, Free Radicals in Biology and Medicine, 2007.

U. Jahn, J. M. Galano, and T. Durand, Beyond prostaglandins-chemistry and biology of cyclic oxygenated metabolites formed by free-radical pathways from polyunsaturated fatty acids, Angew. Chem. Int. Ed, vol.47, pp.5894-5955, 2008.

J. D. Morrow, K. E. Hill, R. F. Burk, T. M. Nammour, K. F. Badr et al., A series of prostaglandin F2-like compounds are produced in vivo in humans by a noncyclooxygenase, free radical-catalyzed mechanism, Proc. Natl. Acad. Sci. U. S. A, vol.87, pp.9383-9387, 1990.

M. B. Kadiiska, B. C. Gladen, D. D. Baird, D. Germolec, L. B. Graham et al., Biomarkers of oxidative stress study II: are oxidation products of lipids, proteins, and DNA markers of CCl4 poisoning? Free Radic, vol.38, pp.698-710, 2005.

G. L. Milne, H. Yin, K. D. Hardy, S. S. Davies, and L. J. Roberts, Isoprostane generation and function, Chem. Rev, vol.111, pp.5973-5996, 2011.

J. Galano, E. Mas, A. Barden, T. A. Mori, C. Signorini et al., Isoprostanes and neuroprostanes: total synthesis, biological activity and biomarkers of oxidative stress in humans, Prostaglandins Other Lipid Mediat, vol.107, pp.95-102, 2013.
URL : https://hal.archives-ouvertes.fr/hal-01822220

J. Nourooz-zadeh, E. H. Liu, E. Anggard, and B. Halliwell, F4-isoprostanes: a novel class of prostanoids formed during peroxidation of docosahexaenoic acid (DHA), Biochem. Biophys. Res. Commun, vol.242, pp.338-344, 1998.

L. J. Roberts, T. J. Montine, W. R. Markesbery, A. R. Tapper, P. Hardy et al., Formation of isoprostane-like compounds (neuroprostanes) in vivo from docosahexaenoic acid, J. Biol. Chem, vol.273, pp.13605-13612, 1998.

J. Nourooz-zadeh, B. Halliwell, and E. E. , Evidence for the formation of F3isoprostanes during peroxidation of eicosapentaenoic acid, Biochem. Biophys. Res. Commun, vol.236, pp.467-472, 1997.

M. Vanrollins, R. L. Woltjer, H. Yin, J. D. Morrow, and T. J. Montine, F2-dihomo-isoprostanes arise from free radical attack on adrenic acid, J. Lipid Res, vol.49, pp.995-1005, 2008.

S. Parchmann and M. J. Mueller, Evidence for the formation of dinor isoprostanes E1 from alpha-linolenic acid in plants, J. Biol. Chem, vol.273, pp.32650-32655, 1998.

N. A. Porter and M. O. Funk, Peroxy radical cyclization as a model for prostaglandin biosynthesis, J. Org. Chem, vol.40, pp.3614-3615, 1975.

W. A. Pryor and J. P. Stanley, Suggested mechanism for the production of malonaldehyde during the autoxidation of polyunsaturated fatty acids. Nonenzymic production of prostaglandin endoperoxides during autoxidation, J. Org. Chem, vol.40, pp.3615-3617, 1975.

D. M. Stafforini, J. R. Sheller, T. S. Blackwell, A. Sapirstein, F. E. Yull et al., Release of free F2-isoprostanes from esterified phospholipids is catalyzed by intracellular and plasma platelet-activating factor acetylhydrolases, J. Biol. Chem, vol.281, pp.4616-4623, 2006.

J. P. Fessel, N. A. Porter, K. P. Moore, J. R. Sheller, and L. J. Roberts, Discovery of lipid peroxidation products formed in vivo with a substituted tetrahydrofuran ring (isofurans) that are favored by increased oxygen tension, Proc. Natl. Acad. Sci, vol.99, pp.16713-16718, 2002.

K. O. Arneson and L. J. Roberts, Measurement of products of docosahexaenoic acid peroxidation, neuroprostanes, and neurofurans, Methods Enzym, vol.433, pp.127-143, 2007.

W. L. Song, J. A. Lawson, D. Reilly, J. Rokach, C. T. Chang et al., Neurofurans, novel indices of oxidant stress derived from docosahexaenoic acid, J. Biol. Chem, vol.283, pp.6-16, 2008.

A. De-la-torre, Y. Y. Lee, C. Oger, P. T. Sangild, T. Durand et al., Synthesis, discovery, and quantitation of dihomo-isofurans: biomarkers for in vivo adrenic acid peroxidation, Angew. Chem, vol.126, pp.6363-6366, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01058061

T. Durand, A. Guy, O. Henry, A. Roland, S. Bernad et al., Total syntheses of iso-, neuro-and phytoprostanes: new insight in lipid chemistry, Chem. Phys. Lipids, vol.128, pp.15-33, 2004.

E. Jahn, T. Durand, J. Galano, and U. Jahn, Recent approaches to the total synthesis of phytoprostanes, isoprostanes and neuroprostanes as important products of lipid oxidative stress and biomarkers of disease, Chem. Listy, vol.108, pp.301-319, 2014.
URL : https://hal.archives-ouvertes.fr/hal-00997141

H. Yin, E. S. Musiek, L. Gao, N. A. Porter, and J. D. Morrow, Regiochemistry of neuroprostanes generated from the peroxidation of docosahexaenoic acid in vitro and in vivo, J. Biol. Chem, vol.280, pp.26600-26611, 2005.

C. Vigor, J. Bertrand-michel, E. Pinot, C. Oger, J. Vercauteren et al., Non-Enzymatic Lipid Oxidation Products in Biological System: Assessment of the Metabolites from Polyunsaturated Fatty Acids

W. L. Song, G. Paschos, S. Fries, M. P. Reilly, Y. Yu et al., Novel eicosapentaenoic acid-derived F3-isoprostanes as biomarkers of lipid peroxidation, J. Biol. Chem, vol.284, pp.23636-23643, 2009.

C. M. Depner, K. A. Philbrick, and D. B. Jump, Docosahexaenoic acid attenuates hepatic inflammation, oxidative stress, and fibrosis without decreasing hepatosteatosis in a Ldlr?/? mouse model of western diet-induced nonalcoholic steatohepatitis, J. Nutr, vol.143, pp.315-323, 2013.

M. L. Chung, K. Y. Lee, and C. Y. Lee, Profiling of oxidized lipid products of marine fish under acute oxidative stress, Food Chem. Toxicol, vol.53, pp.205-213, 2013.

C. F. Labuschagne, E. C. Stigter, M. M. Hendriks, R. Berger, J. Rokach et al., Quantification of in vivo oxidative damage in Caenorhabditis elegans during aging by endogenous F3-isoprostane measurement, Aging Cell, vol.12, pp.214-223, 2013.

K. S. Leung, X. Chen, W. Zhong, A. C. Yu, and C. J. Lee, Microbubble-mediated sonoporation amplified lipid peroxidation of Jurkat cells, Chem. Phys. Lipids, vol.180, pp.53-60, 2014.

J. Nourooz-zadeh, E. H. Liu, B. Yhlen, E. E. Anggard, and B. Halliwell, F4-isoprostanes as specific marker of docosahexaenoic acid peroxidation in Alzheimer's disease, J. Neurochem, vol.72, pp.734-740, 1999.

Y. P. Hsieh, C. L. Lin, A. L. Shiue, H. Yin, J. D. Morrow et al., Correlation of F4-neuroprostanes levels in cerebrospinal fluid with outcome of aneurysmal subarachnoid hemorrhage in humans, Free Radic, Biol. Med, vol.47, pp.814-824, 2009.

E. E. Reich, W. R. Markesbery, L. J. Roberts, I. I. , L. L. Swift et al., Brain regional quantification of F-ring and D-/E-ring isoprostanes and neuroprostanes in Alzheimer's disease, Am. J. Pathol, vol.158, pp.293-297, 2001.

S. A. Back, N. L. Luo, R. A. Mallinson, J. P. O'malley, L. D. Wallen et al., Selective vulnerability of preterm white matter to oxidative damage defined by F2-isoprostanes, Ann. Neurol, vol.58, pp.108-120, 2005.

T. J. Montine, K. S. Montine, W. Mcmahan, W. R. Markesbery, J. F. Quinn et al., F2-isoprostanes in Alzheimer and other neurodegenerative diseases, vol.7, pp.269-275, 2005.

Z. Korade, L. Xu, K. Mirnics, and N. A. Porter, Lipid biomarkers of oxidative stress in a genetic mouse model of Smith-Lemli-Opitz syndrome, J. Inherit. Metab. Dis, vol.36, pp.113-122, 2013.

C. De-felice, F. Della-ragione, C. Signorini, S. Leoncini, A. Pecorelli et al., Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome, Neurobiol. Dis, vol.68, pp.66-77, 2014.
URL : https://hal.archives-ouvertes.fr/hal-00997408

R. Solberg, M. Longini, F. Proietti, P. Vezzosi, O. D. Saugstad et al., Resuscitation with supplementary oxygen induces oxidative injury in the cerebral cortex, Free Radic, Biol. Med, vol.53, pp.1061-1067, 2012.

R. C. Seet, C. Y. Lee, E. C. Lim, J. J. Tan, A. M. Quek et al., Oxidative damage in Parkinson disease: measurement using accurate biomarkers, Free Radic, Biol. Med, vol.48, pp.560-566, 2010.

C. Signorini, C. De-felice, S. Leoncini, A. Giardini, M. D'esposito et al., F4-neuroprostanes mediate neurological severity in Rett syndrome, Clin. Chim. Acta, vol.412, pp.1399-1406, 2011.

R. C. Seet, C. J. Lee, B. P. Chan, V. K. Sharma, H. Teoh et al., Oxidative damage in ischemic stroke revealed using multiple biomarkers, vol.42, pp.2326-2329, 2011.
DOI : 10.1161/strokeaha.111.618835
URL : https://www.ahajournals.org/doi/pdf/10.1161/STROKEAHA.111.618835

R. C. Seet, C. Y. Lee, W. M. Loke, S. H. Huang, H. Huang et al., Biomarkers of oxidative damage in cigarette smokers: which biomarkers might reflect acute versus chronic oxidative stress? Free Radic, Biol. Med, vol.50, pp.1787-1793, 2011.

A. E. Barden, T. B. Corcoran, E. Mas, T. Durand, J. Galano et al., Is there a role for isofurans and neuroprostanes in pre-eclampsia and normal pregnancy?, Antioxid. Redox Signal, vol.16, pp.165-169, 2012.
DOI : 10.1089/ars.2011.4214
URL : https://hal.archives-ouvertes.fr/hal-00662225

M. Ng, J. Lee, W. M. Loke, L. Yeo, A. Quek et al., Does influenza A infection increase oxidative damage?, Antioxid. Redox Signal, vol.21, pp.1025-1031, 2004.
DOI : 10.1089/ars.2014.5907

T. J. Montine, J. F. Quinn, D. Milatovic, L. C. Silbert, T. Dang et al., Peripheral F2-isoprostanes and F4-neuroprostanes are not increased in Alzheimer's disease, vol.52, pp.175-179, 2002.
DOI : 10.1002/ana.10272

D. Milatovic, S. Zaja-milatovic, K. S. Montine, P. J. Horner, and T. J. Montine, Pharmacologic suppression of neuronal oxidative damage and dendritic degeneration following direct activation of glial innate immunity in mouse cerebrum, J. Neurochem, vol.87, pp.1518-1526, 2003.

D. Milatovic, M. Vanrollins, K. Li, K. S. Montine, and T. J. Montine, Suppression of murine cerebral F2-isoprostanes and F4-neuroprostanes from excitotoxicity and innate immune response in vivo by ?-or ?-tocopherol, J. Chromatogr. B, vol.827, pp.88-93, 2005.

S. Zaja-milatovic, R. C. Gupta, M. Aschner, T. J. Montine, and D. Milatovic, Pharmacologic suppression of oxidative damage and dendritic degeneration following kainic acid-induced excitotoxicity in mouse cerebrum, NeuroToxicology, vol.29, pp.621-627, 2008.
DOI : 10.1016/j.neuro.2008.04.009
URL : http://europepmc.org/articles/pmc2517174?pdf=render

J. F. Quinn, J. R. Bussiere, R. S. Hammond, T. J. Montine, E. Henson et al., Chronic dietary ?-lipoic acid reduces deficits in hippocampal memory of aged Tg2576 mice, Neurobiol. Aging, vol.28, pp.213-225, 2007.
DOI : 10.1016/j.neurobiolaging.2005.12.014

W. Balduini, S. Carloni, S. Perrone, S. Bertrando, M. L. Tataranno et al., The use of melatonin in hypoxic-ischemic brain damage: an experimental study, J. Matern. Fetal Neonatal Med, vol.25, pp.119-124, 2012.

Y. Zhang, D. Milatovic, M. Aschner, P. J. Feustel, and H. K. Kimelberg, Neuroprotection by tamoxifen in focal cerebral ischemia is not mediated by an agonist action at estrogen receptors but is associated with antioxidant activity, Exp. Neurol, vol.204, pp.819-827, 2007.
DOI : 10.1016/j.expneurol.2007.01.015
URL : http://europepmc.org/articles/pmc1913768?pdf=render

S. E. Browne, L. J. Roberts, I. I. , P. A. Dennery, S. R. Doctrow et al., Treatment with a catalytic antioxidant corrects the neurobehavioral defect in ataxia-telangiectasia mice, Free Radic, Biol. Med, vol.36, pp.938-942, 2004.

D. R. Euston, A. J. Gruber, and B. L. Mcnaughton, The role of medial prefrontal cortex in memory and decision making, Neuron, vol.76, pp.1057-1070, 2012.

A. C. Andreazza, J. Wang, F. Salmasi, L. Shao, and L. T. Young, Specific subcellular changes in oxidative stress in prefrontal cortex from patients with bipolar disorder, J. Neurochem, vol.127, pp.552-561, 2013.

J. D. Morrow, J. A. Awad, T. Kato, K. Takahashi, K. F. Badr et al., Formation of novel non-cyclooxygenase-derived prostanoids (F2-isoprostanes) in carbon tetrachloride hepatotoxicity. An animal model of lipid peroxidation, J. Clin. Invest, vol.90, pp.2502-2507, 1992.
DOI : 10.1172/jci116143
URL : http://www.jci.org/articles/view/116143/files/pdf

C. Gladine, J. W. Newman, T. Durand, T. L. Pedersen, J. Galano et al., Lipid profiling following intake of the omega 3 fatty acid DHA identifies the peroxidized metabolites f4-neuroprostanes as the best predictors of atherosclerosis prevention, PLoS One, vol.9, p.89393, 2014.
URL : https://hal.archives-ouvertes.fr/hal-00952161

T. A. Mori, R. J. Woodman, V. Burke, I. B. Puddey, K. D. Croft et al., Effect of eicosapentaenoic acid and docosahexaenoic acid on oxidative stress and inflammatory markers in treated-hypertensive type 2 diabetic subjects, Free Radic, Biol. Med, vol.35, pp.772-781, 2003.

L. D. Tobias, F. M. Vane, and J. R. Paulsrud, The biosynthesis of 1a,1b-dihomo-PGE2 and 1a,1b-dihomo-PGF2? from 7,10,13,16-docosatetraenoic acid by an acetonepentane powder of sheep vesicular gland microsomes, Prostaglandins, vol.10, pp.443-468, 1975.

H. Sprecher, M. Vanrollins, F. Sun, A. Wyche, and P. Needleman, Dihomo-prostaglandins and-thromboxane. A prostaglandin family from adrenic acid that may be preferentially synthesized in the kidney, J. Biol. Chem, vol.257, pp.3912-3918, 1982.

W. B. Campbell, J. R. Falck, J. R. Okita, A. R. Johnson, and K. S. Callahan, 16-docosatetraenoic acid) by human endothelial cells, Synthesis of dihomoprostaglandins from adrenic acid, vol.10, pp.67-76, 1985.
DOI : 10.1016/0005-2760(85)90086-4

A. De-la-torre, Y. Y. Lee, C. Oger, P. T. Sangild, T. Durand et al., Synthesis, discovery and quantitation of dihomo-isofurans: novel biomarkers of in vivo adrenic acid peroxidation, Angew. Chem. Int. Ed, 2014.

C. De-felice, C. Signorini, T. Durand, C. Oger, A. Guy et al., F2-dihomo-isoprostanes as potential early biomarkers of lipid oxidative damage in Rett syndrome, J. Lipid Res, vol.52, pp.2287-2297, 2011.
URL : https://hal.archives-ouvertes.fr/hal-00744233

C. De-felice, C. Signorini, T. Durand, L. Ciccoli, S. Leoncini et al., Partial rescue of Rett syndrome by ?-3 polyunsaturated fatty acids (PUFAs) oil, Genes Nutr, vol.7, pp.447-458, 2012.

R. Imbusch and M. J. Mueller, Analysis of oxidative stress and wound-inducible dinor isoprostanes F1 (phytoprostanes F1) in plants, Plant Physiol, vol.124, pp.1293-1304, 2000.
DOI : 10.1104/pp.124.3.1293
URL : http://www.plantphysiol.org/content/plantphysiol/124/3/1293.full.pdf

R. Imbusch and M. J. Mueller, Formation of isoprostane F(2)-like compounds (phytoprostanes F(1)) from alpha-linolenic acid in plants, Free Radic, Biol. Med, vol.28, pp.720-726, 2000.

I. Thoma, C. Loeffler, A. K. Sinha, M. Gupta, M. Krischke et al., Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants, Plant J, vol.34, pp.363-375, 2003.
DOI : 10.1046/j.1365-313x.2003.01730.x
URL : http://onlinelibrary.wiley.com/doi/10.1046/j.1365-313X.2003.01730.x/pdf

C. Loeffler, S. Berger, A. Guy, T. Durand, G. Bringmann et al., B1-phytoprostanes trigger plant defense and detoxification responses, Plant Physiol, vol.137, pp.328-340, 2005.
DOI : 10.1104/pp.104.051714
URL : http://www.plantphysiol.org/content/plantphysiol/137/1/328.full.pdf

A. E. Barden, K. D. Croft, T. Durand, A. Guy, M. J. Mueller et al., Flaxseed oil supplementation increases plasma F1-phytoprostanes in healthy men, J. Nutr, vol.139, pp.1890-1895, 2009.
DOI : 10.3945/jn.109.108316
URL : https://hal.archives-ouvertes.fr/hal-00420110

L. J. Roberts and G. L. Milne, Isoprostanes, J. Lipid Res, vol.50, pp.219-223, 2009.

S. Sethi, A. Y. Eastman, and J. W. Eaton, Inhibition of phagocyte-endothelium interactions by oxidized fatty acids: a natural anti-inflammatory mechanism?, J. Lab. Clin. Med, vol.128, pp.27-38, 1996.

S. Sethi, O. Ziouzenkova, H. Ni, D. D. Wagner, J. Plutzky et al., Oxidized omega-3 fatty acids in fish oil inhibit leukocyte-endothelial interactions through activation of PPAR?, Blood, vol.100, pp.1340-1346, 2002.

A. Mishra, A. Chaudhary, and S. Sethi, Oxidized omega-3 fatty acids inhibit NF-?B activation via a PPAR?-dependent pathway, Arterioscler. Thromb. Vasc. Biol, vol.24, pp.1621-1627, 2004.
DOI : 10.1161/01.atv.0000137191.02577.86
URL : https://www.ahajournals.org/doi/pdf/10.1161/01.ATV.0000137191.02577.86

M. Pan, A. I. Cederbaum, Y. Zhang, H. N. Ginsberg, K. J. Williams et al., Lipid peroxidation and oxidant stress regulate hepatic apolipoprotein B degradation and VLDL production, J. Clin. Invest, vol.113, pp.1277-1287, 2004.
DOI : 10.1172/jci19197

Y. Araki, M. Matsumiya, T. Matsuura, M. Oishi, M. Kaibori et al., Peroxidation of n-3 polyunsaturated fatty acids inhibits the induction of iNOS gene expression in proinflammatory cytokine-stimulated hepatocytes, J. Nutr. Metab, p.374542, 2011.

A. Leaf, Y. Xiao, J. X. Kang, and G. E. Billman, Prevention of sudden cardiac death by n ? 3 polyunsaturated fatty acids, Pharmacol. Ther, vol.98, pp.355-377, 2003.

S. Judé, S. Bedut, S. Roger, M. Pinault, P. Champeroux et al., Peroxidation of docosahexaenoic acid is responsible for its effects on ITO and ISS in rat ventricular myocytes, Br. J. Pharmacol, vol.139, pp.816-822, 2003.

L. Guennec, J. Galano, J. Oger, C. Thireau, J. Roy et al., Methods and pharmaceutical composition for the treatment and prevention of cardiac arrhythmias

V. Saraswathi, L. Gao, J. D. Morrow, A. Chait, K. D. Niswender et al., Fish oil increases cholesterol storage in white adipose tissue with concomitant decreases in inflammation, hepatic steatosis, and atherosclerosis in mice, J. Nutr, vol.137, pp.1776-1782, 2007.

L. Gao, J. Wang, K. R. Sekhar, H. Yin, N. F. Yared et al., Novel n-3 fatty acid oxidation products activate Nrf2 by destabilizing the association between Keap1 and Cullin3, J. Biol. Chem, vol.282, pp.2529-2537, 2007.
DOI : 10.1074/jbc.m607622200

E. S. Musiek, L. Gao, G. L. Milne, W. Han, M. B. Everhart et al., Cyclopentenone isoprostanes inhibit the inflammatory response in macrophages, J. Biol. Chem, vol.280, pp.35562-35570, 2005.
DOI : 10.1074/jbc.m504785200
URL : http://www.jbc.org/content/280/42/35562.full.pdf

J. D. Brooks, E. S. Musiek, T. R. Koestner, J. N. Stankowski, J. R. Howard et al., The fatty acid oxidation product 15-A3t-Isoprostane is a potent inhibitor of NF?B transcription and macrophage transformation, J. Neurochem, vol.119, pp.604-616, 2011.

Z. Majkova, J. Layne, M. Sunkara, A. J. Morris, M. Toborek et al., Omega-3 fatty acid oxidation products prevent vascular endothelial cell activation by coplanar polychlorinated biphenyls, Toxicol. Appl. Pharmacol, vol.251, pp.41-49, 2011.
DOI : 10.1016/j.taap.2010.11.013
URL : http://europepmc.org/articles/pmc3026064?pdf=render

S. Maffei, C. De-felice, P. Cannarile, S. Leoncini, C. Signorini et al., Effects of omega3 PUFAs supplementation on myocardial function and oxidative stress markers in typical Rett syndrome, Mediat. Inflamm, 2014.

M. J. Mueller, Archetype signals in plants: the phytoprostanes, Curr. Opin. Plant Biol, vol.7, pp.441-448, 2004.
DOI : 10.1016/j.pbi.2004.04.001

T. Durand, V. Bultel-ponce, A. Guy, S. E. Fangour, J. C. Rossi et al., Isoprostanes and phytoprostanes: bioactive lipids, vol.93, pp.52-60, 2011.
DOI : 10.1016/j.biochi.2010.05.014

K. Karg, V. M. Dirsch, A. M. Vollmar, J. L. Cracowski, F. Laporte et al., Biologically active oxidized lipids (phytoprostanes) in the plant diet and parenteral lipid nutrition, Free Radic. Res, vol.41, pp.25-37, 2007.
DOI : 10.1080/10715760600939734

C. Traidl-hoffmann, V. Mariani, H. Hochrein, K. Karg, H. Wagner et al., Pollen-associated phytoprostanes inhibit dendritic cell interleukin-12 production and augment T helper type 2 cell polarization, J. Exp. Med, vol.201, pp.627-636, 2005.
DOI : 10.1084/jem.20041065
URL : http://jem.rupress.org/content/jem/201/4/627.full.pdf

A. Barden, E. Mas, P. Henry, T. Durand, J. Galano et al., The effects of oxidation products of arachidonic acid and n3 fatty acids on vascular and platelet function, Free Radic. Res, vol.45, pp.469-476, 2011.
URL : https://hal.archives-ouvertes.fr/hal-00575774

S. Gilles, V. Mariani, M. Bryce, M. J. Mueller, J. Ring et al., Pollen-derived E1-phytoprostanes signal via PPAR-? and NF-?Bdependent mechanisms, J. Immunol, vol.182, pp.6653-6658, 2009.
DOI : 10.4049/jimmunol.0802613
URL : http://www.jimmunol.org/content/182/11/6653.full.pdf

L. Minghetti, R. Salvi, M. L. Salvatori, M. Antonietta-ajmone-cat, C. De-nuccio et al., Nonenzymatic oxygenated metabolites of ?-linolenic acid B1-and L1-phytoprostanes protect immature neurons from oxidant injury and promote differentiation of oligodendrocyte progenitors through PPAR-? activation, Free Radic, Biol. Med, vol.73, pp.41-50, 2014.

J. A. Lawson, S. Kim, W. S. Powell, G. A. Fitzgerald, and J. Rokach, Oxidized derivatives of omega-3 fatty acids: identification of IPF3 alpha-VI in human urine, J. Lipid Res, vol.47, pp.2515-2524, 2006.

T. B. Corcoran, E. Mas, A. Barden, T. Durand, J. M. Galano et al., Are isofurans and neuroprostanes increased after subarachnoid hemorrhage and traumatic brain injury?, Antioxid. Redox Signal, vol.15, pp.2663-2667, 2011.
DOI : 10.1089/ars.2011.4125
URL : https://hal.archives-ouvertes.fr/hal-00631502

H. Yen, H. Wei, and T. Chen, Analytical variables affecting analysis of F 2-isoprostanes and F 4-neuroprostanes in human cerebrospinal fluid by gas chromatography/mass spectrometry, BioMed. Res. Int, p.2013, 2013.

W. R. Markesbery, R. J. Kryscio, M. A. Lovell, and J. D. Morrow, Lipid peroxidation is an early event in the brain in amnestic mild cognitive impairment, Ann. Neurol, vol.58, pp.730-735, 2005.
DOI : 10.1002/ana.20629

R. C. Seet, C. J. Lee, E. C. Lim, A. M. Quek, H. Huang et al., Oral zinc supplementation does not improve oxidative stress or vascular function in patients with type 2 diabetes with normal zinc levels, Atherosclerosis, vol.219, pp.231-239, 2011.
DOI : 10.1016/j.atherosclerosis.2011.07.097

G. L. Milne, J. D. Morrow, and M. J. Picklo-sr, (n-3), in brain regions of rats undergoing ethanol withdrawal, Neurosci. Lett, vol.22, issue.6, pp.172-174, 2006.
DOI : 10.1016/j.neulet.2006.06.058

R. C. Gupta, S. Milatovic, W. Dettbarn, M. Aschner, and D. Milatovic, Neuronal oxidative injury and dendritic damage induced by carbofuran: protection by memantine, Toxicol. Appl. Pharmacol, vol.219, pp.97-105, 2007.
DOI : 10.1016/j.taap.2006.10.028

D. Santos, D. Milatovic, V. Andrade, M. C. Batoreu, M. Aschner et al., The inhibitory effect of manganese on acetylcholinesterase activity enhances oxidative stress and neuroinflammation in the rat brain, Toxicology, vol.292, pp.90-98, 2012.

D. Milatovic, Y. Zhang, S. J. Olson, K. S. Montine, L. J. Roberts et al., Herpes simplex virus type 1 encephalitis is associated with elevated levels of F2-isoprostanes and F4-neuroprostanes, J. Neurovirol, vol.8, pp.295-305, 2002.
DOI : 10.1080/13550280290100743

S. L. Cuddihy, S. S. Ali, E. S. Musiek, J. Lucero, S. J. Kopp et al., Prolonged ?-tocopherol deficiency decreases oxidative stress and unmasks ?-tocopherol-dependent regulation of mitochondrial function in the brain, J. Biol. Chem, vol.283, pp.6915-6924, 2008.

F. E. Harrison, S. S. Yu, K. L. Van-den-bossche, L. Li, J. M. May et al., Elevated oxidative stress and sensorimotor deficits but normal cognition in mice that cannot synthesize ascorbic acid, J. Neurochem, vol.106, pp.1198-1208, 2008.

F. E. Harrison, J. Allard, R. Bixler, C. Usoh, L. Li et al., Antioxidants and cognitive training interact to affect oxidative stress and memory in APP/PSEN1 mice, Nutr. Neurosci, vol.12, pp.203-218, 2009.