comparison of phosphodiesterase mRNA distribution in human brain and peripheral tissues. Neuropharmacology. 2010; 59 (6): 367-74.
- Lipworth BJ. Phosphodiesterase-4 inhibitors for asthma and chronic obstructive pulmonary disease. Lancet. 2005; 365: 167-75.
- Loughney K, Snyder PB, Uher L, Rosman GJ, Ferguson K, et al. (1999). Isolation and characterization of PDE10A, a novel human 3’, 5’-cyclic nucleotide phosphodiesterase. Gene 1999; 234: 109-17.
- MacMullen CM, Vick K, Pacifico R, Fallahi-Sichani M, Davis RL. Novel, primate-specific PDE10A isoform highlights gene expression complexity in human striatum with implications on the molecular pathology of bipolar disorder. Transl Psychiatry 2016; 6: e742.
- Martin C, Burgel PR, Roche N. Inhaled Dual Phosphodiesterase 3/4 Inhibitors for the Treatment of Patients with COPD: A Short Review. Int J Chron Obstruct Pulmon Dis. 2021; 16: 2363-2373.
- Matloka M, Janowska S, Pankiewicz P, Kokhanovska S, Kos T, et al. A PDE10A inhibitor CPL500036 is a novel agent modulating striatal function devoid of most neuroleptic side-effects. Front Pharmacol. 2022; 13: 999685.
- Megens AA, Hendrickx HM, Hens KA, Fonteyn I, Langlois X, et al. Pharmacology of JNJ-42314415, a centrally active phosphodiesterase 10A (PDE10A) inhibitor: a comparison of PDE10A inhibitors with D2 receptor blockers as potential antipsychotic drugs. J Pharmacol Exp Ther. 2014; 349: 138-54.
- Movsesian M, Stehlik J, Vandeput F, Bristow MR. Phosphodiesterase inhibition in heart failure. Heart Fail Rev. 2009; 14: 255-63.
- Mukai Y, Lupinacci R, Marder S, et al. Effects of PDE10A inhibitor MK-8189 in people with an acute episode of schizophrenia: A randomized proof-of-concept clinical trial. Schizophr Res. 2024; 270: 37-43.
- Paronetto MP, Crescioli C. Rethinking of phosphodiesterase 5 inhibition: the old, the new and the perspective in human health. Front Endocrinol (Lausanne). 2024; 15: 1461642.
- Polito M, Guiot E, Gangarossa G, Longueville S, Doulazmi M, et al. Selective Effects of PDE10A Inhibitors on Striatopallidal Neurons Require Phosphatase Inhibition by DARPP-32. eNeuro. 2015; 2: ENEURO.0060-15.2015
- Seeger TF, Bartlett B, Coskran TM, Culp JS, James LC, et al. Immunohistochemical localization of PDE10A in the rat brain. Brain Res. 2003; 985: 113-26.
- Schmidt CJ, Chapin DS, Cianfrogna J, Corman ML, Hajos M, et al. Preclinical characterization of selective phosphodiesterase 10A inhibitors: a new therapeutic approach to the treatment of schizophrenia. J Pharmacol Exp Ther. 2008; 325: 681-90.
- Schudt C, Hatzelmann A, Beume R, Tenor H. Phosphodiesterase inhibitors: history of pharmacology. Handb Exp Pharmacol. 2011; (204): 1-46.
- Smith SM, Uslaner JM, Cox CD, Huszar SL, Cannon CE, et al. The novel phosphodiesterase 10A inhibitor THPP-1 has antipsychotic-like effects in rat and improves cognition in rat and rhesus monkey. Neuropharmacology. 2013; 64: 215-23.
- Smith S, Toolan D, Kandebo M, et al. Preclinical Evaluation of MK-8189: A Novel Phosphodiesterase 10A Inhibitor for the Treatment of Schizophrenia. J Pharmacol Exp Ther. 2024. doi:10.1124/jpet.124.002347.
- Soderling SH, Bayuga SJ, Beavo JA. Isolation and characterization of a dual-substrate phosphodiesterase gene family: PDE10A. Proc Natl Acad Sci 1999; 96: 7071–76.
- Stahl SM. Stahl’s essencial psychopharmacology. Neuroscientific basis and practical applications. Oxford University Press, Cambridge 2021.
- Stangherlin A, Zaccolo M. Phosphodiesterases and subcellular compartmentalized cAMP signaling in the cardiovascular system. Am J Physiol Heart Circ Physiol. 2012; 302: H379-90.
- Suzuki K, Kimura H. TAK-063, a novel PDE10A inhibitor with balanced activation of direct and indirect pathways, provides a unique opportunity for the treatment of schizophrenia. CNS Neurosci Ther. 2018; 24 (7): 604-614.
- Świerczek A, Jankowska A, Chłoń-Rzepa G, Pawłowski M, Wyska E. Advances in the Discovery of PDE10A Inhibitors for CNS-Related Disorders. Part 2: Focus on Schizophrenia. Curr Drug Targets. 2019; 20: 1652-69.
- Uliana DL, Martinez A, Grace AA. THPP-1 PDE10A inhibitor reverses the cognitive deficits and hyperdopaminergic state in a neurodevelopment model of schizophrenia. Schizophr Res. 2024; 274: 315-326.
- Wojtasik-Bakalarz K, Siwek M. New antipsychotic medication. Pharmacotherapy in Psychiatry and Neurology/Farmakoterapia w Psychiatrii i Neurologii 2023, 39 (1), 19-38.
- Yin J, Chen KM, Clark MJ, Hijazi M, Kumari P, et al. Structure of a D2 dopamine receptor-G-protein complex in a lipid membrane. Nature. 2020; 584: 125-29.
- Zagorska A, Partyka A, Bucki A, Gawalska A, Czopek A, et al. Phosphodiesterase 10 Inhibitors – Novel Perspectives for Psychiatric and Neurodegenerative Drug Discovery. Curr Med Chem. 2018; 25: 3455-81.
- Zhu J, Mix E, Winblad B. The antidepressant and antiinflammatory effects of rolipram in the central nervous system. CNS Drug Rev. 2001; 7: 387-98.
