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补充铜对花斑小鼠大脑中铜浓度的影响。

The effect of copper supplementation on the concentration of copper in the brain of the brindled mouse.

作者信息

Wenk G, Suzuki K

出版信息

Biochem J. 1982 Sep 1;205(3):485-7. doi: 10.1042/bj2050485.

Abstract

The brindled mutant mouse is a useful model to study Menkes kinky-hair syndrome. The metabolic dysfunctions in both human and rodent are related to insufficient levels of bioavailable copper. Recently, copper supplementation therapy has been able both to prevent the appearance of various neuropathological changes and to prolong the life of these mutant mice. The optimum conditions for supplementation have been shown to be two intraperitoneal injections on postnatal days 7 and 10. The present study reports on the brain copper concentrations before, during and after the intraperitoneal copper therapy. The results demonstrate that postnatal days 7 and 10 correspond to two important epochs in copper homoeostasis. The supplementation therapy seems to provide sufficient bioavailable copper to respond to the needs of the animal at these crucial time points. The results are discussed in terms of their importance to the human copper disorder.

摘要

花斑突变小鼠是研究门克斯卷发综合征的有用模型。人类和啮齿动物的代谢功能障碍都与生物可利用铜水平不足有关。最近,铜补充疗法既能预防各种神经病理变化的出现,又能延长这些突变小鼠的寿命。已证明补充的最佳条件是在出生后第7天和第10天进行两次腹腔注射。本研究报告了腹腔内铜治疗前、治疗期间和治疗后的脑铜浓度。结果表明,出生后第7天和第10天对应于铜稳态的两个重要时期。补充疗法似乎能提供足够的生物可利用铜,以满足动物在这些关键时间点的需求。根据这些结果对人类铜紊乱的重要性进行了讨论。

相似文献

2
The effect of copper supplementation on the brindled mouse: a clinico-pathological study.
J Neuropathol Exp Neurol. 1981 Jul;40(4):428-46. doi: 10.1097/00005072-198107000-00006.

本文引用的文献

4
The effect of copper supplementation on the brindled mouse: a clinico-pathological study.
J Neuropathol Exp Neurol. 1981 Jul;40(4):428-46. doi: 10.1097/00005072-198107000-00006.
6
Trace element studies in three patients and a fetus with Menkes' disease. Effect of copper therapy.
Pediatr Res. 1981 Mar;15(3):284-9. doi: 10.1203/00006450-198103000-00017.
7
Kinky hair disease. I. Clinical and pathological features.扭发症。一、临床及病理特征。
J Neuropathol Exp Neurol. 1966 Oct;25(4):507-22. doi: 10.1097/00005072-196610000-00001.

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