The isoprostanes—25 years later

Clinical Factors Associated with Plasma F2-Isoprostane Levels in HIV-Infected Adults

Redhage, L. A., Shintani, A., Haas, D. W., Emeagwali, N., Marković, M., Oboho, I., Mwenya, C., Erdem, H., Acosta, E. P., Morrow, J. D., et al. (2009) · HIV Clinical Trials · doi:10.1310/hct1003-181 · Cited by 25

Determination of F2-Isoprostanes in Urine by Online Solid Phase Extraction Coupled to Liquid Chromatography with Tandem Mass Spectrometry

Langhorst, M. L., Hastings, M. J., YOKOYAMA, W. H., Hung, S., Cellar, N. A., Kuppannan, K., & Young, S. A. (2010) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf101146q · Cited by 24

Assessment of oxidative stress in coronary artery bypass surgery: comparison between the global index OXY-SCORE and individual biomarkers

Veglia, F., Werba, J. P., Tremoli, E., Squellerio, I., Sisillo, E., Parolari, A., Minardi, F., & Cavalca, V. (2009) · Biomarkers · doi:10.3109/13547500903134395 · Cited by 22

Gastric cancer in Zambian adults: a prospective case-control study that assessed dietary intake and antioxidant status by using urinary isoprostane excretion

Asombang, A. W., Kayamba, V. J., Lisulo, M. M., Colditz, G. A., Mudenda, V. C., Yarasheski, K. E., Chott, R. C., Rubin, D. C., Gyawali, C. P., Sinkala, E., et al. (2013) · American Journal of Clinical Nutrition · doi:10.3945/ajcn.112.051284 · Cited by 22

Dried blood spot (DBS) sample collection for determination of the oxidative stress biomarker 8‐epi‐PGF 2α in humans using liquid chromatography/tandem mass spectrometry

Bastani, N. E., Gundersen, T. E., & Blomhoff, R. (2012) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.6149 · Cited by 21

E-Ring 8-Isoprostanes Are Agonists at EP2- and EP4-Prostanoid Receptors on Human Airway Smooth Muscle Cells and Regulate the Release of Colony-Stimulating Factors by Activating cAMP-Dependent Protein Kinase

Clarke, D. L., Belvisi, M. G., Hardaker, E. L., Newton, R. C., & Giembycz, M. A. (2004) · Molecular Pharmacology · doi:10.1124/mol.104.006486 · Cited by 21

Sensitive determination of isoprostanes in exhaled breath condensate samples with use of liquid chromatography–tandem mass spectrometry

Janicka, M., Kubica, P., Kot‐Wasik, A., Kot, J., & Namieśnik, J. (2012) · Journal of Chromatography B · doi:10.1016/j.jchromb.2012.03.005 · Cited by 20

Identification of the Major Urinary Metabolite of the Highly Reactive Cyclopentenone Isoprostane 15-A2t-Isoprostane in Vivo

Milne, G. L., Gao, L., Porta, A., Zanoni, G., Vidari, G., & Morrow, J. D. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m502891200 · Cited by 20

Identification of metabolites from Type III F2-isoprostane diastereoisomers by mass spectrometry

Chiabrando, C., Rivalta, C., Bagnati, R., Valagussa, A., Durand, T., Guy, A., Villa, P., Rossi, J., & Fanelli, R. (2002) · Journal of Lipid Research · doi:10.1016/s0022-2275(20)30156-5 · Cited by 20

Electrophilic Cyclopentenone Isoprostanes in Neurodegeneration

Musiek, E. S., McLaughlin, B., & Morrow, J. D. (2007) · Journal of Molecular Neuroscience · doi:10.1007/s12031-007-0042-3 · Cited by 19

Regulation of Activator Protein-1 by 8-iso-Prostaglandin E2 in a Thromboxane A2 Receptor-Dependent and -Independent Manner

Weber, T. J., & Markillie, L. M. (2003) · Molecular Pharmacology · doi:10.1124/mol.63.5.1075 · Cited by 19

Ischemia Reperfusion Unveils Impaired Capacity of Older Adults to Restrain Oxidative Insult

Davies, S., Traustadóttir, T., Stock, A. A., Ye, F., Shyr, Y., Harman, S., & Roberts, L. (2009) · Free Radical Biology & Medicine · doi:10.1016/j.freeradbiomed.2009.07.005 · Cited by 19

Contractile effects of 15-E2t-isoprostane and 15-F2t-isoprostane on chicken embryo ductus arteriosus

van der Sterren, S., & Villamor, E. (2011) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2011.04.010 · Cited by 18

Racial Differences in Urinary F2‐Isoprostane Levels and the Cross‐Sectional Association With bmi

Il’yasova, D., Wang, F. M., Spasojević, I., Baše, K., Agostino, R. B. D., & Wagenknecht, L. E. (2012) · Obesity · doi:10.1038/oby.2012.170 · Cited by 18

Isoprostanes and isofurans as non-traditional risk factors for cardiovascular disease among Canadian Inuit

Alkazemi, D. U. Z., Egeland, G. M., Roberts, L. J., & Kubow, S. J. (2012) · Free Radical Research · doi:10.3109/10715762.2012.702900 · Cited by 17

Assessment of Urinary F 2 -Isoprostanes in Experimental and Clinical Studies: Mass Spectrometry Versus ELISA

Tsikas, D., & Suchy, M.-T. (2012) · Hypertension · doi:10.1161/hypertensionaha.112.199315 · Cited by 16

E-Ring Isoprostanes Stimulate a Cl− Conductance in Airway Epithelium via Prostaglandin E2-Selective Prostanoid Receptors

Seto, V., Hirota, C. L., Hirota, S. A., & Janssen, L. J. (2007) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2007-0117oc · Cited by 15

Daily Consumption of Grapefruit for 6 Weeks Reduces Urine F2-Isoprostanes in Overweight Adults with High Baseline Values but Has No Effect on Plasma High-Sensitivity C-Reactive Protein or Soluble Vascular Cellular Adhesion Molecule

Dow, C. A., Wertheim, B. C., Patil, B. S., & Thomson, C. A. (2013) · Journal of Nutrition · doi:10.3945/jn.113.175166 · Cited by 15

Rational Design of Novel Pyridinol-Fused Ring Acetaminophen Analogues

Shchepin, R. V., Liu, W., Yin, H., Zagol-Ikapitte, I. A., Amin, T., Jeong, B., Roberts, L. J., Oates, J. A., Porter, N. A., & Boutaud, O. G. (2013) · ACS Medicinal Chemistry Letters · doi:10.1021/ml4000904 · Cited by 14

Prenatal exposure to hyperoxia modifies the thromboxane prostanoid receptor-mediated response to H2O2 in the ductus arteriosus of the chicken embryo.

van der Sterren, S., Kessels, L. C. G. A., Pérez‐Vizcaíno, F., Cogolludo, A. L., & Villamor, E. (2014) · PubMed · Cited by 13

Higher Serum Iron Is Associated With Increased Oxidant Stress in HIV-Infected Men

Crist, M. B., Melekhin, V. V., Bian, A., Shintani, A., Milne, G. L., Kallianpur, A. R., Dageforde, L. A., Haas, D. W., & Hulgan, T. (2013) · JAIDS Journal of Acquired Immune Deficiency Syndromes · doi:10.1097/qai.0b013e3182a60f36 · Cited by 13

Quantitation of plasma total 15-series F2-isoprostanes by sequential solid phase and liquid–liquid extraction

Taylor, A. W., & Traber, M. G. (2009) · Analytical Biochemistry · doi:10.1016/j.ab.2009.09.042 · Cited by 13

Perioperative Plasma F2-Isoprostane Levels Correlate With Markers of Impaired Ventilation in Infants With Single-Ventricle Physiology Undergoing Stage 2 Surgical Palliation on the Cardiopulmonary Bypass

Albers, E. L., Donahue, B. S., Milne, G. L., Saville, B. R., Wang, W., Bichell, D. P., & McLaughlin, B. (2012) · Pediatric Cardiology · doi:10.1007/s00246-012-0166-2 · Cited by 13

Quantification of F-Ring and D-/E-Ring Isoprostanes and Neuroprostanes in Alzheimer’s Disease

Reich, E. E., Markesbery, W. R., Roberts, L. J., Swift, L. L., Morrow, J. D., & Montine, T. J. (2001) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-0667-6_39 · Cited by 12

Measurement of urinary F2-isoprostanes by gas chromatography-mass spectrometry is confounded by interfering substances

Mas, E., Barden, A. E., Durand, T., Galano, J., Croft, K. D., & Mori, T. A. (2009) · Free Radical Research · doi:10.3109/10715760903390838 · Cited by 12

C-Nociceptor sensitization by isoprostanes is cyclooxygenase dependent

Junger, H., & Sorkin, L. S. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02306-4 · Cited by 12

Revascularization decreases 8-isoprostaglandin F2α excretion in chronic lower limb ischemia

Rossi, P., Riutta, A., Kuukasjärvi, P., Vehmas, T. I., Mucha, I., & Salenius, J. ‐. (2004) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2004.01.003 · Cited by 10

E-Ring Isoprostane Augments Cholinergic Neurotransmission in Bovine Trachealis via FP Prostanoid Receptors

Paredes, C., Tazzeo, T., & Janssen, L. J. (2007) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2007-0022oc · Cited by 10

Enzyme Immunoassay of Isoprostanes

Callewaert, D. M., & Sloan, C. (2009) · Methods in molecular biology · doi:10.1007/978-1-60327-029-8_26 · Cited by 10

Role of Prostanoid Production and Receptors in the Regulation of Retinal Endogenous Amino Acid Neurotransmitters by 8-Isoprostaglandin E2, Ex Vivo

Zhao, M., Destache, C. J., Ohia, S. E., & Opere, C. A. (2009) · Neurochemical Research · doi:10.1007/s11064-009-0013-x · Cited by 8

Systemic markers of oxidative status and colorectal adenomatous polyps

Siamakpour‐Reihani, S., Scarbrough, P. M., Wang, F. M., Spasojević, I., Baše, K., Sedjo, R. L., D'Agostino, R. B., & Il’yasova, D. (2012) · Annals of Epidemiology · doi:10.1016/j.annepidem.2012.05.001 · Cited by 8

Fatty acids as determinants ofin-vivolipid peroxidation: The EFFGE study in Eastern Finnish hypertensive and non-hypertensive subjects

Kaikkonen, J., Vilppo, T., Asikainen, J., Voutilainen, S., Kurl, S., & Salonen, J. T. (2013) · Annals of Medicine · doi:10.3109/07853890.2013.809915 · Cited by 7

Prostaglandin D2 is metabolized in humans to 9 alpha,11 beta-prostaglandin F2, a novel biologically active prostaglandin.

Te, L., Oates, J. A., & Roberts, L. J. (1985) · PubMed · Cited by 5

Formation of Novel D-Ring and E-Ring Isoprostane-Like Compounds (D4/E4-Neuroprostanes)in Vivo From Docosahexaenoic Acidt

Reich, E. E., Montine, T. J., & Morrow, J. D. (2002) · Advances in experimental medicine and biology · doi:10.1007/978-1-4615-0193-0_79 · Cited by 5

[The application of LC-MS/MS in measurement of oxidative stress parameters].

Yin, H., Gao, F., & An, Y. (2009) · PubMed · Cited by 1

Untitled work

(2000) · doi:10.1002/1531-8249(200012)48:6

Untitled work

(2000) · doi:10.1002/1531-8249(200011)48:5

Reactive Oxygen Species, Toxicity, Oxidative Stress, and Antioxidants: Chronic Diseases and Aging

Jomova, K., Raptova, R., Alomar, S. Y., Alwasel, S. H., Nepovimova, E., Kuca, K., & Valko, M. (2023) · Archives of Toxicology · doi:10.1007/s00204-023-03562-9 · Cited by 2,638

Oxidative stress, dysfunctional glucose metabolism and Alzheimer disease

Butterfield, D. A., & Halliwell, B. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0132-6 · Cited by 1,954

Ferroptosis at the crossroads of cancer-acquired drug resistance and immune evasion

Angeli, J. P. F., Krysko, D. V., & Conrad, M. (2019) · Nature reviews. Cancer · doi:10.1038/s41568-019-0149-1 · Cited by 1,275

Ferroptosis in cancer: from molecular mechanisms to therapeutic strategies

Zhou, Q., Meng, Y., Li, D., Yao, L., Le, J., Liu, Y., Sun, Y., Zeng, F., Chen, X., & Deng, G. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01769-5 · Cited by 1,056

Clinical Relevance of Biomarkers of Oxidative Stress

Frijhoff, J., Winyard, P. G., Žarković, N., Davies, S. S., Stocker, R., Cheng, D., Knight, A. R., Taylor, E., Oettrich, J., Ruskovska, T., et al. (2015) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6317 · Cited by 918

Autour des graisses

(2011) · Médecine des Maladies Métaboliques · doi:10.1016/s1957-2557(11)70232-2

Leadership vs. consensus

Ausman, J. I. (2006) · Surgical Neurology · doi:10.1016/j.surneu.2006.08.052 · Cited by 3

DNA-cleavage caused by resveratrol

Miyata, N., & Fukuhara, K. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)90239-8

Isoprostanes

Roberts, L. J., & Milne, G. L. (2008) · Journal of Lipid Research · doi:10.1194/jlr.r800037-jlr200 · Cited by 107

Recent advances in the biochemistry and clinical relevance of the isoprostane pathway

Musiek, E. S., Yin, H., Milne, G. L., & Morrow, J. D. (2005) · Lipids · doi:10.1007/s11745-005-1460-7 · Cited by 117