» Articles » PMID: 37959659

Analysis of Skin Regeneration and Barrier-Improvement Efficacy of Polydeoxyribonucleotide Isolated from Panax Ginseng (C.A. Mey.) Adventitious Root

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2023 Nov 14
PMID 37959659
Authors
Affiliations
Soon will be listed here.
Abstract

Polydeoxyribonucleotide (PDRN) has the ability to regenerate skin cells and improve the skin barrier and wound healing. This study investigated the possibility of replacing animal-derived PDRN with plant-derived PDRN. To test this, the adventitious roots of Korean ginseng (Panax ginseng C.A. Meyer), which is commonly used to treat various diseases, were suspension-cultivated through tissue culture; subsequently, PDRN was purified using microfluidization, an ultra-high-pressure physical grinding method. The results showed that purified Panax PDRN was effective in healing skin wounds and enhancing the skin barrier. Panax PDRN promoted the proliferation of keratinocytes and fibroblasts by increasing the expression of fibronectin, filaggrin, Ki-67, Bcl-2, inhibin beta A, and Cyclin D1. It also acted as an agonist of the adenosine A2A receptor and induced the phosphorylation of focal adhesion kinase, adenosine triphosphate-dependent tyrosine kinase, and mitogen-activated protein kinase. This activated signal transduction, thereby regenerating skin cells and strengthening the barrier. These results were not only observed in skin cells but also in an artificial skin model (KeraSkin). The use of plant-derived PDRN instead of animal-derived PDRN can promote animal welfare and environmental sustainability. Furthermore, Panax PDRN can potentially be a new plant-derived PDRN (PhytoPDRN) that may be utilized in the treatment of various skin diseases.

Citing Articles

Effects of Chlorella protothecoides-derived polydeoxyribonucleotides on skin regeneration and wound healing.

Park J, Nam G, Lee E, Kim H, Kim H, Myoung K Arch Dermatol Res. 2025; 317(1):483.

PMID: 39994014 DOI: 10.1007/s00403-025-03885-w.


From Polydeoxyribonucleotides (PDRNs) to Polynucleotides (PNs): Bridging the Gap Between Scientific Definitions, Molecular Insights, and Clinical Applications of Multifunctional Biomolecules.

Marques C, Porcello A, Cerrano M, Hadjab F, Chemali M, Lourenco K Biomolecules. 2025; 15(1).

PMID: 39858543 PMC: 11764130. DOI: 10.3390/biom15010148.


First Report on Microbial-Derived Polydeoxyribonucleotide: A Sustainable and Enhanced Alternative to Salmon-Based Polydeoxyribonucleotide.

Chae D, Oh S, Choi Y, Kang D, Park C, Lee J Curr Issues Mol Biol. 2025; 47(1).

PMID: 39852156 PMC: 11763902. DOI: 10.3390/cimb47010041.


The Effect of Polynucleotide-Hyaluronic Acid Hydrogel in the Recovery After Mechanical Skin Barrier Disruption.

Ha Y, Tak K, Jung J, Lee J, Kim C, Ah Y Skin Res Technol. 2024; 30(9):e70068.

PMID: 39300806 PMC: 11413333. DOI: 10.1111/srt.70068.

References
1.
Van den Bossche J, Van Ginderachter J . E-cadherin: from epithelial glue to immunological regulator. Eur J Immunol. 2012; 43(1):34-7. DOI: 10.1002/eji.201243168. View

2.
Valdatta L, Thione A, Mortarino C, Buoro M, Tuinder S . Evaluation of the efficacy of polydeoxyribonucleotides in the healing process of autologous skin graft donor sites: a pilot study. Curr Med Res Opin. 2004; 20(3):403-8. DOI: 10.1185/030079904125003116. View

3.
Noh T, Chung B, Kim S, Lee M, Kim M, Youn C . Novel Anti-Melanogenesis Properties of Polydeoxyribonucleotide, a Popular Wound Healing Booster. Int J Mol Sci. 2016; 17(9). PMC: 5037727. DOI: 10.3390/ijms17091448. View

4.
Thellung S, Florio T, Maragliano A, Cattarini G, Schettini G . Polydeoxyribonucleotides enhance the proliferation of human skin fibroblasts: involvement of A2 purinergic receptor subtypes. Life Sci. 1999; 64(18):1661-74. DOI: 10.1016/s0024-3205(99)00104-6. View

5.
Altavilla D, Squadrito F, Polito F, Irrera N, Calo M, Lo Cascio P . Activation of adenosine A2A receptors restores the altered cell-cycle machinery during impaired wound healing in genetically diabetic mice. Surgery. 2010; 149(2):253-61. DOI: 10.1016/j.surg.2010.04.024. View