›› 2012, Vol. 43 ›› Issue (3): 306-311.doi: 10.3969/j.issn.0529-1356.2012.03.004

• 神经生物学 • 上一篇    下一篇

蛋白酶活化受体1/4参与大鼠蛛网膜下腔出血后脑内小胶质细胞的活化

闫军浩; 张卫光; 周长满*   

  1. 北京大学医学部基础医学院人体解剖学与组织学胚胎学系,北京 100191
  • 收稿日期:2012-01-15 修回日期:2012-02-10 出版日期:2012-06-06
  • 通讯作者: 周长满

Role of protease activated receptor-1 and 4 in the activation of microglia following subarachnoid hemorrhage

  1. Department of Anatomy, Histology and Embryology, School of Basic Medical Sciences, Peking University, Beijing 100191, China
  • Received:2012-01-15 Revised:2012-02-10 Online:2012-06-06
  • Contact: ZHOU Chang-man

关键词: 蛛网膜下腔出血, 蛋白酶活化受体, 小胶质细胞, 炎症, 免疫组织化学, 免疫印迹法, 大鼠

Abstract: Objective To investigate the role of protease activated receptor-1 and 4 (PAR-1, PAR-4) in the activation of microglia following subarachnoid hemorrhage (SAH). Methods One hundred male SD rats were randomly divided into: sham, SAH+control siRNA, SAH+PAR-1 siRNA, SAH+PAR-4 siRNA and SAH+PAR-1/4 siRNA groups, 20 in each group. The drugs were administrated intracerebroventricularly at 1 hour after SAH. At the 6th and 24th hour after SAH, the neurological deficits, brain water content and Evans blue content were evaluated, at the same time, the expression of tumor necrosis factor α(TNF-α) and intercellular cell adhesion molecule-1 (ICAM-1) were also measured by using immunohistochemistry and Western blotting. Results PAR-1siRNA or PAR-4 siRNA could significantly ameliorate the neurological deficits and decrease vascular permeability (EM>P/EM>0.05). In addition, the expression of TNF-α and ICAM-1 was also decreased by PAR-1siRNA or PAR-4 siRNA treatment. The combination of PAR-1and PAR-4 siRNA played more powerful roles than either of them. Conclusion PAR-1 and 4 mediate the activation of microglia in the brain following SAH. Through suppressing the expression of inflammatory factors, PAR-1siRNA and/or PAR-4 s

Key words: Subarachnoid hemorrhage, Protease activated receptor, Microglia, Inflammation, Immunohistochemistry, Western blotting, Rat

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