Wang T, Steel G, Milam A H, Valle D
Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Proc Natl Acad Sci U S A. 2000 Feb 1;97(3):1224-9. doi: 10.1073/pnas.97.3.1224.
Deficiency of ornithine-delta-aminotransferase (OAT) in humans results in gyrate atrophy of the choroid and retina (GA), an autosomal recessive disorder characterized by ornithine accumulation and a progressive chorioretinal degeneration of unknown pathogenesis. To determine whether chronic, systemic reduction of ornithine can prevent this form of retinal degeneration, we used an arginine-restricted diet to maintain long term reduction of ornithine in a mouse model of OAT-deficiency (Oat(-/-)) produced by gene targeting. We evaluated the mice over a 12-month period by measurement of plasma amino acids, electroretinograms, and retinal histologic and ultrastructural studies. We found that an arginine-restricted diet substantially reduces plasma ornithine levels and completely prevents retinal degeneration in Oat(-/-). This result indicates that ornithine accumulation is a necessary factor in the pathophysiology of the retinal degeneration in GA and that restoration of OAT activity in retina is not required for effective treatment of GA.
人类鸟氨酸 - δ - 氨基转移酶(OAT)缺乏会导致脉络膜和视网膜回旋状萎缩(GA),这是一种常染色体隐性疾病,其特征为鸟氨酸积累以及病因不明的进行性脉络膜视网膜变性。为了确定长期全身性降低鸟氨酸是否能预防这种视网膜变性,我们采用了精氨酸限制饮食,以在通过基因靶向产生的OAT缺乏(Oat(-/-))小鼠模型中维持鸟氨酸的长期降低。我们通过测量血浆氨基酸、视网膜电图以及视网膜组织学和超微结构研究,在12个月的时间里对小鼠进行了评估。我们发现,精氨酸限制饮食可大幅降低血浆鸟氨酸水平,并完全预防Oat(-/-)小鼠的视网膜变性。这一结果表明,鸟氨酸积累是GA视网膜变性病理生理学中的一个必要因素,并且有效治疗GA并不需要恢复视网膜中的OAT活性。