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Modulation of nicotinic receptor activity in the central nervous system: a novel approach to the treatment of Alzheimer disease.
Albuquerque EX, Santos MD, Alkondon M, Pereira EF, Maelicke A
Department of Pharmacology and Experimental Therapeutics,
University of
Maryland School of Medicine,
Baltimore MD 21201, USA.
ealbuque@umaryland.edu
Alzheimer Dis Assoc Disord 2001 Aug;15 Suppl 1:S19-25
ABSTRACT
Impaired cholinergic function in the central
nervous system is an early feature of Alzheimer disease (AD). Currently,
cholinergic deficit is usually corrected by increasing the amount of
acetylcholine in the synapse by inhibiting acetylcholinesterase (AChE).
One of the most consistent cholinergic deficits in AD is the reduced
expression of nicotinic acetylcholine receptors (nAChR) in the brain.
Since these receptors are essential for learning and memory, restoring
nicotinic cholinergic function is a promising approach to treating AD.
Allosteric modulation of nAChR is a novel approach, which circumvents
development of tolerance through long-term use of conventional nicotinic
agonists. Allosteric modulators interact with receptor-binding sites
distinct from those capable of recognizing the natural agonist. Positive
allosteric modulation of nAChR activity has no effect on conductance of
single channels; instead, by facilitating channel opening, it
potentiates responses evoked by the interaction of the natural agonist
with presynaptic and postsynaptic nAChR. Allosteric modulation of nAChR
activity could therefore potentially produce a significant benefit in
AD. One such allosteric modulator is galantamine.
In addition to
increasing nAChR activity, galantamine also inhibits AChE. This novel,
dual mechanism of action distinguishes galantamine
from many other AChE
inhibitors. Galantamine has been shown to improve cognitive and daily
function for at least 6 months in placebo-controlled trials, and to
maintain these functions at baseline levels for at least 12 months in a
6-month open-label extension study. Galantamine has positive effects on
nAChR expression, which are likely to contribute to its sustained
efficacy in the treatment of AD patients.
Vinpocetine | Picamilon
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