The Mass Stack contains one bottle each of LGD-4033, Andarine, RAD-140, and MK-677.

***Shake well before each use.***

***Intended for research purposes only.***

Mass Stack Cycle

Mass stack cycles, Testolon RAD140 interacts with the androgen receptor more efficiently than testosterone. Once the androgen receptors are stimulated, release growth proteins. The advantage of TESTOLON RAD140 is that it increases spermiogenesis (sperm production) unlike testosterone which leads to testicular atrophy. In short, RAD 140 is a potent, orally bioavailable, non-steroidal SARM. It works on hormone receptors and is able to mimic the effects of a high dose of testosterone, while providing the same benefits minus the unwanted side effects.

Mass Stack Cycle for sale online

Testolone RAD140, Side effects

Testolone RAD140 is a relatively new SARM on the market and therefore no side effects are clinically reported. The potential risks of using Testolone RAD140 may be similar to those of testosterone. These may include: Abnormal hair growth in women High dose alopecia (hair loss) Mood changing

SARMs Testolone RAD 140, Dosage

Studies on Testolone RAD140 are still in production, but this SARM is known to have similar potency to Ligandrol LGD4033. 20-30 mg / d every 24-36 hours (half-life) is sufficient for maximum muscle enlargement A maximum cycle of use is 12 weeks, but shorter cycles of 6 weeks with 3 weeks off are recommended for total security. dose limit for women not to be exceeded is 10 mg / day In db/db mice, which serve as a model of type 2 diabetes (increased serum TGs, glucose, and insulin), L-165041 causes a modest increase in HDL at a dose that does not cause TG or glucose lowering. GW501516 has been studied in a population of obese rhesus monkeys with metabolic parameters similar to those in humans with metabolic syndrome (dyslipidemia, insulin resistance, hyperinsulinemia, and hypertension). In this model, GW501516 induces a significant increase in HDL-cholesterol levels along with a reduction in TG. Elevated levels of plasma insulin are also suppressed by GW501516 treatment, whereas serum glucose levels are unaffected. These results suggest that PPAR-δ agonists may prove useful in the treatment of dyslipidemia, but it is important to note that this was a limited study with respect to species and compounds. The role of PPAR-δ in dyslipidemia requires further investigation.

Mass Stack Cycle in USA

Ligandrol (LGD-4033) has been originally intended for the treatment of age-related muscle loss and cancer. These days, Ligandrol is also used to increase muscle mass, and it has also positive effects on bone density and sex drive. All this without damage to prostate or liver tissue! Like Testolone, Ligandrol delivers some of the healing benefits of testosterone without the side effects.  Not only that, but Ligandrol is the most potent SARM when it comes to muscle size and gains. Ligandrol also works by selectively tying to androgen receptors, thus showing anabolic activity in the muscles and bones. Thanks to its selectivity, Ligandrol does not affect the prostate and sebaceous glands. When administered consistently, Ligandrol has also been shown to exhibit the following benefits:
  • Increase in lean muscle mass.
  • Increased strength levels.
  • Reduced body fat.
Unlike Testolone, Ligandrol produces a dirtier bulk. This is because the fat-burning properties of Ligandrol are not as prominent. With that said, this isn’t necessarily a downside if you want to not only gain lean body mass but also bodyweight. Andarine, also known as S-40503 or S-4 for short, is a selective androgen receptor modulator, or SARM. Pharmaceutical companies developed andarine for the treatment of osteoporosis and muscle wasting disease. The compound helps build stronger bones and muscle mass but is especially effective at decreasing body fat, providing body builders with “a cut look.” About SARMS

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SARMS is a broad term referring to various substances that bind to androgen receptors and activate in certain tissues such as muscle and bone. Though some early SARMS were steroidal in origin, the term SARMS commonly refers to a new and distinct category of drugs—Non-steroidal Selective Androgen Receptor Modulators—which is part of their appeal. Tissue selectivity is a key component of how SARMS are seen to work, bolstering gains in certain areas with less damage to other body parts such as the liver or prostate. SARMS continue to be evaluated for their potential to serve as effective medicines in combating muscle-wasting conditions and other disorders. The safety and efficacy of SARMS in general, however, has yet to be established and no SARM has been approved as a drug for human use.
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