Masteron and testosterone

Summary: While clearly a powerful anabolic steroid with amazing anti-estrogenic properties, Masteron overdose must be avoided in all circumstances. Like many other steroids, it is not suitable for use by anyone with a prevailing health condition. For the rest of the people though, it is an amazing transformation agent that can help you quickly realize your goals of a stronger body with more muscle density. Its anti-estrogenic properties are essential in taking care of most of the side-effects experienced by use of anabolic steroids, such as high blood pressure and water retention. Post cycle therapy is also essential after the use of Masteron. Depending on your goals, you may choose to stack Masteron with other products to achieve optimal results. The product is highly toxic and dangerous. We advice against using it.

First and foremost, it is important to mention that there is no risk what so ever of any Estrogen related side effects from Masteron Enanthate alone. As mentioned previously, Masteron Enanthate not only avoids aromatization into Estrogen completely, but it even acts as an anti-Estrogen in many cases. Therefore, the typical estrogenic side effects that result from the use of aromatizable anabolic steroids is avoided. This includes: bloating, water retention, blood pressure increases (as a result of water retention), acne, and gynecomastia. Because of Masteron’s anti-estrogenic properties, it can actually help prevent or mitigate these side effects if they are occurring from other anabolic steroids that do aromatize.

Injectable steroids are injected into muscle tissue, not into the veins. They are slowly released from the muscles into the rest of the body, and may be detectable for months after last use. Injectable steroids can be oil-based or water-based. Injectable anabolic steroids which are oil-based have longer half-life than water-based steroids. Both steroid types have much longer half-lives than oral anabolic steroids. And this is proving to be a drawback for injectables as they have high probability of being detected in drug screening since their clearance times tend to be longer than orals. Athletes resolve this problem by using injectable testosterone early in the cycle then switch to orals when approaching the end of the cycle and drug testing is imminent.

Like other AAS, drostanolone is an agonist of the androgen receptor (AR). [3] It is not a substrate for 5α-reductase and is a poor substrate for 3α-hydroxysteroid dehydrogenase (3α-HSD), and therefore shows a high ratio of anabolic to androgenic activity. [3] As a DHT derivative, drostanolone is not a substrate for aromatase and hence cannot be aromatized into estrogenic metabolites . [3] While no data are available on the progestogenic activity of drostanolone, it is thought to have low or no such activity similarly to other DHT derivatives. [3] Since the drug is not 17α-alkylated , it is not known to cause hepatotoxicity . [3]

Masteron and testosterone

masteron and testosterone

Like other AAS, drostanolone is an agonist of the androgen receptor (AR). [3] It is not a substrate for 5α-reductase and is a poor substrate for 3α-hydroxysteroid dehydrogenase (3α-HSD), and therefore shows a high ratio of anabolic to androgenic activity. [3] As a DHT derivative, drostanolone is not a substrate for aromatase and hence cannot be aromatized into estrogenic metabolites . [3] While no data are available on the progestogenic activity of drostanolone, it is thought to have low or no such activity similarly to other DHT derivatives. [3] Since the drug is not 17α-alkylated , it is not known to cause hepatotoxicity . [3]

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