Revuelta M, Venero J L, Machado A, Cano J
Departamento de Bioquímica, Bromatología y Toxicología, Facultad de Farmacia, Universidad de Sevilla, Spain.
Neuroscience. 1999;91(2):567-77. doi: 10.1016/s0306-4522(98)00624-1.
We have previously studied changes in the serotoninergic and dopaminergic nigrostriatal systems following transection of the medial forebrain bundle and found a long-term axotomy-induced increase in the levels of serotonin and its main metabolite, 5-hydroxyindolacetic acid in substantia nigra [Venero et al. (1997) J. Neurochem. 68, 2458-2468]. In an attempt to find a rationale for this effect, we have performed an immunohistochemical study. Transection of the medial forebrain bundle of the rat interrupted most of the ascending serotoninergic pathways from the raphe nuclei as revealed by serotonin immunoreactivity. While serotonin immunostaining was almost absent in striatum, it doubled in the ventral mesencephalon at 21 days postlesion. This axotomy-induced increase was accompanied by an increased density of the serotonin nerve terminal network in the ipsilateral substantia nigra and ventral tegmental area. The increase in serotonin immunoreactivity was in line with the measured levels of serotonin and 5-hydroxyindolacetic acid in substantia nigra. In addition, the distribution pattern of glial fibrillary acidic protein-immunoreactive astrocytes and OX42-immunoreactive microglia correlated highly with the location of increased serotonin fibre density in the ventral mesencephalon, especially in ventral tegmental area and in the most medial part of substantia nigra. We suggest that a pruning effect may underly the axotomy-induced increase in serotonin immunoreactivity in the ventral mesencephalon, and further, that activated astroglia and microglia may play a role in directing serotoninergic axonal regeneration following axotomy.
我们之前研究了内侧前脑束横断后5-羟色胺能和多巴胺能黑质纹状体系统的变化,发现长期轴突切断会导致黑质中5-羟色胺及其主要代谢产物5-羟吲哚乙酸水平升高[Venero等人(1997年),《神经化学杂志》68卷,2458 - 2468页]。为了寻找这种效应的理论依据,我们进行了一项免疫组织化学研究。大鼠内侧前脑束横断中断了大部分来自中缝核的5-羟色胺能上行通路,这通过5-羟色胺免疫反应性得以揭示。虽然纹状体中几乎没有5-羟色胺免疫染色,但在损伤后21天,腹侧中脑的免疫染色增加了一倍。这种轴突切断诱导的增加伴随着同侧黑质和腹侧被盖区5-羟色胺神经终末网络密度的增加。5-羟色胺免疫反应性的增加与黑质中5-羟色胺和5-羟吲哚乙酸的测量水平一致。此外,胶质纤维酸性蛋白免疫反应性星形胶质细胞和OX42免疫反应性小胶质细胞的分布模式与腹侧中脑5-羟色胺纤维密度增加的位置高度相关,特别是在腹侧被盖区和黑质最内侧部分。我们认为,修剪效应可能是腹侧中脑轴突切断诱导的5-羟色胺免疫反应性增加的基础,此外,活化的星形胶质细胞和小胶质细胞可能在轴突切断后引导5-羟色胺能轴突再生中发挥作用。