Suppr超能文献

[获得性、维生素B6反应性、原发性铁粒幼细胞贫血,一种血红素合成中的酶缺乏症]

[Acquired, vitamin B6-responsive, primary sideroblastic anemia, an enzyme deficiency in heme synthesis].

作者信息

Meier P J, Giger U, Brändli O, Fehr J

出版信息

Schweiz Med Wochenschr. 1981 Oct 10;111(41):1533-5.

PMID:7313623
Abstract

The activity of delta-aminolevulinic acid synthetase (ALAS), the rate-limiting enzyme in heme synthesis, has been found to be markedly reduced (13% of controls) in erythroblasts of a patient with acquired, primary sideroblastic anemia. Administration of vitamin B6 (pyridoxin, 200-600 mg/d) resulted in complete reconstitution of erythroblastic ALAS-activity with concomitant disappearance of all hematologic abnormalities. The findings show that the therapeutic efficacy of pyridoxin in primary sideroblastic anemia is due to its effect on defective ALAS. More generally, the data support the view that almost all features of primary sideroblastic anemia can be ascribed to a disturbance of heme synthesis in erythroblasts.

摘要

δ-氨基-γ-酮戊酸合成酶(ALAS)是血红素合成的限速酶,在一名获得性原发性铁粒幼细胞贫血患者的成红细胞中,该酶的活性显著降低(为对照组的13%)。给予维生素B6(吡哆醇,200 - 600mg/天)后,成红细胞的ALAS活性完全恢复,同时所有血液学异常均消失。这些发现表明,吡哆醇对原发性铁粒幼细胞贫血的治疗效果归因于其对缺陷性ALAS的作用。更普遍地说,这些数据支持以下观点:原发性铁粒幼细胞贫血的几乎所有特征都可归因于成红细胞中血红素合成的紊乱。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验