Enriched environment combined with fluoxetine ameliorates depression-like behaviors and hippocampal SYP expression in a rat CUS model

被引:26
作者
Liu, Cong [1 ]
Gu, Jing-Yang [1 ]
Han, Jin-Hong [2 ]
Yan, Fu-Lin [3 ]
Li, Yan [4 ]
Lv, Ting-Ting [1 ]
Zhao, Li-Qin [1 ]
Shao, Qiu-Jing [1 ]
Feng, Yan-Yan [1 ]
Zhang, Xiang-Yang [5 ]
Wang, Chang-Hong [1 ]
机构
[1] Xinxiang Med Univ, Affiliated Hosp 2, Dept Psychiat, Psychiat Hosp Henan Prov, Jianshe Rd 388, Xinxiang 453002, Henan, Peoples R China
[2] Xinxiang Med Univ, Dept Basic Med, Jinsui Rd 601, Xinxiang 453003, Henan, Peoples R China
[3] Xinxiang Med Univ, Pharm Coll, Jinsui Rd 601, Xinxiang 453003, Henan, Peoples R China
[4] Zhengzhou Univ, Publ Hlth Coll, Dept Child & Adolescent, Kexue Rd 100, Zhengzhou 450001, Henan, Peoples R China
[5] Peking Univ, Beijing Hui Long Guar Hosp, Beijing 100096, Peoples R China
关键词
Chronic unpredictable stress; Rat; Hippocampus; Fluoxetine; Enrich environment; CHRONIC MILD STRESS; CHRONIC UNPREDICTABLE STRESS; SYNAPTIC PLASTICITY; ADULT RATS; SYNAPTOPHYSIN; CELLS; DEFICITS; NEUROGENESIS; DYSFUNCTION; PREFERENCE;
D O I
10.1016/j.brainresbull.2017.09.009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Effects of enriched environment (EE) combined with fluoxetine in a chronic unpredictable stress (CUS) rat model were examined in our study. Thirty male Sprague-Dawley rats were randomly divided into control group, CUS group, CUS + EE group, CUS + fluoxetine group, and CUS + EE + fluoxetine group (n = six per group). Rats in the CUS group were bred under conditions of CUS and separation for 6 weeks; Control group animals were bred in group cages (three rats per cage) under standard laboratory conditions for 6 weeks; Rats in CUS + EE group, CUS + fluoxetine group, and CUS + EE + fluoxetine groups were bred under the conditions of CUS and separation for 6 weeks and had an intervention of EE, an oral gavage of fluoxetine, and an intervention of EE + oral gavage of fluoxetine, respectively, every day for the final 3 weeks. Every rat underwent a behavioral assessment at the beginning of the 1st week, at the end of the 3rd week and at the end of the 6th week. Behavioral assessments included sucrose water consumption, weight measurement, and an open field test (measuring horizontal moving distance, rearing behavior, and defecation). Finally, the level of synaptophysin expressed in the hippocampus was measured with immunohistochemistry. We found that EE, fluoxetine, and EE + fluoxetine all reversed the depression-like behaviors of CUS rats. The effect of EE + fluoxetine appeared to be superior to EE or fluoxetine alone; the expression level of synaptophysin in CA1, CA3, and DG of the hippo campus was decreased in CUS rats, however, exposure to EE, fluoxetine, and EE + fluoxetine all reversed this decrease.
引用
收藏
页码:33 / 39
页数:7
相关论文
共 67 条
[1]  
Bambico FR., 2013, Curr Top Behav Neurosci, V15, P243
[2]   Short-term exposure to enriched environment rescues chronic stress-induced impaired hippocampal synaptic plasticity, anxiety, and memory deficits [J].
Bhagya, Venkanna Rao ;
Srikumar, Bettadapura N. ;
Veena, Jayagopalan ;
Rao, Byrathnahalli S. Shankaranarayana .
JOURNAL OF NEUROSCIENCE RESEARCH, 2017, 95 (08) :1602-1610
[3]   Fluoxetine Administration Modulates the Cytoskeletal Microtubular System in the Rat Hippocampus [J].
Bianchi, Massimiliano ;
Shah, Ajit J. ;
Fone, Kevin C. F. ;
Atkins, Alan R. ;
Dawson, Lee A. ;
Heidbreder, Christian A. ;
Hows, Mark E. ;
Hagan, Jim J. ;
Marsden, Charles A. .
SYNAPSE, 2009, 63 (04) :359-364
[4]   Antidepressant Treatment Outcome Depends on the Quality of the Living Environment: A Pre-Clinical Investigation in Mice [J].
Branchi, Igor ;
Santarelli, Sara ;
Capoccia, Sara ;
Poggini, Silvia ;
D'Andrea, Ivana ;
Cirulli, Francesca ;
Alleva, Enrico .
PLOS ONE, 2013, 8 (04)
[5]   The double edged sword of neural plasticity: Increasing serotonin levels leads to both greater vulnerability to depression and improved capacity to recover [J].
Branchi, Igor .
PSYCHONEUROENDOCRINOLOGY, 2011, 36 (03) :339-351
[6]   BDNF protein expression in the hippocampus following exposure of rats to forced swimming stress [J].
Bulygina V.V. ;
Shishkina G.T. ;
Berezova I.V. ;
Dygalo N.N. .
Doklady Biological Sciences, 2011, 437 (1) :82-84
[7]   Neuronal plasticity and antidepressant actions [J].
Castren, Eero ;
Hen, Rene .
TRENDS IN NEUROSCIENCES, 2013, 36 (05) :259-267
[8]   Chronic restraint stress causes anxiety- and depression-like behaviors, downregulates glucocorticoid receptor expression, and attenuates glutamate release induced by brain-derived neurotrophic factor in the prefrontal cortex [J].
Chiba, Shuichi ;
Numakawa, Tadahiro ;
Ninomiya, Midori ;
Richards, Misty C. ;
Wakabayashi, Chisato ;
Kunugi, Hiroshi .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2012, 39 (01) :112-119
[9]   Grand challenges in global mental health [J].
Collins, Pamela Y. ;
Patel, Vikram ;
Joestl, Sarah S. ;
March, Dana ;
Insel, Thomas R. ;
Daar, Abdallah S. .
NATURE, 2011, 475 (7354) :27-30
[10]   Synaptic Dysfunction in Depression: Potential Therapeutic Targets [J].
Duman, Ronald S. ;
Aghajanian, George K. .
SCIENCE, 2012, 338 (6103) :68-72