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GHRP-6

Growth Hormone Releasing Peptide-6, Growth hormone-releasing hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2

Quick Stats
Studies 702
Trials 0
Score 3
2012 pubmed

Protective effect of GHRP-6 and estrogen supplementation against some cardiometabolic risk factors in ovariectomized rats.

Elbassuoni. E E; Ragy. M M; Aziz. N N

Key Findings

  • OVX rats showed higher weight, food intake, fasting glucose, insulin, insulin resistance, total cholesterol and LDL, and lower triglycerides and HDL.
  • Estrogen supplementation reversed all these changes, including weight gain and food intake.
  • GHRP‑6 did not affect weight or food intake but normalized fasting glucose, insulin, insulin resistance, and improved the lipid profile (lower total cholesterol and LDL, higher HDL).

Practical Outcomes

  • For biohackers interested in metabolic health, GHRP‑6 may offer a way to improve blood sugar control and lipid balance without affecting appetite or weight, which could be useful for post‑menopausal or estrogen‑low individuals. However, the evidence is from an animal model, so human dosing, safety, and effectiveness remain uncertain and should be approached cautiously.

Summary

In rats without ovaries (a model of menopause), giving the peptide GHRP‑6 helped lower blood sugar, insulin resistance, and improved cholesterol numbers, even though it didn't stop weight gain. Estrogen did the opposite, fixing weight gain but being less strong on the cholesterol side.

Abstract

This study was aimed to assess the effect of both the estrogen and growth hormone releasing peptide-6 (GHRP-6), on the cardiovascular and metabolic diseases in ovariectomized (OVX) rats. Four groups of adult female rats were used: sham operated, OVX, OVX plus estrogen supplemented, and OVX plus GHRP-6 supplemented. After 8 weeks, blood samples were collected from the retro-orbital plexus and total cholesterol (TC), triglycerides (TGs), high density lipoprotein cholesterol (HDL-C), low density lipoprotein cholesterol (LDL-C), glucose and insulin in serum were estimated. The ovariectomy resulted in significant increase of body weight gain, food intake, fasting serum glucose, insulin, insulin resistance, TC, and LDL-C as well as in significant decrease of serum TGs and HDL-C levels. Estrogen supplementation to OVX rats reversed the effect of OVX on all the above mentioned parameters. However, GHRP-6 supplemented to OVX rats failed to produce significant change in both the body weight gain and food intake, but reversed the effect of OVX on fasting serum glucose, insulin, insulin resistance, and the assessed lipid fractions. The decrease in ovarian hormones produced by OVX resulted in arising of several risk factors related to carbohydrate metabolism and cardiovascular system. It appeared that such negative effects of OVX can be reversed by estrogen or GHRP-6 supplementation. However, the effect of GHRP-6 on improving dyslipidemia after OVX was more potent than that of estrogen, while the effect of estrogen on improving carbohydrate metabolism after OVX was more potent than that of GHRP-6.

Study Information

Provider

pubmed

Year

2012

DOI

10.4149/endo_2012_02_73