Stankiewicz Adrian M, Goscik Joanna, Swiergiel Artur H, Majewska Alicja, Wieczorek Marek, Juszczak Grzegorz R, Lisowski Paweł
Department of Animal Behavior, Institute of Genetics and Animal Breeding, Jastrzebiec, ul. Postepu 36A, 05-552, Magdalenka, Poland.
Faculty of Computer Science, Bialystok University of Technology, Wiejska 45A, 15-351, Bialystok, Poland.
BMC Neurosci. 2014 Dec 4;15:130. doi: 10.1186/s12868-014-0130-6.
In order to better understand the effects of social stress on the prefrontal cortex, we investigated gene expression in mice subjected to acute and repeated social encounters of different duration using microarrays.
The most important finding was identification of hemoglobin genes (Hbb-b1, Hbb-b2, Hba-a1, Hba-a2, Beta-S) as potential markers of chronic social stress in mice. Expression of these genes was progressively increased in animals subjected to 8 and 13 days of repeated stress and was correlated with altered expression of Mgp (Mglap), Fbln1, 1500015O10Rik (Ecrg4), SLC16A10, and Mndal. Chronic stress increased also expression of Timp1 and Ppbp that are involved in reaction to vascular injury. Acute stress did not affect expression of hemoglobin genes but it altered expression of Fam107a (Drr1) and Agxt2l1 (Etnppl) that have been implicated in psychiatric diseases.
The observed up-regulation of genes associated with vascular system and brain injury suggests that stressful social encounters may affect brain function through the stress-induced dysfunction of the vascular system.
为了更好地理解社会压力对前额叶皮层的影响,我们使用微阵列研究了遭受不同持续时间急性和重复社会接触的小鼠的基因表达。
最重要的发现是鉴定出血红蛋白基因(Hbb-b1、Hbb-b2、Hba-a1、Hba-a2、Beta-S)作为小鼠慢性社会压力的潜在标志物。在遭受8天和13天重复应激的动物中,这些基因的表达逐渐增加,并且与Mgp(Mglap)、Fbln1、1500015O10Rik(Ecrg4)、SLC16A10和Mndal的表达改变相关。慢性应激还增加了参与血管损伤反应的Timp1和Ppbp的表达。急性应激不影响血红蛋白基因的表达,但它改变了与精神疾病有关的Fam107a(Drr1)和Agxt2l1(Etnppl)的表达。
观察到的与血管系统和脑损伤相关基因的上调表明,有压力的社会接触可能通过压力诱导的血管系统功能障碍影响脑功能。