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大鼠胆碱能隔海马通路的中度损伤会增加海马神经生长因子的合成:长期代偿性变化的证据?

Moderate lesion of the rat cholinergic septohippocampal pathway increases hippocampal nerve growth factor synthesis: evidence for long-term compensatory changes?

作者信息

Hellweg R, Humpel C, Löwe A, Hörtnagl H

机构信息

Department of Psychiatry, Free University of Berlin, Germany.

出版信息

Brain Res Mol Brain Res. 1997 Apr;45(1):177-81. doi: 10.1016/s0169-328x(96)00310-5.

Abstract

Moderate lesions of the septohippocampal pathway by intraventricular infusions of ethylcholine aziridinium (AF64A) induced a dose-dependent decrease of hippocampal choline acetyltransferase (ChAT) activity, which partially recovered between 1 and 5 weeks after treatment. The cholinergic deficit was associated with an increase in nerve growth factor (NGF) mRNA only within the hippocampal dentate gyrus and hilus by maximally 51% and 111% 3 and 7 weeks after AF64A treatment, respectively, whereas no changes in brain-derived neurotrophic factor- and neurotrophin-3 mRNA were observed. The content of NGF protein transiently increased in the ventral part of the hippocampus 3 weeks after AF64A infusion but returned to control levels at 5 weeks. At that time, however, NGF content as well as ChAT activity were significantly increased in the septum, suggesting an increased utilization of NGF by the remaining cholinergic neurons. Thus, the present data provide correlative evidence for a critical role of endogenous NGF in neuroregeneration and plasticity of the cholinergic basal forebrain in case of incipient damage.

摘要

通过脑室内注入氮丙啶基乙基胆碱(AF64A)对隔海马通路造成中度损伤,可导致海马胆碱乙酰转移酶(ChAT)活性呈剂量依赖性降低,在治疗后1至5周部分恢复。胆碱能缺陷仅在AF64A治疗后3周和7周分别使海马齿状回和门区内神经生长因子(NGF)mRNA最多增加51%和111%,而未观察到脑源性神经营养因子和神经营养素-3 mRNA有变化。注入AF64A后3周,海马腹侧部分NGF蛋白含量短暂增加,但在5周时恢复到对照水平。然而,此时隔区的NGF含量以及ChAT活性显著增加,表明剩余胆碱能神经元对NGF的利用率增加。因此,本研究数据为内源性NGF在初期损伤情况下对胆碱能基底前脑的神经再生和可塑性起关键作用提供了相关证据。

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