Therapeutic Potential of Selectively Targeting the alpha2C-Adrenoceptor in Cognition, Depression, and Schizophrenia-New Developments and Future Perspective.

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Citation

Uys MM, Shahid M, Harvey BH

Therapeutic Potential of Selectively Targeting the alpha2C-Adrenoceptor in Cognition, Depression, and Schizophrenia-New Developments and Future Perspective.

Front Psychiatry. 2017 Aug 14;8:144. doi: 10.3389/fpsyt.2017.00144. eCollection 2017.

PubMed ID
28855875 [ View in PubMed
]
Abstract

alpha2A- and alpha2C-adrenoceptors (ARs) are the primary alpha2-AR subtypes involved in central nervous system (CNS) function. These receptors are implicated in the pathophysiology of psychiatric illness, particularly those associated with affective, psychotic, and cognitive symptoms. Indeed, non-selective alpha2-AR blockade is proposed to contribute toward antidepressant (e.g., mirtazapine) and atypical antipsychotic (e.g., clozapine) drug action. Both alpha2C- and alpha2A-AR share autoreceptor functions to exert negative feedback control on noradrenaline (NA) release, with alpha2C-AR heteroreceptors regulating non-noradrenergic transmission (e.g., serotonin, dopamine). While the alpha2A-AR is widely distributed throughout the CNS, alpha2C-AR expression is more restricted, suggesting the possibility of significant differences in how these two receptor subtypes modulate regional neurotransmission. However, the alpha2C-AR plays a more prominent role during states of low endogenous NA activity, while the alpha2A-AR is relatively more engaged during states of high noradrenergic tone. Although augmentation of conventional antidepressant and antipsychotic therapy with non-selective alpha2-AR antagonists may improve therapeutic outcome, animal studies report distinct yet often opposing roles for the alpha2A- and alpha2C-ARs on behavioral markers of mood and cognition, implying that non-selective alpha2-AR antagonism may compromise therapeutic utility both in terms of efficacy and side-effect liability. Recently, several highly selective alpha2C-AR antagonists have been identified that have allowed deeper investigation into the function and utility of the alpha2C-AR. ORM-13070 is a useful positron emission tomography ligand, ORM-10921 has demonstrated antipsychotic, antidepressant, and pro-cognitive actions in animals, while ORM-12741 is in clinical development for the treatment of cognitive dysfunction and neuropsychiatric symptoms in Alzheimer's disease. This review will emphasize the importance and relevance of the alpha2C-AR as a neuropsychiatric drug target in major depression, schizophrenia, and associated cognitive deficits. In addition, we will present new prospects and future directions of investigation.

DrugBank Data that Cites this Article

Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
QuetiapineAlpha-2C adrenergic receptorProteinHumans
Unknown
Antagonist
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