Reduction in parvalbumin expression in the zona incerta after 6OHDA lesion in rats.

Journal of Neurocytology Pub Date : 2005-12-01 Epub Date: 2006-08-10 DOI:10.1007/s11068-006-8728-y
Claire E Heise, John Mitrofanis
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引用次数: 14

Abstract

In an effort to understand better the neurochemical changes that occur in Parkinson disease, we have examined the expression patterns of the calcium-binding protein parvalbumin in the zona incerta in parkinsonian rats. Sprague-Dawley rats had small volumes of either saline (control) or 6 hydroxydopamine (6OHDA) injected into the medial forebrain bundle, the major tract carrying dopaminergic nigrostriatal axons. After various post-lesion survival periods, ranging from 2 hrs to 84 days, rats were perfused with formaldehyde and their brains processed for routine tyrosine hydroxylase (TH) or parvalbumin immunocytochemistry. In the 3 to 84 days post-lesion cases, there was an overall 50% reduction in the number of parvalbumin(+) cells in the zona incerta on the 6OHDA-lesioned side when compared to control. In the 2 hrs post-lesion cases, there was no substantial loss of parvalbumin(+) cells in the zona incerta after 6OHDA lesion, although in these cases (unlike the longer survival periods), there was limited loss of TH(+) cells in the midbrain on the lesion side. The loss of parvalbumin(+) cells from the zona incerta was due to a loss of antigen expression rather than a loss of the cells themselves, since the number of Nissl-stained cells in the zona incerta was similar on the control and 6OHDA-lesioned sides. In summary, our results indicate that a loss of the midbrain dopaminergic cells induces a major change in parvalbumin expression within the zona incerta. This change may have key functional and clinical implications.

大鼠6OHDA损伤后斑纹带小白蛋白表达降低。
为了更好地了解帕金森病中发生的神经化学变化,我们检查了帕金森病大鼠不动带中钙结合蛋白小白蛋白的表达模式。将小体积生理盐水(对照组)或6 -羟多巴胺(6OHDA)注射到内侧前脑束,内侧前脑束是携带多巴胺能黑质纹状体轴突的主要通道。在病变后2小时至84天的不同生存期后,对大鼠进行甲醛灌注,并对其大脑进行常规酪氨酸羟化酶(TH)或小白蛋白免疫细胞化学处理。在病变后3至84天的病例中,与对照组相比,6ohda病变侧的斑纹带中细小白蛋白(+)细胞数量总体减少了50%。在病变后2小时的病例中,6OHDA病变后无明显的小白蛋白(+)细胞损失,尽管在这些病例中(与更长的生存期不同),病变侧中脑TH(+)细胞有有限的损失。小白蛋白(+)细胞的缺失是由于抗原表达的缺失,而不是细胞本身的缺失,因为在对照组和6ohda损伤侧,小白蛋白(+)细胞的数量相似。综上所述,我们的研究结果表明,中脑多巴胺能细胞的缺失会导致斑带内小蛋白表达的重大变化。这种变化可能具有关键的功能和临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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