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多巴胺去神经支配的纹状体神经元中Fos相关抗原、Jun B和TrkB的长期表达。

Prolonged expression of Fos-related antigens, Jun B and TrkB in dopamine-denervated striatal neurons.

作者信息

Dragunow M, Butterworth N, Waldvogel H, Faull R L, Nicholson L F

机构信息

Department of Pharmacology, School of Medicine, University of Auckland, New Zealand.

出版信息

Brain Res Mol Brain Res. 1995 Jun;30(2):393-6. doi: 10.1016/0169-328x(95)00037-s.

Abstract

Previous studies have demonstrated that striatal dopamine-denervation leads to a long-term increase in Fos-related antigen(s) (FRA's) in striatal neurons. Because Fos-family proteins bind to DNA by dimerizing to Jun-family proteins we investigated the expression of Jun B protein 2 weeks and 1 month after striatal dopamine-denervation, produced by medial forebrain bundle transection. We also investigated the effects of this lesion on TrkB-immunoreactivity in the striatum. FRA's (as previously reported) and Jun B were expressed in striatal neurons following dopamine-denervation, and in addition, there was an increase in expression of TrkB in the striatum on the dopamine-denervated side. These results show that striatal dopamine depletion leads to a long-term up-regulation of FRA's and Jun B in the striatum, and this may be related to other biochemical changes previously reported to occur in striatal neurons (e.g.: D2-dopamine receptor up-regulation) after dopamine depletion. In addition, FRA and Jun B expression may induce increased production of TrkB after dopamine-denervation.

摘要

先前的研究表明,纹状体多巴胺去神经支配会导致纹状体神经元中Fos相关抗原(FRA)长期增加。由于Fos家族蛋白通过与Jun家族蛋白二聚化来结合DNA,我们研究了在前脑内侧束横断导致纹状体多巴胺去神经支配后2周和1个月时Jun B蛋白的表达情况。我们还研究了这种损伤对纹状体中TrkB免疫反应性的影响。如先前报道,FRA和Jun B在多巴胺去神经支配后的纹状体神经元中表达,此外,多巴胺去神经支配侧纹状体中TrkB的表达增加。这些结果表明,纹状体多巴胺耗竭会导致纹状体中FRA和Jun B长期上调,这可能与先前报道的多巴胺耗竭后纹状体神经元中发生的其他生化变化(如:D2-多巴胺受体上调)有关。此外,FRA和Jun B的表达可能会在多巴胺去神经支配后诱导TrkB产生增加。

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