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TB-500 is a synthetic fraction of the protein thymosin beta-4, which is present in virtually all human and animal cells. It consists of 43 amino acids and the gene, TMSB4X encodes it.
Thymosin beta 4 is produced in high concentrations in damaged tissues. TB-500 purports to promote endothelial cell differentiation, angiogenesis, keratinocyte migration, collagen deposition, and decreased inflammation. The healing effect of TB-500 is observed in tendons, ligaments, muscle, skin, heart, and eyes.
After an injury, thymosin beta 4 is released by platelets, macrophages, and many other cell types, to protect cells and tissues from further damage and reduce apoptosis, inflammation and microbial growth. Thymosin beta 4 binds to actin and promotes cell migration, which includes the mobilization, migration, and differentiation of stem/progenitor cells, which form new blood vessels and regenerate the tissue. Thymosin beta 4 also decreases the number of myofibroblasts in wounds, resulting in decreased scar formation and fibrosis.
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CJC-1295 is a synthetic analog of the Growth Hormone-Releasing Hormone. With a substitution of four amino acids, it is more resistant to proteolytic inactivation by dipeptidyl peptidase IV (DPP-IV). When combined with Drug Affinity Complex (DAC), it prolongs its half-life, as well as the duration of action in test subjects.
Studies in animals (rats, pigs, and dogs) show that serum IGF-I levels increase several days after a single administration of CJC-1295 with DAC. It sustained a dose-dependent stimulation of serum GH and IGF-I levels when injected into healthy subjects at intervals of 1-2 weeks.
It increases plasma levels of growth hormone from somatotropic cells in the pituitary gland of animal test subjects, without altering its pulsation. It doesn’t inhibit the effects of somatostatin.
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ABOUT GHRP-6: It belongs in the family of the Growth Hormone secretagogue, meaning that it causes the secretion of growth hormone. It is a synthetic hexapeptide and a met-enkephalin derivative that contains a chain of 6 unnatural D amino acids.
It has no structural similarity with Growth Hormone Releasing Hormone (GHRH) and works by utilizing specific receptors present in cell cultures of the animal pituitary gland or hypothalamus.
GHRP-6 has cytoprotective effects that are non-growth Hormone-related which include neuroprotective, cardioprotective, anti-inflammatory as well as hepatoprotective effects.
Studies in animal test subjects show that GHRP-6 stimulates Ghrelin, “the hunger hormone” through its ghrelin receptor, which in turn signals an increased production of growth hormone (GH) by acting at the level of the pituitary or hypothalamus through a specific receptor different from that of the endogenous Growth Hormone-Releasing Hormone GHRH.
The four parts of the animal test subjects that demonstrate the role of GHRP-6 include the pituitary gland, central nervous system, liver, and stomach.
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Mechano Growth Factor (MGF) is a synthetically manufactured peptide that is an alternative splicing variant of Insulin-like Growth Factor-1 (IGF-1). It serves as a local tissue repair factor that responds to changes in physiological conditions or environmental stimuli inducing muscle cell proliferation. It may function as a neuroprotectant in brain ischemia seen in animal studies.
The level of growth hormone decreases when animals’ age. Several studies show that intensive exercise may stimulate the release of growth hormone in the presence of MGF. This peptide upregulates protein synthesis and activates satellite cells. It is a potent inducer of muscle hypertrophy in experiments.
It has a relatively short half-life of only a few minutes and is often modified to Pegylated-Mechano Growth Factor (PEG-MGF), increasing its stability.
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