Repeated stress increases catalytic TrkB mRNA in rat hippocampus

被引:197
作者
Nibuya, M
Takahashi, M
Russell, DS
Duman, RS [1 ]
机构
[1] Yale Univ, Sch Med, Connecticut Mental Hlth Ctr, Lab Mol Psychiat,Dept Psychiat, New Haven, CT 06508 USA
[2] Yale Univ, Sch Med, Connecticut Mental Hlth Ctr, Lab Mol Psychiat,Dept Neurol, New Haven, CT 06508 USA
[3] Yale Univ, Sch Med, Connecticut Mental Hlth Ctr, Lab Mol Psychiat,Dept Pharmacol, New Haven, CT 06508 USA
关键词
brain-derived neurotrophic factor; TrkB; tyrosine kinase; stress; depression; antidepressant;
D O I
10.1016/S0304-3940(99)00335-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Northern blot analysis was utilized to distinguish between catalytic and truncated TrkB mRNA on the basis of transcript size. Repeated (10 days), but not acute, immobilization stress significantly increased levels of catalytic TrkB mRNA, but did not influence expression of truncated TrkB transcripts in rat hippocampus. Exposure to another paradigm, a combination of different, unpredictable stressors, also increased levels of catalytic, but not truncated, TrkB mRNA. In situ hybridization analysis demonstrated that chronic stress up-regulated TrkB mRNA in CA1 and CA3 pyramidal and dentate gyrus granule cells layers of hippocampus. As previously reported, both acute and chronic immobilization stress decreased expression of BDNF mRNA, suggesting that up-regulation of catalytic TrkB mRNA may be a compensatory adaptation to repeated stress. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:81 / 84
页数:4
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