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* Estrone is weaker than estradiol.
* Estrone is weaker than estradiol.


[[Premarin]], a commonly prescribed estrogenic drug, contains the steroidal estrogens [[equilin]] and [[equilenin]], in addition to [[estrone]] sulfate but due to its healtrisk, genetic Progynova are now more often prescribed.
[[Premarin]], a commonly prescribed estrogenic drug, contains the steroidal estrogens [[equilin]] and [[equilenin]], in addition to [[estrone]] sulfate but due to its healt risk, more genetic estrogen named Progynova are now more often prescribed.


===Nonsteroidal===
===Nonsteroidal===

Revision as of 11:26, 15 February 2009

Estriol. Note two hydroxyl (-OH) groups attached to the D ring (rightmost ring).
Estradiol. Note one hydroxyl group attached to the D ring. The 'di' refers both to this hydroxyl and the one on the A ring (leftmost).
Estrone. Note the ketone (=O) group attached to the D ring.

Estrogens (U.S., otherwise oestrogens or œstrogens) are a group of steroid compounds, named for their importance in the estrous cycle, and functioning as the primary female sex hormone.

Estrogens are used as part of some oral contraceptives, in estrogen replacement therapy of postmenopausal women, and in hormone replacement therapy for transwomen.

Like all steroid hormones, estrogens readily diffuse across the cell membrane; inside the cell, they interact with estrogen receptors.[1] Additionally, estrogens have been shown to activate a G protein-coupled receptor, GPR30.[2]

Types

Steroidal

The three major naturally occurring estrogens in women are estradiol, estriol, and estrone. In the body these are all produced from androgens through actions of enzymes.

Premarin, a commonly prescribed estrogenic drug, contains the steroidal estrogens equilin and equilenin, in addition to estrone sulfate but due to its healt risk, more genetic estrogen named Progynova are now more often prescribed.

Nonsteroidal

A range of synthetic and natural substances have been identified that also possess estrogenic activity.[3]

Unlike estrogens produced by mammals, these substances are not necessarily steroids.

Estrogen production

Steroidogenesis, showing estrogen at bottom right as estrone and estradiol.

Estrogen is produced primarily by developing follicles in the ovaries, the corpus luteum, and the placenta. Follicle-stimulating hormone (FSH) and luteinizing hormone (LH) stimulate the production of estrogen in the ovaries. Some estrogens are also produced in smaller amounts by other tissues such as the liver, adrenal glands, and the breasts. These secondary sources of estrogen are especially important in postmenopausal women.

Synthesis of estrogens starts in theca interna cells in the ovary, by the synthesis of androstenedione from cholesterol. Androstenedione is a substance of moderate androgenic activity. This compound crosses the basal membrane into the surrounding granulosa cells, where it is converted to estrone or estradiol, either immediately or through testosterone. The conversion of testosterone to estradiol, and of androstenedione to estrone, is catalyzed by the enzyme aromatase.

Estradiol levels vary through the menstrual cycle, with levels highest just before ovulation.

Functions

While estrogens are present in both men and women, they are usually present at significantly higher levels in women of reproductive age. They promote the development of female secondary sex characteristics, such as breasts, and are also involved in the thickening of the endometrium and other aspects of regulating the menstrual cycle. In males, estrogen regulates certain functions of the reproductive system important to the maturation of sperm[4][5][6] and may be necessary for a healthy libido.[7][8] Furthermore, there are several other structural changes induced by estrogen in addition to other functions. In dentistry, it reduces hyperkeratinization of the gingiva and increase vascular permeability, exudation, and edema.[citation needed]

, plasminogen

Sexual desire is dependent on androgen levels rather than estrogen levels.[11]

Role in cancer

About 80% of breast cancers, once established, rely on supplies of the hormone estrogen to grow: they are known as hormone-sensitive or hormone-receptor-positive cancers.[12] Suppression of production in the body of estrogen is a treatment for these cancers.

Medical applications

Since estrogen circulating in the blood can negatively feed-back to reduce circulating levels of FSH and LH, most oral contraceptives contain a synthetic estrogen, along with a synthetic progestin. Even in men, the major hormone involved in LH feedback is estradiol, not testosterone.

As more fully discussed in the article on Hormone replacement therapy, estrogen and other hormones are given to postmenopausal women in order to prevent osteoporosis as well as treat the symptoms of menopause such as hot flashes, vaginal dryness, urinary stress incontinence, chilly sensations, dizziness, fatigue, irritability, and sweating. Fractures of the spine, wrist, and hips decrease by 50-70% and spinal bone density increases by ~5% in those women treated with estrogen within 3 years of the onset of menopause and for 5-10 years thereafter.

Before the specific dangers of conjugated equine estrogens were well understood, standard therapy was 0.625 mg/day of conjugated equine estrogens (such as Premarin). There are, however, risks associated with conjugated equine estrogen therapy. Among the older postmenopausal women studied as part of the Women's Health Initiative (WHI), an orally-administered conjugated equine estrogen supplement was found to be associated with an increased risk of dangerous blood clotting. The WHI studies used one type of estrogen supplement, a high oral dose of conjugated equine estrogens (Premarin alone and with medroxyprogesterone acetate as PremPro).[12]

In a study by the NIH, esterified estrogens were not proven to pose the same risks to health as conjugated equine estrogens. Hormone replacement therapy has favorable effects on serum cholesterol levels, and when initiated immediately upon menopause may reduce the incidence of cardiovascular disease, although this hypothesis has yet to be tested in randomized trials. Estrogen appears to have a protector effect on atherosclerosis : it lowers LDL and triglycerides, it raises HDL levels and has endothelial vasodilatation properties plus an anti-inflammatory component.

Research is underway to determine if risks of estrogen supplement use are the same for all methods of delivery. In particular, estrogen applied topically may have a different spectrum of side-effects than when administered orally,[13] and transdermal oestrogens do not affect clotting as they are absorbed directly into the systemic circulation, avoiding first-pass metabolism in the liver. This route of administration is thus preferred in women with a history of thrombo-embolic disease.

Estrogen is also used in the therapy of vaginal atrophy, hypoestrogenism (as a result of hypogonadism, castration, or primary ovarian failure), amenorrhea, dysmenorrhea, and oligomenorrhea. Estrogens can also be used to suppress lactation after child birth.

Hormone-receptor-positive breast cancers are treated with drugs which suppress production in the body of estrogen.[14] This technique, in the context of treatment of breast cancer, is known variously as hormonal therapy, hormone therapy, or anti-estrogen therapy (not to be confused with hormone replacement therapy). Certain foods such as soy may also suppress the proliferative effects of estrogen and are used as an alternative to hormone therapy.[15]

In humans and mice, estrogen promotes wound healing.[16]

At one time, estrogen was used to induce growth attenuation in tall girls.[9] Recently, estrogen-induced growth attenuation was used as part of the controversial Ashley Treatment to keep a developmentally disabled girl from growing to adult size.[17]

Under certain circumstances, estrogen may also be used in males for treatment of prostate cancer.[18]

Most recently, estrogen has been used in experimental research as a way to treat patients suffering from bulimia nervosa, in addition to Cognitive Behavioral Therapy, which is the established standard for treatment in bulimia cases. The estrogen research hypothesizes that the disease may be linked to a hormonal imbalance in the brain.[19]

Estrogen has also been used in studies which indicate that it may be an effective drug for use in the treatment of traumatic liver injury.[20]

Mental health

Estrogen is considered to play a significant role in women’s mental health. A conceptual model of how estrogen affects mood was suggested by Douma et al 2005 based on their extensive literature review relating activity of endogenous, bio-identical and synthetic estrogen with mood and well-being. They concluded the sudden estrogen withdrawal, fluctuating estrogen, and periods of sustained estrogen low levels correlated with significant mood lowering. Clinical recovery from depression postpartum, perimenopause, and postmenopause was shown to be effective after levels of estrogen were stabilized and/or restored.[21][22]

In 2005 Prince Henry's Institute of Medical Research of Australia published an article where it was found that a low Estrogen level in male lab mice may be one cause of Obsessive-Compuslive Disorder. Research has found that when Estrogen levels were raised through the increased activity of the enzyme Aromatase in male lab mice, OCD rituals were dramatically decreased. Hypothalamic protein levels in the gene COMT are enhanced by increasing Estrogen levels which is believed to return lab mice that displayed OCD rituals to normal activity. Aromatase deficiency is ultimately suspected which is involved in the synthesis of Estrogen in humans and has therapeutic implications in humans having Obsessive-Compulsive Disorder.[23]

Health risks and warning labels

The labeling of estrogen-only products in the U.S. includes a boxed warning that unopposed estrogen (without progestagen) therapy increases the risk of endometrial cancer.

Based on a review of data from the WHI, on January 8, 2003 the FDA changed the labeling of all estrogen and estrogen with progestin products for use by postmenopausal women to include a new boxed warning about cardiovascular and other risks. The estrogen-alone substudy of the WHI reported an increased risk of stroke and deep vein thrombosis (DVT) in postmenopausal women 50 years of age or older and an increased risk of dementia in postmenopausal women 65 years of age or older using 0.625 mg of Premarin conjugated equine estrogens (CEE). The estrogen-plus-progestin substudy of the WHI reported an increased risk of myocardial infarction, stroke, invasive breast cancer, pulmonary emboli and DVT in postmenopausal women 50 years of age or older and an increased risk of dementia in postmenopausal women 65 years of age or older using PremPro, which is 0.625 mg of CEE with 2.5 mg of the progestin medroxyprogesterone acetate (MPA).[24][25][26]

Estrogens in cosmetics

Some hair shampoos on the market include estrogens and placental extracts; others contain phytoestrogens. There are case reports of young children developing breasts after exposure to these shampoos.[27] These products are often marketed to African-American consumers.[28]

On September 9, 1993, the FDA determined that not all topically-applied hormone-containing drug products for OTC human use are generally recognized as safe and effective and are misbranded. An accompanying proposed rule deals with cosmetics, concluding that any use of natural estrogens in a cosmetic product makes the product an unapproved new drug and that any cosmetic using the term "hormone" in the text of its labeling or in its ingredient statement makes an implied drug claim, subjecting such a product to regulatory action.[29]

In addition to being considered misbranded drugs, products claiming to contain placental extract may also be deemed to be misbranded cosmetics if the extract has been prepared from placentas from which the hormones and other biologically active substances have been removed and the extracted substance consists principally of protein. The FDA recommends that this substance be identified by a name other than "placental extract" and describing its composition more accurately because consumers associate the name "placental extract" with a therapeutic use of some biological activity.[29]

History

The existence and effects of estrogen were established from 1923 to 1938 in which the formulation was led by a group of scientists instead of pharmaceutical companies. Thereafter, the market for hormonal drug research opened up.

The “first orally effective estrogen”, Emmenin, derived from the late-pregnancy urine of Canadian women, was introduced in 1930 by Collip and Ayerst Laboratories. Estrogens are not water-soluble and cannot be given orally, but the urine was found to contain estriol glucuronide which is water soluble and becomes active in the body after hydrolization.

Scientists continued to search for new sources of estrogen because of concerns associated with the practicality of introducing the drug into the market. At the same time, a German pharmaceutical drug company, formulated a similar product as Emmenin that was introduced to German women to treat menopausal symptoms.

In 1938, British scientists obtained a patent on a newly formulated nonsteroidal estrogen, Diethylstilbestrol (DES), that was cheaper and more powerful than the previously manufactured estrogens. Soon after, concerns over the side effects of DES were raised in scientific journals while the drug manufacturers came together to lobby for governmental approval of DES. It was only until 1941 when estrogen therapy was finally approved by the Food and Drug Administration (FDA) for the treatment of menopausal symptoms. [30]

Hyperestrogenemia

Hyperestrogenemia (elevated levels of estrogen) may be a result of exogenous administration of estrogen or estrogen-like substances, or may be a result of physiologic conditions such as pregnancy. Any of these causes is linked with an increase in the risk of thrombosis. [31]

See also

References

  1. ^ Nussey and Whitehead: Endocrinology, an integrated approach, Taylor and Francis 2001
  2. ^ Prossnitz ER, Arterburn JB, Sklar LA (2007). "GPR30: A G protein-coupled receptor for estrogen". Mol. Cell. Endocrinol. 265–266: 138–42. doi:10.1016/j.mce.2006.12.010. PMID 17222505.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^ Fang H, Tong W, Shi LM, Blair R, Perkins R, Branham W, Hass BS, Xie Q, Dial SL, Moland CL, Sheehan DM (2001). "Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens". Chem. Res. Toxicol. 14 (3): 280–94. doi:10.1021/tx000208y. PMID 11258977.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ Hess RA, Bunick D, Lee KH, Bahr J, Taylor JA, Korach KS, Lubahn DB (1997). "A role for oestrogens in the male reproductive system". Nature. 390 (6659): 509–12. doi:10.1038/37352. PMID 9393999.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  5. ^ J. Raloff (1997-12-06). "Science News Online (12/6/97): Estrogen's Emerging Manly Alter Ego". Science News. Retrieved 2008-03-04. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  6. ^ "Science Blog -- Estrogen Linked To Sperm Count, Male Fertility". Science Blog. Retrieved 2008-03-04. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  7. ^ Hill RA, Pompolo S, Jones ME, Simpson ER, Boon WC (2004). "Estrogen deficiency leads to apoptosis in dopaminergic neurons in the medial preoptic area and arcuate nucleus of male mice". Mol. Cell. Neurosci. 27 (4): 466–76. doi:10.1016/j.mcn.2004.04.012. PMID 15555924.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  8. ^ Ian Muchamore (2004-07-19). "Prince Henry's Institute - Media Release - Male sex drive linked to estrogen". Prince Henry's Institute. Retrieved 2008-03-04. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  9. ^ a b Lee JM, Howell JD (2006). "Tall girls: the social shaping of a medical therapy". Arch Pediatr Adolesc Med. 160 (10): 1035–9. doi:10.1001/archpedi.160.10.1035. PMID 17018462.
  10. ^ Massaro D, Massaro GD (2004). "Estrogen regulates pulmonary alveolar formation, loss, and regeneration in mice". Am. J. Physiol. Lung Cell Mol. Physiol. 287 (6): L1154–9. doi:10.1152/ajplung.00228.2004. PMID 15298854.
  11. ^ Warnock JK, Swanson SG, Borel RW, Zipfel LM, Brennan JJ (2005). "Combined esterified estrogens and methyltestosterone versus esterified estrogens alone in the treatment of loss of sexual interest in surgically menopausal women". Menopause. 12 (4): 374–84. doi:10.1097/01.GME.0000153933.50860.FD. PMID 16037752.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  12. ^ "NIH - Menopausal Hormone Therapy Information". National Institutes of Health. 2007-08-27. Retrieved 2008-03-04. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  13. ^ Menon DV, Vongpatanasin W (2006). "Effects of transdermal estrogen replacement therapy on cardiovascular risk factors". Treat Endocrinol. 5 (1): 37–51. doi:10.2165/00024677-200605010-00005. PMID 16396517.
  14. ^ "Hormonal Therapy". breastcancer.org. 2007-07-26. Retrieved 2008-03-04. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  15. ^ Kurzer MS (2002). "Hormonal effects of soy in premenopausal women and men". J. Nutr. 132 (3): 570S–573S. PMID 11880595.
  16. ^ Oh DM, Phillips, TJ (2006). "Sex Hormones and Wound Healing". Wounds. 18 (1): 8–18.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  17. ^ Gunther DF, Diekema DS (2006). "Attenuating growth in children with profound developmental disability: a new approach to an old dilemma". Arch Pediatr Adolesc Med. 160 (10): 1013–7. doi:10.1001/archpedi.160.10.1013. PMID 17018459.
  18. ^ Oh WK (2002). "The evolving role of estrogen therapy in prostate cancer" ([dead link] – Scholar search). Clin Prostate Cancer. 1 (2): 81–9. PMID 15046698. {{cite journal}}: External link in |format= (help)
  19. ^ Gunilla Andersson (2007-01-09). "Bulimia May Result from Hormonal Imbalance". Karolinska Institutet. Retrieved 2008-03-04. {{cite web}}: Cite has empty unknown parameter: |coauthors= (help)
  20. ^ Hsieh YC, Yu HP, Frink M, Suzuki T, Choudhry MA, Schwacha MG, Chaudry IH (2007). "G protein-coupled receptor 30-dependent protein kinase A pathway is critical in nongenomic effects of estrogen in attenuating liver injury after trauma-hemorrhage". Am. J. Pathol. 170 (4): 1210–8. doi:10.2353/ajpath.2007.060883. PMID 17392161.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  21. ^ Douma, S.L, Husband, C., O’Donnell, M.E., Barwin, B.N., Woodend A.K. (2005). "Estrogen-related Mood Disorders Reproductive Life Cycle Factors". Advances in Nursing Science. 28 (4): 364–375. PMID 16292022.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  22. ^ Lasiuk, GC and Hegadoren, KM (2007). "The Effects of Estradiol on Central Serotonergic Systems and Its Relationship to Mood in Women". Biological Research for Nursing (2007),. 9 (2): 147–160. doi:10.1177/1099800407305600. PMID 17909167.{{cite journal}}: CS1 maint: extra punctuation (link) CS1 maint: multiple names: authors list (link)
  23. ^ "Estrogen deficient male mice develop Compulsive Behavior". Biological Psychiatry. 2007. {{cite journal}}: Cite uses deprecated parameter |authors= (help); Unknown parameter |Volume= ignored (|volume= suggested) (help)
  24. ^ FDA (2003, January 8). "FDA Approves New Labels for Estrogen and Estrogen with Progestin Therapies for Postmenopausal Women Following Review of Women's Health Initiative Data". Retrieved 2006-10-26. {{cite web}}: Check date values in: |date= (help)
  25. ^ Kolata, Gina (2003, January 9). "F.D.A. Orders Warning on All Estrogen Labels". The New York Times. Retrieved 2006-10-26. {{cite web}}: Check date values in: |date= (help)
  26. ^ NLM (2006, April 1). "IMPORTANT WARNING". Drug Information: Estrogen. MedlinePlus. Retrieved 2006-10-26. {{cite web}}: Check date values in: |date= (help)
  27. ^ Sanghavi, DM (October 17, 2006), "Preschool Puberty, and a Search for the Causes", The New York Times, retrieved 2008-06-04
  28. ^ Li ST, Lozano P, Grossman DC, Graham E (2002). "Hormone-containing hair product use in prepubertal children". Arch Pediatr Adolesc Med. 156 (1): 85–6. PMID 11772198.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  29. ^ a b FDA (1995, February). "Products containing estrogenic hormones, placental extract or vitamins". Guide to Inspections of Cosmetic Product Manufacturers. Retrieved 2006-10-24. {{cite web}}: Check date values in: |date= (help)
  30. ^ Rothenberg, Carla J. (2005-04-25). "The Rise and Fall of Estrogen Therapy: The History of HRT" (PDF). Retrieved 2006-10-27.
  31. ^ Chapter 4 in: Mitchell, Richard Sheppard; Kumar, Vinay; Abbas, Abul K.; Fausto, Nelson. Robbins Basic Pathology: With STUDENT CONSULT Online Access. Philadelphia: Saunders. ISBN 1-4160-2973-7.{{cite book}}: CS1 maint: multiple names: authors list (link) 8th edition.

See also

External links and further reading

Template:Sex hormones

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