Peptide Guide
A peptide is a compound consisting of two or more amino acids linked in a chain, the carboxyl group of each acid being joined to the amino group of the next by a bond.
Peptide Guide
BPC 157
BPC 157 is a peptide of a sequence of amino acids with a molecular formula of 62 carbons, 98 hydrogens, 16 nitrogens, and 22 oxygen atoms (C62-H98-N16-O22). BPC stands for ?Body Protecting Compound?. BPC-157 accelerates wound healing, and, via interaction with the Nitric Oxide (NO) system, causes protection of endothelial tissue and an ?angiogenic? (blood vessel building) wound healing effect. BPC 157 is surprisingly free of side effects, and has been shown in research that?s been happening since 1991 to repair tendon, muscle, intestines, teeth, bone and more, both in in-vitro laboratory ?test-tube? studies, in in-vivo human and rodent studies, and when used orally or inject subcutaneously (under your skin) or intramuscularly (into your muscle). BPC-157 is also known as a ?stable gastric pentadecapeptide?, primarily because it is stable in human gastric juice, can cause an anabolic healing effect in both the upper and lower GI tract, has an antiulcer effect, and produces a therapeutic effect on inflammatory bowel disease (IBD) ? all again surprisingly free of side effects.
CJC-1295 with DAC
CJC-1295 is a tetra substituted peptide made up of thirty amino acids. It has been shown through scientific research studies to bio-conjugate to the protein serum albumin which provides an advanced level of homeostasis in animals being tested. The use of CJC-1295 with DAC prevents the production of DPP-IV from occurring as determined in scientific studies with the animal test subjects. This results in the GHRH1-29 experiencing an extended half-life, one which can last over seven days. With the increased stabilization of GHRH1-29, growth hormones are able to function at greater levels and test subjects are then able to experience an increased level of stability in the growth hormones. CJC-1295 with DAC is the preferred and more powerful GHRH component in a peptide protocol. Throughout scientific studies, it has been understood the presence of CJC-1295 with DAC allows for a few elevated processes test subjects experience. This includes Muscular Tissue Growth, Increased Bone Density and Body Fat Reduction.
CJC-1295 w/o DAC
CJC-1295 without DAC is a 30 amino acid peptide hormone, better known in the community as a GHRH (growth hormone releasing hormone). Essentially, what this means is this peptide will release a series of pulses over a long period of time which usually equates to fewer injections. Even though CJC-1295?s main function upon creation was found to boost protein synthesis, increased growth of muscle tissue and many other benefits come with it as well. CJC-1295 also helps injury recovery times, reduce body fat, boost immune system and bone density and cellular repair (skin and organs). The term CJC 1295 without DAC this is really means that they are looking at MOD GRF 1-29. And this modification had resulted in a greater peptide bond, the average user will still likely need to inject two to three times a day with a GHRP to get the maximum effectiveness for releasing endogenous growth hormone. If you prefer to use shorter spikes of GH release then the use of the MOD GRF 1-29 (CJC 1295 without DAC) is optimal.
DSIP
DSIP stands for Delta sleep-inducing peptide. This type of peptide is classified as a neuropeptide and it works by inducing spindle and delta EEG activity and by reducing motor activity. This peptide is utilized in order to help people fall asleep and stay asleep. This peptide is popular with bodybuilders who have learned about the power and potential of peptides through their training and supplementation regimens. DSIP lowers basal corticotropin levels and blocks their release. It also makes it easier for the body to release LH (luteinizing hormone). In addition, it makes it simpler for the body to release somatotrophin (and somatoliberin secretions) and to block the production of somatostatin. This peptide may help people to manage stress. In addition, it may have the power to alleviate the symptoms of hypothermia. It?s also known as an effective means of normalizing blood pressure and contractions which are myocardial. As well, it may offer anti-oxidant benefits (slow down cell damage).
Epitalon
Epitalon (a.k.a. epithalon or epithalone) is a synthetically-derived tetrapeptide, meaning that it consists of four amino acid chains. It was discovered by the Russian scientist Professor Vladimir Khavinson, who then conducted epitalon-related research for the next 35 years in both animal and human clinical trials. Epitalon?s primary role is to increase the natural production of telomerase, a natural enzyme that helps cells reproduce telomeres, which are the protective parts of our DNA. This allows the replication of our DNA so the body can grow new cells and rejuvenate old ones. Furthermore, Epitalon has been shown to inhibit the growth of cancerous tumors, enabling a longer and healthier life in the future. And research has shown that epitalon is a powerful antioxidant that eliminates oxygen-free radicals responsible for damaging and killing cells. As a result of epitalon?s effect on telomerase production, the benefits are unique and far-reaching. Benefits of epitalon include: Increase of human lifespan Significant boosting of energy levels Promotion of deeper sleep Delay and prevention of age-related diseases such as cancer, heart disease and dementia Improvement of skin health and appearance Healing of injured and deteriorating muscle cells
Follistatin
Follistatin is an inhibitor of TGF-β superfamily ligands that repress skeletal muscle growth and promote muscle wasting. Accordingly, follistatin has emerged as a potential therapeutic to ameliorate the deleterious effects of muscle atrophy. In the setting of disease, increasing follistatin expression in musculature has proven beneficial for improving aspects of pathology in dystrophin-deficient mdx mice that model Duchenne and Becker muscular dystrophy (DMD, BMD). Administration of recombinant follistatin has also been shown to promote muscle hypertrophy in wild-type mice, and ameliorate the progression of a mouse model of spinal muscular atrophy (SMA).
GHRP-2
GHRP-2 is a synthetic agonist of ghrelin, the newly-discovered gut peptide which binds to the growth hormone (GH) secretagogue receptor. Ghrelin has been shown to have two major effects, stimulating both GH secretion and appetite/meal initiation. GHRP-2 has been extensively studied for its utility as a growth hormone secretagogue (GHS). Animal studies have shown its effect on food intake. However, whether GHRP-2 can also stimulate appetite in humans when administered acutely is not known. When administered either centrally or peripherally to rodents, ghrelin increases food intake and body weight. Interestingly, its effects on food intake are independent of GH secretion and appear to be mediated via the NPY/Agouti gene-related protein (AGRP) neurons in the hypothalamic arcuate nucleus. Peripheral ghrelin administration has recently been shown to stimulate food intake in lean, healthy men and women and in cancer patients.
GHRP-6
GHRP-6 is an injectable peptide in the category of growth hormone releasing peptides, or GHRP?s. The most common use of these peptides is to increase GH production. Other peptides in this category include GHRP-2, hexarelin, and ipamorelin. With regard to increasing GH, all of these work similarly, and there is no need or advantage to combining them. Instead, the one most suited for the particular case is chosen. The principal use of GHRP-6 is to provide increased GH levels, which also results in increased IGF-1 levels. This aids fat loss and in some instances aids muscle gain as well. Generally, GHRP use is chosen as an alternate to GH use, and only rarely is combined with GH. GHRP-6 is most generally used for the same purposes that GH might be used, but may be chosen where a cost advantage exists favoring GHRP-6, GH is not available, or the individual prefers the idea of stimulating his own GH production to injecting GH. These purposes can include increased fat loss, improved muscle gain when used in combination with anabolic steroids, cosmetic improvement of the skin, and improved healing from injury.
Hexarelin
Hexarelin is a peptide that can promote the secretion of certain hormones. It is a hexipeptide that consists of six amino acids that can release certain hormones as they are needed. It has a half-life of about 70 minutes. Some studies have derived several different effects linked to its use, including elevated levels of fat loss, connective tissues, density of bone minerals, meiosis, mitosis, and elasticity. In turn, these effects have led to animal test subjects experiencing improved endurance, joint rehabilitation, wound healing, and improved muscle strength. Studies also conclude that Hexarelin?s functionality can last a long stretch of time. Furthermore, scientific studies on animal test subjects have determined that Hexarelin does not induce an increased desire for food consumption. The peptide achieves this because it does not increase the levels of ghrelin; the amino acid peptide that clears out the gastric system and induces hunger. Further scientific studies have also determined that the peptide promotes an increase in the secretion of IGF-1 from the liver of animal test subjects. This additional secretion plays a key role in breaking down fat and improving strength.
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