丰富环境联合氟西汀干预对大鼠抑郁样行为及脑内髓鞘碱性蛋白的影响

被引:4
作者
谷景阳 [1 ]
韩金红 [2 ]
詹和琴 [3 ]
王长虹 [1 ]
刘聪 [1 ]
单筱雯 [1 ]
翟飞 [1 ]
机构
[1] 新乡, 新乡医学院第二附属医院
[2] 新乡, 新乡医学院基础医学院
[3] 新乡, 新乡医学院药学院
关键词
抑郁; 髓鞘碱性蛋白; 丰富环境; 氟西汀; 海马; 前额叶;
D O I
暂无
中图分类号
R749.4 [情感性精神病];
学科分类号
100204 [神经病学];
摘要
目的探讨丰富环境联合氟西汀干预对慢性应激所致抑郁大鼠行为学的影响, 以及海马区和前额叶区髓鞘碱性蛋白(myelin basic protein, MBP)变化的影响。方法将50只成年雄性SD大鼠随机分为对照组、氟西汀组、模型组、丰富环境(enriched environment, EE)组和EE+氟西汀组, 后四组在第1~3周接受慢性不可预见性刺激(chronic unpredicted mild stress, CUMS)刺激;第4~6周, 氟西汀组、EE组以及EE+氟西汀组大鼠接受EE和(或)氟西汀干预;采用蔗糖水消耗实验、旷场实验、体质量变化评估大鼠的行为学变化;使用免疫组化法测量大鼠海马各亚区以及前额叶区MBP的含量。结果第3周末, 应激刺激大鼠的各项行为学评估较对照组明显下降, 差异有统计学意义(P<0.05);第6周末, 接受EE和(或)氟西汀干预后的应激大鼠抑郁样行为显著改善, 模型组大鼠海马CA1、DG区以及前额叶区MBP含量较对照组差异均有统计学意义(平均光密度:模型组依次为0.199±0.024, 0.204±0.021, 0.225±0.028;对照组依次为0.279±0.034, 0.288±0.043, 0.308±0.053, P<0.05);氟西汀组、EE组以及EE+氟西汀组大鼠海马CA1、DG区以及前额叶区的MBP含量较模型组明显升高, 差异均有统计学意义(氟西汀组依次为0.259±0.047, 0.266±0.052, 0.284±0.031;EE组依次为0.257±0.038, 0.258±0.042, 0.286±0.037;EE+氟西汀组依次为0.271±0.046, 0.279±0.040, 0.289±0.041, P<0.05)。结论 CUMS所致大鼠抑郁样行为的出现与海马CA1、DG区及前额叶区MBP含量的变化有关, 氟西汀及EE干预均能逆转大鼠的抑郁样行为, 且可使MBP含量恢复正常。
引用
收藏
相关论文
共 22 条
[1]
抗抑郁药物治疗的起效与疗效评价 [J].
季建林 .
世界临床药物, 2012, 33 (07) :385-387+425
[2]
丰富环境对慢性应激大鼠抑郁样行为的影响 [J].
张磊 ;
章军建 ;
孙慧敏 ;
杨英 ;
刘晖 .
中华行为医学与脑科学杂志, 2011, (11)
[3]
慢性应激抑郁模型大鼠海马组织S100B表达及氟西汀的干预作用 [J].
王国栋 ;
董娇 ;
李晏 ;
张晓莉 ;
宁秋芬 ;
刘鲜华 ;
王长虹 .
中华行为医学与脑科学杂志, 2013, 22 (11)
[4]
Role of Hippocampus Mitogen-Activated Protein Kinase Phosphatase-1 mRNA Expression and DNA Methylation in the Depression of the Rats with Chronic Unpredicted Stress [J].
Wang, Chang-Hong ;
Zhang, Xiao-Li ;
Li, Yan ;
Wang, Guo-Dong ;
Wang, Xin-Kai ;
Dong, Jiao ;
Ning, Qiu-Fen .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2015, 35 (04) :473-482
[5]
Changes in proinflammatory cytokines and white matter in chronically stressed rats.[J].Yang P;Gao Z;Zhang H;Fang Z;Wu C;Xu H;Huang QJ.Neuropsychiatric Disease and Treatment.2015, default
[6]
Desvenlafaxine prevents white matter injury and improves the decreased phosphorylation of the rate-limiting enzyme of cholesterol synthesis in a chronic mouse model of depression [J].
Wang, Junhui ;
Qiao, Jinping ;
Zhang, Yanbo ;
Wang, Hongxing ;
Zhu, Shenghua ;
Zhang, Handi ;
Hartle, Kelly ;
Guo, Huining ;
Guo, Wei ;
He, Jue ;
Kong, Jiming ;
Huang, Qingjun ;
Li, Xin-Min .
JOURNAL OF NEUROCHEMISTRY, 2014, 131 (02) :229-238
[7]
Demyelinating evidences in CMS rat model of depression: A DTI study at 7<ce:hsp sp="0.25"/>T.[J].B.S. Hemanth Kumar;S.K. Mishra;R. Trivedi;S. Singh;P. Rana;S. Khushu.Neuroscience.2014,
[8]
Influence of the brain sexual differentiation process on despair and antidepressant-like effect of fluoxetine in the rat forced swim test.[J].M.L. Gómez;L. Martínez-Mota;E. Estrada-Camarena;A. Fernández-Guasti.Neuroscience.2014,
[9]
Etazolate rescues behavioral deficits in chronic unpredictable mild stress model: Modulation of hypothalamic–pituitary–adrenal axis activity and brain-derived neurotrophic factor level.[J].Ankur Jindal;Radhakrishnan Mahesh;Shvetank Bhatt.Neurochemistry International.2013, 5
[10]
A preliminary study of white matter in adolescent depression: relationships with illness severity; anhedonia; and irritability.[J].Sarah E Henderson;Amy R Johnson;Ana I Vallejo;Lev eKatz;Edmund eWong;Vilma eGabbay;Vilma eGabbay.Frontiers in Psychiatry.2013,