EA 481 Laboratory of Integrative and Clinical Neuroscience, University of Franche-Comté/SFR FED 4234, COMUE Bourgogne/Franche-Comté, France.
Department of Cellular and Molecular Pharmacology, The Chicago Medical School, Rosalind Franklin University of Medicine and Science, North Chicago, IL, USA.
Addict Biol. 2017 Sep;22(5):1267-1278. doi: 10.1111/adb.12415. Epub 2016 Jun 6.
Transcranial direct current stimulation (tDCS) is a non-invasive method to modulate cortical excitability. This technique is a promising emerging tool to treat several neuropathologies, including addiction. We have previously shown in mice that repeated tDCS normalizes pathological behaviors associated with chronic nicotine exposure. Here, we evaluated, in adult female mice, the impact of tDCS on cocaine-induced behavior and gene regulation in corticostriatal circuits implicated in psychostimulant addiction. Anodal tDCS was applied transcranially over the frontal cortex. Three weeks after repeated tDCS, we investigated the induction of a gene expression marker (Zif268) by cocaine (25 mg/kg) in 26 cortical and 23 striatal regions using in situ hybridization histochemistry. We also assessed place preference conditioning by cocaine (5, 10 and 25 mg/kg). tDCS pretreatment increased basal expression and attenuated cocaine (25 mg/kg)-induced expression of Zif268 in specific corticostriatal circuits. Cocaine-induced locomotor activation (25 mg/kg) and place preference conditioning (5 and 25 mg/kg) were also reduced. These results demonstrate that tDCS can attenuate molecular and behavioral responses to cocaine for several weeks. Together, our findings provide pre-clinical evidence that such electrical brain stimulation may be useful to modify the psychostimulant addiction risk.
经颅直流电刺激(tDCS)是一种调节皮质兴奋性的非侵入性方法。该技术是一种有前途的新兴工具,可用于治疗多种神经病理学疾病,包括成瘾。我们之前在小鼠中表明,重复 tDCS 可使与慢性尼古丁暴露相关的病理性行为正常化。在这里,我们在成年雌性小鼠中评估了 tDCS 对可卡因诱导的行为和皮质纹状体回路中基因调节的影响,该回路与精神兴奋剂成瘾有关。阳极 tDCS 经颅施加于额叶皮层。在重复 tDCS 3 周后,我们使用原位杂交组织化学法在 26 个皮质和 23 个纹状体区域中研究了可卡因(25mg/kg)诱导的基因表达标志物(Zif268)的诱导。我们还评估了可卡因(5、10 和 25mg/kg)引起的位置偏好条件。tDCS 预处理增加了特定皮质纹状体回路中 Zif268 的基础表达,并减弱了可卡因(25mg/kg)诱导的表达。可卡因诱导的运动激活(25mg/kg)和位置偏好条件(5 和 25mg/kg)也减少了。这些结果表明,tDCS 可以减弱对可卡因的分子和行为反应数周。总之,我们的发现提供了临床前证据,表明这种电脑刺激可能有助于改变精神兴奋剂成瘾的风险。