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Ferroptosis Contributes to Neuronal Death and Functional Outcome After Traumatic Brain Injury*

Kenny, Elizabeth M., BS1,2,3; Fidan, Emin, MD1,2,3; Yang, Qin, MD1,2,3; Anthonymuthu, Tamil S., PhD1,2,3; New, Lee Ann, BS1,2; Meyer, Elizabeth A., BS1,2; Wang, Hong, PhD4; Kochanek, Patrick M., MD2; Dixon, C. Edward, PhD2,5; Kagan, Valerian E., PhD, DSc3,6,7; Bayir, Hülya, MD1,2,3,6,7,8

doi: 10.1097/CCM.0000000000003555
Neurologic Critical Care
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SDC

Objectives: Traumatic brain injury triggers multiple cell death pathways, possibly including ferroptosis—a recently described cell death pathway that results from accumulation of 15-lipoxygenase–mediated lipid oxidation products, specifically oxidized phosphatidylethanolamine containing arachidonic or adrenic acid. This study aimed to investigate whether ferroptosis contributed to the pathogenesis of in vitro and in vivo traumatic brain injury, and whether inhibition of 15-lipoxygenase provided neuroprotection.

Design: Cell culture study and randomized controlled animal study.

Setting: University research laboratory.

Subjects: HT22 neuronal cell line and adult male C57BL/6 mice.

Interventions: HT22 cells were subjected to pharmacologic induction of ferroptosis or mechanical stretch injury with and without administration of inhibitors of ferroptosis. Mice were subjected to sham or controlled cortical impact injury. Injured mice were randomized to receive vehicle or baicalein (12/15-lipoxygenase inhibitor) at 10–15 minutes postinjury.

Measurements and Main Results: Pharmacologic inducers of ferroptosis and mechanical stretch injury resulted in cell death that was rescued by prototypical antiferroptotic agents including baicalein. Liquid chromatography tandem-mass spectrometry revealed the abundance of arachidonic/adrenic-phosphatidylethanolamine compared with other arachidonic/adrenic acid-containing phospholipids in the brain. Controlled cortical impact resulted in accumulation of oxidized phosphatidylethanolamine, increased expression of 15-lipoxygenase and acyl-CoA synthetase long-chain family member 4 (enzyme that generates substrate for the esterification of arachidonic/adrenic acid into phosphatidylethanolamine), and depletion of glutathione in the ipsilateral cortex. Postinjury administration of baicalein attenuated oxidation of arachidonic/adrenic acid-containing-phosphatidylethanolamine, decreased the number of terminal deoxynucleotidyl transferase dUTP nick-end labeling positive cells in the hippocampus, and improved spatial memory acquisition versus vehicle.

Conclusions: Biomarkers of ferroptotic death were increased after traumatic brain injury. Baicalein decreased ferroptotic phosphatidylethanolamine oxidation and improved outcome after controlled cortical impact, suggesting that 15-lipoxygenase pathway might be a valuable therapeutic target after traumatic brain injury.

1Department of Critical Care Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA.

2Safar Center for Resuscitation Research, University of Pittsburgh, Pittsburgh, PA.

3Center for Free Radical and Antioxidant Health, University of Pittsburgh, Pittsburgh, PA.

4Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA.

5Department of Neurosurgery, School of Medicine, University of Pittsburgh, Pittsburgh, PA.

6Department of Environmental and Occupational Health, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA.

7Laboratory of Navigational Redox Lipidomics, Institute of Regenerative Medicine, IM Sechenov Moscow State Medical University, Moscow, Russia.

8Children’s Neuroscience Institute, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA.

*See also p. 480.

Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided in the HTML and PDF versions of this article on the journal’s website (http://journals.lww.com/ccmjournal).

Supported, in part, by National Institutes of Health grants (NS061817, NS076511, AI068021, and NS079061).

Drs. Yang, Mayer, Kochanek, Dixon, Kagan, and Bayir received support for article research from the National Institutes of Health (NIH). Dr. Kochanek’s institution received funding from the NIH; he received funding from Society of Critical Care Medicine (Editor-in-Chief of Pediatric Critical Care Medicine) and from serving as an expert witness and a visiting professor/grand rounds speaker (travel/compensation); and he disclosed other funding separate from that reported in this study by both the NIH, the U.S. Department of Defense, and the state of Pennsylvania. Dr. Kagan disclosed government work. The remaining authors have disclosed that they do not have any potential conflicts of interest.

For information regarding this article, E-mail: bayihx@ccm.upmc.edu

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