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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
2008 pubmed 35 citations

Ghrelin stimulates proliferation of human osteoblastic TE85 cells via NO/cGMP signaling pathway.

Wang. Deng-Hu DH; Hu. Yun-Sheng YS; Du. Jun-Jie JJ; Hu. Yun-Yu YY; Zhong. Wei-De WD; Qin. Wei-Jun WJ

Key Findings

  • Ghrelin at very low concentrations (10⁻Âč⁰‑10⁻⁞ M) increased proliferation of human osteoblastic TE85 cells.
  • Blocking the ghrelin receptor (GHS‑R) with the antagonist D‑Lys3‑GHRP‑6 stopped the growth‑promoting effect.
  • Interfering with NO production or cGMP synthesis prevented ghrelin‑induced cell growth, while supplying NO donors or cGMP analogs mimicked the effect.

Practical Outcomes

  • For biohackers interested in bone health, the data suggest that boosting the NO/cGMP pathway (e.g., with dietary nitrate, beetroot juice, or safe NO donors) might support osteoblast activity. Direct ghrelin supplementation is not yet proven safe or effective in humans, but the findings reinforce the idea that NO‑enhancing strategies could be a low‑risk way to aid bone maintenance alongside exercise and nutrition.

Summary

The study shows that ghrelin, a hormone that makes you feel hungry, can also make bone‑building cells (osteoblasts) multiply, and it does this by turning on a nitric oxide (NO) and cGMP signaling pathway inside the cells.

Abstract

Ghrelin regulates bone formation and osteoblast proliferation, but the detailed signaling pathway for its action on osteoblasts remains unclear. In human osteoblastic TE85 cells, we observed the effects and intracellular signaling pathway of ghrelin on cell proliferation using BrdU incorporation method. Ghrelin, at 10(-10)-10(-8) M concentration, significantly increased BrdU incorporation into TE85 cells. The action of ghrelin was inhibited by D: -Lys3-GHRP-6, a selective antagonist of GHS-R. Nitric oxide (NO) scavenger hemoglobin and the NO synthase inhibitor NAME eliminated the stimulatory action of ghrelin on proliferation, while NO donor SNAP and NO synthase substrate L-AME stimulated proliferation of osteoblastic TE85 cells. The cGMP analogue, 8-Br-cGMP, stimulated TE85 cell proliferation, and ghrelin did not enhance proliferation in the presence of 8-Br-cGMP. Inhibition of cGMP production by the guanylate cyclase inhibitor prevented ghrelin-induced osteoblastic TE85 cell proliferation. In conclusion, ghrelin stimulates proliferation of human osteoblastic TE85 cells via intracellular NO/cGMP signaling pathway.

Study Information

Provider

pubmed

Year

2008

Date

2008-10-25T00:00:00.000Z

DOI

10.1007/s12020-008-9117-3

Citations

35

References

38