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

Marcia R Terluk, Julianne Tieu, Siddhee Anand Sahasrabudhe, Ann Moser, Paul A. Watkins, Gerald V Raymond, Reena V. Kartha

Research output: Contribution to journalArticlepeer-review

23 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)1007-1017
Number of pages11
JournalNeurotherapeutics
Volume19
Issue number3
DOIs
StatePublished - Apr 2022

Bibliographical note

Funding Information:
The authors acknowledge funding from the United Leukodystrophy Foundation and the National Center for Advancing Translational Sciences of the National Institutes of Health (Award Number 1R21TR003941-01).

Funding Information:
Paul A. Watkins is employed at the Kennedy Krieger Institute. He discloses grants from United Leukodystrophy Foundation and Global Foundation for Peroxisomal Disorders. He also has a contract for mouse studies at the Vikings Therapeutics. Gerald V. Raymond is a consultant at Bluebird Bio, Minoryx Therapeutics, and Viking Therapeutics. Reena V. Kartha discloses receiving grants from the United Leukodystrophy Foundation, Cydex Pharmaceuticals Inc., and the NIH. Marcia R. Terluk, Siddhee A. Sahasrabudhe, Ann Moser, and Julianne Tieu declare that they have no conflict of interest. Full conflict of interest disclosures are available in the electronic supplementary material for this article. Acknowledgements Required Author Forms

Publisher Copyright:
© 2022, The American Society for Experimental NeuroTherapeutics, Inc.

Keywords

  • Adrenoleukodystrophy
  • Dietary lipids
  • Fibroblasts
  • Monounsaturated fatty acids
  • Peroxisomes
  • Sphingomyelin
  • Very long-chain fatty acids

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