脑缺血中的多胺。

W Paschen, R Schmidt-Kastner, J Hallmayer, B Djuricic
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引用次数: 70

摘要

本系列实验旨在研究大鼠和蒙古沙鼠可逆性脑缺血中多胺(腐胺、亚精胺和精胺)的区域分布。多胺谱在缺血期间没有变化,但在再循环后发生了变化。最显著的变化是死后腐胺的急剧增加和严重受损区域精胺的显著减少。在给定的脑结构内,脑缺血后腐胺水平与缺血性细胞损伤密度和脑缺血时间密切相关。此外,腐胺在沙鼠海马ca1亚区循环8小时后,即在细胞仍完好无损的情况下,已经显著增加。结果表明,腐胺可能被认为是缺血性细胞损伤的一个很好的生化关联。讨论了死后腐胺水平的变化与该化合物的已知活性的关系。
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Polyamines in cerebral ischemia.

The present series of experiments was designed to study regional profiles of polyamines (putrescine, spermidine, and spermine) in reversible cerebral ischemia produced in rats and Mongolian gerbils. Polyamine profiles did not change during ischemia, but did following recirculation. The most prominent changes were a dramatic postischemic increase in putrescine and a marked decrease in spermine in severely damaged regions. Within a given brain structure, the postischemic putrescine levels correlated closely with the density of ischemic cell injury and the time period of cerebral ischemia. Furthermore, putrescine was already considerably increased in the CA1-subfield of the hippocampus of gerbils after 8 h recirculation, i.e., at a time when the cells are still intact. The results indicate that putrescine may be viewed as an excellent biochemical correlate of ischemic cell injury. The postischemic changes in putrescine levels are discussed in relation to the known activities of this compound.

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The mechanism of ischemia-induced brain cell injury. The membrane theory. Peroxidative damage to cell membranes following cerebral ischemia. A cause of ischemic brain injury? Phosphoinositide turnover and calcium ion mobilization in receptor activation. Polyamines in cerebral ischemia. Reduction of neural damage in irreversible cerebral ischemia by calcium antagonists.
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