Institute of Pharmacology, Polish Academy of Sciences, Laboratory of Pharmacology and Brain Biostructure, Smętna Street 12, 31-343 Kraków, Poland.
Institute of Pharmacology, Polish Academy of Sciences, Laboratory of Pharmacology and Brain Biostructure, Smętna Street 12, 31-343 Kraków, Poland.
Eur Neuropsychopharmacol. 2018 Jan;28(1):97-108. doi: 10.1016/j.euroneuro.2017.11.013. Epub 2017 Nov 22.
In the present study, we investigated whether exposure to an enriched environment (EE) during adolescence might affect the behavioural dysfunction (sensorimotor gating deficit, memory and social interaction impairments) and neurochemical changes (GAD67 expression, histone methylation) induced by methylazoxymethanol (MAM) in the MAM-E17 rat model of schizophrenia. EE was introduced for 7 days in early adolescence (days 23-29), and behavioural and biochemical studies were performed on adult rats at postnatal day 70. The results showed that exposure to EE prevented the development of adult behavioural deficits induced by prenatal MAM administration. EE also prevented the decrease in GAD67 mRNA and protein levels induced by MAM in the medial prefrontal cortex (mPFC). Moreover, EE inhibited the reductions in the amount of Gad1 bound to H3K4me3 and in the total H3K4me3 protein level induced by prenatal MAM administration in the adult mPFC. However, there was no effect of EE on behaviour or levels of the various neurochemical markers in adult rats prenatally treated with vehicle. Thus, these results indicate that EE exposure during early adolescence may inhibit the development of schizophrenia related symptoms through epigenetic mechanisms that regulate the expression of genes (e.g., Gad1) that are impaired in schizophrenia.
在本研究中,我们调查了青春期接触丰富环境(EE)是否会影响亚甲基双氧甲基戊酮(MAM)在精神分裂症 MAM-E17 大鼠模型中引起的行为功能障碍(感觉运动门控缺陷、记忆和社交互动障碍)和神经化学变化(GAD67 表达、组蛋白甲基化)。EE 在青春期早期(第 23-29 天)引入 7 天,在产后第 70 天对成年大鼠进行行为和生化研究。结果表明,暴露于 EE 可预防产前 MAM 给药引起的成年行为缺陷的发展。EE 还可预防 MAM 在中前额皮质(mPFC)中诱导的 GAD67 mRNA 和蛋白水平降低。此外,EE 抑制了产前 MAM 给药引起的成年 mPFC 中与 H3K4me3 结合的 Gad1 量和总 H3K4me3 蛋白水平的降低。然而,EE 对成年大鼠的行为或各种神经化学标志物水平没有影响,这些大鼠在产前用载体处理。因此,这些结果表明,青春期早期暴露于 EE 可能通过调节精神分裂症中受损的基因(例如 Gad1)表达的表观遗传机制来抑制精神分裂症相关症状的发展。