Abstract
The acridine-based, potential Alzheimer's disease therapeutic agents, tacrine and velnacrine, were incubated with rat or gerbil neocortical synaptosomal membranes. Electron paramagnetic resonance employing a protein-specific spin label was used to monitor this interaction. Analogous to their effects in erythrocyte membranes [Butterfield and Rangachari (1992) Biochem. Biophys. Res. Commun. 185: 596-603], in the present studies both agents decreased segmental motion of spin labeled synaptosomal membrane proteins, consistent with increased cytoskeletal protein-protein interactions (0.001<P<0.005), and tacrine was more potent than velnacrine. Thse results are discussed with possible relevance to molecular actions of the agents and molecular alterations in Alzheimer's disease.
| Original language | English |
|---|---|
| Pages (from-to) | 989-994 |
| Number of pages | 6 |
| Journal | Neurochemical Research |
| Volume | 18 |
| Issue number | 9 |
| DOIs | |
| State | Published - Sep 1993 |
Keywords
- Alzheimer's disease
- Synaptosomal membranes
- cytoskeletal protein-protein interactions
- tacrine
- velnacrine
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