Caffino Lucia, Giannotti Giuseppe, Racagni Giorgio, Fumagalli Fabio
Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Via Balzaretti 9, 20133, Milan, Italy.
Psychopharmacology (Berl). 2017 Apr;234(8):1217-1222. doi: 10.1007/s00213-017-4559-z. Epub 2017 Feb 15.
Among the changes caused by repeated exposure to drugs of abuse, structural rearrangements play a critical role, setting the stage for maladaptive responses to environmental challenges and sustaining drug-taking and drug-seeking behaviors. Given that adolescents are more vulnerable to drug abuse than adults and based on our recent data showing that a single exposure to cocaine during adolescence is sufficient to change the adolescent brain, we decided to investigate whether acute cocaine exposure may alter actin remodeling in reward-related brain regions.
Accordingly, we decided to evaluate if F-actin/G-actin ratio was altered by a single injection of cocaine (20 mg/kg) at postnatal day 35. We also evaluated whether the first administration of cocaine influences such a ratio in response to a second injection (10 mg/kg) provided 24 h or 7 days later.
Within the medial prefrontal cortex, a single cocaine injection increases the F-actin/G-actin ratio. This effect lasts 1 week, and it is not affected by the second injection of cocaine, indicating a persistent effect of the first exposure. In the nucleus accumbens, cocaine reduces the F-actin/G-actin ratio 24 h later. Seven days later, instead, such a ratio is markedly increased: notably, the additional exposure to the psychostimulant normalizes the F-actin/G-actin ratio.
These results suggest that a single cocaine injection during adolescence causes possible changes in actin dynamics and influences the response to a second challenge of the psychostimulant, indicating that early cocaine priming might affect mechanisms regulating synaptic structural plasticity in specific brain regions.
在反复接触滥用药物所引起的变化中,结构重排起着关键作用,为对环境挑战的适应不良反应奠定基础,并维持吸毒和觅药行为。鉴于青少年比成年人更容易滥用药物,且基于我们最近的数据表明青春期单次接触可卡因足以改变青少年大脑,我们决定研究急性可卡因暴露是否会改变与奖赏相关脑区的肌动蛋白重塑。
因此,我们决定评估在出生后第35天单次注射可卡因(20毫克/千克)是否会改变F-肌动蛋白/G-肌动蛋白比率。我们还评估了首次注射可卡因是否会影响在24小时或7天后第二次注射(10毫克/千克)时的该比率。
在内侧前额叶皮质内,单次注射可卡因会增加F-肌动蛋白/G-肌动蛋白比率。这种效应持续1周,且不受第二次注射可卡因的影响,表明首次暴露具有持久效应。在伏隔核中,可卡因在24小时后会降低F-肌动蛋白/G-肌动蛋白比率。相反,7天后,该比率会显著增加:值得注意的是,再次接触精神兴奋剂可使F-肌动蛋白/G-肌动蛋白比率恢复正常。
这些结果表明,青春期单次注射可卡因可能会导致肌动蛋白动力学发生变化,并影响对精神兴奋剂第二次挑战的反应,表明早期可卡因预处理可能会影响特定脑区调节突触结构可塑性的机制。