Anti‐inflammatory effect of polydeoxyribonucleotides (PDRN) extracted from red alga ( Porphyra sp.) (Ps‐PDRN) in RAW 264.7 macrophages stimulated with Escherichia coli lipopolysaccharides: A comparative study with commercial PDRN
Abstract
Polydeoxyribonucleotide (PDRN) is a DNA‐derived drug extracted from the sperm cells of Oncorhynchus mykiss or O. keta . PDRN exhibits wound healing and anti‐inflammatory activities by activating adenosine A 2A receptor and salvage pathways. However, commercial PDRN products (e.g., Placentex, Rejuvenex, and HiDr) have limitations as they are exclusively extracted O. mykiss and O. keta , which are expensive and can only be used as extraction sources during a specific period when their sperm cells are activated. Therefore, this study aimed to extract PDRN from Porphyra sp. (Ps‐PDRN) and investigate whether it has anti‐inflammatory activity through a comparative study with commercial product. The results indicated that Ps‐PDRN had an anti‐inflammatory effect on Escherichia coli lipopolysaccharides (LPS)‐stimulated RAW 264.7 macrophages. It inhibited nitric oxide production and inducible nitric oxygen synthase protein expression by suppressing phosphorylation of p38 and ERK, without cytotoxicity. Furthermore, Ps‐PDRN promoted cell proliferation and collagen production in human dermal fibroblast. In conclusion, our study confirms that Ps‐PDRN exhibits both anti‐inflammatory and cell proliferative effects. These results indicated that Ps‐PDRN has the potential as a bioactive drug for tissue engineering.
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PDRN exerts notable anti-inflammatory effects.
“For instance, PDRN has been shown to stimulate the proliferation of skin fibroblasts [52] and osteoblasts [53], accelerate wound healing [25,54], promote angiogenesis [55], and exert notable anti-inflammatory effects [56].”
From Comparison of Polynucleotide and Polydeoxyribonucleotide in Dermatology: Molecular Mechanisms and Clinical Perspectives (2025) · cites this paper as [56]
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Kim, S. T. (2025) · Pharmaceutics · doi:10.3390/pharmaceutics17081024 · Cited by 18 · see citing works
- Authors
- Kim, T., Heo, S., Han, J. S., & Jung, W.
- Affiliations
- Pukyong National University (KR)
- Korea Institute of Ocean Science and Technology (KR)
- All In One GENETECH Busan Republic of Korea
- Corresponding author
- Jung, Won‐Kyo
- Venue
- Cell Biochemistry and Function
- Publisher
- Wiley
- Published
- 2023-08-17
- Volume
- 41
- Issue
- 7
- Pages
- 889-897
- ISSN
- 0263-6484 (ISSN-L)
- 1099-0844
- OpenAlex
- W4385898256
- Cited by
- 21
- References
- 0
- Citations by year
- 2026: 7 · 2025: 10 · 2024: 4
- FWCI
- 4.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell Biochemistry and Function (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Research Foundation of Korea (2019R1A2C1007218, 2021R1A6A1A03039211)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Aquatic Science › Seaweed-derived Bioactive Compounds
- Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Keywords
- polydeoxyribonucleotide, Porphyra, red algae, anti-inflammatory activity, RAW 264.7 macrophages, lipopolysaccharide, nitric oxide, inducible nitric oxide synthase, p38 MAPK, ERK, dermal fibroblasts, collagen synthesis, cell proliferation, tissue engineering, marine biomaterials
- MeSH terms
- RAW 264.7 Cells, Animals, Anti-Inflammatory Agents, Escherichia coli, Lipopolysaccharides, Macrophages, Nitric Oxide, Polydeoxyribonucleotides, Porphyra, Mice
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