期刊文献+

MKP-1在PTSD样大鼠海马组织中表达改变 被引量:6

Study of MKP-1 expression alteration in the hippocampal tissue of the PTSD rats
下载PDF
导出
摘要 目的探讨创伤后应激障碍(PTSD)样大鼠行为学改变与海马组织中丝裂原活化蛋白激酶磷酸酶-1(MKP-1)表达的关系。方法将30只清洁级SD大鼠随机分为Control组、PTSD 1 d组、PTSD 3 d组、PTSD 7 d组、PTSD 14 d组,每组各6只,使用国际认定的单次延长应激(SPS)方法制作大鼠PTSD模型。通过旷场试验、Morris水迷宫观察大鼠的行为学变化。采用实时荧光定量PCR(qRT-PCR)和Western blot法分别检测大鼠海马组织中MKP-1 mRNA和蛋白水平的变化。结果 PTSD 7 d组、PTSD 14 d组与Control组相比直立次数、进格次数以及穿台次数减少,潜伏期延长,差异有统计学意义(P <0. 05)。PTSD 7 d组、PTSD 14 d组与Control组相比,海马组织中MKP-1 mRNA及蛋白表达水平明显升高,差异均具有统计学意义(P <0. 05)。结论 PTSD样大鼠行为改变、记忆下降考虑与海马组织中MKP-1基因及蛋白表达增高有关,MKP-1可能参与了PTSD的发病机制,有望作为PTSD发生发展的参考指标。 Objective To investigate the relationship between the behavioral changes of rats with posttraumatic stress disorder(PTSD)and the expression of mitogen-activated protein kinase phosphatase-1(MKP-1)in hippocampus.Methods Thirty SD rats of clean grade were randomly assigned into control group,PTSD 1 d group,PTSD 3 d group,PTSD 7 d group and PTSD 14 d group with 6 in each group.The PTSD rat model was made by an internationally recognized single prolonged stress(SPS)method.Open-field test and Morris water maze were used to observe the behavior changes in rats.Meanwhile,real time quantitative PCR(qRT-PCR)and Western blot were used to detect the changes of MKP-1 mRNA level and protein level in hippocampus of rats,respectively.Results Compared with the control group,the number of erect times,entry times and frequency of crossing the platform decreased and the incubation period of the rats was prolonged in PTSD 7 d and PTSD 14 d group(P<0.05).The expression level of MKP-1 mRNA and protein in the hippocampus of PTSD 7 d group and PTSD 14 d group were significantly higher than that in the control group(P<0.05).Conclusion Behavioral change and memory decline in rats with PTSD are considered related to the increased expression of MKP-1 gene and protein in hippocampus.MKP-1 probably be involved in the pathogenesis of PTSD,so the MKP-1 may serve as a reference index for the occurrence and development of PTSD.
作者 邢文龙 刘超猛 王梅子 朱志慧 张桂青 Xing Wenlong;Liu Chaomeng;Wang Meizi;ZHU Zhihui;ZHANG Guiqing(Medical College,Shihezi University,Shihezi 832003)
出处 《安徽医科大学学报》 CAS 北大核心 2018年第12期1889-1892,共4页 Acta Universitatis Medicinalis Anhui
基金 "十二五"新疆生产建设兵团医药卫生重点领域科技攻关项目(编号:2012BA023)
  • 相关文献

参考文献3

二级参考文献22

  • 1Walker KR, Tesco G. Molecular mechanisms of cognitive dysfunction following traumatic brain injury [ J ]. Front Ag- ing Neurosci,2013, 5:29.
  • 2Terpolilli NA, Kim SW, Thal SC, et al. Inhaled nitric ox- ide reduces secondary brain damage after traumatic brain injury in mice [ J ]. Cereb Blood Flow Metab,2013,33 : 311 - 318.
  • 3Hlatky R, Lui H, Cherian L, et al. The role of endothelial nitric oxide synthase in the cerebral hemodynamics after controlled cortical impact injury in mice [ J ]. Neurotrau- ma, 2003, 20:995-1006.
  • 4Zhou YF, Li WT, Han HC, et al. A11icin protects rat corti- cal neurons against mechanical trauma injury by regulating nitric oxide synthase pathways [ J ]. Brain Res Bull, 2014, 100:14-21.
  • 5Rangel-Castilla L, Ahmed O, Goodman JC, et al. L-argi- nine reactivity in cerebral vessels after severe traumatic brain injury [J]. Neurol Res. 2010,32:1033-1040.
  • 6Robertson CS, Gopinath SP, Valadka AB, et al. Variants of the endothelial nitric oxide gene and cerebral blood flow after severe traumatic brain injury [ J ]. Neurotrauma, 2011,28:727-737.
  • 7Nelin LD, Wang X, Zhao Q, et al. MKP-1 switches argi- nine metabolism from nitric oxide synthase to arginase fol- lowing endotoxin challenge [ J ]. Am J Physiol Cell Physiol,2007, 293:632-640.
  • 8Yang D, Xie P, Liu ZH. Ischemia/reperfusion-induced MKP-3 impairs endothelial NO formation via inactivation of ERK1/2 pathway [ J]. PLoS one, 2012,7 : 1-14.
  • 9Stefania M, Stefania G, Katia V, et al. Cannabinoid CB2 receptors modulate ERK-1/2 kinase signalling and NO re- lease in microglial cells stimulated with bacterial lipopo- lysaccharide [J]. Br J Pharmacol, 2012,165 : 1773-1788.
  • 10Feeney DM, Boyeson MG, Linn RT, et al. Responses to cortical injury: Methodology and local effects of contusions in the rat [J]. Brain Res,1981,211:67-77.

共引文献10

同被引文献35

引证文献6

二级引证文献9

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部