Effects of GHK peptide and its structural analogues on dynamics of healing and bacterial contamination of infected wound
- Authors: Rakhmetova K.K.1, Bobyntsev I.I.1, Zhilyayeva L.V.1, Bezhin A.I.1, Vorvul' A.O.1
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Affiliations:
- Kursk State Medical University
- Issue: Vol 32, No 4 (2024)
- Pages: 539-548
- Section: Original study
- URL: https://journals.rcsi.science/pavlovj/article/view/279484
- DOI: https://doi.org/10.17816/PAVLOVJ471212
- ID: 279484
Cite item
Abstract
INTRODUCTION: Currently, a promising trend to accelerate wound process seems to be the use of NH2-Gly-L-His-L-Lys-COOH (GHK) tripeptide, which acts on the tissue regeneration, possesses antioxidant, immunotropic and anti-inflammatory effects. At the same time, the disadvantage of all peptides is their rapid degradation by proteolytic enzymes. One method to increase the stability of peptide molecules is the incorporation of D-isomers of amino acids in their structure. It was previously found by us that GHK-D-Ala produces a more marked effect on regenerative processes in the wound and facilitates increase in the number of fibroblast cells and macrophages in the wound with the underlying decrease in the number of granulocytes and lymphocytes; a significant effect of D-Ala-GHK and GHK-D-Ala on the parameters of the inborn immunity and lipid peroxidation was shown.
AIM: To evaluate the healing dynamics and bacterial contamination of an infected wound when using Glycyl-Histidyl-Lysine (GHK) peptide and its structural modifications with D-alanine (D-Ala).
MATERIALS AND METHODS: The experiments were conducted on Wistar rats. In the work, GHK peptide and its structural analogues D-Ala-GHK and GHK-D-Ala were used; they were administered intracutaneously around the wound at doses of 0.5 µg/kg and 1.5 µg/kg every 24 hours for 3rd, 7th and 10th days. The wound area with calculation of the relative wound healing coefficient (RWHC), the healing rate, the time of perifocal edema disappearance, wound cleansing, appearance of granulation and onset of marginal epithelialization were assessed. Bacterial contamination was determined by counting colonies on the nutrient media after inoculation of wound biopsy material on them.
RESULTS: On day 3rd, RWHC increased 3.2–5.3 times (p < 0.05–0.01) after the use of D-Ala-GHK and GHK-D-Ala peptides at both doses with no effect after the injection of GHK. On day 7th, the reduction of the wound area reached statistically significant differences in all experimental groups. By day 10th, the use of peptides resulted in decrease in the wound area most evident after the injection of GHK-D-Ala peptide (by 93%, p < 0.001) in all groups. On days 7th–10th, GHK-D-Ala increased the healing rate 4.7–5.3 times (p < 0.05-0.01) with no significant changes after the injection of GHK and D-Ala-GHK. Also, GHK-D-Ala at both doses resulted in the earliest disappearance of perifocal edema, wound cleansing, emergence of granulation and the onset of marginal epithelialization in all experimental groups. Significant reduction in bacterial contamination was observed after administration of all peptides on days 7th and 10th, being most pronounced after the use of GHK-D-Ala.
CONCLUSION: The application of GHK peptide and its structural analogues D-Ala-GHK and GHK-D-Ala in infected skin wounds accelerated wound healing against the background reduction of bacterial contamination. The most pronounced changes of these parameters were observed after administration of GHK-D-Ala peptide, which indicates the importance of protecting GHK molecule against the impact of carboxypeptidases. A promising continuation of the research in this direction can be the development of local means with antibacterial effect for stimulation of the regeneration processes in the wound.
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##article.viewOnOriginalSite##About the authors
Kamila K. Rakhmetova
Kursk State Medical University
Email: muminovak@mail.ru
ORCID iD: 0000-0001-5511-5962
SPIN-code: 5852-8840
Russian Federation, Kursk
Igor' I. Bobyntsev
Kursk State Medical University
Email: bobig@mail.ru
ORCID iD: 0000-0001-7745-2599
SPIN-code: 3947-0114
MD, Dr. Sci. (Med.), Professor
Russian Federation, KurskLyudmila V. Zhilyayeva
Kursk State Medical University
Email: zhiljaevalv@kursksmu.net
ORCID iD: 0000-0003-0390-4155
SPIN-code: 1726-8119
MD, Cand. Sci. (Med.)
Russian Federation, KurskAleksandr I. Bezhin
Kursk State Medical University
Email: bezhinai@kursksmu.net
ORCID iD: 0000-0003-3776-9449
SPIN-code: 1250-5549
MD, Dr. Sci. (Med.), Professor
Russian Federation, KurskAnton O. Vorvul'
Kursk State Medical University
Author for correspondence.
Email: vorvul1996@mail.ru
ORCID iD: 0000-0002-1529-6014
SPIN-code: 8398-9376
MD, Cand. Sci. (Med.)
Russian Federation, KurskReferences
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