GH-axis research
Sermorelin
Lyophilized endocrine-signaling research peptide for systems review
Sermorelin is a GHRH 1-29 analog studied as a classic pituitary GH-axis research reference.
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Get catalog updates仅供实验室研究使用。不适用于人类或兽医用途。并非旨在诊断、治疗、治愈、减轻或预防疾病。
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研究背景
Sermorelin 研究资料
Sermorelin is a 29-amino-acid analog corresponding to the active amino-terminal region of growth hormone-releasing hormone. It is used as a classic reference for pituitary GHRH-receptor signaling, stimulated GH release, endocrine responsiveness, and downstream IGF-1 measurements. Compared with CJC-1295 with DAC, sermorelin represents a shorter GHRH framework without the same half-life-extension design. Compared with ipamorelin and GHRP peptides, it acts through a different receptor pathway. Researchers generally select sermorelin when the study calls for a well-established GHRH 1-29 reference or a direct comparison of pituitary signaling across GHRH analogs and ghrelin-receptor secretagogues.
Molecular class
44-residue GHRH 1-44 analog
Sequence / composition
A synthetic amino-terminal 44-residue segment corresponding to the receptor-active region of human GHRH.
Research design note
It is a direct GHRH-receptor reference, unlike GH secretagogues that act through GHS-R.
拟议机制
A synthetic GHRH(1-29) peptide that activates the pituitary GHRH receptor, increases cyclic AMP, and stimulates endogenous growth-hormone release from responsive somatotroph cells.
研究中报告的作用
- Human diagnostic and pharmacology studies reported acute GH release and used the response to evaluate pituitary reserve.
- Downstream changes can include transient increases in GH and IGF-1-related markers when repeated exposure is studied.
- Responses vary with age, pituitary function, endogenous somatostatin tone, timing, and prior exposure.
常见研究终点
GHRH receptor signaling, cyclic AMP, peak and integrated GH, IGF-1, pituitary responsiveness, age-related response, pharmacokinetics, and comparison with longer-acting GHRH analogs.
证据与局限
The GHRH stimulation mechanism is well characterized, including historical human diagnostic use. This does not establish therapeutic equivalence of a catalog product.
External reading
Literature for context—not product proof.
Third-party sources describe their own research materials and methods. They do not validate a specific Azure catalog batch.
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