For Research Use Only , ,

Sermorelin, Ipamorelin 10mg (Blend)

$95.00

Sermorelin and Ipamorelin is a research peptide blend that combines a GHRH analog with a ghrelin receptor agonist to examine growth hormone regulation. Sermorelin (GHRH 1–29) activates the GHRH receptor to increase cAMP/PKA signaling, while Ipamorelin stimulates GHS-R1a through Gq/11-coupled calcium flux. This blend is employed in preclinical models investigating endocrine peptide synergy, GH release kinetics, and hypothalamic–pituitary signaling mechanisms.

For research use only. Not for human consumption.

References:
Bowers CY et al., Endocrinology, 1990 126(2):1165–1171
Frohman LA et al., Front Neuroendocrinol, 2002 23(3):257–291
Kojima M et al., Nature, 1999 402(6762):656–660

Overview

Sermorelin and ipamorelin are synthetic peptide analogs frequently examined in parallel within laboratory research settings to study growth hormone axis regulation. Sermorelin is a truncated analog of growth hormone–releasing hormone (GHRH), while ipamorelin is a highly selective agonist of the growth hormone secretagogue receptor (GHS-R1a). Their combined use in experimental models allows investigation of coordinated receptor activation within endocrine signaling networks.

Biochemical Characteristics

Sermorelin is composed of the first 29 amino acids of endogenous GHRH and retains high affinity for the GHRH receptor. Ipamorelin is a pentapeptide engineered for selective ghrelin receptor engagement with minimal interaction with other pituitary hormone pathways in comparative assays. Both peptides demonstrate structural features optimized for receptor specificity in controlled research environments.

Research Applications

In preclinical research, sermorelin is utilized to study GHRH-mediated signaling, somatotroph activation, and downstream transcriptional regulation. Ipamorelin is employed to evaluate ghrelin receptor signaling dynamics, calcium mobilization, and secretagogue pathway selectivity. Combined experimental paradigms focus on endocrine pulsatility, receptor cross-talk, and downstream molecular responses.

Pathway / Mechanistic Context

Sermorelin activates the GHRH receptor, initiating Gs-protein–coupled signaling that elevates intracellular cAMP and activates protein kinase A–dependent transcriptional pathways. Ipamorelin binds to GHS-R1a, stimulating phospholipase C activity and intracellular calcium release. In combination, these peptides are studied for their complementary modulation of growth hormone regulatory circuits in animal and cellular models.

Preclinical Research Summary

Animal and in-vitro studies have investigated GHRH and ghrelin receptor expression in cardiac, neural, skeletal, and gastrointestinal tissues. Experimental findings include observations related to cellular survival signaling, inflammatory marker modulation, vascular remodeling processes, neural receptor interactions, skeletal metabolism markers, pancreatic signaling pathways, and gastrointestinal motility models. All findings originate from preclinical laboratory research and are used solely to advance mechanistic understanding.

Form & Analytical Testing

Sermorelin and ipamorelin are supplied as lyophilized peptides for laboratory research use. Analytical verification commonly includes high-performance liquid chromatography (HPLC) and mass spectrometry to confirm peptide identity, purity, and batch consistency prior to experimental application.

Article Author

Research by L. Edmiston, M.D. for Peptide Sciences. L. Edmiston holds an M.D. from Case Western Reserve University School of Medicine and a B.S. in molecular biology.

Scientific Journal Author

Richard F. Walker, Ph.D, R.Ph, lead author of A better approach to management of adult-onset growth hormone insufficiency?”, received a BS in pharmacy from Rutgers University, a MS in Biochemistry from New Mexico State University and a PhD in a physiology from Rutgers University. He holds postdoctoral fellowships in neuroendocrinology and neuropharmacology at Duke University College of Medicine (Center for the Study of Aging and Human Development) and the University of California, Berkeley, respectively.

Richard F. Walker, Ph.D, R.Ph is being referenced as one of the leading scientists involved in the research and development of Sermorelin. In no way is this doctor/scientist endorsing or advocating the purchase, sale, or use of this product for any reason. There is no affiliation or relationship, implied or otherwise, between Peptide Sciences and this doctor. The purpose of citing the doctor is to acknowledge, recognize, and credit the exhaustive research and development efforts conducted by the scientists studying this peptide. Richard F. Walker, Ph.D, R.Ph is listed in [11] under the referenced citations.

Referenced Citations

  1. L. L. Bagno et al., “Growth Hormone–Releasing Hormone Agonists Reduce Myocardial Infarct Scar in Swine With Subacute Ischemic Cardiomyopathy,” J. Am. Heart Assoc. Cardiovasc. Cerebrovasc. Dis., vol. 4, no. 4, Mar. 2015. [PubMed]
  2. R. M. Kanashiro-Takeuchi et al., “New therapeutic approach to heart failure due to myocardial infarction based on targeting growth hormone-releasing hormone receptor,” Oncotarget, vol. 6, no. 12, pp. 9728–9739, Mar. 2015. [PubMed]
  3. T. Tokudome, K. Otani, M. Miyazato, and K. Kangawa, “Ghrelin and the heart,” Peptides, vol. 111, pp. 42–46, 2019. [PubMed]
  4. S. Tang et al., “Interactions between GHRH and GABAARs in the brains of patients with epilepsy and in animal models of epilepsy,” Sci. Rep., vol. 7, Dec. 2017. [PubMed]
  5. B. S. Shepherd et al., “Endocrine and orexigenic actions of growth hormone secretagogues in rainbow trout (Oncorhynchus mykiss),” Comp. Biochem. Physiol. A. Mol. Integr. Physiol., vol. 146, no. 3, pp. 390–399, Mar. 2007. [PubMed]
  6. N. B. Andersen, K. Malmlöf, P. B. Johansen, T. T. Andreassen, G. Ørtoft, and H. Oxlund, “The growth hormone secretagogue ipamorelin counteracts glucocorticoid-induced decrease in bone formation of adult rats,” Growth Horm. IGF Res. Off. J. Growth Horm. Res. Soc. Int. IGF Res. Soc., vol. 11, no. 5, pp. 266–272, Oct. 2001. [PubMed]
  7. J. Svensson et al., “The GH secretagogues ipamorelin and GH-releasing peptide-6 increase bone mineral content in adult female rats,” J. Endocrinol., vol. 165, no. 3, pp. 569–577, Jun. 2000. [PubMed]
  8. N. K. Aagaard et al., “Growth hormone and growth hormone secretagogue effects on nitrogen balance and urea synthesis in steroid treated rats,” Growth Horm. IGF Res. Off. J. Growth Horm. Res. Soc. Int. IGF Res. Soc., vol. 19, no. 5, pp. 426–431, Oct. 2009. [PubMed]
  9. E. Adeghate and A. S. Ponery, “Mechanism of ipamorelin-evoked insulin release from the pancreas of normal and diabetic rats,” Neuro Endocrinol. Lett., vol. 25, no. 6, pp. 403–406, Dec. 2004. [PubMed]
  10. D. E. Beck, W. B. Sweeney, M. D. McCarter, and Ipamorelin 201 Study Group, “Prospective, randomized, controlled, proof-of-concept study of the Ghrelin mimetic ipamorelin for the management of postoperative ileus in bowel resection patients,” Int. J. Colorectal Dis., vol. 29, no. 12, pp. 1527–1534, Dec. 2014. [PubMed]
  11. R. F. Walker, “Sermorelin: A better approach to management of adult-onset growth hormone insufficiency?,” Clin. Interv. Aging, vol. 1, no. 4, pp. 307–308, Dec. 2006. [PubMed]

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RUO Disclaimer

The products offered on this website are furnished for in-vitro studies only. In-vitro studies (Latin: in glass) are performed outside of the body. These products are not medicines or drugs and have not been approved by the FDA to prevent, treat or cure any medical condition, ailment or disease. Bodily introduction of any kind into humans or animals is strictly forbidden by law.

For Laboratory Research Only. Not for human use, medical use, diagnostic use, or veterinary use.

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