Evidence on the New Drug Lumateperone (ITI-007) for Psychiatric and Neurological Disorders.
Alzheimer Disease
/ drug therapy
Bipolar Disorder
/ drug therapy
Dementia
/ drug therapy
Dopamine D2 Receptor Antagonists
/ pharmacology
Drug Partial Agonism
Heterocyclic Compounds, 4 or More Rings
/ pharmacology
Humans
Receptor, Serotonin, 5-HT2A
/ drug effects
Receptors, Dopamine D1
/ drug effects
Receptors, Dopamine D2
/ drug effects
Schizophrenia
/ drug therapy
Serotonin 5-HT2 Receptor Antagonists
/ pharmacology
Serotonin Plasma Membrane Transport Proteins
/ drug effects
Sleep Wake Disorders
/ drug therapy
Alzheimer`s disease
ITI-007
Lumateperone
novel antipsychotics
personalized medicine
schizophrenia
Journal
CNS & neurological disorders drug targets
ISSN: 1996-3181
Titre abrégé: CNS Neurol Disord Drug Targets
Pays: United Arab Emirates
ID NLM: 101269155
Informations de publication
Date de publication:
2020
2020
Historique:
received:
28
12
2019
revised:
04
04
2020
accepted:
12
04
2020
pubmed:
2
6
2020
medline:
7
9
2021
entrez:
2
6
2020
Statut:
ppublish
Résumé
Lumateperone (ITI-007) is a tosylate salt with binding affinities to receptors implicated in the therapeutic actions of antipsychotic medications, including the serotonin 5HT2A receptors, dopamine D2 and D1 receptors and the serotonin transporter. It has a unique mechanism of action because it simultaneously modulates serotonin, dopamine, and glutamate neurotransmission, implicated in serious mental illness. It can be considered a multi-target-directed ligand and a multifunctional modulator of serotoninergic system with possible precognitive, antipsychotic, antidepressant and anxiolytic properties. Lumateperone has been investigated as a novel agent for the treatment of schizophrenia, but it represents a new potential option for other psychiatric and neurological diseases, such as behavioural symptoms of dementia or Alzheimer's disease, sleep disturbances, bipolar depression. Besides, it has demonstrated a favourable safety profile without significant extrapyramidal side effects, hyperprolactinemia or changes in cardiometabolic or endocrine factors versus placebo. Additional studies are warranted to confirm and examine the benefit of lumateperone and possible therapeutic targets. This paper is a comprehensive and thorough summary of the most important findings and potential future role of this particular compound in personalized treatments.
Identifiants
pubmed: 32479249
pii: CNSNDDT-EPUB-107020
doi: 10.2174/1871527319666200601145653
doi:
Substances chimiques
Dopamine D2 Receptor Antagonists
0
Heterocyclic Compounds, 4 or More Rings
0
Receptor, Serotonin, 5-HT2A
0
Receptors, Dopamine D1
0
Receptors, Dopamine D2
0
Serotonin 5-HT2 Receptor Antagonists
0
Serotonin Plasma Membrane Transport Proteins
0
lumateperone
70BSQ12069
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
243-247Informations de copyright
Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.