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Localization of distinct F2-isoprostanes in human atherosclerotic lesions.
Open accessAbstract
F 2 -Isoprostanes are prostaglandin (PG) isomers formed in situ in cell membranes by peroxidation of arachidonic acid.8-epi PGF 2 ␣ and IPF 2 ␣ -I are F 2 -isoprostanes produced in humans which circulate in plasma and are excreted in urine.Measurement of F 2 -isoprostanes may offer a sensitive, specific, and noninvasive method for measuring oxidant stress in clinical settings where reactive oxygen species are putatively involved.We determined whether isoprostanes were present in human atherosclerotic lesions, where lipid peroxidation is thought to occur in vivo.8-epi PGF 2 ␣ ranged from 1.310-3.450pmol/ mol phospholipid in atherectomy specimens compared with 0.045-0.115pmol/ mol phospholipid ( P Ͻ 0.001) in vascular tissue devoid of atherosclerosis.Corresponding values of IPF 2 ␣ -I were 5.6-13.8 vs. 0.16-0.44pmol/ mol phospholipid ( P Ͻ 0.001).Levels of the two isoprostanes in vascular tissue were highly correlated ( r ϭ 0.80, P Ͻ 0.0001).Immunohistochemical studies confirmed that foam cells adjacent to the lipid necrotic core of the plaque were markedly positive for 8-epi PGF 2 ␣ .These cells were also reactive with anti-CD68, an epitope specific for human monocyte/macrophages. 8-epi PGF 2 ␣ immunoreactivity was also detected in cells positive for anti-␣ -smooth muscle actin antibody, which specifically recognizes vascular smooth muscle cells.Our results indicate that 8-epi PGF 2 ␣ and IPF 2 ␣ -I, two distinct F 2 -isoprostanes and markers of oxidative stress in vivo, are present in human atherosclerotic plaque.Quantitation of these chemically stable products of lipid peroxidation in target tissues, as well as in biological fluids, may aid in the rational development of antioxidant drugs in humans.( J. Clin.Invest.1997.100:2028-2034.)Key words: atherosclerosis • oxidative stress • lipid peroxidation • isoprostanes Methods Sample acquisition and tissue processing.Human atherosclerotic plaques were obtained from 12 patients undergoing carotid endarterectomy.Informed consent was obtained from all patients before surgery.All procedures were approved by the local human ethics committee.
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Citations
Cited by
Carr, A. C., & Frei, B. (1999) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/69.6.1086 · Cited by 940
Reactive oxygen species in cardiovascular disease
Sugamura, K., & Keaney (2011) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2011.05.004 · Cited by 769
Plant polyphenols in cancer and heart disease: implications as nutritional antioxidants
Duthie, G. G., Duthie, S. J., & Kyle, J. A. M. (2000) · Nutrition Research Reviews · doi:10.1079/095442200108729016 · Cited by 759
Oxidative Stress and Cardiovascular Injury: Part II: Animal and Human Studies
Griendling, K. K., & FitzGerald, G. A. (2003) · Circulation · doi:10.1161/01.cir.0000093661.90582.c4 · Cited by 721
Self-citationDisruption of the 12/15-lipoxygenase gene diminishes atherosclerosis in apo E–deficient mice
Cyrus, T., Witztum, J. L., Rader, D. J., Tangirala, R., Fazio, S., Linton, M. F., & Funk, C. D. (1999) · Journal of Clinical Investigation · doi:10.1172/jci5897 · Cited by 523
Metadata
- Authors
- Praticò, D., Iuliano, L., Mauriello, A., Spagnoli, L., Lawson, J. A., Rokach, J., Maclouf, J., Violi, F., & FitzGerald, G. A.
- Venue
- Journal of Clinical Investigation
- Published
- 1997-10-15
- Volume
- 100
- Issue
- 8
- Pages
- 2028-2034
- ISSN
- 0021-9738 (ISSN-L)
- OpenAlex
- W2033539598
- Cited by
- 344
- References
- 0
- FWCI
- 14.66
- Type
- journal article
- Language
- en
- Open access
- bronze
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- Praticò, D., Iuliano, L., Mauriello, A., Spagnoli, L., Lawson, J. A., Rokach, J., Maclouf, J., Violi, F., & FitzGerald, G. A. (1997). Localization of distinct F2-isoprostanes in human atherosclerotic lesions. Journal of Clinical Investigation. https://doi.org/10.1172/jci119735
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