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Air pollution and Alzheimer disease phenotype deplete esterified proresolving lipid mediator reserves in the brain
Ameer Y. Taha, Qing Shen, Yurika Otoki, Nuanyi Liang, Kelley T. Patten, Anthony E. Valenzuela, Christopher D. Wallis, Douglas J. Rowland, Abhijit J. Chaudhari, Keith J. Bein, Anthony S. Wexler, Lee-Way Jin, Brittany N. Dugger, Danielle J. Harvey, Pamela J. Lein
Ameer Y. Taha, Qing Shen, Yurika Otoki, Nuanyi Liang, Kelley T. Patten, Anthony E. Valenzuela, Christopher D. Wallis, Douglas J. Rowland, Abhijit J. Chaudhari, Keith J. Bein, Anthony S. Wexler, Lee-Way Jin, Brittany N. Dugger, Danielle J. Harvey, Pamela J. Lein
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Research Article Aging Neuroscience

Air pollution and Alzheimer disease phenotype deplete esterified proresolving lipid mediator reserves in the brain

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Abstract

BACKGROUND Traffic-related air pollution (TRAP) is a risk factor for Alzheimer disease (AD), where unresolved brain inflammation has been linked to deficits in the levels of free lipid mediators that enable the resolution of inflammation. It is unknown whether these deficits are due to reductions in esterified lipid pools, the main source of free bioactive proresolving lipids in the brain, and whether they are related AD pathophysiology.METHODS This unknown was tested by measuring brain esterified lipid mediators and pathogenic markers of AD in TgF344-AD and WT male and female rats exposed to filtered air or TRAP for 14 months; it was also tested in human postmortem prefrontal cortex of individuals with or without AD.RESULTS Significant reductions in proresolving lipid mediators esterified to neutral lipids and/or phospholipids were seen in AD and TRAP-exposed female rats, where levels were associated with inflammation, synaptic loss, and impaired glucose metabolism. Lower esterified proresolving lipid mediator concentrations were associated with older age in prefrontal cortex of humans with AD compared with controls.CONCLUSION Impaired resolution in AD is due to depletion of esterified proresolving lipid pools that supply the brain with free bioactive mediators involved in inflammation resolution. TRAP exposure alters the same esterified resolution pathways, reflecting convergent mechanisms underlying AD.

Authors

Ameer Y. Taha, Qing Shen, Yurika Otoki, Nuanyi Liang, Kelley T. Patten, Anthony E. Valenzuela, Christopher D. Wallis, Douglas J. Rowland, Abhijit J. Chaudhari, Keith J. Bein, Anthony S. Wexler, Lee-Way Jin, Brittany N. Dugger, Danielle J. Harvey, Pamela J. Lein

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Figure 5

Association between PL-bound oxylipins (log-transformed values) and age in prefrontal cortex of individuals with AD and without AD.

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Association between PL-bound oxylipins (log-transformed values) and age ...
Linear plots and Pearson’s correlation coefficient (r value) between oxylipins and age in the Control (n = 20) and AD (n = 21) groups. These plots are used to visualize associations that reached statistical significance by multiple linear regression analysis applied on log-transformed concentrations of each oxylipin as the dependent variable, and group, sex, mean-centered postmortem interval (PMI), and mean centered age were tested for main effects (independent variables). Interaction effects were tested between group and age as well as between group and sex. (A–D) LA-derived oxylipins (A), DGLA-derived oxylipins (B), AA-derived oxylipins (C), and DHA-derived oxylipins (D). r values in the figure represent Pearson’s correlation coefficient of the linear plot correlating log-transformed oxylipins to age for each of the AD and non-AD groups. EpDPE, epoxydocosapentaenoic acid; EpETE, epoxyeicosatetraenoic acid; EpETrE, epoxyeicosatrienoic acid; HDoHE, hydroxydocosahexaenoic acid; HETE, hydroxyeicosatetraenoic acid; HETrE, hydroxyeicosatrienoic acid; HODE, hydroxyoctadecadienoic acid.

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