Back to all products

GHK-CU

GHK-Cu (Glycyl-L-Histidyl-L-Lysine Copper Complex) is a naturally occurring peptide that binds copper ions and is found in human plasma, saliva, and urine. It is widely studied for its role in tissue regeneration, wound healing, anti-inflammatory activity, and skin and hair rejuvenation. GHK-Cu has demonstrated the ability to stimulate collagen production, promote angiogenesis, modulate gene expression, and protect against oxidative stress in both preclinical and human studies. Its broad biological activity makes it a key molecule of interest in anti-aging, dermatological, and regenerative medicine research.

$59.99

Only 10 left in stock

-
+
COA

COA-GHK

GHK-Cu Summary

Tissue Regeneration & Wound Healing

  • Stimulates production of collagen, elastin, and glycosaminoglycans for structural repair.
    • Promotes re-epithelialization and granulation tissue formation in damaged skin and soft tissues.
    • Enhances angiogenesis (new blood vessel growth) at injury sites.
    • Accelerates healing in preclinical models of skin, corneal, gastric, and bone injuries.

Skin Rejuvenation & Cosmetic Research

  • Increases skin firmness, elasticity, and thickness in photoaged or mature skin.
    • Reduces fine lines, wrinkles, and hyperpigmentation in human clinical trials.
    • Stimulates keratinocyte proliferation and skin barrier repair.
    • Improves overall skin texture and appearance in topical cosmetic research.

Hair Growth & Follicle Health

  • Expands hair follicle size and prolongs the anagen (growth) phase of the hair cycle.
    • Promotes proliferation of dermal papilla and follicular stem cells.
    • Supports reversal of follicle miniaturization in preclinical alopecia models.
    • Enhances scalp health and density in animal studies and topical applications.

Inflammation Modulation

  • Downregulates inflammatory cytokines (e.g., TNF-α, IL-6, TGF-β) in injured or aged tissues.
    • Suppresses NF-κB and p38 MAPK inflammatory pathways.
    • Reduces immune cell infiltration and edema in preclinical wound and lung injury models.
    • Supports resolution-phase macrophage activity for proper tissue cleanup.

 

Antioxidant & Cellular Protection

  • Scavenges reactive oxygen species (ROS) and protects cells from oxidative stress.
    • Increases expression of antioxidant enzymes (e.g., superoxide dismutase).
    • Chelates pro-oxidant metals (e.g., copper, iron), minimizing lipid peroxidation.
    • Shields skin cells and DNA from UV-induced damage and photoaging.

Gene Expression & Epigenetic Modulation

  • Alters expression of over 30% of human genes related to repair, inflammation, and aging.
    • Upregulates regenerative genes (e.g., collagen, stem cell factors, antioxidant proteins).
    • Downregulates pro-aging and pro-inflammatory genes (e.g., MMPs, IL-6, TNF pathways).
    • Reprograms fibroblasts and epithelial cells toward a youthful, healing phenotype.

Cartilage & Connective Tissue Support

  • Enhances synthesis of proteoglycans and collagen in cartilage models.
    • Promotes joint surface regeneration and matrix restoration in osteoarthritis studies.
    • Improves structural integrity of joints, tendons, and ligaments in preclinical research.
    • Potential for use in experimental models of connective tissue aging and degeneration.

Anti-Fibrotic & Scar Remodeling

  • Inhibits overactivation of myofibroblasts, reducing excess collagen deposition.
    • Minimizes scarring in skin and cardiac tissues during regeneration.
    • Promotes balanced ECM remodeling with reduced fibrosis.
    • Encourages regeneration over scar formation in wound healing studies.
GHK-Cu Synergies & Additive Research Compounds

To maximize the utility of GHK-Cu in experimental models, researchers often combine it with compounds that enhance tissue regeneration, antioxidant protection, anti-inflammatory responses, or cosmetic rejuvenation pathways. These combinations are commonly used in studies of skin repair, wound healing, anti-aging, and hair follicle regeneration.

Below is a summary of notable GHK-Cu synergies validated in preclinical and clinical research:

 

GHK-Cu Synergistic Compounds

Compound Mechanism of Synergy Relevant Research / Notes
BPC-157 Promotes angiogenesis and fibroblast migration; complements GHK-Cu’s collagen-stimulating and anti-inflammatory activity. Combined in wound-healing and surgical-recovery models to accelerate closure, reduce oxidative stress, and enhance tissue remodeling.
TB-500 (Thymosin Beta-4) Mobilizes progenitor cells and supports cytoskeletal remodeling; synergizes with GHK-Cu to improve repair quality and minimize fibrosis. Used together in tendon and dermal studies showing improved vascularization, collagen alignment, and reduced scarring.
KPV (Lys-Pro-Val) Tripeptide fragment of α-MSH that suppresses NF-κB-driven inflammation; enhances GHK-Cu’s anti-inflammatory and antioxidant effects. Investigated in inflammatory wound and gut-healing models to reduce cytokine activity and promote balanced tissue recovery.
IGF-1 LR3 Drives anabolic and regenerative pathways in muscle and connective tissue; complements GHK-Cu’s collagen and ECM synthesis. Dual-action pairing studied for post-injury regeneration—GHK-Cu enhances structural repair while IGF-1 supports cellular hypertrophy.
Thymosin Alpha-1 Immune-modulating peptide reducing chronic inflammation; augments GHK-Cu’s wound-healing and vascular effects. Research suggests co-administration may improve immune balance and accelerate repair in systemic injury models.
MOTS-C Mitochondrial peptide that boosts energy metabolism and cellular resilience; works with GHK-Cu’s antioxidant gene activation. Combined use explored in oxidative-stress and metabolic-recovery models to enhance cellular vitality and tissue protection.
Epitalon (Epithalon) Regulates telomere maintenance and circadian rhythm; pairs with GHK-Cu’s rejuvenating and gene-repair effects. Investigated in anti-aging research to support DNA repair, collagen renewal, and overall tissue longevity.
CJC-1295 (No DAC) GHRH analog that elevates GH/IGF-1 levels; may amplify GHK-Cu’s regenerative and collagen-supporting outcomes. Studied in combined metabolic and tissue-healing contexts to synergize growth-axis and extracellular-matrix pathways.
Glutathione Master antioxidant tripeptide; reduces oxidative damage and complements GHK-Cu’s copper-mediated enzymatic defense. Enhances cytoprotective capacity in dermal and systemic regeneration studies.

 

Potential Research Use Cases for GHK-Cu Combinations

  • Skin Repair & Anti-Aging Studies:
    GHK-Cu + BPC-157 / TB-500 / EGF
  • Wound Healing Research:
    GHK-Cu + KPV / Thymosin Alpha-1 / Glutathione
  • Hair Growth & Follicle Activation:
    GHK-Cu + IGF-1 LR3 / CJC-1295 (No DAC)
  • Connective-Tissue & Scar Remodeling:
    GHK-Cu + TB-500 / BPC-157 / KPV
  • Systemic Anti-Aging & Cellular Longevity Models:
    GHK-Cu + Epitalon / MOTS-C / Glutathione
GHK-Cu Research

Below is a breakdown of major research-backed effects by physiological system, showcasing the peptide’s broad experimental utility:

Tissue Regeneration and Wound Healing

GHK-Cu is a naturally occurring copper-binding peptide known for its powerful wound-healing and regenerative properties. It is released from damaged collagen at injury sites and acts as a “repair signal” to activate regenerative pathways (Ref 1). At very low concentrations, GHK-Cu stimulates the production of collagen, elastin, proteoglycans (such as decorin), and angiogenesis, while also regulating metalloproteinases (MMPs) and their inhibitors (TIMPs), resulting in tissue remodeling without fibrosis (Ref 9; Ref 1). In animal models, GHK-Cu accelerates wound contraction, granulation tissue formation, and vascularization. In diabetic wound models, it increased collagen production up to 9-fold and boosted antioxidant levels in the wound bed (Ref 1). Systemically administered GHK-Cu also enhanced healing in distant injuries, suggesting systemic regenerative signaling (Ref 9).

 

Skin Repair and Anti-Aging Cosmetic Research

GHK-Cu is among the most well-studied peptides in skin rejuvenation. Clinical studies consistently show it improves skin firmness, elasticity, and density, while reducing fine lines, hyperpigmentation, and wrinkle depth. In a 12-week clinical trial, GHK-Cu significantly improved aged skin more effectively than vitamin C or retinoic acid (Ref 1). A double-blind comparison trial revealed that GHK-Cu reduced wrinkle volume by 55.8% more than placebo and outperformed Matrixyl® formulations (Ref 6). Histological data confirmed increased collagen I, dermal hydration, and elastic fiber content, while GHK-Cu also stimulated basal-cell integrins and p63, restoring a more stem-like regenerative phenotype (Ref 1). GHK-Cu has shown no adverse effects in trials up to 12 weeks (Ref 5).

Hair Follicle Stimulation

GHK-Cu supports hair-follicle enlargement, prolongs the anagen (growth) phase, and stimulates follicular stem cells. In animal models, it improved hair-shaft thickness and follicle size with a superior safety profile compared to standard treatments (Ref 4). It enhances the health of dermal papilla cells and promotes regeneration of miniaturized follicles, a hallmark of androgenic alopecia. Advanced delivery systems (e.g., ionic microemulsions) have been shown to triple GHK-Cu’s transdermal penetration, enhancing its effects on the scalp (Ref 4).

Anti-Inflammatory and Protective Actions

GHK-Cu exhibits significant anti-inflammatory activity by lowering TNF-α, IL-6, and other cytokines, while inhibiting NF-κB and p38 MAPK signaling pathways (Ref 3). It reduces inflammatory infiltration and edema in lung, skin, and wound models. In models of acute lung injury, GHK-Cu prevented tissue degradation and immune overactivation. Additionally, GHK-Cu supports inflammation resolution by aiding macrophage recruitment for debris clearance and initiating tissue remodeling (Ref 3). In studies on fibroblasts derived from COPD patients, GHK-Cu restored normal cellular function and reduced inflammation-associated gene expression (Ref 7).

Antioxidant and Cell-Protective Effects

GHK-Cu provides protection against oxidative stress by enhancing superoxide dismutase (SOD) activity and reducing reactive oxygen species (ROS) (Ref 8; Ref 3). It neutralizes toxic by-products such as acrolein and malondialdehyde, prevents lipid peroxidation, and shields keratinocytes from UVB-induced damage (Ref 1). GHK-Cu also activates the proteasome, promoting the removal of oxidized proteins and damaged cellular components (Ref 1).

Gene Modulation and Systemic Effects

One of GHK-Cu’s most powerful mechanisms is genetic reprogramming. Research shows it can modulate over 30% of human genes by at least 50%, up-regulating genes linked to repair, regeneration, and antioxidant defenses, while down-regulating those tied to inflammation and apoptosis (Ref 2). In aged fibroblasts and COPD-derived cells, GHK-Cu restored a youthful gene-expression profile and improved cellular function (Ref 7). This broad-scale rebalancing of gene expression supports systemic applications in organ protection, stem-cell regulation, and anti-aging research.

Safety and Compliance

GHK-Cu has been found to be non-toxic in cell-culture and well tolerated in human trials. No irritation, immunogenicity, or adverse events were reported in long-term skin-application studies (Ref 5). Animal studies confirm systemic GHK-Cu administration is safe, even at high doses (Ref 1). However, it is important to note that GHK-Cu is not an approved drug and is provided strictly for laboratory research use only. All effects described are based on pre-clinical studies or limited human data under controlled research conditions.

GHK-Cu Research References
Ref. No. Study / Source Focus / Key Findings Link
1 Pickart L., Vasquez-Soltero J., & Margolina A. (2015). GHK Peptide as a Natural Modulator of Multiple Cellular Pathways in Skin Regeneration. Comprehensive review of GHK-Cu’s roles in wound healing, collagen / elastin synthesis, MMP / TIMP balance, and systemic regenerative signaling. PubMed
2 Pickart L., & Margolina A. (2018). Regenerative and Protective Actions of the GHK-Cu Peptide in the Light of the New Gene Data. Describes modulation of > 30 % of the human genome by GHK-Cu — up-regulating repair / antioxidant genes and down-regulating inflammatory / apoptotic ones. PubMed
3 Park J.R., et al. (2016). The Tripeptide GHK-Cu Complex Ameliorates Lipopolysaccharide-Induced Acute Lung Injury in Mice. Demonstrates strong anti-inflammatory and antioxidant actions via NF-κB / p38 MAPK inhibition; ↓ TNF-α and IL-6 in ALI models. PubMed
4 Liu T., et al. (2023). Thermodynamically Stable Ionic Liquid Microemulsions for Enhanced Topical Delivery of GHK-Cu. Shows 3× transdermal penetration and hair-growth promotion via Wnt/β-catenin activation in murine models. PubMed
5 Margolina A., & Pickart L. (2018). Skin Regenerative and Anti-Cancer Actions of Copper Peptides. Peer-reviewed MDPI cosmetics paper covering dermal repair, anti-inflammatory and oncopreventive mechanisms of GHK-Cu. MDPI
6 Badenhorst T., et al. (2016). Effects of GHK-Cu on MMP and TIMP Expression, Collagen and Elastin Production, and Facial Wrinkle Parameters. Double-blind cosmetic trial showing 55.8 % greater wrinkle reduction vs placebo and enhanced collagen / elastin synthesis. WalshMed(PDF)
7 Campbell J.D., et al. (2012). A Gene Expression Signature of Emphysema-Related Lung Destruction and Its Reversal by the Tripeptide GHK. Genome Medicine 4:67. In COPD fibroblasts, GHK reversed disease-associated gene expression and restored collagen contraction capacity. PubMed
8 Pickart L., Vasquez-Soltero J.M., & Margolina A. (2012). The Human Tripeptide GHK-Cu in Prevention of Oxidative Stress and Degenerative Conditions of Aging: Implications for Cognitive Health. Oxidative Medicine and Cellular Longevity. Summarizes antioxidant and anti-inflammatory effects of GHK-Cu including ↑ SOD and ↓ ROS in pre-clinical models. PubMed
9 Pickart L. (2008). The Human Tripeptide GHK and Tissue Remodeling. Journal of Biomaterials Science, Polymer Edition. Describes GHK-Cu’s regulation of MMPs, TIMPs and collagen remodeling for scar and wound healing. PubMed

Stack With