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Histamine H3 receptor as a potential target for cognitive symptoms in neuropsychiatric diseases.
- Source :
-
Behavioural brain research [Behav Brain Res] 2016 Oct 01; Vol. 312, pp. 415-30. Date of Electronic Publication: 2016 Jun 27. - Publication Year :
- 2016
-
Abstract
- The potential contributions of the brain histaminergic system in neurodegenerative diseases, and the possiblity of histamine-targeting treatments is attracting considerable interests. The histamine H3 receptor (H3R) is expressed mainly in the central nervous system, and is, consequently, an attractive pharmacological target. Although recently described clinical trials have been disappointing in attention deficit hyperactivity disorder (ADHD) and schizophrenia (SCH), numerous H3R antagonists, including pitolisant, demonstrate potential in the treatment of narcolepsy, excessive daytime sleepiness associated with cognitive impairment, epilepsy, and Alzheimer's disease (AD). This review focuses on the recent preclinical as well as clinical results that support the relevance of H3R antagonists for the treatment of cognitive symptoms in neuropsychiatric diseases, namely AD, epilepsy and SCH. The review summarizes the role of histaminergic neurotransmission with focus on these brain disorders, as well as the effects of numerous H3R antagonists on animal models and humans.<br /> (Copyright © 2016 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Brain physiopathology
Clinical Trials as Topic
Disease Models, Animal
Histamine Antagonists administration & dosage
Humans
Memory drug effects
Receptors, Histamine physiology
Alzheimer Disease drug therapy
Brain drug effects
Epilepsy drug therapy
Histamine Antagonists therapeutic use
Receptors, Histamine H3 physiology
Schizophrenia drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1872-7549
- Volume :
- 312
- Database :
- MEDLINE
- Journal :
- Behavioural brain research
- Publication Type :
- Academic Journal
- Accession number :
- 27363923
- Full Text :
- https://doi.org/10.1016/j.bbr.2016.06.051