Catechol estrogens as inhibitors of leukotriene synthesis

Juha Alanko, Eeva Sievi, Tuula Lähteenmäki, István Mucha, Heikki Vapaatalo, Jouko Parantainen

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Estrogens have a beneficial effect on atherosclerosis and osteoporosis after menopause, but their exact mechanism of action is still unknown. The aim of the present study was to investigate the effects of estradiol and its metabolites catechol estrogens on arachidonic acid metabolism in vitro. Estradiol had no effect on arachidonic acid metabolism up to 33 μM in A23187-stimulated human whole blood. All catechol estrogens (2-hydroxyestradiol, 2-hydroxyestrone, 4-hydroxyestradiol and 4-hydroxyestrone) had similar kinds of actions on arachidonic acid metabolism, being over ten times more potent inhibitors of leukotriene synthesis (IC50 values 0.044-0.16 μM) than thromboxane (IC50 values 0.99-2.1 μM) and prostaglandin E2 synthesis (IC50 values 0.84-5.5 μM). It is suggested that some of the protective actions of estrogens - e.g., on atherosclerosis and osteoporosis - may be related to the inhibition of leukotriene synthesis by catechol estrogens.

Original languageEnglish
Pages (from-to)101-104
Number of pages4
JournalBiochemical Pharmacology
Issue number1
Publication statusPublished - Jan 1 1998


  • Estradiol
  • Estrogen
  • Leukotriene
  • Prostaglandin
  • Thromboxane

ASJC Scopus subject areas

  • Biochemistry
  • Pharmacology

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  • Cite this

    Alanko, J., Sievi, E., Lähteenmäki, T., Mucha, I., Vapaatalo, H., & Parantainen, J. (1998). Catechol estrogens as inhibitors of leukotriene synthesis. Biochemical Pharmacology, 55(1), 101-104.