Unit of Research on Psychobiology of Drug Dependence, Department of Psychobiology, Faculty of Psychology, Universitat de València, Valencia, Spain.
Neurobiology of Behavior Research Group (GReNeC-NeuroBio), Department of Health and Experimental Sciences, University Pompeu Fabra, IMIM (Hospital del Mar Medical Research Institute), Barcelona, Spain.
Neuropharmacology. 2019 Mar 1;146:50-64. doi: 10.1016/j.neuropharm.2018.11.011. Epub 2018 Nov 16.
The neuropeptide oxytocin (OXT) plays a critical role in the regulation of social and emotional behaviors. OXT plays a role in stress response and in drug reward, but to date no studies have evaluated its implication in the long-lasting increase of the motivational effects of cocaine induced by repeated social defeat (RSD). During the social defeat procedure, 1 mg/kg of OXT was administered 30 min before each episode of RSD. Three weeks after the last defeat, the effects of cocaine on the conditioned place preference (CPP), locomotor sensitization and the self-administration (SA) paradigms were evaluated. The influence of OXT on the levels of BDNF in the prefrontal cortex (PFC), striatum and hippocampus was also measured. Our results confirm that raising the levels of OXT during social defeat stress can block the long-lasting effects of this type of stress. OXT counteracts the anxiety induced by social defeat and modifies BDNF levels in all the structures we have studied. Moreover, OXT prevents RSD-induced increases in the motivational effects of cocaine. Administration of OXT before each social defeat blocked the social defeat-induced increment in the conditioned rewarding effects of cocaine in the CPP, favored the extinction of cocaine-associated memories in both the CPP and SA, and decreased reinstatement of cocaine-seeking behavior in the SA. In conclusion, the long-lasting effects of RSD are counteracted by administering OXT prior to stress, and changes in BDNF expression may underlie these protective effects.
神经肽催产素(OXT)在调节社会和情感行为方面起着关键作用。OXT 在应激反应和药物奖赏中发挥作用,但迄今为止,尚无研究评估其在反复社交挫败(RSD)引起的可卡因动机效应的长期增加中的作用。在社交挫败程序中,在每次 RSD 之前 30 分钟给予 1mg/kg 的 OXT。在最后一次挫败后 3 周,评估了可卡因对条件位置偏好(CPP)、运动敏化和自我给药(SA)范式的影响。还测量了 OXT 对前额叶皮层(PFC)、纹状体和海马体中 BDNF 水平的影响。我们的结果证实,在社交挫败应激期间提高 OXT 水平可以阻断这种应激的长期影响。OXT 对抗社交挫败引起的焦虑,并调节我们研究的所有结构中的 BDNF 水平。此外,OXT 可防止 RSD 诱导的可卡因动机效应增加。在每次社交挫败之前给予 OXT,可阻断 CPP 中可卡因条件奖励效应的社交挫败诱导增加,有利于 CPP 和 SA 中可卡因相关记忆的消退,并减少 SA 中可卡因寻求行为的复燃。总之,在应激前给予 OXT 可拮抗 RSD 的长期效应,BDNF 表达的变化可能是这些保护作用的基础。