Castro-Blanco Susana, Encinas Juan Manuel, Serrano Julia, Alonso David, Gómez María Benita, Sánchez Jaime, Ríos-Tejada Francisco, Fernández-Vizarra Paula, Fernández Ana Patricia, Martínez-Murillo Ricardo, Rodrigo José
Department of Neuroanatomy and Cell Biology, Instituto de Neurobiologia Santiago Ramón y Cajal, CSIC, E-28002 Madrid, Spain.
Nitric Oxide. 2003 May;8(3):182-201. doi: 10.1016/s1089-8603(03)00003-x.
Changes in the nitric oxide (NO) system of the rat cerebral cortex were investigated by immunohistochemistry, immunoblotting, and NO synthase (NOS) activity assays in adult rats submitted for 30 min to hypoxia, in a hypobaric chamber at a simulated altitude of 38,000 ft (11000 m) (154.9 mm Hg). The cerebral cortex was studied after different survival times, 0 and 24 h, 5, 8, 15, and 30 days of reoxygenation. This situation led to morphological alterations in the large type I interneurons, as well as immunoreactive changes in the appearance and number of the small neurons (type II), both containing neuronal NOS (nNOS). Some of these small neurons showed immunoreactive cytoplasm and short processes; others, the more numerous during all reoxygenation periods, contained the immunoreactive product mainly related to a perinuclear ring. Ultrastructurally, these small neurons exhibited changes in nuclear structures as in the shape of the nuclear membrane, in the distribution of heterochromatin, and in the nucleolar morphology. The reaction product for nitrotyrosine, as a marker of protein nitration, showed modifications in distribution of the immunoreactive product. No expression was found for inducible NOS (iNOS). All these modifications were accompanied by increased nNOS and nitrotyrosine production as demonstrated by Western blotting and calcium-dependent activity, returning to control conditions after 30 days of reoxygenation, suggesting a reversible NO mechanism of action.
通过免疫组织化学、免疫印迹和一氧化氮合酶(NOS)活性测定,对成年大鼠在模拟海拔38,000英尺(11000米)(154.9毫米汞柱)的低压舱中进行30分钟缺氧处理后的大脑皮质一氧化氮(NO)系统变化进行了研究。在复氧后的不同存活时间,即0和24小时、5、8、15和30天,对大脑皮质进行了研究。这种情况导致了大型I型中间神经元的形态改变,以及小型神经元(II型)的外观和数量的免疫反应性变化,两者均含有神经元型一氧化氮合酶(nNOS)。这些小型神经元中的一些显示出免疫反应性细胞质和短突起;其他的,在所有复氧期数量更多,其免疫反应产物主要与核周环有关。在超微结构上,这些小型神经元在核结构上表现出变化,如核膜的形状、异染色质的分布和核仁形态。作为蛋白质硝化标记物的硝基酪氨酸反应产物显示出免疫反应产物分布的改变。未发现诱导型一氧化氮合酶(iNOS)的表达。如蛋白质印迹和钙依赖性活性所示,所有这些改变都伴随着nNOS和硝基酪氨酸产生的增加,在复氧30天后恢复到对照条件,表明存在可逆的NO作用机制。