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普通狨猴急性给予1-甲基-4-苯基-1,2,3,6-四氢吡啶后神经系统形态学变化的演变与分布

The evolution and distribution of morphological changes in the nervous system of the common marmoset following the acute administration of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine.

作者信息

Gibb W R, Terruli M, Lees A J, Jenner P, Marsden C D

机构信息

Department of Neuropathology, National Hospitals for Nervous Diseases, Maida Vale, London.

出版信息

Mov Disord. 1989;4(1):53-74. doi: 10.1002/mds.870040109.

Abstract

Six young adult marmosets received 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine in multiple doses (total 8-16 mg/kg over 2-13 days) sufficient to produce a parkinsonian syndrome and were killed up to 3.5 months later. Cellular changes were found in the substantia nigra, ventral tegmental area, and hypothalamus. The earliest histological abnormalities were axonal swellings in proximal parts of nigrostriatal axons. Subsequent changes in the substantia nigra were reduced Nissl staining, reduced cell volume, and aggregation and loss of melanin granules. Other effects were reduced nuclear and nucleolar volumes, depletion of cells, and hyperplasia of glial cells. Shrunken cytoplasm and nuclei stained uniformly with eosin, and no cells showed cytoplasmic swellings or inclusions. These cellular alterations, with nuclear changes resembling karyolysis, do not occur in Parkinson's disease, which is characterised by Lewy body inclusions and signs of chromatolysis. The rapid appearance of axonal swellings, disruption of Nissl substance, and cell shrinkage suggest an insult to energy producing mechanisms. In this study, the absence of histological evidence of toxicity in the locus coeruleus and also in the substantia innominata and in serotonergic cell groups is unlike the more widespread degenerative changes of Parkinson's disease.

摘要

六只成年狨猴接受了多次剂量的1-甲基-4-苯基-1,2,3,6-四氢吡啶(2至13天内总量为8至16毫克/千克),足以引发帕金森综合征,并在3.5个月内被处死。在黑质、腹侧被盖区和下丘脑发现了细胞变化。最早的组织学异常是黑质纹状体轴突近端的轴突肿胀。黑质随后的变化包括尼氏染色减少、细胞体积减小、黑色素颗粒聚集和丢失。其他影响包括核体积和核仁体积减小、细胞耗竭以及胶质细胞增生。细胞质和细胞核萎缩,伊红染色均匀,没有细胞出现细胞质肿胀或包涵体。这些细胞改变,其核变化类似于核溶解,在帕金森病中不会出现,帕金森病的特征是路易小体包涵体和染色质溶解迹象。轴突肿胀的迅速出现、尼氏体的破坏和细胞萎缩表明对能量产生机制的损害。在本研究中,蓝斑以及无名质和血清素能细胞群中没有毒性的组织学证据,这与帕金森病更广泛的退行性变化不同。

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