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Prolyl oligopeptidase: a potential target for the treatment of cognitive disorders.
- Source :
-
Drug news & perspectives [Drug News Perspect] 2007 Jun; Vol. 20 (5), pp. 293-305. - Publication Year :
- 2007
-
Abstract
- Prolyl oligopeptidase (POP) is a ubiquitous post-proline cleaving enzyme that is highly expressed in brain. Current knowledge about the biochemical features of POP and the pharmacological action of its specific inhibitors has indicated that POP participates in several aspects of the central nervous system (CNS), including learning, memory and mood. Furthermore, a role has been suggested for POP in pathological processes such as eating and mood disorders, hypertension and cell-cycle disturbances, in addition to its proposed connection with the neurodegenerative processes which occur in Alzheimer's, Huntington's and Parkinson's diseases. The milestones responsible for the accelerated development of POP inhibitors include the discovery that these compounds reverse memory loss in animal models of drug- or lesion-induced amnesia and the observation that the expression of POP correlates with age. Today, several POP inhibitors have already been evaluated in preclinical trials as potential drugs for the treatment of natural memory deficits that occur with aging or the pathological memory loss characteristic of Alzheimer's disease. Thus, the results that are emerging from basic research on POP function will facilitate the fine-tuning of more efficient drugs to target this protease.<br /> ((c) 2007 Prous Science. All rights reserved.)
- Subjects :
- Alzheimer Disease drug therapy
Alzheimer Disease enzymology
Animals
Cognition Disorders enzymology
Enzyme Inhibitors chemistry
Humans
Molecular Structure
Phosphorylation drug effects
Prolyl Oligopeptidases
Cognition Disorders drug therapy
Enzyme Inhibitors therapeutic use
Serine Endopeptidases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0214-0934
- Volume :
- 20
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- Drug news & perspectives
- Publication Type :
- Academic Journal
- Accession number :
- 17878957
- Full Text :
- https://doi.org/10.1358/dnp.2007.20.5.1120216