Abstract
Heptylene-linked bis-(9-amino-1,2,3,4-tetrahydroacridine) (bis(7)- tacrine) is a potential palliative therapeutic agent for Alzheimer's disease (AD), on the basis of its superior acetylcholinesterase (ACHE) inhibition and memory-enhancing potency relative to tacrine. In this study we report that bis(7)-tacrine exhibits a potentially complementary central nervous system action, antagonism of GABA(A) receptor function. Bis(7)tacrine displaced [3H]muscimol from rat brain membranes with an apparent K(i) of 6.0 μM; tacrine and physostigmine were shown to be 18 and 170 times less potent, respectively. In whole-cell patch-clamp recordings, bis(7)-tacrine inhibited GABA-induced inward current with an IC50 of 5.6 μM, and shifted the GABA concentration-response curve to the right in a parallel manner. These results suggest that bis(7)-tacrine is a competitive antagonist of the GABA(A) receptor.
| Original language | English |
|---|---|
| Pages (from-to) | 795-800 |
| Number of pages | 6 |
| Journal | NeuroReport |
| Volume | 10 |
| Issue number | 4 |
| Publication status | Published - 17 Mar 1999 |
Keywords
- Acetylcholinesterase
- Bis(7)-tacrine
- Cholinesterase inhibitor
- GABA(A) receptor
- Muscimol
- Physostigmine
- Tacrine
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