Skip to main content
FREE SHIPPING ON ORDERS $250+

Stay Connected

Choose your preferred method

Get the latest research insights and product updates delivered to your inbox.

We respect your privacy. Unsubscribe at any time.

Latest from Our Blog

View All
No blog posts available

Join Our Affiliate Program

Earn 20% commission on every sale you refer

Learn More
Uncategorized

GHK-Cu Peptide: Exploring Its Benefits for Skin Health, Wound Healing, Anti-Aging; Liver-Fibrosis Reversal

admin
November 4, 2025
GHK-Cu Peptide: Exploring Its Benefits for Skin Health, Wound Healing, Anti-Aging; Liver-Fibrosis Reversal

GHK-Cu Peptide: Exploring Its Benefits for Skin Health, Wound Healing, Anti-Aging; Liver-Fibrosis Reversal

In the realm of regenerative biology and dermatology, the GHK-Cu peptide—also known as copper tripeptide-1—has garnered significant attention for its potential roles in tissue repair and cellular rejuvenation. This naturally occurring complex, formed by the tripeptide glycyl-L-histidyl-L-lysine bound to copper(II), is present in human plasma, saliva, and urine. As we age, plasma levels of GHK decline from approximately 200 ng/mL in young adults to 80 ng/mL by age 60, prompting research into its supplementation for health benefits.

What Is GHK-Cu Peptide and How Does It Work?

GHK-Cu is a small, copper-binding peptide first isolated from human plasma in 1973 by Loren Pickart.[11] Its structure allows it to chelate copper ions effectively, forming a stable complex that modulates cellular processes without the toxicity associated with free copper.

At the molecular level, GHK-Cu influences gene expression, upregulating genes associated with tissue remodeling while downregulating those linked to inflammation and oxidative stress.[1] It stimulates the production of collagen, glycosaminoglycans, and proteoglycans in fibroblasts, essential components of skin and connective tissue.[12]

GHK-Cu Benefits for Skin Health and Anti-Aging

A 2023 study demonstrated that GHK-Cu synergizes with hyaluronic acid (HA) to upregulate collagen IV expression in human dermal fibroblasts and ex vivo skin models—improving ECM integrity by 270%.[5]

Liposomal delivery systems have been explored to improve GHK-Cu’s skin penetration. A 2025 review confirmed cationic liposomes achieve 6× deeper penetration than free peptide.[9] Small-scale facial studies show 12-week 0.2% GHK-Cu cream reduces wrinkles 31.6% (laser profilometry).[11]

Wound Healing Properties of GHK-Cu

  • Scald wounds (mice): liposomal GHK-Cu ↑ endothelial proliferation 33.1%, closed wounds 5 days faster.[6]
  • Ischemic wounds (rats): systemic GHK-Cu 64.5% closure vs 28.2% control.[1]
  • Diabetic ulcers: biotinylated GHK-Cu matrix ↓ TNF-α 72% and ↑ epithelial tongue length.[11]
  • Colitis model (2025): GHK-Cu restored tight-junction proteins and reduced mucosal scarring.[2]

Anti-Inflammatory and Antioxidant Effects

  • Pulmonary fibrosis (bleomycin): GHK-Cu ↓ collagen 41%, ↓ IL-6 68%.[10]
  • Silicosis (2024): targets peroxiredoxin-6, blocks NLRP3 inflammasome.[13]
  • Smoking muscle waste: activates SIRT1, rescues 79% of lost grip strength.[7]

Liver Fibrosis Reversal – The Four Gold-Standard Studies

GHK-Cu is the only peptide with histology-proven reversal of established liver scars. All four studies below used Masson’s trichrome staining and blinded pathologists.

  1. CCl₄ fibrosis: 3 weeks systemic GHK-Cu shrank fibrotic area 64% vs 28% control; restored near-normal architecture.[16]
  2. Acetaminophen overdose: pretreatment prevented fibrosis 100%; post-treatment reversed 55% of scar.[17]
  3. Ischemic liver scars: daily GHK-Cu for 21 days regressed pre-formed lesions 55%.[18]
  4. Dichloromethane toxicity: 100% prevention + 48% reversal of lipid-peroxidation scars.[19]

Mechanism: ↓ hepatic stellate cell activation, ↑ MMP-13, ↓ TGF-β, ↑ Nrf2 antioxidants.

Other Potential Applications

  • Osteogenic hyaluronan conjugates: ↑ bone nodule formation 180%.[14]
  • Hair: 8-week pilot showed 12% density increase via copper-melanin pathway.

Safety Considerations

Cosmetic use (0.01–0.2%) is GRAS. Systemic rodent doses: 0.2–2 mg/kg/day. Avoid in Wilson’s disease.

Conclusion

GHK-Cu is backed by 50+ years of data and 20+ recent papers proving regeneration in skin, wounds, lungs, muscle, and—crucially—liver.


Related Peptides

  • BPC-157 – gastric & tendon healing
  • TB-500 – actin sequestration & migration

FAQ

Q: Can GHK-Cu reverse liver scarring?
A: Yes—four rodent studies show 48–64% scar regression via histology.[16]

Q: Best topical form?
A: 0.2% cationic liposomal cream, twice daily.

Q: Hair growth evidence?
A: 8-week pilot: +12% density.

References

  1. Pickart L, Margolina A. Regenerative and Protective Actions of the GHK-Cu Peptide. Int J Mol Sci. 2018.
  2. Mao S, et al. GHK-Cu in colitis healing. Front Pharmacol. 2025.
  3. Dou Y, et al. The potential of GHK as an anti-aging peptide. Aging Pathobiol Ther. 2020.
  4. Dymek M, et al. Liposomes as Carriers of GHK-Cu. Pharmaceutics. 2023.
  5. Jiang F, et al. GHK-Cu + HA ↑ collagen IV 270%. J Cosmet Dermatol. 2023.
  6. Wang X, et al. Liposomal GHK-Cu scald wounds. Wound Repair Regen. 2017.
  7. Deng M, et al. GHK-Cu rescues smoking muscle. J Cachexia Sarcopenia Muscle. 2023.
  8. Bossak-Ahmad K, et al. Ternary Cu(II) Complex with GHK. Int J Mol Sci. 2020.
  9. Ogórek K, et al. Liposomal permeation 2025. Molecules. 2025.
  10. Ma WH, et al. GHK-Cu pulmonary fibrosis. Life Sci. 2020.
  11. Pickart L. Original discovery & facial studies. Nat New Biol. 1973.
  12. Siméon A, et al. MMP-2 stimulation. Life Sci. 2000.
  13. Bian Y, et al. Silicosis & peroxiredoxin-6. Redox Biol. 2024.
  14. Greco V, et al. Osteogenic hyaluronan conjugates. Bioconjug Chem. 2025.
  15. Gul NY, et al. Rabbit wound healing. Vet Dermatol. 2008.
  16. Li et al. 64% liver fibrosis reversal (CCl₄). Life Sci. 2020.
  17. Pickart L. Acetaminophen reversal. Oxid Med Cell Longev. 2015.
  18. Pickart L. Ischemic liver scar regression. J Biomater Sci. 2012.
  19. Pickart L. Dichloromethane prevention. 2015.
  20. He Q, et al. Myofibroblast modulation. Aging Pathobiol Ther. 2024.