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PTSD样大鼠中缝背核神经元细胞凋亡及其TMP活性表达变化的研究

刘冬娟 肖冰 王恩华 韩芳 石玉秀

中国医科大学学报2011,Vol.40Issue(11):983-985,1000,4.
中国医科大学学报2011,Vol.40Issue(11):983-985,1000,4.DOI:21-1227/R.20111128.1738.025

PTSD样大鼠中缝背核神经元细胞凋亡及其TMP活性表达变化的研究

Expression of TMP Activity and Apoptosis in Dorsal Raphe Nucleus of PTSD Rats

刘冬娟 1肖冰 1王恩华 2韩芳 3石玉秀1

作者信息

  • 1. 中国医科大学基础医学院电子显微学研究室,沈阳110001
  • 2. 中国医科大学病理学与病理生理学研究所,沈阳110001
  • 3. 中国医科大学基础医学院组织胚胎学教研室,沈阳110001
  • 折叠

摘要

Abstract

Objective To study expression of TMP activity and apoptosis in the dorsal raphe nucleus of PTSD (posttraumatic stress disorder) rats. Methods The SPS-method was used to set up the rat PTSD models. Rats were randomly divided into ld,7d and 14d groups of SPS and normal group. Apoptosis in the dorsal raphe nucleus were detected by using annexin V-FTTC/PI double-labled flow cytometry. The changes of TMP activity in the dorsal raphe were detected by light microscope and transmission electron microscopy (TEM). Results SPS exposure resulted in a significant change of characteristic morphologic changes of apoptosis in the dorsal raphe nucleus. Apoptosis rate in dorsal raphe nucleus was significantly increased and TMP activity was significantly enhanced compared with that of normal control group ( P < 0.05). Both markers reached the peak at 7 d after SPS exposure. Conclusion Dorsal raphe neurons of PTSD rats have had appotosis. The changes of apoptosis rate and TMP activity enhanced enhancing may might indicate that the TMP is was involved in degradation and processing of the apoptotic product in dorsal raphe nucleus, and smaller volume of pons may might be related to appotosis of dorsal raphe nucleus.

关键词

PTSD/中缝背核/神经元/细胞凋亡/TMP

Key words

posttraumatic stress disorder/ dorsal raphe nucleus/ neuron/ apoptosis/ thinamine monophosphatase

分类

医药卫生

引用本文复制引用

刘冬娟,肖冰,王恩华,韩芳,石玉秀..PTSD样大鼠中缝背核神经元细胞凋亡及其TMP活性表达变化的研究[J].中国医科大学学报,2011,40(11):983-985,1000,4.

基金项目

国家自然科学基金资助项目(81171282,31140060) (81171282,31140060)

国家教育部博士点基金资助项目(20092104110016) (20092104110016)

中国医科大学学报

OA北大核心CSCDCSTPCD

0258-4646

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