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GHK-Cu

Copper Tripeptide-1, Glycyl-L-Histidyl-L-Lysine Copper, Prezatide Copper

Quick Stats
Studies 149
Trials 1
Score 1
1995 pubmed

Effect of the tripeptide glycyl-L-histidyl-L-lysine on the proliferation and synthetic activity of chick embryo chondrocytes.

Pesáková. V V; Novotná. J J; Adam. M M

Key Findings

  • GHK‑Cu boosted proliferation of chick embryo chondrocytes, mainly when they were grown on a denatured skin‑collagen scaffold.
  • GHK increased collagen production; on cartilage‑derived scaffolds it favored type II collagen (the main cartilage collagen), while on the skin‑collagen scaffold it shifted toward types I and III.
  • Different culture supports (plastic, cartilage collagen, ISC‑40) influenced how chondrocytes behaved and responded to GHK.

Practical Outcomes

  • For biohackers, the data suggest GHK might have some potential to support cartilage health, but the evidence is purely in vitro and from chick cells. There’s no clear dosage, delivery method, or safety information for human use, so it isn’t ready to be turned into a real‑world protocol yet.

Summary

The study looked at how a copper‑bound version of the tiny peptide GHK (Gly‑His‑Lys) affects cartilage cells grown in the lab. Adding GHK helped the cells multiply and make more collagen, especially on certain surfaces, but the work was done in chick embryos and in petri dishes, not in people.

Abstract

Under certain conditions chondrocytes form lattices with cartilage collagens, which may serve as cartilage implants. It is necessary to find the optimal conditions for culturing chondrocytes. Three different supports are compared: (a) plastic; (b) cartilage collagens; and (c) insoluble skin collagen solubilized under denaturing conditions (ISC-40). The effect of culture medium supplementation with the tripeptide (Gly-His-Lys)2.Cu.2H2O.2NaCl (GHK) on chondrocyte proliferation and synthetic activity is studied, with particular attention paid to collagen types I, II and III. The collagen supports stimulated chondrocyte proliferation, but on the ISC-40 support they started to dedifferentiate rather early. In the primary culture, chondrocytes on all three supports synthesized mainly collagen type II, and only small amounts of types I and III. In the first passage the synthesis of these two collagen types increased, relative to collagen type II, at least on the cartilage collagen support. Supplementation of culture medium with GHK stimulated chondrocyte proliferation in the primary structure mostly on the ISC-40 support. On the other two types of supports the stimulatory effect of GHK was expressed mostly in the first passages. The collagen synthetic rate was increased by GHK on both of the collagen supports; on the cartilage collagen support collagen type II was synthesized predominantly and on the ISC-40 support types I and III were mostly formed. It is suggested that supplementation of culture medium with GHK may be useful in the preparation of cartilage implants.

Study Information

Provider

pubmed

Year

1995

DOI

10.1016/0142-9612(95)93115-t