What are GHK-cu (Glycyl-Histidyl-Lysine-Copper) injections?

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GHK-Cu Injections: A Research Compound Without Clinical Guidelines

GHK-Cu (Glycyl-Histidyl-Lysine-Copper) injections are an experimental peptide-copper complex that lacks FDA approval, established clinical guidelines, or regulatory oversight for human therapeutic use, and should not be administered outside of approved research protocols.

What is GHK-Cu?

GHK-Cu is a tripeptide-copper complex consisting of the amino acid sequence glycyl-L-histidyl-L-lysine bound to copper (II) ions 1, 2. This compound was originally discovered in 1973 as a component of human albumin that appeared to influence protein synthesis in liver tissue 2.

Natural Occurrence and Age-Related Decline

  • GHK naturally occurs in human serum at concentrations averaging 200 ng/mL at age 20, declining to approximately 80 ng/mL by age 60 3
  • The peptide has high affinity for copper ions and readily forms the copper chelate complex 2, 3

Research Evidence (Not Clinical Practice)

Preclinical Laboratory Studies Only

The available evidence consists entirely of animal models and in vitro cell culture experiments—no human clinical trials, FDA approval, or clinical guidelines exist for therapeutic use:

Animal Studies:

  • In mice exposed to cigarette smoke, intraperitoneal GHK-Cu injections (0.2-20 μg/g/day) reduced emphysematous changes and inflammatory markers (IL-1β, TNF-α) while modulating oxidative stress pathways through Nrf2/Keap1 upregulation 1
  • In lipopolysaccharide-induced acute lung injury in mice, GHK-Cu treatment reduced reactive oxygen species production and suppressed NF-κB p65 and p38 MAPK signaling 4
  • Preliminary observations in aging mice suggested potential effects on cognitive impairment through anti-inflammatory and epigenetic pathways 3

In Vitro Studies:

  • Cell culture experiments with human alveolar epithelial A549 cells showed GHK-Cu inhibited oxidative stress by suppressing malondialdehyde levels and restoring antioxidant capacity 1
  • Gene expression studies using the Broad Institute Connectivity Map demonstrated that GHK modulates expression of multiple genes related to nervous system function 5

Proposed Mechanisms (Experimental Only)

Research suggests GHK-Cu may possess:

  • Antioxidant effects through upregulation of Nrf2 expression 1, 2
  • Anti-inflammatory properties via downregulation of NF-κB signaling 1, 4
  • Modulation of gene expression patterns related to tissue remodeling 2, 5
  • Effects on copper homeostasis and neuroinflammation pathways 2

Critical Clinical Caveats

No established clinical indications exist for GHK-Cu injections:

  • Zero FDA-approved indications for any condition [1-4]
  • No clinical practice guidelines from any major medical society address GHK-Cu use
  • All available evidence comes from animal models and cell culture—not human clinical trials 1, 3, 4
  • Safety profile, appropriate dosing, drug interactions, and long-term effects in humans remain unknown
  • The compound is not regulated as a pharmaceutical agent

Distinction from Approved Therapies

The provided evidence documents discuss established treatments for various conditions (glucocorticoids for inflammatory diseases, immunosuppressants for autoimmune conditions) but none of these guidelines mention or recommend GHK-Cu [6-7]. This absence from clinical guidelines reflects the lack of human efficacy and safety data.

Current Status

GHK-Cu remains an investigational compound used in:

  • Preclinical research settings only 1, 3, 4
  • Some cosmetic skin care products (topical formulations, not injections) 2, 3
  • Unregulated supplement markets without quality control or safety oversight

Any use of GHK-Cu injections in clinical practice would be considered experimental and should only occur within IRB-approved research protocols with informed consent, safety monitoring, and regulatory oversight.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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