Abstract |
We have reported that the antidementia drug tetrahydroaminoacridine (THA; 30 microM) is neuroprotective and neurotrophic and selectively increases m3-muscarinic acetylcholine receptor (mAChR) mRNA levels in differentiating cerebellar granule cells. Here, we examined whether novel prolyl endopeptidase inhibitor ONO-1603, a potential antidementia drug, induces similar effects in these cerebellar neurons. Supplement of ONO-1603 (0.03 microM) to cultures grown in 15 mM KCl-containing media was found to markedly promote neuronal survival and neurite outgrowth and enhance [3H] N-methylscopolamine binding to mAChRs. Moreover, ONO-1603 increased the level of m3-mAChR mRNA and stimulated mAChR-mediated phosphoinositide turnover. The common actions of ONO-1603 and THA suggest that these properties could be related to their putative antidementia activities and that this model system may be used to screen for drugs effective in the treatment for Alzheimer's disease.
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Authors | N Katsube, K Sunaga, D M Chuang, R Ishitani |
Journal | Neuroscience letters
(Neurosci Lett)
Vol. 214
Issue 2-3
Pg. 151-4
(Aug 23 1996)
ISSN: 0304-3940 [Print] Ireland |
PMID | 8878106
(Publication Type: Journal Article)
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Chemical References |
- Cholinesterase Inhibitors
- Muscarinic Agonists
- Neuroprotective Agents
- ONO 1603
- Phosphatidylinositols
- Pyrrolidines
- RNA, Messenger
- Receptors, Muscarinic
- Serine Proteinase Inhibitors
- Physostigmine
- Serine Endopeptidases
- Prolyl Oligopeptidases
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Topics |
- Animals
- Brain Edema
(drug therapy)
- Cell Differentiation
(drug effects)
- Cell Survival
(drug effects)
- Cells, Cultured
- Cerebellum
(cytology, drug effects)
- Cholinesterase Inhibitors
(pharmacology)
- Muscarinic Agonists
(pharmacology)
- Neurons
(drug effects)
- Neuroprotective Agents
(pharmacology)
- Phosphatidylinositols
(metabolism)
- Physostigmine
(pharmacology)
- Prolyl Oligopeptidases
- Pyrrolidines
(pharmacology)
- RNA, Messenger
(biosynthesis)
- Rats
- Rats, Sprague-Dawley
- Receptors, Muscarinic
(biosynthesis, metabolism)
- Serine Endopeptidases
(metabolism)
- Serine Proteinase Inhibitors
(pharmacology)
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