Journal
FREE RADICAL BIOLOGY AND MEDICINE
Volume 177, Issue -, Pages 313-325Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2021.11.003
Keywords
Natural products; Quinones; Aging; Lipid peroxidation; Oxytosis; ferroptosis; Neurodegenerative disease; Drug discovery
Funding
- Shiley-Marcos Alzheimer's Disease Research Center at University of California San Diego
- Salk Institute
- Shiley Foundation
- Paul F. Glenn Center for Biology of Aging Research at the Salk Institute
- National Institutes of Health [R01AG069206]
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The study identified potent anti-oxytotic/ferroptotic compounds in plant quinones that can protect against oxidative damage and cell death in nerve cells, which are relevant to Alzheimer's disease. These compounds target and prevent lipid peroxidation through the reducing activity of cellular redox enzymes, offering new approaches for future neurotherapies.
Because old age is the greatest risk factor for Alzheimer's disease (AD), it is critical to target the pathological events that link aging to AD in order to develop an efficient treatment that acts upon the primary causes of the disease. One such event might be the activation of oxytosis/ferroptosis, a unique cell death mechanism characterized by mitochondrial dysfunction and lethal lipid peroxidation. Here, a comprehensive library of >900 natural compounds was screened for protection against oxytosis/ferroptosis in nerve cells with the goal of better understanding the chemical nature of inhibitors of oxytosis/ferroptosis. Although the compounds tested spanned structurally diverse chemical classes from animal, microbial, plant and synthetic origins, a small set of very potent anti-oxytotic/ferroptotic compounds was identified that was highly enriched in plant quinones. The ability of these compounds to protect against oxytosis/ferroptosis strongly correlated with their ability to protect against in vitro ischemia and intracellular amyloid-beta toxicity in nerve cells, indicating that aspects of oxytosis/ ferroptosis also underly other toxicities that are relevant to AD. Importantly, the anti-oxytotic/ferroptotic character of the quinone compounds relied on their capacity to target and directly prevent lipid peroxidation in a manner that required the reducing activity of cellular redox enzymes, such as NAD(P)H:quinone oxidoreductase 1 (NQO1) and ferroptosis suppressor protein 1 (FSP1). Because some of the compounds increased the production of total reactive oxygen species while decreasing lipid peroxidation, it appears that the pro-oxidant character of a compound can coexist with an inhibitory effect on lipid peroxidation and, consequently, still prevent oxytosis/ferroptosis. These findings have significant implications for the understanding of oxytosis/ ferroptosis and open new approaches to the development of future neurotherapies.
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