Dysfunctional lipid metabolism and peroxidation in chronic pain and neurodegeneration

National Institute On Aging

Investigators

Linked publications & trials

Abstract

The mission of the Lipid Peroxidation Unit (LPU) is to (1) discover new mediators and mechanisms linking lipids to age-related diseases, with an emphasis on chronic pain and Alzheimer's disease, and (2) to translate these discoveries into targeted, safe, and effective nutrition-based and drug treatments. Our long-term goal is to develop and advance non-addictive diet and drug-based interventions to prevent and treat age-related diseases. We apply an interdisciplinary, translational approach comprising randomized controlled trials, postmortem studies, synthetic and analytical chemistry, immunohistochemistry, and cellular assays to achieve these objectives. Randomized controlled trials Our team is leading or collaborating on several randomized controlled trials testing the clinical efficacy and biochemical effects of targeted alterations in dietary fatty acids, which are precursors to bioactive lipid mediators including oxylipins and endocannabinoids. These trials include a total of more than 500 randomized participants, including 350 suffering with chronic pain syndromes that are refractory to conventional medical management. These five trials grew out of the promising results of small randomized trial conducted at UNC-Chapel Hill testing targeted dietary manipulation as an adjunct strategy for managing treatment-resistant chronic headaches in collaboration with Doug Mann, M.D., and the Department of Physical Medicine and Rehabilitation Medicine. We recently published the results of a follow-up randomized controlled trial demonstrating clinical efficacy and biochemical effects of a targeted dietary intervention in n=182 patients with frequent migraines (https://www.bmj.com/content/374/bmj.n1448). We are leading an analysis of a completed NIH intramural RCT testing the effects of targeted alterations in dietary fatty acids on endocannabinoids, craving, satiety, and body composition. This trial is led by NIAAA and includes investigators from NIA, NIDDK, the NIH Clinical Center, and UNC-Chapel Hill. Mediators and mechanisms linking lipids to disease Our team is investigating the potential roles of oxidized lipids that are present in human tissues in pain, itch, and age-related diseases. Synthetic chemistry and drug discovery Our team uses the interdisciplinary, translational approach described above to inform the design and total synthesis of stable analogs and small molecules as potential drug candidates. The long-term goal of these efforts is to develop targeted, effective, non-addictive drugs to treat chronic pain and neurodegenerative diseases. Analytical chemistry Our team applies liquid chromatography-tandem mass spectrometry and related techniques to identify and quantify bioactive lipid mediators, pathway precursors, and inactivation products in human and rodent tissues. These approaches provide key biochemical insights into the mechanisms of action linking lipid mediators and their precursor fatty acids to inflammation, pain, and related clinical endpoints in randomized controlled trials and other studies. Immunohistochemistry Our team applies immunohistochemistry and related techniques to characterize lipid-related derangements in human neurological tissues. We are currently investigating lipid-related derangements in postmortem hippocampus, entorhinal cortex, amygdala and several brainstem nuclei specimens from cases with Alzheimer's disease, Parkinson's disease and matched controls. Cellular assays In the past year our Unit expanded use of iPSC derived human neuron and astrocyte cell lines which will be used for modeling and investigating lipid-related molecular mechanisms relevant for neuroinflammatory and neuro-degenerative diseases. These collective efforts are directed toward discovery of new mediators and mechanisms underlying age-related diseases, and the translation of findings into effective, non-addictive treatments for chronic pain neurodegenerative diseases.