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Voluntary wheel running during adolescence prevents the increase in ethanol intake induced by social defeat in male mice
被引:2
|作者:
Reguilon, Marina D.
[1
]
Ferrer-Perez, Carmen
[2
]
Manzanedo, Carmen
[1
]
Minarro, Jose
[1
]
Rodriguez-Arias, Marta
[1
]
机构:
[1] Univ Valencia, Fac Psychol, Dept Psychobiol, Unit Res Psychobiol Drug Dependence, Avda Blasco Ibanez 21, Valencia 46010, Spain
[2] Univ Valencia, Fac Psicol, Dept Psicol Evolut, Valencia, Spain
来源:
关键词:
Physical exercise;
Wheel running;
Social stress;
Resilience;
Ethanol;
BDNF;
Self-administration;
VENTRAL TEGMENTAL AREA;
NEUROTROPHIC FACTOR;
CORTICOSTRIATAL BDNF;
SYNAPTIC PLASTICITY;
ALCOHOL-CONSUMPTION;
ACCUMBAL DOPAMINE;
GENE-EXPRESSION;
RAT MODEL;
EXERCISE;
STRESS;
D O I:
10.1007/s00213-023-06461-0
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
RationaleExposure to social defeat (SD) induces a depressive phenotype, increased ethanol seeking and consumption, accompanied by activation of the neuroinflammatory response. However, a resilient response can be potentiated through physical exercise in the form of voluntary wheel running (VWR) during or after exposure to social stress. Therefore, the aim of this study was to test whether physical exercise during adolescence prior to being exposed to SD can enhance resilience to the increase in ethanol intake.MethodsMale mice had access to VWR during adolescence and the effects of social defeat (4 sessions every 72 h) on oral ethanol self-administration (SA) was evaluated. Based on the social interaction test, mice were classified as resilient or susceptible to depressive-like behavior. Two weeks after the last encounter, mice were subjected to the drinking in the dark and oral ethanol SA paradigms. Mice were then sacrificed to measure brain-derived neurotrophic factor (BDNF) levels in the striatum and hippocampus.ResultsAs expected, susceptible mice increased ethanol intake in the oral SA protocol. However, susceptible mice in the exercise condition did not increase ethanol intake, showing similar consumption and motivation for ethanol than the control and resilient groups. On the other hand, decreased BDNF levels were observed in susceptible mice in both experimental conditions compared to the control groups after ethanol SA.ConclusionsThe pre-exposure of VWR prevented the increase in consumption and motivation for ethanol induced by SD in susceptible mice. On the other hand, it appears that VWR did not exhibit any significant long-term effects on BDNF signaling, which is mainly affected in susceptible mice after ethanol intake.
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页数:18
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