GHRP-6
Growth Hormone Releasing Peptide-6, Growth hormone-releasing hexapeptide, His-D-Trp-Ala-Trp-D-Phe-Lys-NH2
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 (10â»Âčâ°â10â»âžâŻM) increased proliferation of human osteoblastic TE85 cells.
- Blocking the ghrelin receptor (GHSâR) with the antagonist DâLys3âGHRPâ6 stopped the growthâpromoting effect.
- Interfering with NO production or cGMP synthesis prevented ghrelinâinduced 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 NOâenhancing strategies could be a lowârisk 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 boneâbuilding 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
pubmed
2008
2008-10-25T00:00:00.000Z
10.1007/s12020-008-9117-3
35
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