ANADOIL-40 (5-androstene-3b-17b-Diol)
5-Androstenedoil-Designed to dramatically increase levels of testosterone in the human body. The substance 5-Androstene-3b-17b-Doil is a hormone precursor that has a direct one-way conversion into testosterone in the body.

5-AD is actually the demethlated version of the schedule III ANABOLIC STEROID METHANDROIL.

Testosterone is a steroid hormone from the androgen group. In mammals, testosterone is primarily secreted in the testes of males and the ovaries of females, although small amounts are also secreted by the adrenal glands. It is the principal male sex hormone and an anabolic steroid.

In both men and women, testosterone plays a key role in health and well-being as well as in sexual functioning. Examples include enhanced libido, increased energy, increased production of red blood cells and protection against osteoporosis. On average, an adult human male body produces about forty to sixty times more testosterone than an adult female body, but females are, from a behavioral perspective (rather than from an anatomical or biological perspective), more sensitive to the hormone. However the overall ranges for male and female are very wide, such that the ranges actually overlap at the low end and high end respectively.

Virilizing and effects on humans
In general, androgens promote protein synthesis and growth of those tissues with androgen receptors. Testosterone effects can be classified as virilizing and anabolic, although the distinction is somewhat artificial, as many of the effects can be considered both.
— Anabolic effects include growth of muscle mass and strength, increased bone density and strength, and stimulation of linear growth and bone maturation.
— Virilizing effects include maturation of the sex organs, particularly the penis and the formation of the scrotum in unborn children, and after birth (usually at puberty) a deepening of the voice, growth of the beard and axillary hair. Many of these fall into the category of male secondary sex characteristics.

Testosterone effects can also be classified by the age of usual occurrence. For postnatal effects in both males and females, these are mostly dependent on the levels and duration of circulating free testosterone.

Prenatal androgen effects
Most of the prenatal androgen effects occur between 7 and 12 weeks of gestation.
— Genital virilization (midline fusion, phallic urethra, scrotal thinning and rugation, phallic enlargement); although the role of testosterone is far smaller than that of Dihydrotestosterone.
— Development of prostate and seminal vesicles

Early infancy androgen effects
Early infancy androgen effects are the least understood. In the first weeks of life for male infants, testosterone levels rise. The levels remain in a pubertal range for a few months, but usually reach the barely detectable levels of childhood by 4-6 months of age. The function of this rise in humans is unknown. It has been speculated that «brain masculinization» is occurring since no significant changes have been identified in other parts of the body.

Early postnatal effects
Early postnatal effects are the first visible effects of rising androgen levels in childhood, and occur in both boys and girls in puberty.
— Adult-type body odour
— Increased oiliness of skin and hair, acne
— Pubarche (appearance of pubic hair)
— Axillary hair
— Growth spurt, accelerated bone maturation
— Develop hair on upper lip and sideburns.

Advanced postnatal effects
Advanced postnatal effects begin to occur when androgen has been higher than normal adult female levels for months or years. In males these are usual late pubertal effects, and occur in women after prolonged periods of heightened levels of free testosterone in the blood.
— Phallic enlargement or clitoromegaly
— Increased libido and frequency of erection or clitoral engorgement
— Pubic hair extends to thighs and up toward umbilicus
— Facial hair (sideburns, beard, moustache)
— Chest hair, periareolar hair, perianal hair
— Subcutaneous fat in face decreases
— Increased muscle strength and mass
— Deepening of voice
— Growth of the Adam’s apple
— Growth of spermatogenic tissue in testes, male fertility
— Growth of jaw, brow, chin, nose, and remodeling of facial bone contours
— Shoulders become broader and rib cage expands
— Completion of bone maturation and termination of growth. This occurs indirectly via estradiol metabolites and hence more gradually in men than women.

Adult testosterone effects
Adult testosterone effects are more clearly demonstrable in males than in females, but are likely important to both sexes. Some of these effects may decline as testosterone levels decline in the later decades of adult life.
— Libido and clitoral engorgement/penile erection frequency.
— Mental and physical energy
— The most recent and reliable studies have shown that testosterone does not cause Prostate cancer, but that it can increase the rate of spread of any existing prostate cancer. Recent studies have also shown its importance in maintaining cardio vascular health.
— Increase eumelanin and reduce pheomelanin

Testosterone regulates the population of thromboxane A2 receptors on megakaryocytes and platelets and hence platelet aggregation in humans ( Ajayi and Halushka 2005, Ajayi et al 1995).

Effects on the brain
As testosterone affects the entire body (often by enlarging; men have bigger hearts, lungs, liver, etc.), the brain is also affected by this «sexual» advancement; the enzyme aromatase converts testosterone into estradiol that is responsible for masculinization of the brain in a male fetus.

There are some differences in a male and female brain (the result of different testosterone levels). A clear difference is the size: the male human brain is, on average, larger; however, in females (who generally do not have as high testosterone levels) the corpus callosum is proportionally larger. This means that the effect of testosterone is a greater overall brain volume, but a decreased connection between the hemispheres.

A study conducted in 1996 found no effects on mood or behavior from the administration of supraphysiologic doses of Testosterone for 10 weeks to healthy men.

The literature suggests that attention, memory, and spatial ability are key cognitive functions affected by testosterone in humans, though the literature is rather sparse. Preliminary evidence suggests that low testosterone levels may be a risk factor for cognitive decline and possibly for dementia of the Alzheimer?s type, a key argument in Life Extension Medicine for the use of testosterone in anti-aging therapies. Much of the literature, however, suggests a curvilinear or even quadratic relationship between spatial performance and circulating testosterone, where both hypo- and hypersecretion of circulating androgens have negative effects on cognition and cognitively-modulated aggressivity, as detailed above.

Contrary to what has been postulated in outdated studies and by certain sections of the media, aggressive behaviour is not typically seen in hypergonadal men who have their testosterone replaced adequately to the eugonadal/normal range. In fact aggressive behaviour has been associated with hypogonadism and low testosterone levels and it would seem as though supraphysiological and low levels of testosterone and hypogonadism cause mood disorders and aggressive behaviour, with eugondal/normal testosterone levels being important for mental well-being. Testosterone depletion is a normal consequence of aging in men. One consequence of this is an increased risk for the development of Alzheimer?s Disease (Pike et al, 2006, Rosario 2004).

Mechanism
The effects of testosterone in humans and other vertebrates occur by way of two main mechanisms: by activation of the androgen receptor (directly or as DHT), and by conversion to estradiol and activation of certain estrogen receptors.

Free testosterone (T) is transported into the cytoplasm of target tissue cells, where it can bind to the androgen receptor, or can be reduced to 5α-dihydrotestosterone (DHT) by the cytoplasmic enzyme 5-alpha reductase. DHT binds to the same androgen receptor even more strongly than T, so that its androgenic potency is about 2.5 times that of T. The T-receptor or DHT-receptor complex undergoes a structural change that allows it to move into the cell nucleus and bind directly to specific nucleotide sequences of the chromosomal DNA. The areas of binding are called hormone response elements (HREs), and influence transcriptional activity of certain genes, producing the androgen effects. It is important to note that if there is a 5-alpha reductase deficiency, the body (of a human) will continue growing into a female with testicles.

Androgen receptors occur in many different vertebrate body system tissues, and both males and females respond similarly to similar levels. Greatly differing amounts of testosterone prenatally, at puberty, and throughout life account for a share of biological differences between males and females.

The bones and the brain are two important tissues in humans where the primary effect of testosterone is by way of aromatization to estradiol. In the bones, estradiol accelerates maturation of cartilage into bone, leading to closure of the epiphyses and conclusion of growth. In the central nervous system, testosterone is aromatized to estradiol. Estradiol rather than testosterone serves as the most important feedback signal to the hypothalamus (especially affecting LH secretion). In many mammals, prenatal or perinatal «masculinization» of the sexually dimorphic areas of the brain by estradiol derived from testosterone programs later male sexual behavior.

The human hormone testosterone is produced in greater amounts by males, and less by females. The human hormone estrogen is produced in greater amounts by females, and less by males. Testosterone causes the appearance of masculine traits (i.e., deepening voice, pubic and facial hairs, muscular build, etc.) Like men, women rely on testosterone to maintain libido, bone density and muscle mass throughout their lives. In men, inappropriately high levels of estrogens lower testosterone, decrease muscle mass, stunt growth in teenagers, introduce gynecomastia, increase feminine characteristics, and decrease susceptibility to prostate cancer, reduces libido and causes erectile dysfunction and can cause excessive sweating and hot flushes. However, an appropriate amount of estrogens is required in the male in order to ensure well-being, bone density, libido, erectile function, etc.

acquistare la testosterone anadoil in malta, testosterone anadoil in malta, malta, buy testosterone anadoil, order testosterone anadoil, cheap testosterone anadoil, testosterone anadoil online, of , in , testosterone, is , effects, to , a , levels, by , androgen, as , growth, or , on , brain, females, males, estradiol, adult, it , increased, hormone, humans, human, occur, libido, an , postnatal, maturation, female, important, receptor,  , be , anabolic, normal, prostate, muscle, receptors, amounts, women, increase, prenatal, deepening, circulating, voice, certain, months, pubic, «, cancer, studies, facial, puberty, decline, phallic, suggests, literature, greater, weeks, strength, aggressive, include, virilizing, at , behaviour, tissues, density, steroid, et , throughout, affected, enzyme, ajayi, differences, causes, estrogens, mental, erectile, recent, different, shown, produced, bones, larger, hypogonadism, cognitive, spatial, later, alzheimer, decrease, aging, consequence, activation, alpha, reductase, areas, effect, estrogen, directly, behavior, system, enlargement, overall, biological, perspective, times, ranges, androgens, beard, usually, classified, average, cells, secreted, mammals, actually, conversion, testes, health, blood, energy, sexual, axillary, characteristics, advanced, sideburns, appearance, no , frequency, erection, tissue, engorgement, clitoral, masculinization», function, development, dihydrotestosterone, androstene, infancy, first, childhood, range, pubertal, hence, of  the, in  the, of  testosterone, testosterone is , testosterone levels, testosterone in , growth of , is  a , levels of , the brain, androgen effects, postnatal effects, to  the, in  humans, males and, testosterone effects, 8212 growth, has been, the androgen, effects on , bone maturation, muscle mass, into the, androgen receptor, and females, aggressive behaviour, prostate cancer, occur in , 8212 increased, libido and, in  men, in  a , free testosterone, effects are, to  estradiol, the literature, bone density, well being, and the, by  the, in  both, effects can, the body, can be , the human, important to , by  males, as  testosterone, the most, amounts by , greater amounts, it  can, studies have, less by , by  females, of  estrogens, clitoral engorgement, of  growth, and hence, in  females, adult testosterone, affected by , and less, a  male, by  way, in  many, consequence of , and low, females the, way of , activation of , receptor or , of  certain, areas of , in  males, and by , the bones, effect of , the male, produced in , alpha reductase, is  produced, suggests that, growth in , for the, human hormone, low testosterone, in  greater, infancy androgen, although the, many of , be  classified, androgen receptors, virilizing and, the effects, effects include, maturation of , strength and, density and, and strength, that the, and female, is  the, a  key, it  is , from the, anabolic steroid, on  average, an  adult, male and, for male, rather than, adult female, at  puberty, deepening of , the first, for a , are the, effects early, early infancy, of  this, early postnatal, pubic hair, appearance of , and occur, effects of , development of , that of , these are, on  the, both males, of  these, axillary hair, the levels, levels and, phallic enlargement, weeks of , prenatal androgen, of  circulating, advanced postnatal