Please use this identifier to cite or link to this item: https://repositorio.uca.edu.ar/handle/123456789/10847
Título : Lovastatin di erentially regulates 7 and 4 neuronal nicotinic acetylcholine receptor levels in rat hippocampal neurons
Autor : Borroni, María Virginia 
Kamerbeek, Constanza B. 
Pediconi, María F. 
Barrantes, Francisco José 
Palabras clave : MEDICINACOLESTEROLRECEPTORESENFERMEDAD DE ALZHEIMERNEURONASHIPOCAMPO
Fecha de publicación : 2020
Editorial : MDPI
Cita : Borroni, M. V., Kamerbeek; C. B., Pediconi, M. F., Barrantes, F. J. Lovastatin di erentially regulates 7 and 4 neuronal nicotinic acetylcholine receptor levels in rat hippocampal neurons [en línea]. Molecules. 2020, 25 (4838). Disponible en: https://repositorio.uca.edu.ar/handle/123456789/10847
Resumen : Abstract: Neuronal 7 and 4 2 are the predominant nicotinic acetylcholine receptor (nAChR) subtypes found in the brain, particularly in the hippocampus. The e ects of lovastatin, an inhibitor of cholesterol biosynthesis, on these two nAChRs endogenously expressed in rat hippocampal neuronal cells were evaluated in the 0.01–1 M range. Chronic (14 days) lovastatin treatment augmented cell-surface levels of 7 and 4 nAChRs, as measured by fluorescence microscopy and radioactive ligand binding assays. This was accompanied in both cases by an increase in total protein receptor levels as determined byWestern blots. At low lovastatin concentrations (10–100 nM), the increase in 4 nAChR in neurites was higher than in neuronal cell somata; the opposite occurred at higher (0.5–1 M) lovastatin concentrations. In contrast, neurite 7 nAChRs raised more than somatic 7 nAChRs at all lovastatin concentrations tested. These results indicate that cholesterol levels homeostatically regulate 7 and 4 nAChR levels in a di erential manner through mechanisms that depend on statin concentration and receptor localization. The neuroprotective pleomorphic e ects of statins may act by reestablishing the homeostatic equilibrium.
URI : https://repositorio.uca.edu.ar/handle/123456789/10847
ISSN : 1420-3049
Disciplina: MEDICINA
DOI: 10.3390/molecules25204838
Derechos: Acceso abierto
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