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1 See also  





2 References  














Template:Selected biological properties of endogenous estrogens in rats






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  • t
  • e
  • Selected biological properties of endogenous estrogens in rats
    Estrogen ERTooltip Estrogen receptor RBATooltip relative binding affinity (%) Uterine weight (%) Uterotrophy LHTooltip Luteinizing hormone levels (%) SHBGTooltip Sex hormone-binding globulin RBATooltip relative binding affinity (%)
    Control 100 100
    Estradiol (E2) 100 506 ± 20 +++ 12–19 100
    Estrone (E1) 11 ± 8 490 ± 22 +++ ? 20
    Estriol (E3) 10 ± 4 468 ± 30 +++ 8–18 3
    Estetrol (E4) 0.5 ± 0.2 ? Inactive ? 1
    17α-Estradiol 4.2 ± 0.8 ? ? ? ?
    2-Hydroxyestradiol 24 ± 7 285 ± 8 +b 31–61 28
    2-Methoxyestradiol 0.05 ± 0.04 101 Inactive ? 130
    4-Hydroxyestradiol 45 ± 12 ? ? ? ?
    4-Methoxyestradiol 1.3 ± 0.2 260 ++ ? 9
    4-Fluoroestradiola 180 ± 43 ? +++ ? ?
    2-Hydroxyestrone 1.9 ± 0.8 130 ± 9 Inactive 110–142 8
    2-Methoxyestrone 0.01 ± 0.00 103 ± 7 Inactive 95–100 120
    4-Hydroxyestrone 11 ± 4 351 ++ 21–50 35
    4-Methoxyestrone 0.13 ± 0.04 338 ++ 65–92 12
    16α-Hydroxyestrone 2.8 ± 1.0 552 ± 42 +++ 7–24 <0.5
    2-Hydroxyestriol 0.9 ± 0.3 302 +b ? ?
    2-Methoxyestriol 0.01 ± 0.00 ? Inactive ? 4
    Notes: Values are mean ± SD or range. ER RBA = Relative binding affinitytoestrogen receptors of rat uterine cytosol. Uterine weight = Percentage change in uterine wet weight of ovariectomized rats after 72 hours with continuous administration of 1 μg/hour via subcutaneously implanted osmotic pumps. LH levels = Luteinizing hormone levels relative to baseline of ovariectomized rats after 24 to 72 hours of continuous administration via subcutaneous implant. Footnotes: a = Synthetic (i.e., not endogenous). b = Atypical uterotrophic effect which plateaus within 48 hours (estradiol's uterotrophy continues linearly up to 72 hours). Sources: [1][2][3][4][5][6][7][8][9]
  • Template:Affinities of estrogen receptor ligands for the ERα and ERβ
  • Template:Relative affinities of estrogens for steroid hormone receptors and blood proteins
  • References

    1. ^ Martucci C, Fishman J (March 1976). "Uterine estrogen receptor binding of catecholestrogens and of estetrol (1,3,5(10)-estratriene-3,15alpha,16alpha,17beta-tetrol)". Steroids. 27 (3): 325–333. doi:10.1016/0039-128x(76)90054-4. PMID 178074. S2CID 54412821.
  • ^ Martucci C, Fishman J (December 1977). "Direction of estradiol metabolism as a control of its hormonal action--uterotrophic activity of estradiol metabolites". Endocrinology. 101 (6): 1709–1715. doi:10.1210/endo-101-6-1709. PMID 590186.
  • ^ Fishman J, Martucci C (December 1978). "Differential biological activity of estradiol metabolites". Pediatrics. 62 (6 Pt 2): 1128–1133. doi:10.1542/peds.62.6.1128. PMID 724350. S2CID 29609115.
  • ^ Martucci CP, Fishman J (December 1979). "Impact of continuously administered catechol estrogens on uterine growth and luteinizing hormone secretion". Endocrinology. 105 (6): 1288–1292. doi:10.1210/endo-105-6-1288. PMID 499073.
  • ^ Fishman J, Martucci CP (1980). "New Concepts of Estrogenic Activity: the Role of Metabolites in the Expression of Hormone Action". In Pasetto N, Paoletti R, Ambrus JL (eds.). The Menopause and Postmenopause. pp. 43–52. doi:10.1007/978-94-011-7230-1_5. ISBN 978-94-011-7232-5.
  • ^ Fishman J, Martucci C (September 1980). "Biological properties of 16 alpha-hydroxyestrone: implications in estrogen physiology and pathophysiology". The Journal of Clinical Endocrinology and Metabolism. 51 (3): 611–615. doi:10.1210/jcem-51-3-611. PMID 7190977.
  • ^ Martucci CP (July 1983). "The role of 2-methoxyestrone in estrogen action". Journal of Steroid Biochemistry. 19 (1B): 635–638. doi:10.1016/0022-4731(83)90229-7. PMID 6310247.
  • ^ Fishman J, Martucci C (1980). "Dissociation of biological activities in metabolites of estradiol". In McLachlan JA (ed.). Estrogens in the Environment: Proceedings of the Symposium on Estrogens in the Environment, Raleigh, North Carolina, U.S.A., September 10-12, 1979. Elsevier. pp. 131–145. ISBN 9780444003720.
  • ^ Kuhl H (August 2005). "Pharmacology of estrogens and progestogens: influence of different routes of administration". Climacteric. 8 Suppl 1: 3–63. doi:10.1080/13697130500148875. PMID 16112947. S2CID 24616324.

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