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纹状体苍白球或纹状体黑质通路的自杀性运输损伤对纹状体超微结构的影响。

Effects of suicide transport lesions of the striatopallidal or striatonigral pathways on striatal ultrastructure.

作者信息

Roberts R C, Strain-Saloum C, Wiley R G

机构信息

Maryland Psychiatric Research Center, University of Maryland School of Medicine, Baltimore 21228, USA.

出版信息

Brain Res. 1995 Dec 1;701(1-2):227-37. doi: 10.1016/0006-8993(95)01004-3.

Abstract

In the basal ganglia, centrally active suicide transport agents produce selective lesions of the striatopallidal and striatonigral pathways based on receptor binding and neuropeptide mRNA studies. Anatomical analyses indicate a selective, albeit modest, loss of projection neurons. In the present study, we sought to determine the ultrastructural sequelae in the striatum of suicide transport injections of the globus pallidus (GP) or substantia nigra (SN). Neostriata of adult rats were examined 10 days after lesions of the striatopallidal or striatonigral pathways with OX7-saporin or volkensin. Controls consisted of normal unoperated rats and animals injected into either target with ricin, a toxic lectin that is not transported in the central nervous system. Injections with OX7-saporin or volkensin into the GP or SN produced a decrease in striatal synaptic density of approximately 20%, relative to the contralateral side. Dark degenerating profiles, though very rare in the contralateral striata, were present throughout the neuropil in the ipsilateral striata. In animals with striatopallidal lesions, axospinous synapses of both the asymmetric and symmetric type were decreased in density, while the number of synapses formed with dendritic shafts was unaffected. In addition, the number of striatal mitochondrial profiles was decreased ipsilateral to the lesions. In animals with striatonigral lesions, the number of axospinous and axodendritic synapses of the asymmetric type was decreased ipsilateral to the lesions. Synaptic density and ultrastructural integrity remained unaffected in the striata of animals receiving ricin injections and in the contralateral striata of animals receiving OX7-saporin or volkensin injections. Our results, taken together with previous studies showing marked loss of receptors, uptake sites and mRNA, suggest that while most synapses are present and intact, the efficacy of synaptic transmission may be altered.

摘要

基于受体结合和神经肽mRNA研究,中枢活性自杀转运剂在基底神经节产生纹状体苍白球和纹状体黑质通路的选择性损伤。解剖学分析表明投射神经元有选择性的、尽管程度不大的损失。在本研究中,我们试图确定向苍白球(GP)或黑质(SN)进行自杀转运注射后纹状体中的超微结构后遗症。成年大鼠的新纹状体在纹状体苍白球或纹状体黑质通路用OX7-皂草素或 Volkensin损伤后10天进行检查。对照组包括正常未手术的大鼠以及用蓖麻毒素注射到任一靶点的动物,蓖麻毒素是一种不在中枢神经系统中转运的有毒凝集素。向GP或SN注射OX7-皂草素或Volkensin导致纹状体突触密度相对于对侧降低约20%。暗变性轮廓在对侧纹状体中非常罕见,但在同侧纹状体的整个神经毡中都存在。在有纹状体苍白球损伤的动物中,不对称和对称类型的轴棘突触密度均降低,而与树突干形成的突触数量未受影响。此外,损伤同侧的纹状体线粒体轮廓数量减少。在有纹状体黑质损伤的动物中,损伤同侧不对称类型的轴棘和轴树突突触数量减少。接受蓖麻毒素注射的动物纹状体以及接受OX7-皂草素或Volkensin注射的动物对侧纹状体中的突触密度和超微结构完整性未受影响。我们的结果与先前显示受体、摄取位点和mRNA明显丢失的数据相结合,表明虽然大多数突触存在且完整,但突触传递的效能可能会改变。

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