Drugs profiles

Insulin is peptide hormone produced in the pancreas. The release of this hormone in the human body is most closely tied to blood glucose levels, although a number of other factors including pancreatic and gastrointestinal hormones, amino acids, fatty acids, and ketone bodies are also  involved. The main biological role of insulin is to promote the intracellular utilization and storage of amino acids, glucose, and fatty acids, while simultaneously inhibiting the breakdown of glycogen, protein, and fat. It is most notably identified with the control of blood sugar levels, and insulin medications are typically prescribed to people with diabetes, a metabolic disorder characterized by high  blood  sugar. While insulin targets many organs in the body, this hormone is both anabolic and anti-catabolic to muscle tissue. Insulin first became available as a medicine during the 1920’s. The first insulin preparations made were produced from crude pancreatic extracts taken from dogs. At one point when the supply of dead dogs ran out, the group actually started taking stray dogs off the streets in order to use. Soon after it was  discovered that cows and pigs worked as well that had been slaughtered and this made the research and development much more convenient and acceptable to the public. In 1974, chromatographic purification techniques allowed the manufacture of animal insulin with extreme purity. The pharmaceutical company Novo was the first to release a drug made with this technology.

Melanotan II was developed originally as potential preventative treatments for various forms of skin cancer. It was thought that by artificially stimulating the internal tanning process among members of the population that were at high risk to develop skin cancer due to sun exposure that one may be able to lower the chances of these individuals from developing the disease later in life. While these findings have been relatively inconclusive in terms of the original intent of the product a few secondary uses for the drug have been found and are now utilized by many.

Isotretinoin is an anti-acne medication that is chemically related to retinoic acid and retinol (vitamin A). Although its exact mode of action is unknown, this agent works by inhibiting sebaceous gland functioning, which diminishes oil production in the skin and hinders acne development. This product is sold in many countries throughout the world, and is largely recognized as one of the most effective medications available for treating severe acne. Studies also suggest that it has one of the highest success rates with even the strongest cases of clinical acne. Given that acne is one of the most common side effects of anabolic/androgenic steroid use, isotretinoin is utilized by bodybuilders and athletes to reduce or eliminate this cosmetic issue  during steroid therapy. Isotretinoin was developed by the pharmaceutical company Hoffmann-La Roche, and was first introduced as a drug medication in 1982. The company marketed it under the brand name of Accutane, and retained the patent rights until 2002. Now that the patent has expired, there are a number of generic versions of the drug available. Isotretinoin is not a controlled substance, but has been regulated by the FDA in recent years due to potential side effects. Due to this, there are some very strict guidelines in place for prescribing the drug. Isotretinoin is most  commonly supplied in soft gel like capsules of 10, 20, and 40mg.

Albuterol sulfate is a selective beta-2 adrenergic agonist, very similar in structure and action to the popular weight loss aid clenbuterol. Unlike clenbuterol, however, albuterol is readily available as a prescription drug in the United States. It is also sold under other brand names in a number of  other countries worldwide. Albuterol is most commonly found in the form of a rescue inhaler, which is designed to disperse a measured amount of the drug immediately and directly to the bronchial tubes in times of crisis (asthma attack). This form provides the least amount of systemic drug activity possible, which is great for minimizing unwanted cardiovascular side effects. Albuterol oral tablets are also available, however, and provide a systemic drug activity possible, which is great for minimizing unwanted cardiovascular side effects. Albuterol sulfate was introduced to the U.S drug market in 1980, sold under the Ventolin brand name. Albuterol sulfate has grown to be one of the most popular drugs in history for the management of acture asthma attacks. As a result, many other companies have invested in the market. The FDA has approved a number of generic preparations of the drug.

Bromocriptine mesylate is a dopaminomimetic ergot derivative with D2 dopamine receptor agonist and D1 dopamine receptor antagonist activities. It is used most commonly as a prolactin inhibitor in cases of hyperprolactinemia, a growth hormone suppressant in acromegaly, and as an adjunctive medication to elodea in the management of Parkinson’s disease. The structure and activity of this drug are very similar to that of cabergoline. In the bodybuilding and athletic communities, bromocriptine is sometimes used to induce fat loss or combat elevated prolactin levels. The human medical data concerning the potential role this drug might play in supporting ongoing fat loss is encouraging. In cases where it was given while dieting, bromocriptine was capable of increasing total fat loss by a statistically significant degree, and seemed to extend the duration in which the diet was most effective. Bromocriptine has been used widely in clinical medicine for its indicated use since the 1970s. It is also much more widely distributed than its counterpart medication cabergoline, which is used for a similar set of clinical indications. In the U.S., the most common brand name for this drug Parlodel, which is sold by the pharmaceutical company Novartis.

Cialis is a drug used for the treatment of erectile dysfunction in men. The drug is FDA approved in the U.S. and is available from the pharmaceutical company Eli Lilly. There are also several generic preparations available worldwide. This drug has became on the most popular drugs for erectile dysfunction today. For the purposes of steroid users the use of tadalafil citrate is rather limited beyond that of a “recreational” purpose. One exception to this may be once a steroid user is coming off of anabolic-androgenic steroids and have suffered a significant reduction in their ability to perform sexually and/or their sex drive. The use of drugs such as tadalafil citrate can help to alleviate some of the difficulty many have during this period of time.

Clenbuterol is an anti asthma medication that belongs to a broad group of drugs known as sympathomimetics. These drugs affect that sympathetic nervous system in a wide number of ways, largely mediated by the distribution of adrenoceptors. There are actually nine different types of these receptors in the body, which are classified as either alpha or beta and further subcategorized by type number of ways, largely mediated by the distribution of adrenoceptors. Clenbuterol has been available as a bronchodilator for decades and is widely used in many parts of the world. Although it has a good safety record and approval in a wide number of other countries, this compound has never been made available for human use in the United States. The fact that there are a number of similar effective asthma medications already approved by the FDA and available may have something to do with this.

Liothyronine sodium is a synthetically manufactured prescription thyroid hormone. It specially consist of the the L-isomer of the natural thyroid hormone triiodothyronine (T3). Thyroid hormone stiumlate basal metabolic rate, and are involved with many cellular functions including protein, fat, and carbohydrate metabolism. Liothyronine sodium is used medically to treat hypothyroidism, a condition where the thyroid gland does not produce sufficient levels of thyroid hormone. Hypothyroidism is usually diagnosed with a serum hormone profile, and may manifest itself with symptoms including loss of energy, lethargy, weight gain, hair loss, and changes in skin texture. The first medication that included T3 was technically a thyroid extract, first given to a patient with my edema in 1891. Natural thyroid extracts contained therapeutically viable levels of the thyroid hormones T3 and T4, and were widely used in medical practice for more than 60 years. In the 1950s, however, these drugs slowly start giving way to new synthetic thyroid medications, namely liothyronine sodium and levothyroxine sodium, which were consistent in dosage and effect, and more desirable to consumers than prepared animal extracts. Although liothyronine sodium and levothyroxine sodium are both widely available in the U.S. and abroad to this day, liothyronine retains a significantly smaller portion of the global thyroid market. Given its more potent and fast acting effect, however, liothyronine sodium remains a popular thyroid drug with bodybuilders and athletes. Liothyronine sodium is most commonly supplied in oral tablets of 5mcg, 25mcg, and 50mcg.

DNP is one of the most controversial drugs in use by bodybuilders. This agent is not sold for human use anywhere in the world at this time, but is readily available as an industrial chemical. Among other things, it is used an intermediary for the production of certain dyes, for photographic development, as a fungicide, in wood pressure treatment to prevent rotting, and as insecticide. It  is technically classified as a posion. The fat loss properties of DNP were reportedly first noticed during World War 1, when overweight men working with DNP in munitions plants started losing substantial amounts of weight. It did not take very long for this chemical to be identified as the cause. Soon after, it ws packaged as a drug product. By 1935, more than 100,000 Americans had already used “patent mediine” remedies that included the drug. DNP was the first synthetic drug that was ever used for weight loss in the United States. There were several popular brand names for the drug when it was marketed and was found in pharmacies all across the country. This drug was introduced before the time of government reviewed safety concerning drugs and medications. It wasn’t long after the drug was on the market that reports of severe side effects started coming in. There was a report of women who went blind temporarily in California. After this, reports of cases severe as death started being reported and by 1938 DNP was off the market for good. It has never since been re introduced as a medicine of any kind for humans or animals.

Cabergoline is a selective dopamine receptor agonist. This agent is highly specific in its actions, with a strong affinity for the dopamine D2 receptor, and a low affinity for dopamine D1, A1-adrenergic, A2-adrenergic, 5-HT1-serotonin, and 5-HT2-serotonin receptors. Its main clinical use is for the treatment of hyperprolactinemia, or the hyper secretion of prolactin from lacto tropes in the anterior pituitary. It is also used in the management of Parkinson’s disease. This drug effectively inhibits prolactin secretion by mimicking the actions of dopamine on the D2 receptor. Cabergoline was developed during the 1980s. The most popular brand name for the drug is Dostinex, which is produced in the United States and many other countries around the world by the large pharmaceutical company Pharmacia. This company did have exclusive rights to the sale of the drug until 2005 when the FDA began approving several generic brands of the drug for use. The Dostinex brand still dominates the global market. Cabergoline is most commonly found in tablets of 500mcg each.