Department of Neurology, The First People's Hospital of Changde City, Changde, Hunan, China 415000.
Comput Math Methods Med. 2021 Dec 24;2021:1574109. doi: 10.1155/2021/1574109. eCollection 2021.
The aim was to investigate the role that enriched environment (EE) plays in the regulation of inflammation in cerebral infarction (CI) lesions and further explore the relationship between this regulation and dendritic cells (DCs).
72 Sprague-Dawley rats were randomly divided into sham operation group (CON group, = 24) and CI model group ( = 48). On completion of the establishment of CI rat models by Longa's method, rats in the models group were further assigned to standard environment group (NC group, = 24) and EE group ( = 24). HE staining was utilized for evaluation of neuronal injury in the lesions. The number of CD74- and integrin E-positive cells was detected by immunofluorescence. The expression of the IL-1, IL-6, and TNF- in the brain tissue and serum of rats was measured by immunohistochemistry and ELISA, respectively.
In comparison with the CON group, the NC and EE groups showed significant increases in neuronal injury, CD74- and Integrin E-positive cells, DC content, as well as IL-1, IL-6, and TNF- expression in brain tissue and serum. According to the further comparison between the NC group and EE group, the latter showed decreases in each indicator, and these decreases were in a time-dependent manner.
EE avoids the accumulation of DCs in the lesions and reduces the contents of IL-1, IL-6, and TNF-, consequently promoting the recovery of CI. And better recovery results can be obtained through increasing the time to stay in EE.
探讨丰富环境(EE)在脑梗死(CI)病灶炎症调节中的作用,并进一步探讨这种调节与树突状细胞(DC)之间的关系。
72 只 Sprague-Dawley 大鼠随机分为假手术组(CON 组,n=24)和 CI 模型组(n=48)。采用 Longa 法建立 CI 大鼠模型后,模型组大鼠进一步分为标准环境组(NC 组,n=24)和 EE 组(n=24)。采用 HE 染色评估病灶神经元损伤情况。免疫荧光法检测 CD74-和整合素 E 阳性细胞数。免疫组化和 ELISA 分别检测脑组织和血清中大鼠 IL-1、IL-6 和 TNF-的表达。
与 CON 组相比,NC 组和 EE 组神经元损伤、CD74-和整合素 E 阳性细胞、DC 含量以及脑组织和血清中 IL-1、IL-6 和 TNF-的表达均明显升高。进一步比较 NC 组和 EE 组,后者各指标均降低,且呈时间依赖性。
EE 可避免 DC 在病灶中的堆积,降低 IL-1、IL-6 和 TNF-的含量,从而促进 CI 的恢复。通过增加在 EE 中的停留时间,可以获得更好的恢复效果。