Stanolone is identical to the body's own dihydrotestosterone which, as we know, is formed by the peripheral conversion of testosterone. Some therefore call Stanolone a synthetic dihydrotestosterone. Stanolone has a predominantly androgenic effect and, due to its structure, cannot be converted into estrogen.
For a fast buildup of power and muscle mass Stanolone is of little value. Stanolone used to be the athlete's favorite competition steroid since it helped to obtain a harder muscle through a lower fat content by increasing the androgen level without aromatizing. Numerous athletes used Stanolone during workouts for doping tested championships since the substance remains in the body for only a short time and the testosterone/epitestosterone value is not influenced.
Another positive characteristic is that the injectable version is not liver toxic. Today, however, Stanolone is rarely used by athletes. One reason for this is that almost all European and American compounds are no longer commercially available. The other reason is that most athletes use the still readily available Masteron which has similar effects. Neither the original nor a fake of Stanolone is available on the black market.
Androgen and the body’s own dihydrotestosterone the same, as we know, it is formed by the transformation of testosterone peripheral. Some are therefore referred to as male and steroidal ketone synthesis of dihydrotestosterone. Androgen has a major androgenic effect due to its structure and can not be converted to estrogen. For the rapid accumulation of functional and muscle mass, Stanolone is of little value.
Stanolone was once the athlete’s favorite competitive steroid because it did not aromatize by increasing the level of androgen, thereby gaining harder muscles with lower fat content. Many athletes use Stanolone to conduct doping tests during exercise during the tournament because the substance remains in the body only for a short period of time and the testosterone / testosterone values are not affected.
Another positive feature is that the injected version is not hepatotoxic. However, today, Stanolone is rarely used by athletes. One reason is that almost all of the European and American compounds are no longer commercialized. Another reason is that most athletes use Masteron with similar effects that can still be used. There are no Stanolone originals or fakes on the black market.
Stanolone can be used as pharmaceutical material. Its main function is to promote metabolism. Anabolic effects include growth of muscle mass and strength, increased bone density and strength, and stimulation of linear growth and bone maturation.It doesn’t metabolize in the body long enough to make it to the muscles.
The main androgen which is secreted by the testes is of course testosterone. However, in most of the body, the androgenic sign is not carried through by testosterone. In these tissues inluding brain (CNS), skin, genitals – practically everything but muscle – the active androgen is actually dihydrotestosterone (DHT).
Stanolone is use for chronic wasting disease, osteoporosis, severe infection and trauma, burn, etc caused by the negative nitrogen balance, promote the growth of premature infants and immature, etc. The fracture is not easy to heal. Hypercholesterolemia and postpartum depression can also be used.
stanolone can be used for chronic wasting disease, osteoporosis, severe infections and wounds caused
by burns negative nitrogen balance.stanolone can promote premature children and the growth of immature children and so on. stanolone can also be used on fracture healing, hypercholesterolemia, postpartum weakness. stanolone is dht.
it to be better than and not as problematic as many might guess, at least at moderate doses. i'd consider it as part of stack, for example as an added 100-200 mg/week, rather than being the base or the sole steroid used. there's been at least one medical study on use by injection, which went well.
the oral bioavailability is very low.the propionate powder may be available.if used orally, there would be no liver harshness. no harshness at all really.dht really does only one thing that other anabolic steroids that strongly bind the androgen receptor don't and that is convert to 5a-androstanediol, which itself has some adverse effect on the scalp but doesn't appear to be thought a really major player in hair loss.still, i don't know what might happen with really high doses of dht.
there really seems no reason to do it. but for example, adding it at 100-200 mg/week, by injection, for reason of getting positive effect on the nervous system would be an interesting thing to do, and i think entirely reasonable.oral use, i would not bother with, but if doing it, would expect to have to work up to say 200-300 mg two or three times per day, which might get expensive fast.
The dosage of stanolone is around 50-80milligrams (mgs) per day. Since it is not liver toxic, users will sometimes run it for up to 10 weeks. However, new users should not exceed 6 weeks in order to determine how they react to its strong DHT properties.
Users get the DHT type results of muscle hardness, some fat loss, water loss, increased lean muscle mass, and an increase in libido. Nonetheless, the results are not dramatic in those looking to move the scale upwards, or put on a lot of large muscle mass, so if that is your goal you should look elsewhere.
stanolone converts to DHT in the body. DHT is our male sex hormone, so it will cause an increase in strength, and it will help maintain muscle mass. What's more, DHT helps inhibit estrogen conversion in the body, so it will help dry out the user and give the impression of a loss of body fat, since water is shed from within cells.
Another secret is its ability to bind to SHBG (sex hormone binding globulin), leading to a greater ratio of free testosterone to total testosterone. In the end of the day, it is this 'free testosterone' that really matters, not the total testosterone.
Adverse effects of Stanolone are similar to those of other AAS and include androgenic side effects like oily skin, acne, seborrhea, increased facial/body hair growth, scalp hair loss, and increased aggressiveness and sex drive.In women,
Stanolone can cause partially irreversible virilization, for instance voice deepening, hirsutism, clitoromegaly, breast atrophy, and muscle hypertrophy, as well as menstrual disturbances and reversible infertility.In men, the drug may also cause hypogonadism, testicular atrophy, and reversible infertility at sufficiently high dosages.
Stanolone can have adverse effects on the cardiovascular system, especially with long-term administration of high dosages.AAS like Stanolone stimulate erythropoiesis (red blood cell production) and increase hematocrit levels and at high dosages can cause polycythemia (overproduction of red blood cells),
which can greatly increase the risk of thrombic events such as embolism and stroke.Unlike many other AAS, Stanolone is not aromatized and has no risk of estrogenic side effects like gynecomastia, fluid retention, or edema.In addition, as it is not a 17α-alkylated AAS and is administered parenterally, Stanolone has no risk of hepatotoxicity.
Estrogen is not an issue when using Stanolone. Consequently, the user does not have to worry about water retention and the domino effect of side effects that accompany it. Furthermore, they also do not have to worry about gynecomastia (bitch tits), as it is not possible to have any estrogen aromatization with epi-andro.
However, there is one problem with Stanolone, and it is related to its effects on head hair loss. DHT will fry your head hair, especially if you are predisposed to such condition. Another issue is possible joint discomfort from the dryness the user can experience.
Although it is tempting to use such DHT inhibitors (5a reductase inhibitor) as finasteride or dutasteride to help protect the hair, one must keep in mind that DHT is our sex hormone, and it is what gives males penises in the first place. Inhibiting this hormone brings along the risk of short and long term sexual dysfunction.
In spite of the fact that Stanolone is considered a mild compound, just like any hormone, the user must respect it and expect some organ strain, even though it is safe on the liver. Due to its effects on blood pressure, and the heart in general, a support supplement such as N2Guard would be a wise choice.
Moreover, like all exogenous hormones it will cause suppression, so a post cycle therapy (PCT) should always be used. Please see the perfect PCT for the optimal PCT protocol.
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