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神经酸可减轻极长链脂肪酸的蓄积,是治疗肾上腺脑白质营养不良症的潜在疗法。

Nervonic Acid Attenuates Accumulation of Very Long-Chain Fatty Acids and is a Potential Therapy for Adrenoleukodystrophy.

机构信息

Center for Orphan Drug Research, University of Minnesota, McGuire Translational Research Facility, 2001 6th St SE, Minneapolis, MN, 55455, USA.

Department of Experimental and Clinical Pharmacology, College of Pharmacy, University of Minnesota, Minneapolis, MN, 55455, USA.

出版信息

Neurotherapeutics. 2022 Apr;19(3):1007-1017. doi: 10.1007/s13311-022-01226-7. Epub 2022 Apr 4.

Abstract

Adrenoleukodystrophy (ALD) is an X-linked inherited peroxisomal disorder due to mutations in the ALD protein and characterized by accumulation of very long-chain fatty acids (VLCFA), specifically hexacosanoic acid (C26:0). This can trigger other pathological processes such as mitochondrial dysfunction, oxidative stress, and inflammation, which if involves the brain tissues can result in a lethal form of the disease called childhood cerebral ALD. With the recent addition of ALD to the Recommended Uniform Screening Panel, there is an increase in the number of individuals who are identified with ALD. However, currently, there is no approved treatment for pre-symptomatic individuals that can arrest or delay symptom development. Here, we report our observations investigating nervonic acid, a monounsaturated fatty acid as a potential therapy for ALD. Using ALD patient-derived fibroblasts, we examined whether nervonic acid can reverse VLCFA accumulation similar to erucic acid, the active ingredient in Lorenzo's oil, a dietary intervention believed to alter disease course. We have shown that nervonic acid can reverse total lipid C26:0 accumulation in a concentration-dependent manner in ALD cell lines. Further, we show that nervonic acid can protect ALD fibroblasts from oxidative insults, presumably by increasing intracellular ATP production. Thus, nervonic acid can be a potential therapeutic for individuals with ALD, which can alter cellular biochemistry and improve its function.

摘要

肾上腺脑白质营养不良(ALD)是一种 X 连锁遗传性过氧化物酶体疾病,由于 ALD 蛋白的突变导致,其特征是极长链脂肪酸(VLCFA),特别是二十六烷酸(C26:0)的积累。这可能会引发其他病理过程,如线粒体功能障碍、氧化应激和炎症,如果涉及脑组织,则可能导致一种致命形式的疾病,称为儿童脑 ALD。随着 ALD 最近被添加到推荐的统一筛选面板中,被诊断为 ALD 的人数有所增加。然而,目前对于有症状前的个体,还没有批准的治疗方法可以阻止或延迟症状的发展。在这里,我们报告了我们关于神经酸的观察结果,神经酸是一种单不饱和脂肪酸,可能是 ALD 的一种潜在治疗方法。使用 ALD 患者来源的成纤维细胞,我们研究了神经酸是否可以像芥酸(Lorenzo 油中的活性成分)一样逆转 VLCFA 的积累,Lorenzo 油是一种饮食干预措施,被认为可以改变疾病进程。我们已经表明,神经酸可以以浓度依赖的方式逆转 ALD 细胞系中总脂质 C26:0 的积累。此外,我们还表明,神经酸可以保护 ALD 成纤维细胞免受氧化损伤,推测是通过增加细胞内 ATP 的产生。因此,神经酸可能是 ALD 个体的一种潜在治疗方法,它可以改变细胞的生化特性并改善其功能。

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