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Variable response of selected cuproproteins in rat choroid plexus and cerebellum following perinatal copper deficiency

机译:围产期铜缺乏后大鼠脉络丛和小脑中所选铜蛋白的可变反应

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Recent immunohistochemical characterization of the copper transport protein, Ctr1, reported enriched levels in mouse choroid plexus, and enhancement by copper deficiency. To extend and confirm this, experiments were conducted with Holtzman rats. Following perinatal copper deficiency there was an 80% reduction in brain copper of 24–27 day old copper-deficient (Cu-) rat pups compared to copper-adequate (Cu+) controls. Choroid plexus immunoblot analysis with rabbit anti-hCtr1 demonstrated a 50% higher Ctr1 protein expression in Cu-samples. However, levels of copper chaperone for superoxide dismutase (CCS) were unchanged, suggesting that Ctr1 buffers the choroid plexus against copper deficiency, since CCS normally is much higher in Cu-tissues. There were 13% lower levels of cytochrome c oxidase subunit IV (COX IV) detected in Cuchoroid plexus. In contrast, in cerebellum of Cu-rats CCS was 2-fold higher and COXIV 1.7-fold lower than Cu+ rats consistent with severe copper deficiency. Brain mitochondria from Cu-rats had severe reductions in COXIV content and CCO activity and modest but significant elevations in CCS and reductions in Cu, Zn-superoxide dismutase. COXIV may be a more sensitive marker for copper deficiency than CCS and may prove useful to assess copper status.
机译:铜转运蛋白Ctr1的最新免疫组织化学表征报告了小鼠脉络丛中的富集水平以及铜缺乏引起的增强。为了扩展和证实这一点,对霍尔茨曼大鼠进行了实验。围产期铜缺乏后,与铜充足(Cu +)对照相比,24-27日龄缺铜(Cu-)大鼠幼崽的脑铜减少了80%。兔抗hCtr1的脉络丛免疫印迹分析表明,Cu样品中的Ctr1蛋白表达高50%。然而,用于超氧化物歧化酶(CCS)的铜伴侣蛋白水平没有变化,这表明Ctr1缓冲了脉络丛以防止铜缺乏,因为CC组织中的CCS通常更高。在脉络丛中检测到的细胞色素C氧化酶亚基IV(COX IV)的水平降低了13%。相比之下,在Cu-大鼠的小脑中,CCS比Cu +大鼠高2倍,而COXIV则低1.7倍,这与严重的铜缺乏相一致。 Cu大鼠的脑线粒体COXIV含量和CCO活性显着降低,CCS适度但显着升高,Cu,Zn超氧化物歧化酶降低。与CCS相比,COXIV可能是铜缺乏症更敏感的标志物,并且可能被证明对评估铜的状态有用。

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