Life Extension Magazine April 2006
By Dr. Sergey Dzugan and Armond Scipione
Progesterone and the Brain
The brain is highly responsive to progesterone. In fact, progesterone concentrations in the brain have been shown to be 20 times higher than in the blood.2 Insomnia, anxiety, and migraine are just a few of the conditions linked to an imbalance of progesterone and estrogen.19-22 In the brain as elsewhere in the body, progesterone counterbalances the effects of estrogen. Whereas estrogen has an excitatory effect on the brain, progesterone’s effect is calming.9 Clinical and anecdotal experience indicates that women with estrogen dominance sleep restlessly, whereas progesterone replenishment enhances sleep.
It remains unexplained why anxiety disorders are more prevalent in women than in men, and how female hormone-related events (such as menstrual cycle and postpartum) influence the course of anxiety disorders. However, it would appear logical that female hormones and their derivatives play a major role in these observations.23 Several studies have shown progesterone to have anxiolytic (anti-anxiety) effects by acting on gamma-aminobutyric acid (GABA) receptors in the brain.20-22 GABA is an inhibitory neurotransmitter that aids in relaxation and sleep. In the brain, GABA helps balance excitation with inhibition. Furthermore, withdrawal from endogenous progesterone supplementation after chronic administration increases anxiety via declining levels of its potent GABA-modulatory metabolites.24
A variety of evidence suggests a link between migraine and the female sex hormones. According to the American Migraine Study, 17.6% of females versus only 6% of males in the US currently suffer from severe migraine.25 Many women with migraine, especially those with a history of menstrual migraine, experience an exacerbation of the condition as they approach menopause. During this time, the orderly pattern of estrogen and progesterone secretion is lost.26
In 1953, two English physicians, Drs. Katharina Dalton and Raymond Greene, published the first medical report on premenstrual syndrome (PMS). Dr. Dalton observed that progesterone injections relieved her own menstrual migraine headaches. Dr. Dalton then injected progesterone into other women and found that their PMS was cured.11 Hormone replacement with estrogen exacerbates migraine, and oral contraceptives can change the character and frequency of migraine.27 Higher levels of estradiol and the estradiol:progesterone ratio are directly correlated to increased headache activity.19
Migraine syndromes, particularly in women, are associated with deficits in brain and serum ionized magnesium levels.28 Scientists believe that magnesium’s ability to relieve premenstrual distress may be due to the mineral’s ability to relax vascular smooth muscle.29 Researchers have demonstrated that with each increase in estrogen, a decrease in ionized magnesium occurs. However, as progesterone levels rise, ionized magnesium levels increase as well.30
In one study, physicians set out to test the hypothesis that migraine is a specific consequence of an imbalance between neurohormonal and metabolic integrity. Restoration of progesterone along with several other steroid hormones led to a complete resolution of migraine.8
Progesterone and Osteoporosis
Bone is a very metabolically active tissue, and bone remodeling continues throughout life. The remodeling process is an active coupling of bone formation and bone resorption. Bone loss occurs when the cellular events of bone resorption are quantitatively greater than the events of bone formation.
Conventional medicine widely attributes osteoporosis to a decline in estrogen. Before the onset of menopause, however, luteal levels of progesterone decline, whereas levels of estrogen, lutenizing hormone, follicle stimulating hormone, and other reproductive hormones remain intact. In addition, we know that bone loss begins in women well before menopause. In fact, a woman attains her peak bone density at approximately 30 years of age, after which she begins to lose bone at a rate of about 1-1.5% per year.9 Countless women who use estrogen therapy and consume the proper nutrients still have disappointing bone density test results. These facts raise an interesting question: is the decline in estrogen responsible for bone loss, or is progesterone involved, possibly even more so than estrogen?
The two types of bone-regulating cells are osteoclasts and osteoblasts. Osteoclasts function to dissolve older bone, leaving tiny unfilled spaces behind. Osteoblasts are then able to move into these spaces to produce new bone. Like all living cells, osteoblasts and osteoclasts require hormonal guidance to function properly. Estrogen is able to help slow bone loss by curbing the activity of bone-dissolving osteoclasts.31,32 On the other hand, osteoblasts depend primarily on progesterone and testosterone to facilitate the building of new bone. In the absence of these hormones, osteoblasts and osteoclasts cease to function properly, and rapid deterioration of bone occurs. Natural progesterone stimulates the new bone formation required to prevent and reverse osteoporosis.7 Progesterone also appears to increase levels of insulin-like growth factor 1, which promotes bone formation.33 It remains uncertain whether progesterone or estrogen plays a more prominent role in bone remodeling. An optimal balance of both hormones appears to be most efficient in preventing and treating osteoporosis.
Progesterone and Cancer
Disturbances in gonadal hormones have been associated with an increased risk of both breast and endometrial cancers. As previously stated, most controlled studies and observational studies in the past five years suggest that the addition of synthetic progestins to synthetic estrogen in hormone replacement therapy, particularly in a continuous combined regimen, increases breast cancer risk compared to synthetic estrogen alone.1 By contrast, recent studies suggest that the addition of natural progesterone does not affect breast cancer risk.1,2 In fact, a large base of evidence suggests that progesterone is a protective agent against, as well as a potential adjunctive treatment for, breast and endometrial cancers.34-44 Whereas estrogen is pro-proliferative, causing the cells in the breast and uterus to multiply, progesterone does not promote proliferation of these tissues.
One of the most significant studies of the relationship between low levels of natural progesterone and increased breast cancer risk was published in the American Journal of Epidemiology in 1981. The study followed 1,083 women with a history of difficulty becoming pregnant for periods ranging from 13 to 33 years. The researchers found that infertile women who demonstrated a progesterone deficiency had a premenopausal breast cancer risk that was 540% greater than that of women whose infertility was due to non-hormonal causes. Furthermore, the women with a progesterone deficiency had a 1,000% greater chance of death from all types of cancer.34
In a study conducted at the National Taiwan University Hospital, researchers showed that transdermal estradiol increased breast cell proliferation by 230%, while transdermal progesterone decreased cell proliferation by over 400%.6 A combination of estradiol and progesterone cream was able to maintain the normal proliferation rate. This provides direct evidence that estradiol stimulates hyperproliferation of breast tissue cells and progesterone decreases hyperproliferation.
Serum progesterone levels at the time of breast cancer surgery influence survival rates, according to a 1996 study published in the British Journal of Cancer. Women who had progesterone levels of 4 ng/mL or greater at the time of breast cancer surgery had significantly better survival rates at 18 years than those with lower serum levels of progesterone at the time of surgery. In women with higher progesterone levels at the time of surgery, approximately 65% were alive 18 years later, whereas only 35% of the women with low progesterone levels survived 18 years.45
Conventional estrogen replacement therapy with synthetic estrogens increases the incidence
of endometrial (uterine lining) abnormalities, including cancer.37 However, co-administration of progesterone counteracts this effect.36-44
Women are also becoming increasingly aware of other serious health conditions that may result from an imbalance of their gonadal hormones. Some scientists believe that conditions such as ovarian cysts, uterine fibroids, fibrocystic breast disease, and cervical erosions may stem from an imbalance between progesterone and estrogen.12
Progesterone After a Hysterectomy?
Hysterectomy is the surgical removal of the uterus, which is sometimes performed in conjunction with an oophorectomy or ovariectomy, which is the surgical removal of the ovaries. Doctors often perform a hysterectomy to alleviate patient discomforts associated with conditions such as uterine fibroids, endometriosis, and heavy menses. These conditions, however, are often related to a relative dominance of estrogen.12 Removal of the uterus does not correct the underlying imbalance that may have contributed to these conditions in the first place.
Many medical professionals believe that once the uterus has been removed, there is no need to supplement with progesterone. Clinical experience and a review of the scientific literature, however, make it is clear that unopposed estrogen therapy can lead to many undesirable health conditions. When women are young, they have optimal levels of all the steroid hormones, not just estrogen. Replacing only estrogen after a complete hysterectomy is a sure-fire way to increase existing estrogen dominance. Whether a woman has a uterus or not, research suggests that estrogen replacement therapy should not be given without natural progesterone.
Progesterone and Men
Typically thought of as a female hormone, progesterone can also be an invaluable tool in hormone modulation in men. Progesterone is manufactured in men by the adrenal glands and testes. Just as estrogen dominance can severely affect the quality of life for women, excess estrogen can be equally detrimental to men. Elevated estrogen in men has been linked to gynecomastia (breast enlargement in men), decreased sexual function, weight gain, and prostate enlargement.46-48
Benign prostatic hyperplasia seems to be related to long-term exposure of the prostate gland to the strong androgen dihydrotestosterone and possibly to estrogens. In fact, the late Dr. John R. Lee, considered a pioneer in natural progesterone therapy, believed that excessive exposure to estrogen was a primary cause of prostate enlargement and prostate cancer. In addition to counterbalancing the negative aspects of estrogen, progesterone may also inhibit 5-alpha-reductase, the enzyme that converts testosterone to dihydrotestosterone.49
In the past century, progesterone and hormone restoration has become increasing popular with men and women alike. In the early 1900s, the average life expectancy was only 49 years.50 Men and women simply did not live long enough to experience the detrimental effects of an imbalance of progesterone and estrogen. Since then, advances in health and medicine have significantly extended the human life span. Today, it is up to each individual to ensure that his or her quality of life is also extended.
The risks and side effects of synthetic progestins like medroxyprogesterone acetate have clouded the true health benefits of progesterone supplementation and restoration. Due to monetary interest, research has focused almost exclusively on synthetic derivatives rather than the natural hormones found within the human body. Natural progesterone is associated with few side effects, and is less expensive than its synthetic counterpart.51
Assessing levels of progesterone and other hormones through regular blood testing is essential to attaining optimal health. Life Extension suggests using individually modified doses of progesterone in a cyclical manner. Such an approach will mimic a youthful physiology, resulting in much-improved quality of life.
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