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G-protein coupled receptors as therapeutic targets for neurodegenerative and cerebrovascular diseases.
- Source :
-
Neurochemistry international [Neurochem Int] 2016 Dec; Vol. 101, pp. 1-14. Date of Electronic Publication: 2016 Sep 09. - Publication Year :
- 2016
-
Abstract
- Neurodegenerative and cerebrovascular diseases are frequent in elderly populations and comprise primarily of dementia (mainly Alzheimer's disease) Parkinson's disease and stroke. These neurological disorders (NDs) occur as a result of neurodegenerative processes and represent one of the most frequent causes of death and disability worldwide with a significant clinical and socio-economic impact. Although NDs have been characterized for many years, the exact molecular mechanisms that govern these pathologies or why they target specific individuals and specific neuronal populations remain unclear. As research progresses, many similarities appear which relate these diseases to one another on a subcellular level. Discovering these similarities offers hope for therapeutic advances that could ameliorate the conditions of many diseases simultaneously. G-protein coupled receptors (GPCRs) are the most abundant receptor type in the central nervous system and are linked to complex downstream pathways, manipulation of which may have therapeutic application in many NDs. This review will highlight the potential use of neurotransmitter GPCRs as emerging therapeutic targets for neurodegenerative and cerebrovascular diseases.<br /> (Copyright © 2016 Elsevier Ltd. All rights reserved.)
- Subjects :
- Alzheimer Disease drug therapy
Alzheimer Disease metabolism
Animals
Cerebrovascular Disorders drug therapy
Humans
Neurodegenerative Diseases drug therapy
Parkinson Disease drug therapy
Parkinson Disease metabolism
Receptors, G-Protein-Coupled therapeutic use
Cerebrovascular Disorders metabolism
Neurodegenerative Diseases metabolism
Neurotransmitter Agents pharmacology
Receptors, G-Protein-Coupled metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1872-9754
- Volume :
- 101
- Database :
- MEDLINE
- Journal :
- Neurochemistry international
- Publication Type :
- Academic Journal
- Accession number :
- 27620813
- Full Text :
- https://doi.org/10.1016/j.neuint.2016.09.005