Abstract
β-Amyloid(1-42) peptide (βAP) was injected into the right nucleus basalis magnocellularis (nbm) of rats. After a 14-day survival time, the acetylcholinesterase and choline acetyltransferase activities and the number of muscarinic receptors were found biochemically to be significantly reduced in the ipsilateral frontal cortices. Confirmation of these data with silver staining also revealed degeneration of the projective fibers of the nbm to the frontal cortex. These results demonstrate the cholinotoxicity of βAP in an in vivo animal model.
| Original language | English |
|---|---|
| Pages (from-to) | 71-75 |
| Number of pages | 5 |
| Journal | Brain Research |
| Volume | 695 |
| Publication status | Published - 1995 |
Keywords
- Cholinotoxicity
- Cholinergic system
- Frontal cortex
- Nucleus basalis magnocellularis
- β-Amyloid(1-42) peptide
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