畜牧兽医学报 ›› 2010, Vol. 41 ›› Issue (7): 878-882.

• 基础兽医 • 上一篇    下一篇

替来他明诱导大鼠中枢神经系统c-fos基因的表达

卢德章,范宏刚,于世明,张栾松,马昆,马海鹍,王洪斌*   

  1. 东北农业大学 动物医学学院,哈尔滨 150030
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2010-07-20 发布日期:2010-07-20
  • 通讯作者: 王洪斌

Tiletamine Induced c-fos Oncogene Expression within Central Nervous System of Rats

LU De-zhang, FAN Hong-gang, YU Shi-ming, ZHANG Luan-song,MA Kun, MA Hai-kun, WANG Hong-bin*   

  1. College of Veterinary Medicine, Northeast Agricultural University, Harbin 150030, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2010-07-20 Published:2010-07-20

摘要: 本研究旨在观察替来他明麻醉后大鼠中枢神经系统c-fos基因的表达,了解替来他明在中枢神经系统的作用部位,探讨替来他明对中枢神经系统的作用机制。72只SD大鼠,随机分为生理盐水组、给药后10、30、60、90、100、120和180 min组,每组9只。腹腔注射替来他明50 mg·kg-1后,分别于给药前(生理盐水组)和给药后10、30、60、90、100、120和180 min经4%多聚甲醛(0.1 mol·L-1, PB, pH 7.4)灌注后,取脑,将脑分为大脑皮层、海马、丘脑、小脑、脑干5个脑区,置于20%蔗糖溶液中24 h(4 ℃)脱水。冰冻切片,片厚10 μm,按照Elivision法进行免疫组化染色,观察鉴别Fos阳性神经元并做阳性神经元计数。结查显示,对照组中仅发现少量Fos阳性神经元,试验组中Fos阳性神经元在大脑皮层、海马、丘脑、小脑、脑干内都有表达。替来他明腹腔注射10 min后Fos阳性神经元表达开始增加,60 min表达至高峰,90 min表达下降,180 min下降至基线水平,与给药前相比无显著性差异(P>0.05)。结果提示,替来他明能诱导大鼠大脑皮层、海马、丘脑、小脑、脑干c-fos基因的表达,大脑皮层、海马、丘脑、小脑和脑干是替来他明的作用位点。

关键词: 替来他明, c-fos基因, 中枢神经系统

Abstract: To investigate the distribution of c-fos oncogene expression in rats central nervous system following tiletamine anesthesia. Tiletamine action sites in CNS were studied, and general anesthetic mechanisms were also discussed. 72 SD rats were randomly divided into 8 groups. At 0, 10, 30, 60, 90, 100, 120 and 180 min after given tiletamine 50 mg·kg-1 intraperitoneally, rats were perfused with 4% Paraformaldehyde (0.1 mol·L-1, PB, pH 7.4). The whole brain was separated into cerebral cortex, hippocampus, thalamus, cerebellum and brain stem. Then these brain tissues were dehydrated 24 h by 20% sucrose (4 ℃). Cryosections were 10 μm and Elivision Immunohistochemical technique for Fosprotein was used to observe and count on the Fos-like immunoreactive neurons. In normal saline group, there was few Fos-like immunoreactive neurons appeared. And Fos-like immunoreactive neurons were observed in cerebral cortex, hippocampus, thalamus, cerebellum and brain stem in experimental groups. Fos-like immunoreactive neurons expression increased at 10 min after tiletamine administrated by intraperitoneal injection, peaked at 60 min and decreased at 90 min. At 180 min after injection, Fos-like immunoreactive neurons recovered to base level, which had no significant difference compared with that before given tiletamine (P>0.05). The results showed that tiletamine induce expression of c-fos oncogene in the rats′ cerebral cortex, hippocampus, thalamus, cerebellum and brain stem. And the cerebral cortex, hippocampus, thalamus, cerebellum and brain stem at the action sites of tiletamine.

Key words: Tiletamine, c-fos oncogene, central nervous system