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卒中后抑郁大鼠模型的建立及评估 被引量:14

Establishment and Evaluation of Post-stroke Depression Rat Model
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摘要 目的建立卒中后抑郁(post stroke depression,PSD)有效动物模型。方法大脑中动脉闭塞(MCAO)制备大鼠局灶脑缺血模型,加以慢性不可预见的温和刺激结合孤养建立PSD模型并予氟西汀干预。分为对照组、卒中组、抑郁组、PSD组和PSD+氟西汀组。分别采用糖水消耗试验、旷野试验(open-fieldtest,OFT)、强迫游泳评估大鼠快感缺失、活动减少、行为绝望等行为。结果应激14d时,与对照组及卒中组相比,PSD组体重增长幅度显著降低(P<0.05),经氟西汀干预后体重增长幅度明显增加(P<0.01)。PSD组水平得分在应激第7天时与对照组相比显著降低(P<0.05);到应激14d时,PSD组与对照组及卒中组相比水平得分进一步下降(P<0.01),并持续到应激18d(P<0.01)。PSD组垂直得分在应激14d时与对照组、卒中组相比均显著下降(P<0.05或P<0.01),强迫游泳的不动时间明显延长(P<0.05);而氟西汀干预后水平得分与垂直得分均显著增加(P<0.05或P<0.01),不动时间明显缩短(P<0.01)。结论PSD模型大鼠较充分而持续表现快感缺乏、活动减少等"抑郁"核心症状,可操作性和重复性较好,是研究PSD较为理想的大鼠模型。氟西汀能改善PSD模型大鼠行为学异常。 Objective To establish the rat model of post-stroke depression (PSD). Methods The focal cerebral ischemia model was set up by blocking the middle cerebral artery (MCA). Then the model rats were separately raised and put into chronic unpredictable mild stress (CUMS) to induce the PSD model and some of them were intervened by ? uoxertine. The rats were divided into control, stroke, depression, post-stroke depression and PSD treated with ? uoxertine groups and all of them were examined dynamically by Open-fi eld test (OFT), sucrose consumption test and forced swimming test. Results The animal models of PSD had significantly less weight gain than control group and stroke group(P<0.01)at day 14 after CUMS. After given ? uoxertin the animals' body weight in PSD group increased signifi cantly than before. The scores of horizontal and vertical movement activities in OFT of PSD group were signifi cantly less than in control and stroke groups(P<0.05 or P<0.01). The fi xed time in forced-swimming test was signifi cantly longer in PSD group when compared with control and stroke groups(P<0.05). Fluoxertin markedly increased open-fi eld activities(P<0.05 or P<0.01) and decreased the fi xed time in forced-swimming test(P<0.01). Conclusion Anhedonia and underactivity, the core symptoms in the PSD patients, can be found completely and persistently in the PSD group rats. With good operability and repeatability, the rats PSD model is an ideal model for the PSD research. Fluoxetine can improve the behavior abnormality of the PSD rats.
出处 《中国卒中杂志》 2007年第11期891-894,共4页 Chinese Journal of Stroke
基金 国家自然科学基金项目(30570656 30600206) 江苏省自然科学基金重点项目(BK2006708)
关键词 卒中 抑郁 模型 动物 氟西汀 Stroke Depressive disorder Models Animal Fluoxertin
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参考文献8

  • 1[1]Leentjens AF,Aben I,Lodder,et al.General and diaease-specific risk factors for depression after ischemic stroke:a two-step Cox regression analysis[J].Int Psychogeriatr,2006,18:739-748. 被引量:1
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二级参考文献8

  • 1Willner P. Animal models of depression: an overview. Trends Pharmacol Sci, 1991,12: 131-136. 被引量:1
  • 2Sugo N, Hum PD, Morahan MB, et al. Social stress exacerbates focal cerebral ischemia in mice. Stroke, 2002,33 : 1660-1664. 被引量:1
  • 3Willner P. The validity of animal model of depression. Psychopharmacology, 1984,83 : 1-16. 被引量:1
  • 4Koizumi J, Yoshida Y, Nakazawa T, et al. Experimental studies of iscbemie brain edema: A new experimental model of cerebral embolism in rats in which recirculation can be introduced in the ischemie area. Jpn J Stroke, 1986,8:1-8. 被引量:1
  • 5Longa EZ, Weistein PR, Carlson S. Reversible middle cerebral artery occlusion without craniectomy in rats. Stroke, 1989,20 : 84- 89. 被引量:1
  • 6Willner P, Towell A, Sampson D, et al. Reduction of sucrose preference by chronic mild unpredictable stress and its restoration by a tricyclic antidepressant. Psychopharmacology, 1987,93:358- 364. 被引量:1
  • 7Katz R J, Roth KA, Carroll BJ. Acute and chronic stress effects on open field activity in the rat: implications for a model of depression. Neurosci Biobehav Rev, 1981,5:247-251. 被引量:1
  • 8唐启盛,裴清华,侯秀娟,曲淼.脑卒中后抑郁状态动物模型的建立[J].北京中医药大学学报,2004,27(3):33-36. 被引量:51

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