Category: pct cycle
PCT has two main functions: 1. Restart gonad axis. 2. Impedance muscle decomposition.
To restart the gonad axis
Long-term external injection results in the suppression of testosterone secretion, and there is no external testosterone after the withdrawal of the drug. At this time, we need to turn on the natural testosterone secretion process again.
LH and FSH are essential for promoting the natural secretion of testosterone and sperm, and it is important to mention that several drugs commonly used in PCT are HCG, tamoxifen, and clomiphene, all of which belong to SERM.
HCG acts like LH, which means it stimulates the release of testosterone and sperm.
But using HCG alone does not make our LH and FSH return to normal levels (if are used individually in the PCT HCG to resume their normal secretion of testosterone, your testosterone can resume normal is really amazing), the introduction of SERM tamoxifen, club, and lack of estrogen receptor binding to estrogen signal stimulate hypothalamus GnRH secretion, and then spread to the pituitary gland to further stimulate the secretion of LH and FSH, tamoxifen, Clomid stimulation on LH and FSH recovery respectively, in other words, both be short of one cannot.
While using SERM, not only improve the level of androgen and estrogen levels can ascend, after a period of time after the stop using SERM may result in higher estrogen in our body, our usual practice is to late to join the AI is also mentioned in a series (estrogen) or the testosterone used to suppress estrogen, and the benefits of the testosterone will not just against female so I tend to choose the testosterone.
To impedance muscle decomposition
In fact, many people have asked me a question before: how much muscle can I retain in a cycle? It’s an open question, like a beginner going to the gym and asking me how to practice. It depends on your training level, your diet level, your pharmacist level. The PCT does a good job of impedance muscle breakdown, including your muscle mass and body fat rate, etc., which of course means that the impedance muscle breakdown in the PCT is completely optional, the gonadal axis must be restored first and foremost, as far as you want to retain more muscle, recover faster and better, you need to increase your budget.
Because during the PCT phase we generally avoid any drugs that suppress our own testosterone, the use of peptides can both resist muscle breakdown and promote the recovery of the gonadal axis.
Whether you use human growth hormone or growth hormone-releasing peptide, it can stimulate the secretion of IGF-1, burn fat, reduce the breakdown of protein, and stimulate the late gene expression of GnRH, increasing the concentration of free testosterone, so that your testosterone level increases.
You will feel like a superhero while you are on a cycle. PR’s every time you go to the gym, confidence is through the roof, it’s amazing! And if you are smart about it, you can keep most of your gains after a proper PCT.
Steroids multiple muscle protein synthesis rate and time, which means: from the same workout you will build 10 fold more muscle.
They help lose weight because your metabolic rate goes up since muscle building and keeping needs a lot of calories. Which means if you keep eating normally, you will build muscle and lose weight at the same time. Although I wouldn’t recommend that because that means you are wasting time not building muscle, which would benefit your weight loss in the long run much more!
Steroids are safe, as long as you don’t overdo it and you have proper knowledge about the usage and PCT.
You can reach similar physique with only a few testosterone cycles, of course, you have to have proper training and nutrition too.
Before you start, you should have at least 5 years of training history and knowledge of proper nutrition, don’t do steroid if you are under 20 years old, your test levels are probably in their peak, suggest doing a hormone test to see where you at (Total and Free Testosterone, Estrogen, LH, FSH, TSH, T3, T4), where they will help you analyze your results: Pharma
I would ask how old you are? If you’re 35 or older, you may have low testosterone levels and; therefore, eligible for hormone replacement/testosterone replacement therapy. If you’re in your 20s, you’ll want to seriously consider whether you want to take steroids and shut down your body’s ability to make your own testosterone unless you do proper post cycle therapy, which is also difficult to come by, unless prescribed by a physician.
The following cycle is for a woman who uses anabolic steroids before and successfully doing so. She has used Anavar and has no serious side effects, and she is looking for more. The following cycle can be used to both cutting and bulking cycle, but most women will find it most suitable for cutting.
Technically, some women can use both Anavar and Masteron; However, such use would present a high rate of masculine symptoms. The cutting above allows for the initial use of Anavar and the gradual use of Masteron. They were also separated to reduce the risk of masculinity.
Masteron’s association with steroid use in women is not as strong as Anavar’s and is even smaller than steroids such as Primobolan and Winstrol. However, Masteron is less likely to promote masculine symptoms than Winstrol and Primobolan. It has almost the same androgen activity as Anavar. It is a good steroid to promote strength and hardness, although it is often not associated with building quality, and it can provide lean benefits far beyond the credit many people give it, especially female steroid users. Keep in mind that women are far more sensitive to anabolic steroids than men, and milder steroids can still produce considerable impact at lower doses. If you choose to use Masteron, the propionate version is the only one we can recommend. If a failure occurs, once the use is stopped, it will quickly clear the body. If you choose to use the version based on Enanthate, it will remain on your system for a long time after stopping.
HGH: even without HGH, the cycle itself is beneficial, but HGH increases its value tenfold.
Aromatase inhibitors (AI) are not required in female cycles. Unlike men, women don’t need to worry about estrogen dominance as much as men do. In addition, no aromatic steroids are introduced into this cycle.
HCG: women do not need to use HCG during a cycle, which is often recommended for men. Men use it to maintain testicular function, which is irrelevant for women. Like men, women do not need post-cycle therapy (PCT) because they do not need the stimulation of testicular activity.
Steroid Cycle For Women
The following cycle is for women who have never used anabolic steroids or performance-enhancing drugs. However, this is often the only style cycle a woman will use, as it is all that many people need. For fitness conscious women, you can use the following methods to do breast enhancement or cutting; The diet you follow will determine where it goes. For a woman who wants more muscle mass/quality, this will increase the lean tissue she craves, rather than the puffy look she doesn’t want. If you want to lose weight and get in shape, assuming you’re not eating enough calories, the following tips will help her stay lean while dieting, while also making her harder.
Unlike men, women do not use testosterone. In some cases, late-stage steroid use in women is the exception. Testosterone is highly masculine, which means the deepening of the vocal cords, the growth of body hair, and the enlargement of the clitoris. These side effects are undesirable for most women, so testosterone generally needs to be avoided. There are exceptions, of course. Women sometimes take low doses of testosterone, but that’s not one of them. Most women will find it best to choose a steroid with the lowest masculine activity, usually one with a lower androgen rating.
Anavar could start with a lower dose, say 5 milligrams a day, but few women respond worse to 10 milligrams a day, which seems to be the optimal dose for most women. If you start experiencing masculine symptoms at any time, stop using them immediately and they will disappear quickly. However, if the symptoms are present and are ignored, and if you continue to use them, you may find that the negative effects become permanent. Ignoring these effects usually does not cause irreversible damage after 6-8wk runs, but is usually associated with several cycles that ignore these effects. In some cases, however, the negative effects of neglect can be permanent.
B12, it’s not a steroid, but a lot of the things that we add to the menstrual cycle are not steroids. Since women are bound to be limited in their use, we must find other options. This is not a requirement for this cycle, we just provide you with high-quality options. If B12 is used, it is highly recommended that you choose to inject B12, especially methyl cobalamin, as it is by far the most effective. This will provide a lot of energy for your training and greatly improve recovery, which is the most important factor.
HGH: if this is your first cycle, you are unlikely to add HGH, but the outline above shows where you should choose to add HGH in future code. The cycle itself is not as beneficial, but HGH increases its value tenfold.
Aromatase inhibitors (AI) are not required in female cycles. Unlike men, women don’t need to worry about estrogen dominance as much as men do. In addition, no aromatic steroids are introduced into this cycle.
HCG: women do not need to use HCG into their cycle, which is often recommended for men. Men use it to maintain testicular function, which is irrelevant for women. Like men, women do not need post-cycle therapy (PCT) because they do not need stimulation of testicular activity.
Nolvadex powder with domestic Canada delivery
Nolvadex is a popular and potent selective estrogen receptor modulator (SERM), commonly referred to as anti-estrogen. However, as an antagonist, it is also an agonist because it ACTS as an estrogen in some parts of the body and as an anti-estrogen in others. One of the oldest SERM on the market, it’s still used in medicine, and Nolvadex is also used by users of anabolic steroids, it’s not an anabolic steroid. This is an important note because some people often confuse it with the steroid cycle. Nolvadex is just a SERM.
The official name of Nolvadex is the Tamoxifen Citrate, which was originally developed by ICI in 1961 and is now the Nolvadex trademark of astrazeneca. SERM was developed to treat breast cancer, particularly hormone-reactive breast cancer. However, it is also effective in the prevention of breast cancer. And then we have the users of anabolic steroids, who long ago identified Nolvadex as having a place in this group. Nova is known to act as an anti-estrogen during anabolic steroid cycles to prevent estrogen-related side effects. It is also used as part of a post-cycle treatment (PCT) recovery program, which is its most common and beneficial for users of steroids.
Nolvadex functions and features
Tamoxifen citrate is an estrogen agonist and antagonist of SERM. Nolvadex works as an anti-estrogen drug by binding to estrogen receptors that take the place of estrogen. This combination prevents estrogen from working in certain parts of the body, which is why it is beneficial for breast cancer patients. Many types of breast cancer actually rely on estrogen when it attaches to receptors in the breast. By blocking the attachment of these receptors, it also protects women with gynecomastiosis who use anabolic steroids, which may be partly caused by the aromatization of anabolic steroids such as testosterone, dianabol, nandrolone and boldenone.
Nolvadex is primarily thought of as an anti-estrogen, but it also has estrogenic effects, particularly in the liver. This is a benefit because the estrogen activity in the liver is associated with healthier cholesterol levels. This is particularly beneficial for steroid users because many anabolic steroids tend to have negative effects on cholesterol. We will explore the direct effects of Nolvadex further later.
Novadex is mainly anti-estrogen but also has strong testosterone stimulating properties. Nolvadex has the ability to block estrogen-induced negative feedback from the hypothalamus and pituitary gland. Thus, this stimulated the enhanced release of pituitary luteinizing hormone (LH) and follicle-stimulating hormone (FSH). Luteinizing hormone and follicle-stimulating hormone are both important for natural testosterone production. Without luteinizing hormone and follicle-stimulating hormone, and with more emphasis on luteinizing hormone, there is no natural production of testosterone.
The influence of Nolvadex
The Nolvadex effect is very direct for breast cancer patients. By preventing estrogen from attaching to cancer cells, cancer cells can’t get the hormones they need to survive. While it works, it’s not always the only compound used, or even the first. Aromatase inhibitors (AI) are usually used early because of their ability to lower serum estrogen levels. Over time, ai like Nolvadex will be converted to SERM. In the case of prevention, those with a strong family history of breast cancer can be prevented with Nolvadex at an early age.
For users of anabolic steroids, Nolvadex’s primary role in the menstrual cycle is to prevent male breast development. Nolvadex does not seem to have a strong effect on the other major estrogenic effects in water retention, but these can usually be controlled by other means. As for female breast protection, this is enough for many men, if you can complete the work, this should be your first choice. If not, you’ll need an ai like Arimidex (Anastrozole) or Femara (Letrozole). However, ai can have a negative effect on cholesterol. Ai alone does not seem to have a strong, negative effect, but when added to aromatic steroids, the effect seems to worsen. You can use ai to control cholesterol, but if it can do the job, SERM with Nolvadex should be your first choice. As an added benefit, keep in mind that this SERM will have a positive effect on your cholesterol levels.
The Nolvadex final effect is the most valuable for users of anabolic steroids. The use of anabolic steroids inhibits the production of natural testosterone. The inhibition rate will depend on the steroid used, but in most cases it will be significant. Once the anabolic steroid use is completed, natural testosterone production will resume assuming that the individual does not have a previous low testosterone status and does not damage his hypothalamic-pituitary-testicular reticulum axis (HPTA) through inappropriate behavior. However, this natural production will begin on its own, but there is a problem. Once you get out of the cycle, your natural testosterone levels will be very low, and production will start again, and they will stay low for a long time. It takes months and months for the body to fully return to its natural testosterone levels. In fact, it can take as long as a year or more, depending on the severity of the cycle and the person’s overall personality. This means that an individual’s testosterone levels will be low for quite some time, which can be accompanied by a series of annoying symptoms. This condition may include all the symptoms associated with low testosterone. In addition, because of low testosterone levels, and because cortisol is the main hormone in the body, individuals are likely to lose large amounts of muscle tissue gained through steroid use.
Because of low testosterone levels after the hormone anabolic cycle, most men are encouraged to undergo a PCT program, which includes discontinuing hormone anabolic. Solid state PCT programs often include novadex as well as SERM (clomiphene citrate) and the powerful peptide hormone HCG(human chorionic gonadotropin). By implementing the PCT program, you will greatly stimulate natural testosterone production, speed up the recovery process, and greatly protect your body. Once the PCT program is over, contrary to popular belief, your testosterone levels won’t stay at their normal high levels. Full recovery will still take a long time. However, PCT programs including Nolvadex will ensure that you have enough testosterone to function properly and that your testosterone levels continue to rise naturally.
There are many performance-enhancing athletes who scoff at PCT programs, and it’s time to abandon them. If you only plan to stop your cycle for a short time, say 4-6 weeks, or if you’re stuck with low testosterone levels throughout your cycle, there’s no good reason for a PCT program. This is common in core fitness circles, but not realistic for most people who use anabolic steroids. Most people who use steroids have a fair amount of time to stop using them, and in the name of health and well-being, that’s the best way to do it. If this is the case, then there is no logical reason to abandon PCT, and we can guarantee that those who implement PCT will be better off.
For the purpose of protecting estrogen side effects during the use of anabolic steroids, 10-20 mg per day is common. If 20 mg per day does not protect you from male breast development, then you will need AI. If you can’t control water retention with this dose, you may want to consider using artificial intelligence, but if the calorie content in your diet is too high, especially carbohydrates, you should control the water. Many performance athletes often blame steroids for huge moisture retention, and in fact many times they eat more than they need. Overeating can cause you to hold water and add aromatic steroids, which is even worse. Control your diet and control estrogen through SERM, most should be no problem. Controlling cholesterol will become even more important if artificial intelligence is required and during the usual cycle and competition cycles.
For the PCT, the standard dose of Nolvadex usually starts at 40 mg per day. The dose is usually 40 mg per day for several weeks, reduced to 20 mg per day for several weeks, and then completed in a week or two with 10 mg per day. How your cycle ends will determine when you start Nolvadex treatment. This also affects time if HCG is included.
There are several SERM’s available, with Nolvadex and Clomid being the most common, but Nolvadex is probably the most beneficial of all SERM’s. There is no doubt that this is beneficial for breast cancer patients. In terms of performance capabilities, individuals should not expect any kind of real performance boost. Of course, it can stimulate natural testosterone production.
Aromatase Inhibitors (AIs) vs. Selective Estrogen Receptor Modulators (SERM)
Anyone who wants to use anabolic steroids as performance enhancers should take the time to learn about the various products and supplements that will prevent unwanted side effects. Aromatase inhibitors (AIs) and selective estrogen receptor modulators (SERMs) are two very popular – and very important – parts of an anabolic steroid cycle. Understanding the difference between the two is vital to maintaining your health and your physique.
What Do AIs and SERMs Do in the Body?
Just as AIs and SERMs are very different, they are also very much the same. Both of these compounds provide ways to control the amount of estrogen in the body, which is vital for preventing some significant side effects.
Many of the most popular anabolic steroids convert to estrogen, and when too much estrogen is present, you may notice some of the following:
Gynecomastia (a condition in which men develop female breast tissue)
AIs and SERMs both prevent these side effects, but they do so in very different ways.
What Is an AI?
An AI, or aromatase inhibitor, prevents a steroid from converting to estrogen. Androgen is common in anabolic steroids, and some are more androgenic than others are. Once these androgens are in the body, they turn into estrogen over time with the help of an enzyme known as aromatase. An aromatase inhibitor binds to the aromatase enzyme, thereby making it ineffective at converting androgens into estrogen. However, it takes time for AIs to build up in the bloodstream. Arimidex is the most popular aromatase inhibitor among steroid users, but Letrozole is another option for men who are particularly sensitive to the effects of estrogen or who want to reverse existing gynecomastia.
What Is a SERM?
On the other hand, a SERM, or a selective estrogen receptor modulator, binds to the estrogen receptor itself rather than the aromatase. While a SERM blocks some of the actions of estrogen, it allows others. Even in the male body, some estrogen is important. While an AI inhibits all estrogen, a SERM just prevents its negative effects by blocking estrogen’s androgenic properties. Two of the most popular SERMs in terms of performance enhancement are Nolvadex and Clomid.
Which Is the Best Choice?
While an AI blocks estrogen production and may ward off side effects, bear in mind that the body continues to send chemical signals that it needs more estrogen. As such, the body continues to produce more estrogen, resulting in an endless cycle and sometimes a “rebound” effect in which estrogen levels suddenly spike after stopping the AI. A SERM only affects the way the body uses estrogen, and as far as the body knows, there is plenty of estrogen to go around. Thus, while an AI can prevent unwanted side effects during anabolic steroid cycles, it is imperative to use a SERM during post-cycle therapy to combat rebounds and bring levels back to normal.
Both AIs and SERMs play important roles for people who choose to enhance their performance with anabolic steroids. However, knowing which product to use in which situation can make all of the difference when it comes to preventing potentially serious side effects.
Letrozole (Femara) is an oral nonsteroidal aromatase inhibitor used as an adjunct treatment for hormone-responsive breast cancer.
Estrogen is produced by converting aromatase activity into aromatase activity. The drug blocks estrogen production by reversibly binding in this way by competing with hemoglobin P450 units of heme. This effect is specific and the product does not reduce the production of minerals or corticosteroids. In contrast, tamoxifen’s anti-estrogen effect is due to its interference with estrogen receptors rather than its inhibition of estrogen production.
The drug has also been shown to slow the fusion of growth plates in adolescents. This may increase the effectiveness of growth hormone, so the drug is used to treat teenagers and small children.
The drug is approved by the food and drug administration (FDA) to treat postmenopausal women with localized or metastatic breast cancer that is hormone-receptor-positive or whose receptor status is unknown.
The product’s anti-estrogen effect has been shown to be useful in pre-treatment of pregnancy termination combined with misoprostol. It can replace mifepristone, which is expensive and not available in many countries.
This drug is sometimes used to treat gynecomastia, although it may be most effective if detected early (as in the use of anabolic steroids).
Some studies have shown that the drug can be used to promote sperm production in men with non-obstructive azoospermia.
This medicine is most effective when taken regularly.
If you miss the dose of this medicine, take it as soon as possible. If it’s almost the next dose, skip the missed dose and go back to your regular dose plan. Don’t take two doses at a time.
If you have any questions about how to use this product, please consult your healthcare provider.
Comparism with tamoxifen
Tamoxifen is also used to treat hormone-reactive breast cancer, but it is treated by interfering with estrogen receptors. However, the drug is only effective in postmenopausal women because estrogen is mainly produced in surrounding tissues (such as adipose tissue, such as breast tissue) and many parts of the brain. In premenopausal women, the main source of estrogen is the ovary, not the peripheral tissue, and the drug is ineffective.
In the 1-98 study, the drug reduced cancer recurrence but did not change survival compared with tamoxifen in postmenopausal women with hormone-responsive breast cancer.
The drug is an aromatase inhibitor for the treatment of breast cancer. Aromatase inhibitors inhibit the action of aromatic hydrocarbons, which convert androgens into estrogen through aromatization. Because breast tissue is stimulated by estrogen, reducing the production of estrogen is a way to inhibit the recurrence of breast tumor tissue.
Mainly through the liver of CYP3A4 and CYP2A6. This product inhibits aromatase by competitively binding to the heme of the enzyme’s cytochrome P450 subunit, resulting in reduced estrogen biosynthesis in all tissues. It is slowly metabolized into inactive metabolites, and its glucuronic acid conjugates are excreted in the kidneys as major pathways of clearance.
Rapid and complete absorption. Absorption is not affected by food.
Exemestane for pct cycle
Exemestane is a steroidal aromatase inhibitors/suicide irreversible aromatase inactivator, by blocking aromatase reduces the production of estrogen in the body. The drug, which is structurally similar to formestan, is used in the treatment of estrogen-dependent breast cancer, are most aromatase inhibitors. It is popular among bodybuilders when it was used to the post pct-cycle.
The function of Exemestane
For strength athletes and bodybuilders, Exemestane several useful features. First of all, Exemestane estrogen can be 85% lower. Doing so will certainly help prevent estrogen-related side effects from aromatase steroids. The drug also boosts users’ testosterone levels, which may be beneficial if used during post-cycle therapy. In addition, there is evidence that Exemestane is likely to raise the level of insulin growth factor of IGF.
Effects of Exemestane
Like other aromatase inhibitors, the effects of Exemestane lipid/cholesterol to the users, there are conflicting information and research. Some studies have shown that Exemestane lipid/cholesterol almost has no impact to the user, and the influence of other research shown that it can be rather serious.
After oral 25 milligrams, Exemestane2 hours peak plasma concentration. The effective life of this medicine is between 24 and 30 hours. This is important because it is much shorter than nsaids. Single oral 25 milligrams Exemestane will result in plasma and urine estrogen levels decline in a relatively long time, about 2 to 3 days after taking a maximum inhibition, and last about 4 to 5 days.
Research shows that 25 milligrams of Exemestane improves the level of testosterone and estrogen as welll as levels of IGF is basically as effective as 50 mg. Therefore, a daily dose of more than 25 milligrams is not necessary. Due to the activity of Exemestane, it is suggested taking it about every 24 hours.
The only negative effect of the compound from the dose plan is that it takes about seven days to reach stable plasma levels. However, this is not the main barrier to its use. It simply needs a week before the users fully realize the effect of compound Exemestane came into use.
Side effects when using Exemestane
Exemestane under the dose of 600 mg/day is no significant drug toxicity. Most users are well tolerated and the maximum tolerable dose of toxicity has not been determined. Adverse side effects associated with the use of this compound are usually very mild and may include transient gastrointestinal reactions, hot flashes, nausea and/or fatigue. As noted earlier, the effect of esimetan on lipids/cholesterol is unknown and should therefore be monitored when the compound is used.
Exemestane is a relatively safe in aromatic steroid inhibitors, due to the compound has a moderate negative side effects, should be used under the guidance.
Anastrozole is an aromatase inhibitor. Aromatase inhibitors prevent the conversion of androgens from fat, muscle, breast and brain into estrogen. The main medical use of anastrozole is to inhibit the progression and growth of breast cancer in women by blocking aromatase. It is also used by some doctors to treat testosterone deficiency in men and in combination with testosterone replacement therapy.
For bodybuilders and strength athletes, anastrozole is used to reduce the aromatization of anabolic steroids, in part because it boosts users’ testosterone levels. By reducing the amount of estrogen in a steroid user’s body, he will be able to avoid estrogen-related side effects, such as water retention and breast development in women.
Interestingly, in addition to lowering estrogen, anastrozole also increased testosterone levels by 58 percent, as well as increasing levels of the moisturizing hormone. This is very important. Considering that anastrozole can be used in combination with other compounds, it can increase users’ natural testosterone levels in the post-cycle.
Anastrozole powder uses
In most users, 0.5 mg per day should be sufficient to prevent estrogenic side effects associated with anabolic steroid use. Even when the dose was increased to 1 mg per day there was no change in the amount of estrogen compared to 0.5 mg per day. This suggests that if estrogen side effects are still a problem at 0.5mg, increasing your dose will have no further effect. If symptoms persist, users may have to try a more potent compound, such as femara.
However, most users can reduce any water retention or other estrogen-related side effects they may have by taking a dose less than 0.5 mg per day. Interestingly, users reported that a dose of 0.25 mg daily or 0.5 mg every other day was sufficient to achieve this result. It is possible to take anastrozole every other day because it has 48 hours of activity.
The same dose of anastrozole should be used in patients who take anastrozole during the postcycle treatment period. There is no need to increase or decrease the dose. It can run the entire post-cycle without any adverse effects.
Blood levels of the compound should stabilize and peak 7 to 10 days after the first dose. As a result, it is unlikely that users will have to load anastrozole in advance or start using it before they start managing the anabolics they plan to use.
Side effects of taking Arimidex
Arimidex appears to have a mild effect on blood lipids (cholesterol) and has not been shown to have a negative effect on blood lipids (cholesterol). However, it should be noted that if a person consistently suppresses your natural estrogen levels over a long period of time, this could have negative effects on your health (including your cholesterol). Nevertheless, there is no scientific evidence that anastrozole is dangerous for healthy individuals, even in the long term.
It appears that the use of anastrozole has few side effects. It is by far one of the safest compounds available to athletes. It helps to increase natural testosterone levels.
At the end of the anabolic androgen cycle, the two most important things are:
1. Reactivate natural hormonal functions that have been suppressed during the cycle, primarily to bring testosterone back to normal levels.
2. In order to maintain the gains from the cycle, this is actively achieved when the first point is satisfied.
SERMs & AIs
In order to fully resume your natural test production, you need something to stimulate your pituitary gland to restart its regular activity. These drugs are divided into two families: SERM(selective estrogen receptor modulators) and AI(aromatase inhibitors). Common SERMs are Nolvadex (tamoxifen) and Clomid (clomiphene). The most commonly used AIs are: Femara, Arimidex, aromatin, and liquidex. Proviron is also an androgen with high e – resistance.
SERMs: these compounds bind to estrogen receptors and show good estrogen effects, which are associated with our recovery.
They are used in post-cycle therapy because they stimulate the pituitary gland to release more gonadotropins, promoting faster and higher release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH).
Both hormones make the testes produce more sperm and testosterone, allowing the body to return to normal production levels.
AIs: they’re not like SERMs, they’re not estrogen. Their role is to prevent the conversion of androgens to estrogen. At the end of a cycle, the body no longer acquires exogenous hormones, and its natural hormone production is partially inhibited. Here are the risks of any estrogen-related side effects, such as increased fat and water, male breast development, low libido, and all the others mentioned earlier.
Using artificial intelligence to suppress estrogen receptors would suppress any temptation to question them. Therefore, they are often used over a cycle to prevent the aromatization of estrogen from being tested by aromatase.
When do I start my post-cycle therapy?
It depends on the cycle of medication use.
What is HCG and when is it used?
HCG, the human chorionic gonadotropin hormone, is recommended when your body’s sperm production needs rapid fixation. In fact, when boys are shrinking, they need nourishment.
Sometimes people find it useful to run at 500IU twice a week even in the last few weeks of a long cycle.
It should never be used alone without SERM, as it will replace the normal function of LH for a period of time and need to be supplemented again after the intake of HCG. That’s why I usually only advise when I have to.
Diet on the PCT
Don’t reduce calories when you think your body is in a highly anabolic state on PCT.
You have to maintain what you’re getting, and the PCT drugs themselves don’t work miracles, like the AAS, so keep them at high levels to maintain what you’re getting and change your diet with your goals.