青春期的自愿车轮运动可以防止雄性小鼠因社交失败而导致的乙醇摄入增加。

IF 3.5 3区 医学 Q2 NEUROSCIENCES
Psychopharmacology Pub Date : 2025-05-01 Epub Date: 2023-09-22 DOI:10.1007/s00213-023-06461-0
Marina D Reguilón, Carmen Ferrer-Pérez, Carmen Manzanedo, José Miñarro, Marta Rodríguez-Arias
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引用次数: 0

摘要

理由:暴露于社会失败(SD)会诱导抑郁表型,增加乙醇的寻求和消耗,并伴有神经炎症反应的激活。然而,在暴露于社会压力期间或之后,可以通过自愿轮跑(VWR)形式的体育锻炼来增强弹性反应。因此,本研究的目的是测试暴露于SD之前的青春期体育锻炼是否可以增强对乙醇摄入量增加的抵抗力。方法:雄性小鼠在青春期获得VWR,并评估社交失败(每72小时4次)对口服乙醇自给药(SA)的影响。根据社会互动测试,小鼠被归类为有弹性或易受抑郁样行为影响。在最后一次接触后两周,小鼠接受了在黑暗中饮用和口服乙醇SA的模式。然后处死小鼠以测量纹状体和海马中的脑源性神经营养因子(BDNF)水平。结果:正如预期的那样,易感小鼠在口服SA方案中增加了乙醇摄入。然而,运动条件下的易感小鼠没有增加乙醇摄入,表现出与对照组和弹性组相似的乙醇消耗和动机。另一方面,在乙醇SA后,与对照组相比,在两种实验条件下,易感小鼠的BDNF水平都有所下降。结论:VWR的预暴露防止了易感小鼠SD诱导的乙醇消耗和动机的增加。另一方面,VWR似乎对BDNF信号传导没有表现出任何显著的长期影响,BDNF信号主要在摄入乙醇后的易感小鼠中受到影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Voluntary wheel running during adolescence prevents the increase in ethanol intake induced by social defeat in male mice.

Voluntary wheel running during adolescence prevents the increase in ethanol intake induced by social defeat in male mice.

Rationale: Exposure 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.

Methods: Male 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.

Results: As 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.

Conclusions: The 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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来源期刊
Psychopharmacology
Psychopharmacology 医学-精神病学
CiteScore
7.10
自引率
5.90%
发文量
257
审稿时长
2-4 weeks
期刊介绍: Official Journal of the European Behavioural Pharmacology Society (EBPS) Psychopharmacology is an international journal that covers the broad topic of elucidating mechanisms by which drugs affect behavior. The scope of the journal encompasses the following fields: Human Psychopharmacology: Experimental This section includes manuscripts describing the effects of drugs on mood, behavior, cognition and physiology in humans. The journal encourages submissions that involve brain imaging, genetics, neuroendocrinology, and developmental topics. Usually manuscripts in this section describe studies conducted under controlled conditions, but occasionally descriptive or observational studies are also considered. Human Psychopharmacology: Clinical and Translational This section comprises studies addressing the broad intersection of drugs and psychiatric illness. This includes not only clinical trials and studies of drug usage and metabolism, drug surveillance, and pharmacoepidemiology, but also work utilizing the entire range of clinically relevant methodologies, including neuroimaging, pharmacogenetics, cognitive science, biomarkers, and others. Work directed toward the translation of preclinical to clinical knowledge is especially encouraged. The key feature of submissions to this section is that they involve a focus on clinical aspects. Preclinical psychopharmacology: Behavioral and Neural This section considers reports on the effects of compounds with defined chemical structures on any aspect of behavior, in particular when correlated with neurochemical effects, in species other than humans. Manuscripts containing neuroscientific techniques in combination with behavior are welcome. We encourage reports of studies that provide insight into the mechanisms of drug action, at the behavioral and molecular levels. Preclinical Psychopharmacology: Translational This section considers manuscripts that enhance the confidence in a central mechanism that could be of therapeutic value for psychiatric or neurological patients, using disease-relevant preclinical models and tests, or that report on preclinical manipulations and challenges that have the potential to be translated to the clinic. Studies aiming at the refinement of preclinical models based upon clinical findings (back-translation) will also be considered. The journal particularly encourages submissions that integrate measures of target tissue exposure, activity on the molecular target and/or modulation of the targeted biochemical pathways. Preclinical Psychopharmacology: Molecular, Genetic and Epigenetic This section focuses on the molecular and cellular actions of neuropharmacological agents / drugs, and the identification / validation of drug targets affecting the CNS in health and disease. We particularly encourage studies that provide insight into the mechanisms of drug action at the molecular level. Manuscripts containing evidence for genetic or epigenetic effects on neurochemistry or behavior are welcome.
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