Fat Burning / Anti - Aging 2mg Peptide CAS 140703-51-1

For Fat Burning 2mg Herarelin CAS 140703-51-1 Human Growth Hormone PeptideQuick Detail:

Name: PeptideSpecification: 2mg/vial 10vials/kit Supply Ability: 880 kits/month

191aa Human Growth Hormone kit for sale. . is a lyolized (freeze-dried) white powder packed in a sealed box containing 10 x 10 iu/vials.Detailed Description: is another hexapeptide like GHRP-6. Unlink the other GHRP’s out there, is the dark horse, the black sheep, the underdog not usually mentioned and often over looked for certain qualities. This grossly underestimated peptide shouldn’t be pushed to the side, but rather examined to understand its benefits and usability for bodybuilders and athletes alike.For starters is not your average GHRP. The structure of the amino acid is that of a hexapeptide known to help promote the release of growth hormone (GH). The mechanism of action is not yet fully understood by scientists. However, what we know is that has the ability to act both on the pituitary gland and the hypothalamus. It is known to give the largest release of GH than any other GHRP.Benefit:Interestingly, the most amazing finding with was its ability to act on cardiac receptors separate from the GH releasing properties. The peptide can directly aid in cardio protective left ventricular pressure issues, as well as, help healing scar tissue on the heart. Studies on lean and obese lab rats concluded that while lean rats were able to take advantage of the GH plasma increase better than the obese rats (the healthier the rat the more effectively produced and utilized GH), obese rats did not see the same advantage. Separate from the studies that monitored GH, both lean and obese rats both received all of the cardio protective properties of .

How does it work?When is given as a subcutaneous injection, it activates the pituitary via a pulse, just like GHRP-6, and helps circulate growth hormone in the body. Unlike GHRP-6, it does not induce any hunger side effects. has the ability to not only raise the level of GH in the body but to also suppress somatostatin, which is the main culprit that inhibits GH from being released. This means that there will be more GH in abundance. In addition, is the strongest GHRP available, so users should notice that desensitization can come much quicker than other GHRP’s. This makes it less ideal for long term use, but with ’s ability to raise healthy levels of IGF-1 and GH it can work perfect as a PCT tool for those coming off a synthetic GH/IGF-1 cycle. The potency of this peptide should not be underestimated and it comes with an increase in cortisol production as well as prolactin. Nothing close to what might be seen in elevated levels from use, but compared to other GHRP’s it has the strongest affinity to raise cortisol/prolactin.Dosage and Usage: comes in a freeze dried powder just like the other GHRP peptides and storage should be done in a cool dry place until reconstituted and placed in a refrigerator. Bacteriostatic water is used to reconstitute the powder and an insulin syringe is the preferred method for administering subcutaneous injections of . Users will notice 200mcgs is the saturation dose for and over a few weeks of use total desensitization may begin to take place. Also, the occasional flare up of the pituitary has been noted when dosing far beyond saturation doses. Desensitization can be cleared easily by taking a break from hexerlin usage for a few days to a few weeks. This GHRP is the strongest, and because of the desensitization factor, I believe the optimal way to use this peptide would be to blend it at low doses with other GHRP’s like GHRP2, GHRP6 or iPamorelin. By combining a low dose of hexearelin with another GHRP, you are going to increase your ability to put out a greater pulse of growth hormone. Combine this with GHRH’s and you have a synergistic blend that will release GH more effectively. In fact, for synthetic HGH users, this may be a viable way to save money on using less exogenous GH by combining it with in a GHRP+GHRH cycle. As a result, utilizing in this protocol would establish the maximum GH release in the body.Applications:The peak GH secretion rate following the first intravenous bolus of was greater than that following the first bolus of GHRH-(1-29)-NH2 (P < 0.001), and was greatest following the administration of with GHRH-(1-29)-NH2 (P < 0.001). The coadministration of the two secretagogues resulted in peak GH secretion rates significantly greater than the arithmetic sum of those following their isolated administration (P = 0.001), demonstrating synergism. Compared to sa administration of a second bolus of , GHRH-(1-29)-NH2 or both resulted in significant further GH secretion (P = 0.02, P = 0.002, P = 0.03, respectively). The administration of a second bolus of or with GHRH-(1-29)-NH2 120 minutes after the first bolus resulted in lower peak GH secretion rates (P = 0.03). The reductions in peak GH secretion rates following the 60-minute boluses were not statistically significant. The peak GH secretion rates following the first GHRH-(1-29)-NH2 boluses were similar to those following the 60 and 120-minute GHRH-(1-29)-NH2 boluses (P = NS). Irrespective of the interval between the boluses of with GHRH-(1-29)-NH2, the peak GH secretion rates following the second boluses were not significantly different from the arithmetic sum of those following the administration of the second boluses of or GHRH-(1-29)-NH2, indicating loss of synergism on repeated administration.