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Mod GRF 1-29

Sermorelin, Growth Hormone Releasing Hormone (1-29), hGRF(1-29)NH2

A synthetic peptide analog of growth hormone-releasing hormone that stimulates the pituitary gland to secrete growth hormone.

Quick Stats
Studies 227
Trials 47
Formula C149H246N44O42S
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Utility 2
pubmed 1987

Mechanisms of calcitonin-induced growth hormone (GH) suppression: roles of somatostatin and GH-releasing factor.

Lengyel. A M AM; Tannenbaum. G S GS

The study shows that giving calcitonin directly into the brain of rats sharply cuts down the natural pulses of growth hormone (GH). This suppression isn’t because more somatostatin (a hormone that blocks GH) is released, and it also makes the pituitary less responsive to GH‑releasing factor (GRF). In short, calcitonin can blunt GH spikes via a central brain mechanism.

Utility 2
pubmed 1986

Superactive amidated COOH-terminal glucagon analogues with no methionine or tryptophan.

Murphy. W A WA; Coy. D H DH; Lance. V A VA

Researchers made modified versions of glucagon, a hormone that raises blood sugar, and found some changes made it work much better at breaking down glycogen in rats. The most active version was over five times stronger than normal glucagon, while other tweaks made it weaker. These results show that certain spots on the glucagon molecule can be altered without losing function, and sometimes even improve it.

Utility 2
pubmed Oct 15, 1984

Administration of human pancreatic growth hormone-releasing factor (GRF) analogs enhances responsiveness of cultured rat pituitary cells to GRF.

Heiman. M L ML; Murphy. W A WA; Nekola. M V MV; Lance. V A VA; Coy. D H DH

In rats, giving a growth hormone‑releasing factor (GRF) peptide for a few days made the pituitary gland more sensitive to that same peptide later on, but it didn’t change how the gland responded to a different hormone. This shows the gland can be “primed” by repeated GRF exposure.

Utility 2
pubmed 1985

Interaction of growth hormone-releasing factor (GRF) and 14 GRF analogs with vasoactive intestinal peptide (VIP) receptors of rat pancreas. Discovery of (N-Ac-Tyr1,D-Phe2)-GRF(1-29)-NH2 as a VIP antagonist.

Waelbroeck. M M; Robberecht. P P; Coy. D H DH; Camus. J C JC; De Neef. P P; Christophe. J J

The study shows that the natural growth‑hormone‑releasing factor (GRF‑1‑29) and several modified versions can bind to the same receptors that the hormone VIP uses in the rat pancreas. One specially modified peptide, (N‑Ac‑Tyr1,D‑Phe2)‑GRF(1‑29)‑NH2, blocks both VIP and GRF actions, acting like a VIP antagonist. Changing certain amino‑acid positions (especially 6 and 7) or swapping them for D‑forms makes the peptides less effective at stimulating the cell’s adenylate‑cyclase enzyme, while other swaps can make them even more active.

Utility 2
pubmed 1995

Effects of peptide T derivatives on the proliferation of cultured human keratinocytes.

Marastoni. M M; Scaranari. V V; Fantini. F F; Sevignani. C C; Tomatis. R R

The study tested three versions of peptide T and a related peptide (VIP) on human skin cells grown in the lab. Two forms of peptide T and VIP each boosted cell growth, while a cyclic version of peptide T did not. Blocking VIP's receptor stopped VIP's effect but didn’t affect peptide T, suggesting they work through different pathways.

Utility 2
pubmed Jun 15, 1996

Vasoactive intestinal peptide and pituitary adenylate cyclase-activating polypeptides (PACAP27) and PACAP38) protect CD4+CD8+ thymocytes from glucocorticoid-induced apoptosis.

Delgado. M M; Garrido. E E; Martinez. C C; Leceta. J J; Gomariz. R P RP

The study shows that two brain‑derived peptides, VIP and PACAP, can protect young immune cells (CD4+CD8+ thymocytes) from dying when the body releases stress hormones like dexamethasone. When a short fragment of a related peptide, called GRF‑1‑29, blocks the VIP receptor, this protection is reduced, proving the effect works through that specific receptor.

Utility 2
pubmed 1991

Comparison of enzymatic semisyntheses of peptide amides: human growth hormone releasing factor and analogs.

Bongers. J J; Offord. R E RE; Felix. A M AM; Lambros. T T; Liu. W W; Ahmad. M M; Campbell. R M RM; H...

The paper compares different enzyme‑based ways to turn precursor forms of growth‑hormone‑releasing factor (GRF) into the active, amidated version. It shows that a recombinant enzyme can make the full‑length peptide almost completely, while trypsin can also do the job but with lower yields, especially for the shorter, super‑active 1‑29 version.

Utility 2
pubmed Jun 2, 1990

[Relations between Sheehan's syndrome and empty sella turcica. A functional study apropos of 6 cases].

López de la Torre Casares. M M; Gargallo Fernández. M M; Moreno Esteban. B B; Rodrígu...

The study looked at six people with Sheehan's syndrome (a pituitary problem) and tested how their hormones responded to various challenges, including a dose of GRF‑1‑29, which normally makes the pituitary release growth hormone. All patients showed severe pituitary damage, and the GRF test helped show how the gland was functioning.

Utility 2
pubmed 1990

Vasoactive intestinal peptide (VIP) as transmitter of inhibitory motor neurons of the gut: evidence from the use of selective VIP antagonists and VIP antiserum.

Grider. J R JR; Rivier. J R JR

The study shows that a peptide called GRF‑1‑29, normally known for stimulating growth hormone, can also block the action of another peptide, VIP, which relaxes the gut. In lab experiments on guinea pig and rat intestines, GRF‑1‑29 reduced VIP‑driven muscle relaxation, though it was less potent than other VIP blockers.

Utility 2
pubmed 1991

Carboxypeptidase mediated C-terminal amidation of polypeptide acids.

Aasmul-Olsen. S S; Christensen. K A KA; Widmer. F F

Scientists showed that a special enzyme called carboxypeptidase can turn peptide acids into the more stable peptide amides that we usually want, like the active form of GRF‑1‑29. By using bigger, water‑loving side‑chains (like threonine) as the leaving group, they got better yields, and the method works even for longer peptides when the enzyme is made in a recombinant form.

Utility 2
pubmed 1990

GRF-induced GH response in attention-deficit hyperactivity disorder.

Cacabelos. R R; Albarrán. M M; Diéguez. C C; Fariñas. F F; del Pino. J L JL; Exp&#xf3...

The study looked at how a growth‑hormone‑releasing peptide (GRF‑1‑29) makes the body release GH in kids with ADHD compared to healthy kids. ADHD kids started with lower GH levels and showed a different pattern of GH release after the peptide, with some showing a strong response and others a weak one.

Utility 2
pubmed 1988

[Effects of GRF 1-29 in normal and hypotrophic lambs].

Pastoureau. P P; Barenton. B B; Blanchard. M M; Boivin. G G; Charrier. J J; Dulor. J P JP; Theriez....

Injecting GRF‑1‑29 into lambs quickly boosted their growth hormone levels, especially in under‑nourished animals. The treatment also shifted body composition by lowering fat storage and raising calcium and phosphorus in the bones, suggesting it can influence both metabolism and skeletal growth in ruminants.

Utility 2
pubmed 1987

[Diagnostic use of the GRF test in the study of GH secretion].

Ramos. M M; Fernández. A A; Ferrández. A A; Mayayo. E E; Guallar. A A

Giving a single IV dose of the peptide GRF‑1‑29 can help doctors figure out whether a person’s growth‑hormone problem comes from the brain (hypothalamus) or the pituitary gland. Some people who seem to have a hypothalamic issue don’t react to a one‑time dose, so they may need a longer or pulsed GRF regimen and thyroid hormone support. If there’s no reaction at all, the problem is likely in the pituitary and direct growth‑hormone therapy is needed.

Utility 2
pubmed 1987

[Growth hormone secretion following administration of growth hormone releasing hormone in constitutional short stature and idiopathic growth hormone deficiency].

Butenandt. O O; Kiess. W W

The study tested a tiny dose of the peptide GRF‑1‑29 in kids with different types of short stature. It showed that the peptide can make growth hormone (GH) rise, but the rise is much smaller in kids who truly lack GH. However, some GH‑deficient kids still had a normal GH spike, so the test isn’t reliable for telling who has a GH problem.

Utility 1
pubmed Sep 1, 2009

Vasoactive intestinal peptide acts via multiple signal pathways to regulate hippocampal NMDA receptors and synaptic transmission.

Yang. Kai K; Trepanier. Catherine H CH; Li. Hongbin H; Beazely. Michael A MA; Lerner. Ethan A EA; Ja...

The study shows that a tiny amount of the hormone VIP can boost brain cell communication (NMDA receptors) through specific VPAC receptors and a cAMP/PKA signaling route, while a higher dose uses a different receptor (PAC1) and other pathways. The peptide GRF‑1‑29 blocks the VPAC‑mediated boost, meaning it can stop this effect.

Utility 1
pubmed Nov 1, 1995

Pituitary adenylate cyclase-activating polypeptides (PACAP27 and PACAP38) inhibit the mobility of murine thymocytes and splenic lymphocytes: comparison with VIP and implication of cAMP.

Delgado. M M; De la Fuente. M M; Martínez. C C; Gomariz. R P RP

The study shows that two brain‑derived peptides, PACAP27 and PACAP38, can slow down the movement of mouse immune cells in a dish, likely by raising cAMP levels, and that a related peptide (VIP) does the same. It also suggests that the receptors these peptides use are similar, and that a specific antagonist can partly block their effect.

Utility 1
pubmed Apr 1, 1994

Effects in vitro of new growth hormone releasing peptide (GHRP-1) on growth hormone secretion from ovine pituitary cells in primary culture.

Wu. D D; Chen. C C; Zhang. J J; Katoh. K K; Clarke. I I

In a lab test using sheep pituitary cells, the new peptide GHRP‑1 (also called KP‑101) was shown to make the cells release growth hormone, but it needed a higher concentration to work and never reached the maximum effect that the classic hormone‑releasing factor (GRF) could achieve. The effect depended on calcium channels, and the peptide behaved similarly to the older GHRP‑6. These results come from an in‑vitro experiment, not from human trials.

Utility 1
pubmed Dec 1, 1999

Vasoactive intestinal polypeptide stimulates the proliferation of HaCaT cell via TGF-alpha.

Sung. K J KJ; Chang. S E SE; Paik. E M EM; Lee. M W MW; Choi. J H JH

The study shows that the peptide VIP makes skin cells (keratinocytes) grow faster, but it does this by boosting a growth factor called TGF‑alpha rather than the usual cAMP pathway. This effect happens even when the usual PKA blocker is present, and short pieces of VIP work the same way. The finding is mainly about skin biology, not about overall health or performance.