首页> 外文期刊>Die Pharmazie >The role of 8-OH-DPAT on the rat neuronal apoptosis after diffuse brain injury coupled with secondary brain injury
【24h】

The role of 8-OH-DPAT on the rat neuronal apoptosis after diffuse brain injury coupled with secondary brain injury

机译:8-OH-DPAT在弥漫性脑损伤与继发性脑损伤后大鼠神经元凋亡中的作用

获取原文
获取原文并翻译 | 示例
           

摘要

The potential role of 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) on rat neuronal apoptosis after diffuse brain injury (DBI) coupled with secondary brain injury (SBI) was investigated. One hundred and twelve adult male Wister rats weighing 305-355 g were randomly divided into four groups and received an intraperitoneal injection of 8-OH-DPAT (0.5 mg/kg) or an equal volume of normal saline. Neurological severity score (NSS) was recorded and the injured extent was observed after hematoxylin-eosin (HE) staining. The neuronal cell apoptosis index and the expression of Bax and BcI-2 were detected by TUNEL method and immunohistochemistry respectively. We found a higher NSS value for rats in the DBI + SBI groups compared with those in normal control and sham-operated control groups (P<0.01). HE staining showed that 8-OH-DPAT treatment could alleviate the occurrence of injury in rats CA3 hippocampus and PFC. The neuronal apoptosis index decreased in the 8-OH-DPAT treatment group compared with the NS group (P<0.05) and gradually increased at 6h, reached the peak level at 72h and still had a high performance at 168 h in not only CA3 hippocampus but also PFC. Expression of Bax and BcI-2 increased after DBI + SBI, however, with 8-OH-DPAT treatment BcI-2 expression increased while Bax expression decreased. 8-OH-DPAT had an inhibitory effect on the rat neuronal apoptosis in CA3 hippocampus and PFC after DBI coupled with SBI.
机译:研究了弥散性脑损伤(DBI)继发性继发性脑损伤(SBI)后8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)对大鼠神经元凋亡的潜在作用。将一百一十二只体重为305-355 g的成年雄性Wister大鼠随机分为四组,并腹膜内注射8-OH-DPAT(0.5 mg / kg)或等体积的生理盐水。记录神经系统严重程度评分(NSS),苏木精-伊红(HE)染色后观察损伤程度。分别采用TUNEL法和免疫组化法检测神经细胞凋亡指数以及Bax和Bcl-2的表达。我们发现,与正常对照组和假手术对照组相比,DBI + SBI组的大鼠的NSS值更高(P <0.01)。 HE染色显示8-OH-DPAT治疗可减轻大鼠CA3海马和PFC的损伤。与NS组相比,8-OH-DPAT治疗组的神经元凋亡指数下降(P <0.05),并在6h逐渐升高,在72h达到峰值,并且在168h不仅在海马CA3海马中还具有较高的表现。而且还有PFC。在DBI + SBI后,Bax和BcI-2的表达增加,但是,通过8-OH-DPAT处理,BcI-2的表达增加而Bax的表达减少。 8-OH-DPAT对DBI联合SBI后海马CA3海马和PFC的神经细胞凋亡具有抑制作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号