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What Will You Gain After Methenolone Enanthate Cycle


Primo (Methenolone Enanthate) is a mild anabolic steroid with minimal androgen production. Henolone can be used in combination with almost any steroid, with the most suitable environment being arranged in the reduced-fat/backup cycle. Known as “the safest of all steroids,” it has no side effects on your liver, few estrogen-related side effects, and high blood pressure, which is often associated with high estrogen levels, is rare. The most common Methenolone type is Methenolone Enanthate. Using Methenolone Enanthate, you are advised to inject twice a week to keep plasma levels stable. As a long-acting injection, Methenolone Enanthate takes 4-6 weeks to achieve full efficacy. For optimal results, I recommend continuous use of Methenolone Enanthate for 12-16 weeks. Although you can use it for short periods of time, once you see the results, you will find that the longer Cycle works best. The result of Methenolone Enanthate is a high muscle mass that will last long after your cycle is over. With proper diet and training, you will retain up to 90-95% of the cycle yield. Speaking of diet, you can maintain a low-calorie diet with the Methenolone muscle cycle. High protein (twice my weight) medium carbohydrate and low fat. You can also do a lot of cardio. I do cardio twice a day: after strength training and after dinner. Arnold Schwarzenegger’s slender waist is largely thanks to Methenolone.

What you can expect when using Methenolone Enanthate is that it makes your muscles angular and makes them hard, like concrete, and it polishes away all the excess and makes your muscles visible. Your breasts are getting wider and thicker, and the lines in the middle of your breasts are becoming very visible. Your shoulders will become fuller, as if someone had taken a softball, cut it in half and placed it on top of your shoulder. Your back is like a cobra with a very thin waistline, which makes your back look bigger. The leg muscles become so obvious that when you walk or run, everyone can see that every muscle in your leg is moving.

Now let’s talk about dose, 400mg/ week is your minimum dose. But the magic number is 600mg per week. The increase from 400 to 600mg/ week was dramatic, but the change from 600 to 800mg/ week was less dramatic. In my opinion, the 600-800mg/ week increase is not worth it. It’s like throwing money out the window. This is because of the high cost of methenolone, and some people may not be able to afford up to 600mg/ week for 16 consecutive weeks. In this case, I recommend using primo at 400mg/ week for 8 weeks, then increasing it to 600mg/ week for 8 weeks. This will save you quite a bit of money.

Finally, let’s talk about a cycle with Methenolone. This is where your thinking has to change. When arranging cycles, we always use Testosterone as the basis of a cycle, but when you have Methenolone, Methenolone is the basis of a cycle. You should use the lower dose of Methenolone along with the 600mg/ week dose. 250mg/ week testosterone is enough for this because high doses of this might cause water retention and reduce the effects of Methenolone. Believe me, at this point, my clients have tried all types of Testosterone, and at the same time use the Arimidex to control estrogen, finally, he found out that low Testosterone is the best solution, and keep low doses of Testosterone also make AI becomes unnecessary. He used a Methenolone + Dromostanplone cycle/Anavar + Methenolone + Anavar cycle/Methenolone + Dromostanolone cycle/Methenolone + Stanozolol cycle/Anavar + Methenolone + Stanozolol cycle. Although the combination of Methenolone and Anavar is a good cycle, the problem is that the cost of the cycle is very high.

The favorite cycle of my customer is as follows:
Week 1-18, 250mg/ week
Week 1-16, Methenolone 600mg/ week
Week 10-16 Stanozolol 50mg/ day
Weeks 8-16, Nandrolone Phenylpropionate 100mg/ week (to protect against joint pain caused by Winstrol)


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Structural characteristics of Mesterolone

Mesterolone is a modified form of dihydrotestosterone. It differs by the addition of a methyl group at carbon 1, which helps protect the hormone from hepatic metabolism during oral administration. The same structural modification is also used with oral Primobolan® (methenolone) tablets. Alkylation at the one position slows hepatic metabolism of the steroid during the first pass, although much less profoundly than c-17 alpha alkylation. Mesterolone is resistant enough to breakdown to allow therapeutically beneficial blood levels to be achieved, although the overall bioavailability remains much lower than c-17 alpha-alkylated oral steroids. Mesterolone also has a very strong binding affinity for Sex Hormone Binding Globulin.572 This may act to displace other steroids more weakly bound to SHBG into a free (active) state.

Side Effects (Estrogenic)

Mesterolone is not aromatized by the body and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as the drug is unlikely to induce gynecomastia, water retention, or other estrogen-related side effects.

Mesterolone is actually believed to act as an anti-aromatase in the body, preventing or slowing the conversion of steroids into estrogen. The result is somewhat comparable to Arimidex, although less profound. The anti-estrogenic properties of mesterolone are not unique, and a number of other steroids have demonstrated similar activity.

Dihydrotestosterone and Masteron (2-methyl dihydrotestosterone), for example, have been successfully used as therapies for gynecomastia and breast cancer due to their strong androgenic and potentially anti-estrogenic effect. It has also been suggested that nandrolone may even lower aromatase activity in peripheral tissues where it is more resistant to estrogen conversion (the most active site of nandrolone aromatization seems to be the liver). The antiestrogenic effect of all of these compounds is presumably caused by their ability to compete with other substrates for binding to the aromatase enzyme. With the aromatase enzyme bound to the steroid, yet being unable to alter it, an inhibiting effect is achieved as it is temporarily blocked from interacting with other hormones.

Side Effects (Androgenic)

Mesterolone is classified as an androgenic steroid. Androgenic side effects are common with this substance, especially with higher doses. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement.

Additionally, the 5-alpha-reductase enzyme does not metabolize mesterolone, so its relative androgenic is not affected by finasteride or dutasteride.

Side Effects (Hepatotoxicity)

Mesterolone is not c17-alpha alkylated, and not known to produce hepatotoxic effects; liver toxicity is unlikely.

Side Effects (Cardiovascular)

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendency to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependant on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or nonaromatizable), and level of resistance to hepatic metabolism.0

Mesterolone is an oral non-aromatizable androgen and expected to have a notable negative effect on lipids. Studies administering 100 mg of mesterolone per day to hypogonadal men for approximately 6 months demonstrated a significant increase in total cholesterol (18.8%) and LDL cholesterol (65.2%), accompanied by a significant decrease in HDL cholesterol (-35.7%).573Mesterolone should not be used when cardiovascular risk factors preclude the use of other oral steroids. To help reduce cardiovascular strain it is advised to maintain an active cardiovascular exercise program and minimize the intake of saturated fats, cholesterol, and simple carbohydrates at all times during active AAS administration.

Supplementing with fish oils (4 grams per day) and a natural cholesterol/antioxidant formula such as Lipid Stabil or a product with comparable ingredients is also recommended. Side Effects (Testosterone Suppression): Mesterolone has a very weak suppressive effect on gonadotropins and serum testosterone. Studies show that when given in moderate doses (150 mg per day or less), significant suppression of testosterone levels does not occur.574 In studies with higher doses (300 mg per day and above), the agent strongly suppressed serum testosterone.575The above side effects are not inclusive. For a more detailed discussion of potential side effects, see the Steroid Side Effects section of this book.

Administration (Men)

To treat androgen insufficiency, mesterolone is usually given in a dose of 1 tablet (25 mg) three times per day at the initiation of therapy. The drug is later continued at a lower maintenance dose, which usually consists of taking 1 tablet(25 mg) one to two times per day. Similar doses are used to support male fertility, usually in conjunction with other fertility drugs like injectable FSH. The usual dosage among male athletes is between 50 mg and 150 mg of mesterolone per day, or two to six 25 mg tablets. The drug is typically taken in cycles of 6-12 weeks in length, which is usually a sufficient period of time to notice the benefits of drug therapy.

Many bodybuilders favor the use of mesterolone during dieting phases or contest preparation when low estrogen and high androgen levels are particularly desirable. This is especially beneficial when anabolics like Winstrol, Anavar, or Primobolan are being used alone, as the androgenic content of these drugs is relatively low.

Mesterolone can be effectively used here to adjust the androgen to estrogen ratio upwards, bringing about an increase in the hardness and density of the muscles,

supporting libido and a general sense of well being, and increasing the tendency to burn body fat. It is also commonly used (at a similar dosage) to prevent gynecomastia when other aromatizable steroids are being administered, often in

conjunction with 10-20 mg per day of Nolvadex.

Administration (Women)

Mesterolone is not approved for use in women. This agent is not recommended for women for physique- or performance-enhancing purposes due to its strong androgenic nature and tendency to produce virilizing side effects. Some women do favor the drug, however, and find a single 25 mg tablet enough to efficiently shift the hormone balance in the body, greatly impacting the look of definition to the physique.

Intake is usually limited to no longer than four or five weeks in such situations to minimize the chance of developing lasting virilizing effects. One tablet used in conjunction with 10 or 20 mg of Nolvadex® can be even more efficient for muscle hardening, creating an environment where the body is much more inclined to burn off extra body fat, especially in female trouble areas like the hips and thighs. Extreme caution should be taken with such use, however.


Methenolone & Nandrolone Deca


Metenolone and Nandrolone are actually two different things. Methenolone has nothing to do with Nandrolone. Metenolone is not derived from Nandrolone but derived from dihydrotestosterone (DHT). These two things sound a lot alike, but they are two things.

Deca

1. “Nandrolone” category is the safest steroid because Nandrolone has low ability to switch to androgens and to estrogen;
2. Nandrolone Decanoate is what we call Deca. Deca, known as the king of Bulking, is definitely not a name! Deca became famous at the end of the last century, and it can definitely compete with oral drugs like Dianabol and Anadrol in terms of muscle gain;
3. Compared with testosterone, Deca is definitely a crushing grade in terms of protein synthesis ability, and the protein synthesis ability is 130% of testosterone;
4. Compared with Dianabol, Anadrol, etc., Deca is quite gentle and quiet in the muscle gain, Deca’s muscle gain process will not bring blush, chest redness and other characteristics. And you won’t get violent and sweaty because of using Deca.
5. However, Deca can’t be used alone like Dianabol. The biggest risk of using Deca alone is the possibility of “wilting”. This must not be ignored. If you use Deca alone, it must be done with the help of testosterone.

Methenolone

1. Methenolone does not belong to the nandrolone class;
2. Methenolone and testosterone play the same principle, but the anabolic capacity of metoprolol is about 88% of testosterone, there will be no violent bulking like Deca, and its male hormone ability declines more, only the original testosterone 44%;
3. Methenolone is not suitable for non-season weft increase, it is more suitable for long-term use during the preparation period because it has mild nature and does not turn estrogen; no hepatotoxicity, very safe. It effectively protects muscles during fat loss, prevents muscle loss and improves muscle mass. It is suitable for use during fat loss or e preparation;
4. Methenolone often used in conjunction with Stanozolol, Clenbuterol during the preparation period, and finally achieved the effect of increasing lean body mass, dry, and fat reduction.

Therefore, Deca is suitable for the non-season injection cycle, while Methenolone is suitable for the preparation period.


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Methenolone is a medium anabolic but very low androgen steroid. The Methenolone is very versatile. It is often stacked with other (usually stronger) steroids for faster and stronger effects. Metenolone is suitable for both cutting cycles and quality cycles; In both cases, it will restore and grow lean and tight muscle mass faster. Welcome to buy Methenolone powder from us. We have free reship service if your parcel was intercepted.

Methenolone was made in 1960. Squibb began making injectable drugs in 1962. Metenosaurus was originally used for aggressive treatment after surgery for muscle loss, infection, long-term illness, corticosteroids or malnutrition, and in some cases for osteoporosis and breast cancer. Methenolone is often used to promote weight gain, with Methenolone being less than normal and having no side effects.

One notable feature is that it binds firmly to androgen receptors, stronger than testosterone. This quality makes the original brown a good burner.

Methenolone does not convert to estradiol; So you can take it without the risk of estrogen side effects (gynecomastia, water retention).

Methenolone is one of the safest steroids on the market, so women, older athletes, and teenagers often find it the best way to improve their health and avoid side effects.

Overall, Methenolone, one of the safest anabolic steroids available on the market, is a relatively weak compound that takes time to show the best effects. If the drug is used for at least 10 weeks with other steroids, good results will be found.


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Methenolone profile

Methenolone is a medium anabolic but very low androgen steroid. Methenolone is very versatile. It is often stacked with other (usually stronger) steroids for faster and stronger effects. Methenolone is appropriate during cutting cycles and bulking cycles; In both cases, it will restore and grow lean and tight muscle mass faster.

Methenolone was made in 1960. Squibb began making injectable drugs in 1962. Methenolone was originally used as an aggressive treatment for post-operative muscle loss, infection, long-term illness, corticosteroids or malnutrition, and in some cases for osteoporosis and breast cancer. Methenolone is often used to promote weight gain, with Methenolone being less than normal and having no side effects.

Methenolone functions

One notable feature is that it binds firmly to androgen receptors, stronger than testosterone. Methenolone does not convert to estradiol; So you can take it without the risk of estrogen side effects (gynecomastia, water retention). Methenolone increases protein synthesis, increases lean tissue, and increases the number of red blood cells. The increase of red blood cells can increase the muscle endurance of users, improve nitrogen retention, help users to save more muscle as much as possible under extreme diet and training conditions, and promote the decomposition of fat. Metenosaurus has a very strong binding ability to androgen receptors. The ability to bind to androgen receptors is linked to increased fat breakdown, and Methenolone also boosts the user’s immune system.

Methenolone Enanthate and Methenolone Acetate

Methenolone is one of the safest steroids on the market, so women, older athletes, and teenagers often find it the best way to improve their health and avoid side effects. Many athletes and enthusiasts struggle to find the right balance between gaining lean weight and losing subcutaneous fat as they prepare to compete. Methenolone is an indispensable artifact for the preparation of the game because of its mild nature and extremely unnatural nature. This property is that Methenolone can maintain muscle fullness and synthesis capacity in a low-carb environment. In this way, in the early and middle stages of the backup race, an appropriate amount of Methenolone Enanthate can be added in cycles (the recommended starting dose is 500mg/ week) to reduce fat without affecting the rate of muscle growth. Meanwhile, Methenolone’s extremely mild nature can also be used continuously for a long period in the backup race or other cycles. If you have a good budget and your level is high, you can use Methenolone Enanthate in very high doses (even two bottles per week, that’s 2,000 mg/ week).

As for Methenolone Acetate, I personally suggest to add it at the later stage of the preparation. Methenolone Acetate also has the miracle effect of maintaining muscle satiation in a low-carb water environment. However, due to the low utilization rate of Methenolone Acetate in oral form, it is not as cost-effective as Methenolone Enanthate.

Overall, Methenolone, one of the safest anabolic steroids available on the market, is looking to make the most of the weaker compounds and needs time to show the best effects. If the drug is used for at least 10 weeks with other steroids, good results will be found.

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