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灵长类动物腹内侧中脑被盖损伤后多巴胺神经元的肥大。

Hypertrophy of dopamine neurons in the primate following ventromedial mesencephalic tegmentum lesion.

作者信息

Janson A M, Fuxe K, Goldstein M, Deutch A Y

机构信息

Department of Histology and Neurobiology, Karolinska Institutet, Stockholm, Sweden.

出版信息

Exp Brain Res. 1991;87(1):232-8. doi: 10.1007/BF00228526.

Abstract

Morphological changes in ventral mesencephalic dopamine (DA) neurons of a monkey sustaining a unilateral electrolytic lesion of the ventromedial mesencephalic tegmentum four years earlier were examined. Substantia nigra (A9) DA neurons lateral to the lesion underwent hypertrophic changes. The mean area of these neurons was enlarged by approximately 30% relative to corresponding neurons in the contralateral substantia nigra. Semi-quantitative immunohistochemical measurements of the intensity of tyrosine hydroxylase-like immunoreactivity (TH-li) indicated an increase in the amount of TH-li protein per cell in the hypertrophied neurons. Hypertrophic changes were also observed in ipsilateral A11 DA neurons of the caudal hypothalamus, suggesting that the increase in size was related to transection of the axons of DA neurons as they pass through the midbrain in their projections to target sites. The lesion did not overtly change the density or pattern of the substance P innervation of the substantia nigra, indicating that the striato- and pallido-nigral projections were spared by the lesion. These data suggest that hypertrophy may be a compensatory mechanism of dopaminergic neurons in response to partial lesions of the nigrostriatal system, and thus represent a morphological counterpart to the compensatory biochemical processes effected in response to partial lesions of the striatal dopaminergic innervation.

摘要

对一只四年前遭受腹内侧中脑被盖单侧电解损伤的猴子腹侧中脑多巴胺(DA)神经元的形态变化进行了检查。损伤侧外侧的黑质(A9)DA神经元发生了肥大性改变。相对于对侧黑质中的相应神经元,这些神经元的平均面积增大了约30%。酪氨酸羟化酶样免疫反应性(TH-li)强度的半定量免疫组织化学测量表明,肥大神经元中每个细胞的TH-li蛋白量增加。在下丘脑尾部的同侧A11 DA神经元中也观察到了肥大性改变,这表明大小的增加与DA神经元轴突在向靶位点投射过程中穿过中脑时的横断有关。该损伤并未明显改变黑质中P物质神经支配的密度或模式,表明纹状体和苍白球-黑质投射未受该损伤影响。这些数据表明,肥大可能是多巴胺能神经元对黑质纹状体系统部分损伤的一种代偿机制,因此代表了对纹状体多巴胺能神经支配部分损伤所产生的代偿性生化过程的形态学对应物。

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