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兴奋性毒性(喹啉酸)诱导大鼠纹状体变性后一氧化氮合酶活性双向变化的证据。

Evidence for bidirectional changes in nitric oxide synthase activity in the rat striatum after excitotoxically (quinolinic acid) induced degeneration.

作者信息

Schmidt W, Wolf G, Calka J, Schmidt H H

机构信息

Institute of Medical Neurobiology, University of Magdeburg, Germany.

出版信息

Neuroscience. 1995 Jul;67(2):345-56. doi: 10.1016/0306-4522(95)00027-g.

Abstract

Nitric oxide, a gaseous inter- and intracellular messenger, is thought to mediate neurotoxicity via excitatory amino acid receptors which may contribute to the pathogenesis of a variety of neuronal diseases. Excitotoxin lesions induced by quinolinic acid were made unilaterally in the rat striatum to study biochemically, light- and electron microscopically the possible involvement of the nitric oxide synthesizing enzyme nitric oxide synthase in degeneration processes. 5 days after quinolinic acid injection nitric oxide synthase activity in the striatum was elevated to 196.5% (P < 0.005% as compared to controls). There was no requirement of Ca2+ for the enzyme activity measured indicating that the elevation is due to the inducible isoform of nitric oxide synthase. Parallel to the depletion of neurons by quinolinic acid a massive gliosis was seen. Whereas quiescent astroglial cells in the normal striatum did not show any light microscopically detectable nicotinamide adenine dinucleotide phosphate diaphorase reaction, reactive astroglia revealed a substantial labeling distributed over the cell body and their stellar processes. Within the lesion and, particularly, close to the needle tract the number of microglia/macrophages labeled by isolectin B4 increased dramatically. Reactive microglial cells macrophages, situated along the needle tract and characterized by a pseudopodic or a globular shape, contained highest staining activity. At the ultrastructural level only disintegrated, if any, neuronal perikarya were seen five days after quinolinic acid injection while numerous reactive glial cells were observed. Reactive astroglia showed nicotinamide adenine dinucleotide phosphate diaphorase activity by displaying a substantial labeling of the nuclear envelope and endoplasmic membranes. Occasionally stained mitochondria were encountered. Globular-shaped (ameboidal) microglia near the needle tract were rich in phagocytotic debris and, apart from formazan-positive endomembranes, their plasmalemma was often nicotinamide adenine dinucleotide phosphate diaphorase stained. Additionally, in those cells regions of highly electron-dense puncta were seen which differ sharply from other cytoplasmic areas. Such sand-like accumulations of nicotinamide adenine dinucleotide phosphate diaphorase positive grains have never been observed in other cell types, indicating a special type of nitric oxide synthase representation, possibly that of the inducible isoform.

摘要

一氧化氮是一种气态的细胞间和细胞内信使,被认为通过兴奋性氨基酸受体介导神经毒性,这可能与多种神经元疾病的发病机制有关。在大鼠纹状体单侧制造喹啉酸诱导的兴奋毒素损伤,以从生物化学、光学显微镜和电子显微镜角度研究一氧化氮合成酶(NOS)在变性过程中可能发挥的作用。注射喹啉酸5天后,纹状体中的一氧化氮合酶活性升高至196.5%(与对照组相比,P<0.005)。所测酶活性不需要Ca2+,这表明活性升高是由于诱导型一氧化氮合酶亚型所致。与喹啉酸导致的神经元减少同时出现的是大量的胶质细胞增生。正常纹状体中静止的星形胶质细胞在光学显微镜下未显示出任何可检测到的烟酰胺腺嘌呤二核苷酸磷酸黄递酶反应,而反应性星形胶质细胞则显示出大量分布在细胞体及其星状突起上的标记。在损伤部位,特别是靠近针道处,被异凝集素B4标记的小胶质细胞/巨噬细胞数量急剧增加。沿着针道分布的、具有伪足状或球状形态的反应性小胶质细胞/巨噬细胞具有最高的染色活性。在超微结构水平上,注射喹啉酸5天后仅可见解体的神经元胞体(若有的话),同时观察到大量反应性胶质细胞。反应性星形胶质细胞通过显示核膜和内质网的大量标记而呈现烟酰胺腺嘌呤二核苷酸磷酸黄递酶活性。偶尔可见染色的线粒体。靠近针道的球状(阿米巴样)小胶质细胞富含吞噬碎片,除了甲臜阳性的内膜外,其质膜通常也被烟酰胺腺嘌呤二核苷酸磷酸黄递酶染色。此外,在这些细胞中可见高电子密度的点状区域,与其他细胞质区域明显不同。这种烟酰胺腺嘌呤二核苷酸磷酸黄递酶阳性颗粒的沙样聚集从未在其他细胞类型中观察到,表明存在一种特殊类型的一氧化氮合酶表现形式,可能是诱导型亚型。

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