Departments of Neuroscience, Psychiatry and Psychology, University of Pittsburgh, A210 Langley Hall, Pittsburgh, PA 15260, USA; Institute of Genetic and Molecular Neurobiology, Otto-von-Guericke University, University of Magdeburg, Universitätsplatz 2, 39106 Magdeburg, Germany.
Departments of Neuroscience, Psychiatry and Psychology, University of Pittsburgh, A210 Langley Hall, Pittsburgh, PA 15260, USA; Department of Pharmacology, Ribeirao Preto Medical School, University of Sao Paulo, 3900 Bandeirantes Ave, Ribeirao Preto, SP, 14049-900, Brazil.
Eur Neuropsychopharmacol. 2019 Oct;29(10):1127-1137. doi: 10.1016/j.euroneuro.2019.07.134. Epub 2019 Jul 29.
Stress during adolescence is a risk factor for neuropsychiatric diseases, including schizophrenia. We recently observed that peripubertal male rats exposed to a combination of daily footshock plus restraint stress exhibited schizophrenia-like changes. However, numerous studies have shown sex differences in neuropsychiatric diseases as well as on the impact of coping with stress. Thus, we decided to evaluate, in adolescent female rats, the impact of different stressors (restraint stress [RS], footshock [FS], or the combination of FS and RS [FS+RS]) on social interaction (3-chamber social approach test/SAT), anxiety responses (elevated plus-maze/EPM), cognitive function (novel object recognition test/NOR), and dopamine (DA) system responsivity by evaluating locomotor response to amphetamine and in vivo extracellular single unit recordings of DA neurons in the ventral tegmental area (VTA) in adulthood. The impact of FS+RS during early adulthood was also investigated. Adolescent stress had no impact on social behavior, anxiety, cognition and locomotor response to amphetamine. In addition, adolescent stress did not induce long-lasting changes in VTA DA system activity. However, a decrease in the firing rate of VTA DA neurons was found 1-2 weeks post-adolescent stress. Similar to adolescent stress, adult stress did not induce long-lasting behavioral deficits and changes in VTA DA system activity, but FS+RS decreased VTA DA neuron population activity 1-2 weeks post-adult stress. Our results are consistent with previous studies showing that female rodents appear to be more resilient to developmental stress-induced persistent changes than males and may contribute to the delayed onset and lesser severity of schizophrenia in females.
青春期压力是神经精神疾病的一个风险因素,包括精神分裂症。我们最近观察到,青春期雄性大鼠在经历每日足底电击加束缚应激的组合后,表现出类似精神分裂症的变化。然而,许多研究表明,神经精神疾病以及应对压力的影响存在性别差异。因此,我们决定在青春期雌性大鼠中评估不同应激源(束缚应激[RS]、足底电击[FS]或 FS 和 RS 的组合[FS+RS])对社交互动(3 腔社交接近测试/SAT)、焦虑反应(高架十字迷宫/EPM)、认知功能(新物体识别测试/NOR)和多巴胺(DA)系统反应性的影响,方法是评估成年后对安非他命的运动反应和腹侧被盖区(VTA)中 DA 神经元的体外单细胞记录。还研究了成年早期 FS+RS 的影响。青春期应激对社交行为、焦虑、认知和安非他命的运动反应没有影响。此外,青春期应激不会引起 VTA DA 系统活性的持久变化。然而,在青春期应激后 1-2 周发现 VTA DA 神经元的放电率降低。与青春期应激相似,成年应激不会引起持久的行为缺陷和 VTA DA 系统活性的改变,但 FS+RS 在成年应激后 1-2 周会降低 VTA DA 神经元群体的活性。我们的研究结果与先前的研究一致,表明雌性啮齿动物似乎比雄性更能抵抗发育性应激引起的持久变化,这可能有助于解释女性精神分裂症发病较晚且程度较轻。