IN CHARGE OF A CHANGE

Testosterone Propionate is the shortest-estered testosterone steroid. It’s an injectable compound with a slower rate of release than un-esterified Testosterone, but a faster rate of release than all the rest of esterified testosterones. it is used in hormone replacement therapy, anti-aging and in treatment of muscular catabolism.

Androgen replacement therapy (ART), often referred to as testosterone replacement therapy (TRT), is a hormone treatment often prescribed to counter the effects of male hypogonadism. ART typically involves the administration of testosterone.

Testosterone Cypionate is an eight-carbon ester form of Testosterone. The number of ester carbon atoms correlate with the half-life of the prodrug. Testosterone inhibits gonadotropin secretion from the pituitary gland and ablates estrogen production in the ovaries, thereby decreasing endogenous estrogen levels. In addition, this agent promotes the maintenance of male sex characteristics and is indicated for testosterone replacement in hypogonadal males.

Testosterone suspension is a potent androgenic steroid and major product secreted by the leydig cells of the testis. Its production is stimulated by luteinizing hormone from the pituitary gland. In turn, testosterone exerts feedback control of the pituitary LH and FSH secretion. Depending on the tissues, testosterone can be further converted to dihydrotestosterone or estradiol.

Sustabolin contains, per mL, short-acting testosterone propionate, 60 mg of testosterone phenylpropionate, 60 mg of testosterone isocaproate, and 100 mg of testosterone decanoate. The first, testosterone propionate, is short-acting and gives Sustabolin a quick onset of action in a steroid cycle. The other esters are medium to long-acting.olves the administration of testosterone.

Bolde Depot can promote erythropoietin (EPO) stimulating factor that, in turn, stimulates the bone marrow growth that leads to an increased production of red blood cells. More red blood cell means more hemoglobin, and a higher oxygen carrying capacity. It may also result in changes to electrolyte levels because of its potent mineralocorticoid properties.

Nandrolone is the base hormone, commonly known by the trade name Deca Durabolin, which contains Nandrolone Decanoate. This popular preparation takes the nandrolone hormone and adds a decanoate ester chain. This ester chain is attached during the manufacturing process and it serves dual purposes. The main purpose is to make the hormone oil soluble, so it can be put in an amp or multi-dose vial. The second purpose of this ester chain is to slow-release the steroid by keeping deca from interacting with androgen receptors until the ester chain is cleaved off by enzymes in your body.

Nandrolone Phenylpropionate, also known as “NPP” is very similar to the very popular steroid “Deca” which is Nandrolone with a longer ester (Decanoate). Nandrolone Phenylpropionate is, therefore, a shorter acting “Deca” for all practical intents and purposes. Anecdotally, it seems to produce less water retention than its longer acting cousin, and this would be very consistent with injectable testosterones, where we find that shorter esters provide much less water retention..

Maste Depot is a synthetic anabolic steroid related to dihydrotestosterone that has antiestrogenic effects. Dromostanolone inhibits the growth of estrogen receptor-presenting breast cancers; its virilizing effects limit its clinical usefulness.

Winstrol has a unique ability to lower the amount of sex hormone-binding globulin (SHBG), more than any other steroid on the market. SHBG is a hormone that binds to other steroids in your cycle making them useless; in simple terms, it makes taking too much steroids useless as it neutralizes them. However, stanozolol allows you to stack multiple steroids in your cycle without the need to lower your dosages. An interesting stack would be winstrol and proviron, allowing for maximum SHBG reduction and maximizing cycle effectiveness.

As a derivative of DHT, metenolone, the active form of metenolone enanthate, is not aromatized, and so has no propensity for producing estrogenic side effects like gynecomastia.[6] As an AAS, metenolone enanthate is antigonadotropic and can suppress the hypothalamic–pituitary–gonadal axisand produce reversible hypogonadism and infertility.

As a derivative of DHT, metenolone, the active form of metenolone enanthate, is not aromatized, and so has no propensity for producing estrogenic side effects like gynecomastia.[6] As an AAS, metenolone enanthate is antigonadotropic and can suppress the hypothalamic–pituitary–gonadal axisand produce reversible hypogonadism and infertility.

Trenbolone has both anabolic and androgenic effects. Once metabolized, trenbolone esters have the effect of increasing ammonium ion uptake by muscles, leading to an increase in the rate of protein synthesis.

Trenbolone has both anabolic and androgenic effects. Once metabolized, trenbolone esters have the effect of increasing ammonium ion uptake by muscles, leading to an increase in the rate of protein synthesis.

Trenbolone (Tren) has been regarded by many as one of the strongest and most effective steroids to change your physique quickly. This steroid is part of the 19-nor family of steroids which are characterized by a modification at the 19th position. Like trenbolone, another popular steroid in this 19-nor family is the very popular Nandrolone (Deca Durabolin and NPP), although the real-world actions of these two steroids are very different.

Nicotinamide adenine dinucleotide (NAD⁺) is a coenzyme for redox reactions, making it central to energy metabolism. NAD⁺ is also an essential cofactor for non-redox NAD⁺-dependent enzymes, including sirtuins, CD38 and poly(ADP-ribose) polymerases. NAD⁺ can directly and indirectly influence many key cellular functions, including metabolic pathways, DNA repair, chromatin remodelling, cellular senescence and immune cell function. These cellular processes and functions are critical for maintaining tissue and metabolic homeostasis and for healthy ageing.

Semaglutide belongs to a class of medications known as glucagon-like peptide-1 receptor agonists, or GLP-1 RAs. It mimics the GLP-1 hormone, released in the gut in response to eating.

One role of GLP-1 is to prompt the body to produce more insulin, which reduces blood sugar (glucose). For that reason, health care providers have used semaglutide for more than 15 years to treat Type 2 diabetes.