Behavioural Neuroscience Laboratory, Department of Animal Science, School of Life Sciences, Bharathidasan University, Tiruchirappalli, India.
Departamento de Neurobiología Celular y Molecular, Instituto de Neurobiología, Universidad Nacional Autónoma de México, Juriquilla, Querétaro 76230, Mexico.
Gen Comp Endocrinol. 2021 Jan 1;300:113641. doi: 10.1016/j.ygcen.2020.113641. Epub 2020 Oct 2.
Environmental enrichment (EE) dynamically regulates gene expression and synaptic plasticity with positive consequences on behavior. The present study was performed on field-mice to explore the effects of EE on both captive-condition inducing social stress and epigenetic changes of molecules resilience stress. For this purpose, field-mice were caught and allowed to habituate in standard laboratory conditions for 7 days. The next day animals were randomly assigned to three groups: i) mice at short-term standard condition (STSC); which were subjected to social interaction test (SIT) on day 9, ii) mice continuously maintainedfor additional 30 days, with these long-term standard conditions (LTSC), and iii) mice maintained in an EE cage for additional 30 days. After achieving SIT, we examined epigenetic changes of a repertory of molecules associated with resilience stress, by determining their levels by Western blot. Thus, the main findings were that during SIT, EE exerted more social interaction of field-mice with the strangers compared with STSC and LTSC mice. Related with social behavior results, we found that in mice subjected to EE the levels of histone 3 lysine 9 di-methylation (H3K9me2), glucocorticoid receptor (GR), N-methyl-D asparate (NMDA) receptor subunits NR2A and NR2B, postsynaptic density protein-95 (PSD-95), and mature brain-derived neurotrophic factor (mBDNF) were significantly elevated; whereas the levels of DNA methyltransferase-3A (DNMT3A), methyl-CpG-binding protein-2 (MeCP2), repressor element-1 silencing transcription factor (REST), H3K4me2 and lysine demethylase-1A (KDM1A) decreased. These results suggest that enhanced sociability of EE mice could be mediated, in part, by altered expression of molecules regulating glutamate signaling pathway through GR by epigenetic mechanisms.
环境富集(EE)通过对行为产生积极影响来动态调节基因表达和突触可塑性。本研究在野外小鼠中进行,旨在探索 EE 对圈养条件诱导的社会应激和分子应激弹性的表观遗传变化的影响。为此,将野外小鼠捕获并使其在标准实验室条件下适应 7 天。第二天,动物被随机分配到三个组:i)短期标准条件(STSC)下的小鼠,在第 9 天进行社会互动测试(SIT),ii)连续维持 30 天的长期标准条件(LTSC)下的小鼠,和 iii)在 EE 笼中维持 30 天的小鼠。在完成 SIT 后,我们通过 Western blot 确定其水平,检查与应激弹性相关的一系列分子的表观遗传变化。因此,主要发现是,在 SIT 期间,与 STSC 和 LTSC 小鼠相比,EE 使野外小鼠与陌生小鼠的社会互动更多。与社会行为结果相关,我们发现,在接受 EE 的小鼠中,组蛋白 3 赖氨酸 9 二甲基化(H3K9me2)、糖皮质激素受体(GR)、N-甲基-D-天冬氨酸(NMDA)受体亚基 NR2A 和 NR2B、突触后密度蛋白-95(PSD-95)和成熟脑源性神经营养因子(mBDNF)的水平显著升高;而 DNA 甲基转移酶 3A(DNMT3A)、甲基-CpG 结合蛋白 2(MeCP2)、抑制元件 1 沉默转录因子(REST)、H3K4me2 和赖氨酸去甲基酶 1A(KDM1A)的水平降低。这些结果表明,EE 小鼠社交能力增强可能部分通过表观遗传机制通过 GR 调节谷氨酸信号通路分子的表达来介导。