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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 1
pubmed 1991

Lack of effect of vasoactive intestinal peptide antagonists on blood flow in the rat thyroid.

Michalkiewicz. M M; Huffman. L J LJ; Hedge. G A GA

Scientists tested three chemicals that were supposed to block a hormone called VIP, to see if they could change blood flow in the thyroid gland of rats. The drugs didn't affect thyroid blood flow or hormone release, even at much higher doses than the hormone itself. This means those particular blockers don't work for influencing thyroid blood flow.

Utility 1
pubmed Oct 31, 1991

Radioimmunoassay of growth hormone-releasing hormone (GHRH) with a polyclonal antibody against synthetic GHRH(1-29)-Gly4-Cys-NH2: method and clinical studies.

Zhang. C Y CY; Yamasaki. R R; Mitsuhashi. S S; Takahashi. H H; Bando. H H; Saito. S S

Scientists created a very sensitive blood test to measure the hormone GHRH and used it to see how much of the hormone is in healthy people and in several disease groups. They found normal levels around 20 ng/L, higher levels in kidney‑failure patients, and extremely high levels in a rare tumor case. The study mainly shows the test works, not how to use GHRH for performance or health.

Utility 1
pubmed Jun 14, 1991

Low-dose intrathecal morphine facilitates the spinal flexor reflex by releasing different neuropeptides in rats with intact and sectioned peripheral nerves.

Wiesenfeld-Hallin. Z Z; Xu. X J XJ; Håkanson. R R; Feng. D M DM; Folkers. K K

In rats, tiny amounts of morphine injected into the spine make a reflex stronger by causing the release of different brain chemicals, depending on whether the leg nerves are still connected. When the nerves are intact, the chemical substance P is involved; when the nerves are cut, a different chemical called VIP takes over. A peptide called GRF‑1‑29 was used to block VIP and stop the reflex boost in the nerve‑cut rats.

Utility 1
pubmed 1991

An analogue of growth hormone releasing factor (GRF), (Ac-Try1, D-Phe2)-GRF-(1-29), specifically antagonizes the facilitation of the flexor reflex induced by intrathecal vasoactive intestinal peptide in rat spinal cord.

Xu. X J XJ; Wiesenfeld-Hallin. Z Z

In rats, a modified growth‑hormone‑releasing‑factor peptide (Ac‑Try1, D‑Phe2‑GRF‑1‑29) blocks the pain‑enhancing effects of vasoactive intestinal peptide (VIP) in the spinal cord, showing it works as a specific VIP antagonist but doesn’t affect other pain‑related signals.

Utility 1
pubmed 1990

VIP antagonist [N-Ac-Tyr1,D-Phe2]-GRF-(1-29)-NH2: an inhibitor of vasodilation in the feline colon.

Blank. M A MA; Kimura. K K; Fuortes. M M; Jaffe. B M BM

Scientists tested a modified peptide called [N-Ac-Tyr1,D-Phe2]-GRF-(1-29)-NH2 in anesthetized cats and found it can blunt the widening of blood vessels in the colon that normally happens when certain nerves are stimulated. The peptide didn’t change the amount of the natural signaling molecule VIP that was released, just blocked its effect on blood flow.

Utility 1
pubmed Aug 24, 1990

Plasticity of the peptidergic mediation of spinal reflex facilitation after peripheral nerve section in the rat.

Wiesenfeld-Hallin. Z Z; Xu. X J XJ; Håkanson. R R; Feng. D M DM; Folkers. K K

In rats, a peptide called GRF‑1‑29 (used as a VIP blocker) can stop a certain spinal reflex that normally gets stronger after nerve injury. The study shows that after cutting a nerve, the body switches from using one type of signaling molecule (tachykinins) to another (VIP) to boost that reflex.

Utility 1
pubmed 1990

Evidence for vasoactive intestinal peptide as a mediator of non-adrenergic non-cholinergic neurotransmission in the trachea.

Venugopalan. C S CS; Holmes. E P EP; O'Malley. N A NA

In guinea‑pig trachea, the peptide VIP makes the airway muscles relax. Two synthetic versions of a related peptide (one based on GRF‑1‑29) can block this relaxation, but only at relatively high concentrations. The study shows how these compounds interfere with VIP’s effect in a lab setting.

Utility 1
pubmed 1990

High affinity receptors for vasoactive intestinal peptide on a human glioma cell line.

Nielsen. F C FC; Gammeltoft. S S; Westermark. B B; Fahrenkrug. J J

The study shows that the hormone VIP sticks tightly to receptors on a type of brain cancer cell, gets pulled inside the cell, and is broken down. Some specially modified versions of the growth‑hormone‑releasing peptide (GRF‑1‑29) can block VIP from binding, but only at fairly high concentrations. The findings are mostly about cell‑culture chemistry and don’t give clear guidance for everyday supplement or dosing strategies.

Utility 1
pubmed 1990

[The predictive value of the GRF-stimulation test].

Andler. W W; Eiden. S S

The study looked at using a short version of growth‑hormone‑releasing factor (GRF‑1‑29) to test if kids have growth‑hormone problems. It found the test is good at confirming normal pituitary function but often gives false positives for hypothalamic issues, so it isn’t reliable for diagnosing growth‑hormone deficiency.

Utility 1
pubmed 1990

Analogues of growth hormone-releasing factor (1-29) amide containing the reduced peptide bond isostere in the N-terminal region.

Hocart. S J SJ; Murphy. W A WA; Coy. D H DH

Scientists tried swapping a normal peptide bond for a special chemical link in a growth‑hormone‑releasing peptide (GRF‑1‑29) to see how it changes activity. Most of the modified versions barely activated the hormone release, and one version actually blocked the natural peptide at relatively high concentrations.

Utility 1
pubmed 1990

The novel VIP-like hypothalamic polypeptide PACAP interacts with high affinity receptors in the human neuroblastoma cell line NB-OK.

Cauvin. A A; Buscail. L L; Gourlet. P P; De Neef. P P; Gossen. D D; Arimura. A A; Miyata. A A; Coy....

The study shows that the brain peptide PACAP binds strongly to specific receptors on human neuroblastoma cells, while similar peptides like VIP are much weaker and the growth hormone‑releasing peptide GRF‑1‑29 does not bind these receptors at all.

Utility 1
pubmed May 15, 1990

A glucagon-secretin-like peptide stimulates the intrinsic nervous plexus of guinea pig gallbladder.

Greco. A V AV; Mancinelli. R R; Mingrone. G G; Racanicchi. C C

In guinea pig gallbladders, a peptide called GRF‑1‑29 (a glucagon‑secretin family member) makes the muscle contract more strongly and often, while blocking VIP (another gut peptide) does nothing. This suggests that the natural nerve signal that relaxes the gallbladder isn’t VIP but something like GRF‑1‑29.

Utility 1
pubmed 1990

The effect of orchidectomy on rat pituitary responsiveness to GHRH depends on age.

Pinilla. L L; López. F J FJ; Aguilar. E E

In rats, the ability of the pituitary gland to release growth hormone (GH) after a GHRH injection changes with age and whether the testes are removed. Removing the testes early (when the rats are young) makes the pituitary more responsive to GHRH a week later, while removing them later (when the rats are older) reduces the response. Overall, the age‑related increase in GH response happens regardless of testicular function.

Utility 1
pubmed 1990

Opioid control of growth hormone in the suckled sow is primarily mediated through growth hormone releasing factor.

Armstrong. J D JD; Esbenshade. K L KL; Coffey. M T MT; Heimer. E E; Campbell. R R; Mowles. T T; Feli...

In nursing mother pigs, blocking the hormone GRF‑1‑29 with a vaccine lowered their growth hormone (GH) levels, and giving an opioid blocker (naloxone) also reduced GH and prolactin. The study shows that opioids can influence GH both through GRF‑dependent and independent routes, but it was done in sows, not humans.

Utility 1
pubmed Apr 1, 1986

Lack of effect of muscarinic cholinergic blockade on the GH responses to GRF 1-29 and TRH in acromegalic subjects.

Jordan. V V; Dieguez. C C; Valcavi. R R; Artioli. C C; Portioli. I I; Rodriguez-Arnao. M D MD; Gomez...

In people with acromegaly (a condition with too much growth hormone), blocking muscarinic cholinergic receptors with the drug pirenzepine did not change how their bodies responded to the growth‑hormone‑releasing peptide GRF‑1‑29 or to TRH. This is different from what happens in healthy people, where such blockade can lower the hormone response.

Utility 1
pubmed 1987

Growth hormone, somatomedin levels and growth regulation in Turner's syndrome.

Ranke. M B MB; Blum. W F WF; Haug. F F; Rosendahl. W W; Attanasio. A A; Enders. H H; Gupta. D D; Bie...

The study looked at growth hormone (GH) and related proteins in girls with Turner syndrome, a rare genetic condition. It found that the basic GH system works normally, but the levels change over time because these girls lack normal ovarian hormones. Some individuals may still have unusually low GH or IGF levels.

Utility 1
pubmed 1987

Plasma somatotropin and somatomedin C concentrations following GRF or TRH injections in newborn calves.

Coxam. V V; Davicco. M J MJ; Opmeer. F A FA; Ravault. J P JP; Barlet. J P JP

In newborn calves, injecting the short version of growth hormone‑releasing factor (GRF‑1‑29) makes the pituitary release more growth hormone (GH), but it doesn't change the downstream hormone IGF‑1 or blood sugar. A similar hormone, TRH, also boosts GH and other hormones, but the effect is weaker in slightly older calves.

Utility 1
pubmed 1985

Structural requirements for the activation of rat anterior pituitary adenylate cyclase by growth hormone-releasing factor (GRF): discovery of (N-Ac-Tyr1, D-Arg2)-GRF(1-29)-NH2 as a GRF antagonist on membranes.

Robberecht. P P; Coy. D H DH; Waelbroeck. M M; Heiman. M L ML; de Neef. P P; Camus. J C JC; Christop...

Scientists tested many versions of the growth‑hormone‑releasing peptide (GRF) to see how changes in its building blocks affect its ability to turn on an enzyme in rat pituitary cells. They found that swapping a specific amino‑acid at position 2 to its mirror‑image form (D‑Arg) made the peptide work even better, while the same swap in a slightly modified version turned the peptide into a blocker that stops the normal GRF from working.

Utility 1
pubmed 1993

The entire vasoactive intestinal polypeptide molecule is required for the activation of the vasoactive intestinal polypeptide receptor: functional and binding studies on opossum internal anal sphincter smooth muscle.

Chakder. S S; Rattan. S S

The study shows that the full vasoactive intestinal peptide (VIP) molecule is needed to relax gut smooth muscle, while shorter pieces and a growth‑hormone‑releasing‑factor (GRF) analog can stick to the VIP receptor but do not really relax the muscle.