isoprostane

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Introduction

Isoprostanes are formed in situ by peroxidation

Structure

* It would appear that these are the prostaglandins

Laboratory

More general terms

References

  1. Montine KS, Quinn JF, Zhang J, Fessel JP, Roberts LJ 2nd, Morrow JD, Montine TJ. Isoprostanes and related products of lipid peroxidation in neurodegenerative diseases. Chem Phys Lipids. 2004 Mar;128(1-2):117-24. PMID: https://www.ncbi.nlm.nih.gov/pubmed/15037157
  2. Musiek ES, Cha JK, Yin H, Zackert WE, Terry ES, Porter NA, Montine TJ, Morrow JD. Quantification of F-ring isoprostane-like compounds (F4-neuroprostanes) derived from docosahexaenoic acid in vivo in humans by a stable isotope dilution mass spectrometric assay. J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Jan 5;799(1):95-102. PMID: https://www.ncbi.nlm.nih.gov/pubmed/14659440
  3. 3.0 3.1 Pratico D, Clark CM, Liun F, Rokach J, Lee VY, Trojanowski JQ. Increase of brain oxidative stress in mild cognitive impairment: a possible predictor of Alzheimer disease. Arch Neurol. 2002 Jun;59(6):972-6. Erratum in: Arch Neurol 2002 Sep;59(9):1475. PMID: https://www.ncbi.nlm.nih.gov/pubmed/12056933
  4. 4.0 4.1 Urine Testing for Alzheimer's Disease Lab Tests Online http://www.labtestsonline.org/news/alzheimer020717.html

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