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    What Are Aromatase Inhibitors? Copy and paste :)

    Aromatase inhibitors stop the production of estrogen in post-menopausal women. Aromatase inhibitors work by blocking the enzyme aromatase, which turns the hormone androgen into small amounts of estrogen in the body. This means that less estrogen is available to stimulate the growth of hormone-receptor-positive breast cancer cells.

    Aromatase inhibitors can't stop the ovaries from making estrogen, so aromatase inhibitors only work in post-menopausal women.

    There are three aromatase inhibitors:

    Arimidex (chemical name: anastrozole)

    Aromasin (chemical name: exemestane)

    Femara (chemical name: letrozole)

    Each is a pill, usually taken once a day. Arimidex and Femara are available as generic medicines.

    Benefits of Aromatase Inhibitors

    A number of studies have compared aromatase inhibitors with tamoxifen to see which type of medicine was more effective in treating early-stage, hormone-receptor-positive breast cancer in post-menopausal women. Based on the results, most doctors recommend that after initial treatment (surgery and possibly chemotherapy and radiation therapy):

    An aromatase inhibitor is the best hormonal therapy to start with. When treating early-stage, hormone-receptor-positive breast cancer, aromatase inhibitors have more benefits and fewer serious side effects than tamoxifen.

    switching to an aromatase inhibitor after taking tamoxifen for 2 to 3 years (for a total of 5 years of hormonal therapy) offers more benefits than 5 years of tamoxifen.

    taking an aromatase inhibitor for 5 years after taking tamoxifen for 5 years continues to reduce the risk of the cancer coming back, compared to no treatment after tamoxifen.

    Aromatase Inhibitors for Men

    The enzyme aromatase converts testosterone into estradiol and converts androstenedione into estrone.

    Treatment for Increased Estrogen and Decreased Testosterone

    Inappropriate diet is considered the main cause of insulin resistance, which is the primary pathophysiologic feature of metabolic syndrome. Increased insulin levels stimulate aromatase activity.

    In obese men, increased aromatase activity results in reduced testosterone and increased estradiol and estrone concentrations, ultimately resulting in a decrease in muscle mass and an increase in total fat mass. Increased total fat mass contributes to oxidative stress, inflammation, and further increased aromatase activity (wrong diet Ă* hyperinsulinism Ă* hyperaromatization Ă* excess obesity).3-5

    Cohen proposed that aromatase inhibitors could be potential therapeutic agents for men with obesity. Leder recommended their use during testosterone therapy in older men to prevent adverse effects of estradiol.

    Male gynecomastia is usually caused by increased estrogen activity, decreased testosterone activity, or the use of numerous medications. Excess aromatase activity is also a cause of gynecomastia.7-12

    Hyperaromatization

    Hyperaromatization is a term used to describe excessive aromatase activity, which results in conversion of testosterone into estrogen. Although possible in both sexes, hyperaromatization is particularly found in men and often accompanies low testosterone concentration and obesity related to metabolic syndrome and insulin resistance.13

    Myomin and Chrysin

    Available natural formulas that help reverse hyperaromatization include myomin and chrysin. Myomin is a combination of Smilax glabra Roxb, Curcuma zedoria, Cyperus rotundus, and Aralia dasyphylla.

    A fluorescent antibody study in animals showed that myomin significantly reduced the population of hepatic aromatase within 30 days. In another study, myomin significantly inhibited aromatase expression in in vivo ovary, ectopic endometrium, and in vitro–cultured primary ovarian granulosa cells of rats.

    Chrysin is a naturally occurring flavone. It is chemically extracted from the blue passion flower (Passiflora caerulea).

    While these aromatase inhibitors of natural origin appear to be harmless, they are not known to correct hyperinsulinism. It is important for men with excess testosterone-to-estrogen transformation to undergo testing for insulin resistance21 and, if found, to follow appropriate diet, exercise, and supplementation to decrease or stop hyperinsulinism, thus reducing or eliminating the excess conversion and in many cases rendering aromatase inhibitor use of any sort less necessary or unnecessary at all.

    Aromataste Inhibitor Drugs

    Aromatase inhibitor drugs (patent pharmaceuticals) are “approved” for estrogen receptor positive (ER+) early breast cancer and following Tamoxifen therapy. They include Aromasin ® (exemestane), an irreversible steroidal inhibitor; Femara ® (letrozole) and Arimidex ® (anastrozole), which are non-steroidal inhibitors. Aromatase inhibitors are generally not used to treat breast cancer in premenopausal women, since the decrease in estrogen stimulates androgen production by the ovaries, which will counteract their effect. The most common side effects of aromatase inhibitors are joint stiffness or joint pain. Regular bone density testing is recommended for those taking aromatase inhibitor drugs.

    Alcohol Consumption

    Alcohol consumption increases estrogen levels and breast cancer risk.26,27 A study28 proposed that increased aromatization may be a mechanism for feminization in some male alcoholics and for plasma estrogen level increases in postmenopausal women who consumed moderate levels of alcohol.

    In conclusion, metabolic syndrome presents a unique challenge because of its multiple mechanisms. Addressing glucose metabolism with diet, exercise, and natural therapies is a mainstay of naturopathic treatment. In addition, several natural aromatase inhibitors may be useful for men with metabolic syndrome accompanied by increased estrogen and decreased testosterone concentrations. They may be particularly useful as an adjunct to testosterone therapy in these patients.

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    thanx for the info.

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    This information is well represented in an easy to understand format. Thank you.

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