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定性酶组织化学和微量分析揭示了内侧缰核微波照射后钙及钙激活ATP酶超微结构分布的变化。

Qualitative enzyme histochemistry and microanalysis reveals changes in ultrastructural distribution of calcium and calcium-activated ATPases after microwave irradiation of the medial habenula.

作者信息

Kittel A, Siklós L, Thuróczy G, Somosy Z

机构信息

Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, Hungary.

出版信息

Acta Neuropathol. 1996 Oct;92(4):362-8. doi: 10.1007/s004010050531.

Abstract

The localization of calcium and calcium-activated ATPases was investigated electron microscopically in the medial habenula of mice after whole body irradiation with modulated microwaves. In non-irradiated animals calcium-containing precipitates were seen in different subcellular compartments and were often localized on the luminal side of membranes of synaptic vesicles in nerve terminals. At 1 h after 16-Hz modulated microwave irradiation, the number of synaptic vesicles containing calcium precipitates decreased, and reaction products appeared at new locations: in the synaptic clefts and on non-synaptic surfaces of the neuronal plasma membrane. This modified calcium distribution remained unchanged for 24 h following irradiation. Calcium-activated "ecto"-localized ATPase was detected as a punctuated-linear distribution of the reaction product outlining whole areas of glial and neuronal plasma membrane in the habenula of control animals. This pattern did not change on microwave irradiation. However, a quercetin-sensitive "endo"-localized Ca(2+)-ATPase activity appeared in some nerve terminals 24 h after irradiation. Thus, microwave irradiation can influence neuronal calcium homeostasis by inducing Ca2+ redistribution across the plasma membrane and by modifying Ca(2+)-ATPase activity. However, no direct correlation between these effects could be demonstrated by the present study.

摘要

在用调制微波对小鼠进行全身照射后,通过电子显微镜研究了内侧缰核中钙和钙激活的ATP酶的定位。在未照射的动物中,含钙沉淀物可见于不同的亚细胞区室,且常位于神经末梢突触小泡膜的腔面。在16赫兹调制微波照射后1小时,含有钙沉淀物的突触小泡数量减少,反应产物出现在新的位置:突触间隙和神经元质膜的非突触表面。这种改变后的钙分布在照射后24小时保持不变。在对照动物的缰核中,钙激活的“胞外”定位ATP酶被检测为反应产物的点状线性分布,勾勒出胶质和神经元质膜的整个区域。这种模式在微波照射后没有改变。然而,照射后24小时,一些神经末梢出现了对槲皮素敏感的“胞内”定位Ca(2+)-ATP酶活性。因此,微波照射可通过诱导Ca2+跨质膜重新分布和改变Ca(2+)-ATP酶活性来影响神经元钙稳态。然而,本研究未能证明这些效应之间存在直接相关性。

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