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Comparison of ex vivo inhibitory effect between 2-hydroxyestradiol and its 17-sulfate on rat hepatic microsomal lipid peroxidation.

Abstract
Two endogenous antioxidants that are speculated to be defense substances against preeclampsia, 2-hydroxyestradiol (2-OH-E2) and its 17-sulfate, 2-hydroxyestradiol 17-sulfate (2-OH-E2-17-S), were administered to rats to compare their inhibitory effects on hepatic microsomal lipid peroxidation, and the lipid peroxides were determined in NADPH- and ascorbic acid-dependent systems. The two catechols showed a strong inhibitory effect on lipid peroxidation in both systems, and the effect was dose dependent. However, a large difference was observed in their inhibition patterns. After administration of 2-OH-E2, the effect appeared immediately and decreased gradually with time. In contrast, the effect of 2-OH-E2-17-S appeared some time after administration and persisted for a longer time. Both catechols also showed a striking difference in their dynamics. After administration, 2-OH-E2 was detected in the blood together with its metabolites, 2-methoxyestradiol and 2-methoxyestrone, and they disappeared immediately. In contrast, 2-OH-E2-17-S was present in the blood for a longer time together with its O-methylated product, 2-methoxyestradiol 17-sulfate, but disappeared from liver microsomes within 2 h after administration. The results imply no occurrence of a direct inhibition effect of 2-OH-E2-17-S.
AuthorsKaori Takanashi, Yasunori Osanai, Takahiro Kyo, Itsuo Yoshizawa
JournalLipids (Lipids) Vol. 38 Issue 8 Pg. 847-54 (Aug 2003) ISSN: 0024-4201 [Print] United States
PMID14577664 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Estrogens
  • Estradiol
  • 2-hydroxyestradiol 17-sulfate
  • 2-hydroxyestradiol
Topics
  • Animals
  • Dose-Response Relationship, Drug
  • Estradiol (analogs & derivatives, blood, pharmacology)
  • Estrogens (blood, pharmacology)
  • Lipid Peroxidation (drug effects)
  • Liver (drug effects)
  • Male
  • Microsomes, Liver (drug effects, metabolism)
  • Models, Molecular
  • Molecular Structure
  • Rats
  • Rats, Wistar
  • Time Factors

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