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Ketotifen is an antihistimine that inhibits down regulation of beta receptors, which are often degraded by fat-burners such as Albuterol and Clenbuterol.
It can be used in combination with these other drugs in order to keep feeling their fat-burning effects for longer periods of time with out the need for periods of on and off cycling.
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So what will ketotifen do with regards to our research that no other compound will? Well when administered with a beta 2 adrenergic agents such as clenbuterol or albuterol it will allow the compound to remain effective for a longer duration, at a lower effective dose. This eliminates the need for dangerously administering very high doses to research subjects which may come along with higher risks and undesirable side effects. It also allows us to administer the beta 2 agonist continuously without a reduction in effectiveness. This will lead to us observing much faster results in our research than if we were required to stop administration or adapt a 2 week on, 2 week off protocol to our research subjects.
Ketotifen has 2 primary effects. First off it is an h1 antihistamine. There are 2 types of antihistamines, h1 and h2. A primary difference is h1 antihistamines cross the blood brain barrier in research subjects and are known to induce drowsiness as a result of this. Ketotifen, being an h1 antihistamine is known to induce this effect. Secondly it is a mast cell stabilizer. Mast cells are cells that are rich in histamine. They are activated via calcium channel transfer; ketotifen blocks this calcium channel transfer. This is of particular note as clenbuterol , via cAMP, activates this calcium channel transfer.
The synergy between clenbuterol and ketotifen in research subjects is complicated to say the least. I mean in all reality they BOTH exhibit antihistamine effects, yet while displaying a synergy at making the other more effective. Just as ketotifen prevents the down regulation of beta 2 receptors, clenbuterol prevents the very same effect in histamine receptors! Luckily for our purposes there is a definitive study which proves that the addition of ketotifen increases the effectiveness of clenbuterol in research subjects. There is also a study which proves its effects on prevention of down regulation of b2 adrenergic receptors. Sometimes science makes it a bit easier. Published, peer reviewed studies proving the effectiveness and synergy of 2 research compounds.
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Using CJC 1295 in conjunction with a GHRP product as a means of enhancing general anabolism / fat burning as part of a wider stack containing steroid hormones if you are looking to achieve the highest level of anabolism possible.
PT-141 is also known as Bremelanotide and is most known for its ability to treat sexual dysfunction in men and women. It is a derivative of Melanotan 2. It’s a synthetic peptide blend, as it isn’t naturally produced in the body like growth hormones are. PT 141 was developed from the Melanotan 2 hormone which is known to help darken pigmentation of the skin. It has often been linked to individuals treating sexual disorders (including ED or hypoactive sexual desire in women).
An ideal peptide in muscular development, IGF-1 – LR3 (insulin-like growth factor) peptide by Axiom Peptides belongs to the family of peptides with an identical structure to that of insulin. This is a highly anabolic hormone that is released in the liver and in peripheral tissues in response to GH so that new muscle fibers are constructed.
Peptides play a very important role in sports. They provide the body with the necessary building blocks to be able to produce amino acids, which are used in building muscle mass. They also contain the perfect arrangement of amino acids. Remember, they do not require digestion because they have been broken down into smaller peptides. This means that they are quickly absorbed into the body. They are also the perfect choice for any athlete.
