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Issue title: HNE and Further Lipid Peroxidation Products
Article type: Research Article
Authors: Yoshida, Yasukazu | Hayakawa, Mieko | Niki, Etsuo
Affiliations: National Institute of Advanced Industrial Science and Technology (AIST), Human Stress Signal Research Center, Ikeda 563-8577, Japan
Note: [] Address for correspondence: Yasukazu Yoshida, AIST, Human Stress Signal Research Center, 1-8-31 Midorigaoka, Ikeda 563-8577, Japan. Tel.: +81 72 751 8183; Fax: +81 72 751 9964; E-mail: yoshida-ya@aist.go.jp
Abstract: An improved method for the measurement of lipid peroxidation in vivo has been recently developed, where total hydroxyoctadecadienoic acid (HODE) and 7-hydroxycholesterol (FCOH) were determined by GC/MS analysis from physiological samples after reduction with sodium borohydride and saponification by potassium hydroxide. In this method, both free and ester forms of hydroperoxides and ketones as well as hydroxides of linoleic acid and cholesterol are measured as HODE and FCOH, respectively. The ratio of stereo-isomer, (Z, E)-HODE/(E, E)-HODE, could be also measured. In the present study, in order to examine the effect of continuous, slow flux of free radicals in vivo, a water-soluble radical generator was administered to rats and mice and the amounts of HODE and 8-isoprostane in plasma and liver were measured. It was found that the administration of free radical-generating azo compound increased the level of HODE and decreased the (Z, E)-HODE/(E, E)-HODE ratio in both plasma and liver. The level of HODE was much higher than 8-isoprostane.
Keywords: Lipid peroxidation, oxidative stress, HODE, oxycholesterol
Journal: BioFactors, vol. 24, no. 1-4, pp. 7-15, 2005
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