Level D· Scientific groundwork from lab and animal studiesLaboratory StudyEurope PMCOpen access

Effect of Photobiomodulation with 980nm Diode Laser and Vitamin D on Proliferation and Osteoblastic Differentiation of Periodontal Ligament Stem Cells : Effects of Photobiomodulation and Vitamin D on Differentiation of S

Moussavi Jahanabadi SAH., Taleghani F., Tehranchi M., Hakimiha N., Hodjat M., Saberi Haghighi R.

Laboratory Study on Ligament Injury, published in Galen Med J (2024) — summary generated from the PubMed abstract.

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Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
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This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Laboratory Study
Journal
Galen Med J (2024)
Reported sample size
—
Source database
Europe PMC
PMID
42039994
PMCID
PMC12107314
DOI
10.31661/gmj.v13isp1.3624

Abstract (original English)

Background It has been established that periodontal ligament stem cells (PDLSCs) have a significant impact on restoration of periodontal tissues, and optimizing their differentiation into osteoblast is critical to improving clinical outcomes in periodontal regeneration. Different non-invasive method, including photobiomodulation (PBM) and vitamin D supplementation, hold potential for enhancing Osteoblastic Differentiation. the present work aimed at investigating the synergic impact of PBM by the use of a 980 nm diode laser and vitamin D on the osteogenic differentiation and cell viability of PDLSCs. Materials and methods Cultured PDLSCs were separated into six groups: 1. Control (no treatment), 2. Vitamin D, 3. PBM at 2 J/cm², 4. PBM at 2 J/cm² with Vitamin D (VD- 2 J/cm²), 5. PBM at 4 J/cm², and 6. PBM at 4 J/cm² with Vitamin D (VD- 4 J/cm²). We evaluated cell viability using the methyl thiazolyl tetrazolium assay at 24 and 72 hours post-irradiation. For the osteogenic differentiation assessment, we measured expression of osteogenic genes, including Runt-related transcription factor 2(RUNX2), Osteocalcin (OCN), alkaline phosphatase (ALP), and Osteopontin(OPN), through quantitative reverse transcription-polymerase chain reaction. Additionally, Alizarin red staining was utilized for detecting calcification. Results All study groups demonstrated enhanced viability in comparison w

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is preclinical work; animal or laboratory results cannot be applied to humans.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

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