UFR2709, an Antagonist of Nicotinic Acetylcholine Receptors, Delays the Acquisition and Reduces Long-Term Ethanol Intake in Alcohol-Preferring UChB Bibulous Rats
Primer Autor |
Rivera-Meza, Mario
|
Co-autores |
Galvez, Gabriel
Gonzalez-Gutierrez, Juan Pablo
Hodar-Salazar, Martin
Sotomayor-Zarate, Ramon
Quintanilla, Maria Elena
Quilaqueo, Maria Elena
Iturriaga-Vasquez, Patricio
|
Título |
UFR2709, an Antagonist of Nicotinic Acetylcholine Receptors, Delays the Acquisition and Reduces Long-Term Ethanol Intake in Alcohol-Preferring UChB Bibulous Rats
|
Editorial |
MDPI
|
Revista |
BIOMEDICINES
|
Lenguaje |
en
|
Resumen |
Alcoholism is a worldwide public health problem with high economic cost and which affects health and social behavior. It is estimated that alcoholism kills 3 million people globally, while in Chile it is responsible for around 9 thousand deaths per year. Nicotinic acetylcholine receptors (nAChRs) are ligand-gated ion channels expressed in the central nervous system, and they were suggested to modulate the ethanol mechanism involved in abuse and dependence. Previous work demonstrated a short-term treatment with UFR2709, a nAChRs antagonist, which reduced ethanol intake using a two-bottle free-choice paradigm in University of Chile bibulous (UChB) rats. Here, we present evidence of the UFR2709 efficacy in reducing the acquisition and long-term ethanol consumption. Our results show that UFR2709 (2.5 mg/kg i.p.) reduces the seek behavior and ethanol intake, even when the drug administration was stopped, and induced a reduction in the overall ethanol intake by around 55%. Using naive UChB bibulous rats, we demonstrate that UFR2709 could delay and reduce the genetically adaptive impulse to seek and drink ethanol and prevent its excessive intake.
|
Tipo de Recurso |
artículo original
|
Description |
This work was supported by the National Agency of Research and Development (ANIDChile) through FONDECYT Grants N ffi116-0398 and 120-0474 to R.S.-Z., 120-1577 to M.R.-M., 115-0615 to P.I.-V. and 322-0275 to J.P.G.-G. Partial support was received from DIUV-CI Grant Nffi 01/2006 (to R.S.-Z.). ANID [ACT210012] M.R.-M. M.H.-S. is a fellow of the CONICYT National Ph.D. Scholar Fellowship.
Este trabajo contó con el apoyo de la Agencia Nacional de Investigación y Desarrollo (ANIDChile) a través de los Becas FONDECYT N° ffi116-0398 y 120-0474 a R.S.-Z., 120-1577 a M.R.-M., 115-0615 a P.I.-V. y 322-0275 a J.P.G.-G. Se recibió apoyo parcial de la subvención DIUV-CI Nffi 01/2006 (a R.S.-Z.). ANID [ACT210012] M.R.-M. M.H.-S. Es becario del Doctorado Nacional de CONICYT. Beca académica.
|
doi |
10.3390/biomedicines10071482
|
Formato Recurso |
PDF
|
Palabras Claves |
UFR2709
voluntary ethanol intake
UChB rats
nicotinic antagonist
PARTIAL AGONIST VARENICLINE
ACCUMBAL DOPAMINE OVERFLOW
VENTRAL TEGMENTAL AREA
CONSUMPTION
HIPPOCAMPAL
SENSITIVITY
DEPENDENCE
CYTISINE
SMOKING
DRUGS
|
Ubicación del archivo | |
Categoría OCDE |
Bioquímica y Biología Molecular
Medicina
Investigación y Experimental
Farmacología y farmacia
|
Materias |
UFR2709
ingesta voluntaria de etanol
ratas UChB
antagonista nicotínico
AGONISTA PARCIAL VARENICLINA
DESBORDAMIENTO DE DOPAMINA ACUMBARAL
ÁREA TEGMENTAL VENTRAL
CONSUMO
HIPOCAMPAL
SENSIBILIDAD
DEPENDENCIA
CITISINA
FUMAR
DROGAS
|
Título de la cita (Recomendado-único) |
UFR2709, an Antagonist of Nicotinic Acetylcholine Receptors, Delays the Acquisition and Reduces Long-Term Ethanol Intake in Alcohol-Preferring UChB Bibulous Rats
|
Identificador del recurso (Mandatado-único) |
artículo original
|
Versión del recurso (Recomendado-único) |
version publicada
|
License |
CC BY 4.0
|
Condición de la licencia (Recomendado-repetible) |
CC BY 4.0
|
Derechos de acceso |
acceso abierto
|
Access Rights |
acceso abierto
|
Referencia del Financiador (Mandatado si es aplicable-repetible) |
ANID-FONDECYT 116-0398
ANID-FONDECYT 120-0474
ANID-FONDECYT 120-1577
ANID-FONDECYT 115-0615
ANID-FONDECYT 322-0275
UV DIUV-CI 01/2006
ANID ACT210012
ANID FONDECYT 116-0398
ANID FONDECYT 120-0474
ANID FONDECYT 120-1577
ANID FONDECYT 115-0615
ANID FONDECYT 322-0275
|
Id de Web of Science |
WOS:000833892500001
|