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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 4

Pearson’s correlation between brain in vivo imaging markers of AD pathology and brain esterified oxylipins in female rats.

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Pearson’s correlation between brain in vivo imaging markers of AD pathol...
The figures show linear plots and significant Pearson’s correlation coefficient r values between in vivo imaging markers of AD pathogenesis and log oxylipin concentrations within PL or NL in female rats (n = 27). (A) 18F-PBR111 average whole brain SUV and log-transformed PL-bound oxylipins. (B) 18F-UCB-H average whole brain SUV and log-transformed proresolving PL-bound oxylipins. (C) 18F-UCB-H average whole brain SUV and log-transformed proinflammatory PL-bound oxylipins. (D) 18F-FDG average whole brain SUV and log-transformed NL-bound oxylipins. *P < 0.05 and **P < 0.01. DiHETrE, dihydroxyeicosatrienoic acid; DiHDPA, dihydroxydocosapentaenoic acid; EpDPE, epoxydocosapentaenoic acid; EpETE, epoxyeicosatetraenoic acid; EpETrE, epoxyeicosatrienoic acid; HDoHE, hydroxydocosahexaenoic acid; HEPE, hydroxyeicosapentaenoic acid; HETE, hydroxyeicosatetraenoic acid; HETrE, hydroxyeicosatrienoic acid; HODE, hydroxyoctadecadienoic acid; HOTrE, hydroxyoctadecatrienoic acid.

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