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Orexin receptors: possible therapeutic targets for psychiatric disorders.

作者信息

Chaki Shigeyuki

机构信息

Taisho Pharmaceutical Co., Ltd, Toshima-Ku, Tokyo, 170-8633, Japan.

Chiba University Center for Forensic Mental Health, Chiba, 260-8670, Japan.

出版信息

Psychopharmacology (Berl). 2025 Mar 28. doi: 10.1007/s00213-025-06767-1.


DOI:10.1007/s00213-025-06767-1
PMID:40153060
Abstract

RATIONALE: Orexins, comprising orexin-A and orexin-B, are neuropeptides with extensive projections throughout the central nervous system. They are implicated in a variety of physiological processes through their receptors, orexin type 1 (OX) and orexin type 2 (OX) receptors. Among the physiological functions of orexins, their role in sleep/wake regulation has garnered significant attention. Consequently, three orexin receptor antagonists that block both OX and OX receptors (dual orexin receptor antagonist; DORA) are available on the market for the treatment of insomnia. Additionally, another DORA, vornorexant, has been submitted for approval. OBJECTIVE: Beyond sleep disorders, the orexin system is deeply implicated in the pathophysiology of several psychiatric disorders, including depression, anxiety, and substance use disorders. RESULTS: Accumulating evidence indicates that orexin receptor antagonists improve behavioral abnormalities that mimic certain psychiatric disorders in animal models and are effective in treating these disorders or their symptoms in humans. Moreover, orexin receptor antagonists are expected not only to alleviate core symptoms of psychiatric disorders but also to improve sleep disturbances, which are often comorbid with these conditions. CONCLUSION: Drug discovery and development targeting orexin receptors should provide novel therapeutic options for the treatment of psychiatric disorders.

摘要

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本文引用的文献

[1]
Treatment effect and safety of seltorexant as monotherapy for patients with major depressive disorder: a randomized, placebo-controlled clinical trial.

Mol Psychiatry. 2025-6

[2]
Pivotal role of orexin signaling in the posterior paraventricular nucleus of the thalamus during the stress-induced reinstatement of oxycodone-seeking behavior.

J Psychopharmacol. 2024-7

[3]
Plasma Orexin Levels Related to Altered Brain Activity During Abstinence in Patients with Alcohol Dependence.

Psychiatry Clin Psychopharmacol. 2021-9-1

[4]
Higher orexin-A levels are associated with treatment response to clozapine in patients with schizophrenia: A cross-sectional study.

J Psychopharmacol. 2024-3

[5]
Improvement of autistic-like behaviors in adult rats prenatally exposed to valproic acid through early suppression of orexin receptor.

Ann Med Surg (Lond). 2023-11-22

[6]
Suvorexant improves mitochondrial dynamics with the regulation of orexinergic and mTOR activation in rats exhibiting PTSD-like symptoms.

J Affect Disord. 2024-4-1

[7]
Pharmacokinetics, pharmacodynamics and safety profile of the dual orexin receptor antagonist vornorexant/TS-142 in healthy Japanese participants following single/multiple dosing: Randomized, double-blind, placebo-controlled phase-1 studies.

Basic Clin Pharmacol Toxicol. 2023-11

[8]
Use of drug purchase tasks in medications development research: orexin system regulation of cocaine and drug demand.

Behav Pharmacol. 2023-8-1

[9]
Dual orexin/hypocretin receptor antagonism attenuates NMDA receptor hypofunction-induced attentional impairments in a rat model of schizophrenia.

Behav Brain Res. 2023-7-26

[10]
Evaluation of the delirium preventive effect of dual orexin receptor antagonist (DORA) in critically ill adult patients requiring ventilation with tracheal intubation at an advanced emergency center: A single-center, retrospective, observational study.

Gen Hosp Psychiatry. 2023

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