设为首页 | 加入收藏
网站首页 本刊简介 编委会 投稿指南 过刊浏览 广告合作 网上订购 下载专区 联系我们  
慢性应激对不同月龄大鼠前额叶皮质、纹状体脑源性神经营养因子表达的影响
作者:王一赫1  江虹1  冀永娟2  李颖3  樊淑娟1  潘芳1  刘德祥1 
单位:1. 山东大学医学院 山东济南 250012 
2.
 青岛妇幼医院 山东青岛 266011 
3.
 中国人民公安大学 北京 100038 
关键词:应激 衰老 前额叶 纹状体 脑源性神经营养因子 
分类号:R395.1
出版年,卷(期):页码:2012,20(6):765-768
摘要:

目的:观察慢性应激对不同月龄大鼠行为、前额叶皮质、纹状体脑源性神经营养因子(BDNF)表达的影响。方法:采用慢性轻度不可预知性应激建立动物模型,观察2月龄和15月龄48只Wistar大鼠的行为学、前额叶皮层和纹状体细胞形态学及BDNF的表达。结果:与对照组相比,青年应激大鼠水平运动、直立次数均明显减少,这一变化在老年应激组更明显。应激组糖水偏爱百分比显著低于对照组,并持续到应激结束后一周;老年应激组的糖水偏爱百分比低于青年组。应激组前额叶皮层和纹状体神经细胞呈程度不同的损伤现象,且老年应激组的损伤较青年组严重。应激组前额叶皮质和纹状体BDNF表达明显下调,老年应激组下调明显。应激后一周,青年应激组BDNF表达有一定程度的升高,但仍显著低于对照组。结论:慢性轻度不可预知性应激引起老年大鼠明显的行为学改变,提示老年大鼠对应激的反应性和耐受性降低。应激导致前额叶皮层和纹状体细胞的变性、萎缩和死亡及BDNF表达下降,这一变化在老年组更为明显。

Objective: To study the chronic stress effects on the behavior and BDNF expression in PFC and caudate putamen in different aged rats.Methods: Chronic unpredictable mild stress(CUMS) was used to build 2 month and 15 month old Wistar rats depressive animal model,and to observe the behavior in open field test,sucrose preference,morphologic changes and BDNF expression in PFC and caudate putamen.Results: Compared with the control groups,the young stress groups displayed less square crossing and vertical movement,and the aged stress animals had more remarkable changes in those behavior.The young stress rats showed obviously decreased tendency in sucrose preference compared with the control groups.Meanwhile,the aged stress group exhibited obvious decreases of sucrose preference after stress,and persisted 1 week after stress than the young stress group.The young stress groups displayed obviously morphologic damage in PFC and caudate putamen,the aged stress group showed more cell atrophy and cellular necrosis compared with the young stress group.The young stress rats had significant lower BDNF expression in PFC and caudate putamen than the control groups;the aged stress rats showed even lower BDNF expression than the young stress rats at every testing time.Conclusion: CUMS induces aged rats to more serious abnormal behavior than young animals,indicating aging is one of the important influence factors in stress.The aged rats have more serious cell atrophy and cellular necrosis than the young rats under CUMS.Stress induces significant reduction of BDNF expression in PFC and caudate putamen.The aged stress rats have much lower BDNF expression than the young rats.

基金项目:
山东省自然基金(ZR2011CM015)
作者简介:
参考文献:

1.Astin JA,Forys K. Psychosocial determinants of health and illness:Integrating mind,body,and spirit[J].Advances In Mind-body Medicine,2004,(04):14-21.
2.Mastorakos G,Pavlatou M,Diamanti-Kandarakis E. Exercise and the stress system[J].Hormones,2005,(02):73-89.
3.Tafet GE,Bernardini R. Psychoneuroendocrinological links between chronic stress and depression[J].Progress in Neuro-Psychopharmacology & Biological Psychiatry,2003,(06):893-903.
4.McEwen BS. Protective and damaging effects of stress mediators:central role of the brain[J].Journal of Clinical Neuroscience,2006,(04):367-381.
5.鲁燕霞,刘萌,石寿森. 不同时程心理应激对支气管哮喘大鼠免疫功能的影响[J].中国临床心理学杂志,2010,(02):146-148.
6.Sousa N,Lukoyanov NV,Madeira MD. Reorgnization of the morphology of hippocampal neuritis and synapses after stress-induced damage correlates with behavioral imorovement[J].Neuroscience,2000,(02):253-266.
7.肖晶,朱雪玲,罗英姿. 抑郁症的脑结构异常--结构性核磁共振成像研究[J].中国临床心理学杂志,2011,(05):589-590.
8.Smith MA,Makinl S,Kvetnasky R. Stress and glucocorticoids affect the expression of brain-derived neurotrophic factor and neurotrophin-3mRNAs in the hippocampus[J].Journal of Neuroscience,1995,(03):1768-1777.
9.Roceri M,Cirulli F,Pessina C. Postnatal repeated maternal deprivation produces age-dependent changes of brain-derived neurotrophic factor expression in selected rat brain regions[J].Biological Psychiatry,2004,(07):708-714.
10.Schabitz WR,Berger C,Kollmar R. Effect of brainderived neurotrophic factor treatment and forced arm use on functionalmotor recovery after small cortical ischemia[J].Stroke,2004,(04):992-997.
11.Fernandez-Espejo E. Pathogenesis of Parkinson's disease:prospects of neuroprotective and restorative therapies[J].Molecular Neurobiology,2004,(01):15-30.
12.Willner P,Towell A,Sampson D. Reduction of sucrose preference by chronic unpredictable mild stress,and its restoration by a tricyclic antidepress-ant[J].Psychopharmacology(Berlin),1987,(03):358-364.
13.许晶,李晓秋. 慢性应激抑郁模型的建立及其评价[J].中国行为医学杂志,2003,(01):14-17.doi:10.3760/cma.j.issn.1674-6554.2003.01.006.
14.Lapchak PA,Araujo DM,Beck KD. BDNF and trkB mRNA expression in the hippocampal formation of aging rats[J].Neurobiology of Aging,1993,(02):121-126.
15.Croll SD,Nancy Y,Ronald M. Expression of BDNF and trkB as a function of age and cognitive performance[J].Brain Research,1998,(1-2):200-218.
16.Mizoguchi K,Ishige A,Aburada M. Chronic stress attenuates glucocorticoid negative feedback:Involvement of the prefrontal cortex and hippocampus[J].Neuroscience,2003,(03):887-897.
17.Tam SY,Roth RH. Mesoprefrontal dopaminergic neurons:Can tyrosine availability influence their functions[J].Biochemical Pharmacology,1997,(04):441-453.
18.江雪华,张敏,陆大祥. 新生期孤养对成年大鼠行为与5-羟色胺转运体表达的影响[J].中国临床心理学杂志,2010,(04):411-414.
19.Schildkraut JJ. The catecholamine hypothesis of affective disorders:A review of supporting evidence[J].American Journal of Psychiatry,1965,(05):509-512.
20.Erickson KI,Prakash RS,Voss MW. Brain-derived neurotrophic factor is associated with age-related decline in hippocampal volume[J].Journal of Neuroscience,2010,(15):5368-5375.
21.司银楚,朱培纯. 去脑皮层血管对大鼠前脑大细胞基底核AchE,ChAT,BDNF,TrkB及其mRNA的影响[J].神经解剖学杂志,2001,(02):161-165.
22.赖红,曾亮,赵海花. 老龄大鼠海马结构脑源性神经营养因子表达的改变[J].解剖学杂志,2005,(86):673-675.
23.Bjornebekk A,Math6 AA,Gruber SH. Housing conditions modulate escitalopram effects on antidepressive-like behaviour and brain neurochemistry[J].International Journal of Neuropsychopharmacology,2008,(08):1135-1147.

服务与反馈:
文章下载】【加入收藏
您是第访问者

《中国临床心理学杂志》编辑部
地址:湖南省长沙市中南大学湘雅二医院内, 410011
电 话:0731-85292472    电子邮件:cjcp_china@163.com
本系统由北京博渊星辰网络科技有限公司设计开发 技术支持电话:010-63361626