Meier P J, Giger U, Brändli O, Fehr J
Schweiz Med Wochenschr. 1981 Oct 10;111(41):1533-5.
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.
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。