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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 1
2025 pubmed

Growth hormone-releasing peptide 6 (GHRP-6) hydrogel for acute kidney injury therapy via metabolic regulation.

Zhao. Xiaotong X; Pan. Kai K; Li. Rui R; Liu. Meina M; Li. Duo D; Jia. Pingping P; Han. Zhibo Z; Han. Zhong-Chao ZC; Guo. Zhikun Z; Li. Zongjin Z; Li. Qiong Q

Key Findings

  • A self‑assembling GHRP‑6 hydrogel was created for targeted delivery to kidney cells.
  • Treatment increased levels of spermidine, L‑glutamine, and acetyl‑CoA, indicating enhanced amino‑acid and fatty‑acid metabolism.
  • GHRP‑6 hydrogel activated the mTOR‑P70 signaling pathway, improving survival of tubular epithelial cells in an ischemic environment.

Practical Outcomes

  • The study shows a promising experimental approach for protecting kidneys after acute injury, but it is limited to animal models and a specialized gel formulation. It does not provide a ready‑to‑use protocol, dosage, or safety data for self‑administration, so biohackers should view it as early‑stage research rather than an actionable supplement strategy.

Summary

Scientists made a gel that slowly releases the peptide GHRP‑6 and tested it in mice with sudden kidney damage. The gel boosted certain metabolites and turned on a cell‑growth pathway, helping kidney cells survive and recover better.

Abstract

Renal tubular epithelial cells (TECs), which are highly susceptible to injury during acute kidney injury (AKI), have notable regenerative effects on renal recovery after AKI. AKI-driven metabolic reprogramming of TECs plays a critical role in determining whether kidneys recover functionally or develop fibrosis. Targeting the metabolism of TECs offers valuable insights into AKI treatment. Growth hormone-releasing hormone (GHRH) and its analog GHRH peptide (GHRP) play beneficial roles in the field of regenerative medicine. Here, we designed a self-assembling GHRP-6 peptide hydrogel, and we hypothesized that this hydrogel could reprogram the metabolism of TECs, further enhancing recovery from AKI. Metabolomic sequencing analysis revealed that spermidine, L-glutamine, and acetyl-CoA, which are involved in amino acid and fatty acid metabolism, were highly enriched in a mouse model of AKI treated with the GHRP-6 hydrogel. Further study revealed that GHRP-6 hydrogel treatment enhanced the survival of TECs in the ischemic microenvironment by activating the mTOR-P70 pathway. In conclusion, GHRP-6 hydrogel treatment has beneficial therapeutic effects on AKI through the targeting of metabolic reprogramming, which offers a novel therapeutic strategy to protect TECs in AKI treatment.

Study Information

Provider

pubmed

Year

2025

Date

2025-12-01T00:00:00.000Z

DOI

10.1186/s12951-025-03888-9

References

41