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

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.