Zinc and imipramine reverse the depression-like behavior in mice induced by chronic restraint stress

被引:67
|
作者
Ding, Qin [1 ]
Li, Hongxia [1 ]
Tian, Xue [1 ]
Shen, Zhilei [1 ]
Wang, Xiaoli [1 ]
Mo, Fengfeng [1 ]
Huang, Junlong [1 ]
Shen, Hui [1 ]
机构
[1] Second Mil Med Univ, Dept Naval Hyg, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Depression; Zinc; Imipramine; Chronic restraint stress; GPR39; UP-REGULATION; ANTIDEPRESSANT ACTIVITY; NEUROTROPHIC FACTOR; SERUM ZINC; RECEPTOR; GPR39; HIPPOCAMPUS; BRAIN; MODEL; NEUROBIOLOGY;
D O I
10.1016/j.jad.2016.03.017
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Depression is a common psychopathological disorders. Studies of depression have indicated that zinc play a role in the depression pathophysiology and treatment. In present study, we examined the effects of zinc and imipramine supplement alone or combination of zinc and imipramine in mice induced by chronic restraint stress (CRS). Moreover, the possible roles of zinc receptor (G protein-coupled receptor 39, GPR39)-related pathway was investigated. Decreased weight and increased corticosterone (CORT) were observed after 3 weeks CRS exposure. It was shown that CRS induced lower serum zinc, higher hippocampal zinc, increased immobility time in tail suspension test and decreased movement distance in spontaneous activity test, which could be normalized by zinc (30 mg/kg) and imipramine (20 mg/kg) supplement alone and combination of zinc (15 mg/kg) and imipramine (5 mg/kg) for 3 weeks after CRS exposure. Moreover, the changes in mRNA expressions of GPR39, cAMP-response element binding protein (CREB), brain-derived neurotropic factor (BDNF) and n-methytl-D-aspartate receptors (NMDAR) could be reversed by the same treatment mentioned above. These results suggested that zinc dyshomeostasis in serum and hippocampus and depression-like behavior in CRS exposure animals observed in present study could be normalized by zinc and imipramine. The combination of zinc and imipramine in low dose has synergetic effects. The possible mechanism might be correlated to GPR39 receptor-related pathway. (c) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:100 / 106
页数:7
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