Cited by 65Wound Healing and TreatmentsBurn Injury Management and OutcomesDermatologic Treatments and Research

Polydeoxyribonucleotide improves angiogenesis and wound healing in experimental thermal injury

Bitto, Alessandra, Galeano, Mariarosaria, Squadrito, Francesco, Minutoli, Letteria, Polito, Francesca, Dye, Julian F., Clayton, Elizabeth A., Calò, Margherita +3 more·2008·Critical Care Medicine

Abstract

Objective Polydeoxyribonucleotide contains a mixture of nucleotides and interacts with adenosine receptors, stimulating vascular endothelial growth factor expression and wound healing. The purpose of this study was to investigate the effect of polydeoxyribonucleotide on experimental burn wounds. Design Randomized experiment. Setting Research laboratory at a university hospital. Subjects Thermal injury in mice. Interventions Mice were immersed in 80 degrees C water for 10 secs to achieve a deep-dermal second-degree burn. Animals were randomized to receive either polydeoxyribonucleotide (8 mg/kg/day intraperitoneally for 14 days) or its vehicle alone (0.9% NaCl solution at 100 microL/day intraperitoneally). On days 7 and 14 the animals were killed. Blood was collected for tumor necrosis factor-alpha measurement; burn areas were used for histologic and immunohistochemical examination, for the evaluation of vascular endothelial growth factor and nitric oxide synthases by Western blot, and for the determination of wound nitric oxide products. Measurements and main results Polydeoxyribonucleotide increased burn wound re-epithelialization and reduced the time to final wound closure. Polydeoxyribonucleotide improved healing of burn wound through increased epithelial proliferation and maturation of the extracellular matrix as confirmed by fibronectin and laminin immunostaining. Polydeoxyribonucleotide also improved neoangiogenesis as suggested by the marked increase in microvessel den…

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Crossref · 10.1097/ccm.0b013e318170ab5c

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  • Upon enzymatic degradation, PDRN yields a pool of bioavailable nucleosides and nucleotides that can be rapidly reincorporated into cellular processes, promoting tissue regeneration and accelerating wound healing.

    “Upon enzymatic degradation, PDRN yields a pool of bioavailable nucleosides and nucleotides that can be rapidly reincorporated into cellular processes, thereby promoting tissue regeneration and accelerating wound healing [50,75,76,77].”

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Authors
Bitto, A., Galeano, M., Squadrito, F., Minutoli, L., Polito, F., Dye, J. F., Clayton, E. A., Calò, M., Venuti, F. S., Vaccaro, M., & Altavilla, D.
Affiliations
University of Messina (IT)
Venue
Critical Care Medicine
Published
2008-05
Volume
36
Issue
5
Pages
1594-1602
ISSN
0090-3493 (ISSN-L)
OpenAlex
W2015613680
Cited by
65
References
0
Citations by year
2026: 7 · 2025: 6 · 2024: 3 · 2023: 4 · 2022: 2 · 2021: 2 · 2020: 4 · 2019: 4 · 2018: 5 · 2017: 5 · 2016: 4 · 2015: 2 · 2014: 4 · 2013: 3
FWCI
3.56
Type
journal article
Language
en
Open access
closed
Locations
  • Critical Care Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
  • Health Sciences › Medicine › Epidemiology › Burn Injury Management and Outcomes
  • Health Sciences › Medicine › Dermatology › Dermatologic Treatments and Research
Keywords
polydeoxyribonucleotide, burns, burn wounds, wound healing, angiogenesis, re-epithelialization, vascular endothelial growth factor, nitric oxide synthase, inducible nitric oxide synthase, TNF-α, CD31, microvessel density, extracellular matrix, fibronectin, laminin, adenosine receptors
MeSH terms
Animals, Burns, Male, Mice, Inbred C57BL, Polydeoxyribonucleotides, Wound Healing, Neovascularization, Physiologic, Mice

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