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成年大鼠脑中抗抑郁药治疗对脑源性神经营养因子转录本的差异调节。

Differential regulation of brain derived neurotrophic factor transcripts by antidepressant treatments in the adult rat brain.

作者信息

Dias Brian G, Banerjee Sunayana B, Duman Ronald S, Vaidya Vidita A

机构信息

Department of Biological Sciences, Tata Institute of Fundamental Research, Homi Bhabha Road, Colaba, Mumbai, 400 005, India.

出版信息

Neuropharmacology. 2003 Sep;45(4):553-63. doi: 10.1016/s0028-3908(03)00198-9.

DOI:10.1016/s0028-3908(03)00198-9
PMID:12907316
Abstract

Antidepressants are known to increase brain derived neurotrophic factor (BDNF) mRNA in the adult rat brain. The BDNF gene has four differentially regulated promoters that generate four transcript forms, each containing a unique non-coding 5' exon (exon I-IV) and a common 3' coding exon. Using in situ hybridization with exon-specific riboprobes, we have examined whether diverse classes of antidepressants recruit a single or multiple BDNF promoters to regulate BDNF mRNAs. The antidepressants tested were electroconvulsive seizure (ECS) and the pharmacological antidepressants tranylcypromine, desipramine and fluoxetine. The effects of both acute and chronic ECS were the most prominent on exon I and II containing BDNF mRNAs in hippocampal and cortical subfields. Chronic ECS enhanced the acute induction of exon I, II and IV mRNAs but did not influence the acute upregulation of exon III mRNAs. Acute pharmacological antidepressants resulted in region-specific decreases in distinct exon-specific BDNF transcripts. In contrast, chronic administration with tranylcypromine and desipramine enhanced exon II and exon III mRNAs, respectively, in discrete hippocampal and cortical subfields. Chronic fluoxetine treatment did not have a significant effect on the exon-specific BDNF transcripts. The results indicate that distinct antidepressants differentially regulate BDNF mRNAs through a region-specific recruitment of the four BDNF promoters and suggest that diverse signaling mechanisms may be recruited to regulate BDNF transcripts.

摘要

已知抗抑郁药可增加成年大鼠脑中脑源性神经营养因子(BDNF)的mRNA。BDNF基因有四个差异调节的启动子,可产生四种转录本形式,每种形式都包含一个独特的非编码5'外显子(外显子I-IV)和一个共同的3'编码外显子。我们使用外显子特异性核糖探针进行原位杂交,研究了不同类别的抗抑郁药是募集单个还是多个BDNF启动子来调节BDNF mRNA。所测试的抗抑郁药为电惊厥发作(ECS)以及药理抗抑郁药反苯环丙胺、地昔帕明和氟西汀。急性和慢性ECS对海马和皮质亚区中含外显子I和II的BDNF mRNA的影响最为显著。慢性ECS增强了外显子I、II和IV mRNA的急性诱导,但不影响外显子III mRNA的急性上调。急性药理抗抑郁药导致不同外显子特异性BDNF转录本出现区域特异性减少。相反,反苯环丙胺和地昔帕明的慢性给药分别增强了离散海马和皮质亚区中外显子II和外显子III的mRNA。慢性氟西汀治疗对外显子特异性BDNF转录本没有显著影响。结果表明,不同的抗抑郁药通过对四个BDNF启动子的区域特异性募集来差异调节BDNF mRNA,并提示可能募集多种信号传导机制来调节BDNF转录本。

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