Poulos A, Singh H, Paton B, Sharp P, Derwas N
Clin Genet. 1986 May;29(5):397-408. doi: 10.1111/j.1399-0004.1986.tb00511.x.
The accumulation of very long chain fatty acids in plasma and skin fibroblasts was measured in at least four separate inherited disease states. Both the magnitude and the nature of the fatty acid changes reflected the clinical status of individual patients. In Zellweger's syndrome, and to a lesser extent in infantile Refsum's disease, there was an increase in 24:0, 26:0, 26:1, and a number of even longer chain fatty acids, while in the X-linked form of adrenoleukodystrophy these changes were less pronounced. Zellweger fibroblasts in culture took up lignoceric, phytanic and stearic acids and incorporated them into a variety of lipids in a manner comparable to control fibroblasts. However, these cells were unable to convert phytanic or lignoceric acid to CO2. Infantile Refsum's and X-linked adrenoleukodystrophy fibroblasts showed normal conversion of these acids to CO2. Normal fibroblast homogenates produced radioactive acetate from [1-14C] stearic and [1-14C] lignoceric acids indicating that both substrates were beta-oxidised under these conditions. Homogenates of fibroblasts from all patients patients with biochemical evidence of accumulation of very long chain fatty acids showed normal or near-normal stearic acid beta-oxidation, but were deficient in lignoceric acid beta-oxidation. Residual lignoceric acid beta-oxidation activity varied from approximately 15% in Zellweger syndrome up to 50% in X-linked adrenoleukodystrophy. It is postulated that the accumulation of very long chain fatty acids results from defects in peroxisomal beta-oxidation. In Zellweger's syndrome, and possibly in infantile Refsum's disease, it is probable that this defect is secondary to a primary abnormality affecting the structure and/or function of peroxisomes, while the primary defect in X-linked adrenoleukodystrophy may be confined to a pathway specific for the oxidation of very long chain fatty acids.
在至少四种不同的遗传性疾病状态下,对血浆和皮肤成纤维细胞中极长链脂肪酸的积累情况进行了测定。脂肪酸变化的程度和性质均反映了个体患者的临床状况。在泽尔韦格综合征中,以及在程度较轻的婴儿型Refsum病中,二十四烷酸、二十六烷酸、二十六碳烯酸以及一些更长链脂肪酸的含量均有所增加,而在X连锁肾上腺脑白质营养不良中,这些变化则不太明显。培养的泽尔韦格成纤维细胞摄取了木蜡酸、植烷酸和硬脂酸,并以与对照成纤维细胞类似的方式将它们整合到各种脂质中。然而,这些细胞无法将植烷酸或木蜡酸转化为二氧化碳。婴儿型Refsum病和X连锁肾上腺脑白质营养不良的成纤维细胞显示出这些酸向二氧化碳的正常转化。正常成纤维细胞匀浆可由[1-¹⁴C]硬脂酸和[1-¹⁴C]木蜡酸产生放射性乙酸盐,这表明在这些条件下两种底物均发生了β氧化。所有有极长链脂肪酸积累生化证据的患者的成纤维细胞匀浆均显示出正常或接近正常的硬脂酸β氧化,但木蜡酸β氧化存在缺陷。残余的木蜡酸β氧化活性在泽尔韦格综合征中约为15%,在X连锁肾上腺脑白质营养不良中高达50%。据推测,极长链脂肪酸的积累是由过氧化物酶体β氧化缺陷所致。在泽尔韦格综合征中,可能在婴儿型Refsum病中,这种缺陷可能继发于影响过氧化物酶体结构和/或功能的原发性异常,而X连锁肾上腺脑白质营养不良的原发性缺陷可能局限于极长链脂肪酸氧化特有的一条途径。