6533b871fe1ef96bd12d0d56

RESEARCH PRODUCT

Galantamine is an allosterically potentiating ligand of the human α4/β2 nAChR

Alfred MaelickeAlfred MaelickeMarion ZerlinMarek SamochockiWalter LuytenEdson X. AlbuquerqueP. J. Groot KormelinkRuth Jostock

subject

Rivastigminemedicine.medical_specialtyChemistryGeneral MedicinePharmacologyAcetylcholinesterasechemistry.chemical_compoundEndocrinologyNicotinic agonistNeurologyMechanism of actionTacrineInternal medicinemental disordersmedicineGalantamineNeurology (clinical)Metrifonatemedicine.symptomMode of actionmedicine.drug

description

Galantamine (ReminyI ) is a novel drug treatment for mild to moderate Alzheimer's disease (AD). Originally established as a reversible inhibitor of the acetylcholine-degrading enzyme acetylcholinesterase (AChE), galantamine also acts as an allosterically potentiating ligand (APL) on nicotinic acetylcholine receptors (nAChR). Having previously established this second mode of action on nAChRs from murine brain, we demonstrate here the same action of galantamine on the most abundant nAChR in the human brain, the α4/β2 subtype. This nAChR-sensitizing action is not a common property of all, or most, AChE inhibitors, as is shown by the absence of this effect for other therapeutically applied AChE inhibitors including tacrine, metrifonate, rivastigmine and donepezil. The possible benefits for therapy of AD of an APL action on nicotinic receptors is discussed.

https://doi.org/10.1034/j.1600-0404.2000.00310.x