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Breakthrough by Moran Eye Center Scientist, Colleagues Fuels New Line of Disease Research

Chemical synthesis of a retina-specific VLC-PUFA (32:6 n-3) from docosahexaenoic acid (DHA).
Chemical synthesis of a retina-specific VLC-PUFA (32:6 n-3) from docosahexaenoic acid (DHA).

 

Scientists like the John A. Moran Eye Center鈥檚 Paul S. Bernstein, MD, PhD, know a special class of lipids, or fatty acids, found in the retina of the eye and in just a few other parts of the body play an important role in maintaining vision.

But it鈥檚 been difficult to study whether giving these lipids, called very-long-chain polyunsaturated fatty acids (VLC-PUFAs), to patients as a supplement could prevent blinding eye diseases like age-related macular degeneration, diabetic retinopathy, and some inherited retinal diseases. Made in the body by the ELOVL4 enzyme but rarely consumed as part of a normal diet, VLC-PUFAs weren鈥檛 commercially available in enough quantities for animal or human research.

Now Bernstein and colleagues from the University of Utah鈥檚 Chemistry Department have changed the paradigm, inventing a method for synthesizing large enough quantities of VLC-PUFAs to evaluate their potential sight-preserving properties. The method and the results of the first study to use it were published in Proceedings of the National Academy of Sciences of the United States of America (PNAS) this week.

The study determined that VLC-PUFA supplementation increased levels of the lipids in the retina and also improved visual function in normal mice and in mice with a defect in the ELOVL4 enzyme. While Bernstein says there鈥檚 more work to be done, the results are an exciting first step.

"Synthesizing VLC-PUFAs opens up a whole new area of study, and these first results are very promising," said Bernstein, the paper鈥檚 corresponding author. "Our results raise interesting questions about how orally administered VLC-PUFAs improve vision, how they are carried in the bloodstream, and how they are selectively targeted to the retina. The VLC-PUFA formulation, dosage, and timing of the intervention first need to be optimized, and then the underlying mechanisms will need to be defined."

Organic Chemistry Professor , a co-author on the research, said the group is confident it can synthesize additional VLC-PUFA variants.

"There are a number of VLC-PUFA variants that are present in the human eye," said Rainier, second author on the research.

Paul S. Bernstein, MD, PhD, is the vice-chair for clinical and basic science research at the John A. Moran Eye Center at the University of Utah.
Paul S. Bernstein, MD, PhD, is the vice-chair for clinical and basic science research at the John A. Moran Eye Center at the University of Utah.

"So far we have only made one member of this family, but we are confident that our new synthetic method will enable us to both synthesize and study the other variants and by doing that get a much better idea of what it is that each of the individual VLC-PUFAs do."

Bernstein鈥檚 laboratory focuses on the biochemistry and biophysics of nutritional interventions against inherited and acquired ocular disorders. Bernstein, Moran鈥檚 vice-chair for clinical and basic science research and the Val A. and Edith D. Green Presidential Professor of Ophthalmology and Visual Sciences, helped develop the protective AREDS2 supplement formulation for patients with age-related macular degeneration.

Additional authors on the PNAS study, , were: Aruna Gorusupudi, Rameshu Rallabandi, Binxing Li, Ranganathan Arunkumar, J. David Blount, Gergory T. Rognon, Fu-Yen Chang, Alexander Wade, Steven Lucas, and John C. Conboy.

The research was supported by a Knights Templar Career Starter Grant, a University of Utah Center on Aging Seed Grant, a Foundation Fighting Blindness Grant, a Carl Marshall Reeves and Mildred Almen Reeves Foundation Grant, and departmental core grants from Research to Prevent Blindness and the National Institutes of Health.