Effect of Photobiomodulation on Transforming Growth Factor-β1, Platelet-Derived Growth Factor-BB, and Interleukin-8 Release in Palatal Wounds After Free Gingival Graft Harvesting: A Randomized Clinical Study

Ilker Keskiner, Muge Lutfioğlu, Ahmet Aydogdu, N Isil Saygun, Muhittin A Serdar, Ilker Keskiner, Muge Lutfioğlu, Ahmet Aydogdu, N Isil Saygun, Muhittin A Serdar

Abstract

Objective: This study evaluated the impact of photobiomodulation (PBM) on the healing of the donor palatal area following free gingival graft (FGG) harvesting by examining changes in transforming growth factor (TGF)-β1, platelet-derived growth factor (PDGF)-BB, and interleukin (IL)-8 levels in palatal wound fluid (PWF).

Material and methods: Thirty patients were selected and randomly assigned to receive PBM (laser group) or PBM sham (sham group) in the palatine area after FGG harvesting. A neodymium-doped yttrium aluminum garnet (Nd:YAG) laser (1064 nm) was applied to the test sites immediately after surgery and every 24 h thereafter for 4 days. PWF was collected on Days 7 and 12, and PWF TGF-β1, PDGF-BB, and IL-8 levels were analyzed by enzyme-linked immunosorbent assays (ELISA).

Results: PWF TGF-β1, PDGF-BB, and IL-8 levels were significantly lower on Day 12 than on Day 7 for both groups. PWF TGF-β1, PDGF-BB, and IL-8 levels of the laser group were significantly higher than those of sham group on Day 7 (p < 0.05). PWF TGF-β1 levels were also significantly higher in laser group than in the sham group on Day 12; however, differences in PDGF-BB and IL-8 levels between groups on Day 12 were statistically nonsignificant.

Conclusions: Observed increases in PWF TGF-β1, PDGF-BB, and IL-8 levels suggest that PBM may accelerate wound healing by stimulating production of selected mediators.

Figures

FIG. 1.
FIG. 1.
Consolidated Standards of Reporting Trials (CONSORT) patient flow chart.
FIG. 2.
FIG. 2.
Clinical views of wound area of the laser group: (a) before surgery, (b) after harvesting free gingival graft (FGG), (c) healing on Day 7, (d) healing on Day 12. Sham group: (e) before surgery, (f) after harvesting FGG, (g) healing on Day 7, (h) healing on Day 12.
FIG. 3.
FIG. 3.
Palatal wound fluid sampling.

References

    1. Aoki A, Mizutani K, Schwarz F, et al. . Periodontal and peri-implant wound healing following laser therapy. Periodontol 2000 2015;68:217–269
    1. Ishikawa I, Aoki A, Takasaki AA, Mizutani K, Sasaki KM, Izumi Y. Application of lasers in periodontics: true innovation or myth? Periodontol 2000 2009;50:90–126
    1. Firat ET, Dağ A, Günay A, et al. . The effects of low-level laser therapy on palatal mucoperiosteal wound healing and oxidative stress status in experimental diabetic rats. Photomed Laser Surg 2013;31:315–321
    1. Saygun I, Nizam N, Ural AU, Serdar MA, Avcu F, Tözüm TF. Low-level laser irradiation affects the release of basic fibroblast growth factor (bFGF), insulin-like growth factor-I (IGF-I), and receptor of IGF-I (IGFBP3) from osteoblasts. Photomed Laser Surg 2012;30:149–154
    1. Saygun I, Karacay S, Serdar M, Ural AU, Sencimen M, Kurtis B. Effects of laser irradiation on the release of basic fibroblast growth factor (bFGF), insulin like growth factor-1 (IGF-1), and receptor of IGF-1 (IGFBP3) from gingival fibroblasts. Lasers Med Sci 2008;23:211–215
    1. Choi EJ, Yim JY, Koo KT, et al. . Biological effects of a semiconductor diode laser on human periodontal ligament fibroblasts. J Periodontal Implant Sci 2010;40:105–110
    1. Lee JY, Kim IR, Park BS, et al. . Effect of low-level laser therapy on oral keratinocytes exposed to bisphosphonate. Lasers Med Sci 2015;30:635–643
    1. Basso FG, Pansani TN, Soares DG, et al. . Biomodulation of inflammatory cytokines related to oral mucositis by low-level laser therapy. Photochem Photobiol 2015;91:952–956
    1. Medrado AR, Pugliese LS, Reis SR, Andrade ZA. Influence of low level laser therapy on wound healing and its biological action upon myofibroblasts. Lasers Surg Med 2003;32:239–244
    1. Al-Watban FA, Delgado GD. Burn healing with a diode laser: 670 nm at different doses as compared to a placebo group. Photomed Laser Surg 2005;23:245–250
    1. Fahimipour F, Mahdian M, Houshmand B, et al. . The effect of He-Ne and Ga-Al-As laser light on the healing of hard palate mucosa of mice. Lasers Med Sci 2013;28:93–100
    1. Al-Watban FA, Andres BL. Laser biomodulation of normal and neoplastic cells. Lasers Med Sci 2012;27:1039–1043
    1. Cambier DC, Vanderstraeten GG, Mussen MJ, van der Spank JT. Low-power laser and healing of burns: a preliminary assay. Plast Reconstr Surg 1996;97:555–558
    1. Walker MD, Rumpf S, Baxter GD, Hirst DG, Lowe AS. Effect of low-intensity laser irradiation (660 nm) on a radiation-impaired wound- healing model in murine skin. Lasers Surg Med 2000;6:41–47
    1. Schlager A, Kronberger P, Petschke F, Ulmer H. Low-power laser light in the healing of burns: a comparison between two different wavelengths (635 nm and 690 nm) and a placebo group. Lasers Surg Med 2000;27:39–42
    1. Jahangiri Noudeh Y, Shabani M, Vatankhah N, Hashemian SJ, Akbari K. A combination of 670 nm and 810 nm diode lasers for wound healing acceleration in diabetic rats. Photomed Laser Surg 2010;28:621–627
    1. Firat ET, Dağ A, Günay A, et al. . The effect of low-level laser therapy on the healing of hard palate mucosa and the oxidative stress status of rats. J Oral Pathol Med 2014;43:103–110
    1. Dias SB, Fonseca MV, Dos Santos NC, et al. . Effect of GaAIAs low-level laser therapy on the healing of human palate mucosa after connective tissue graft harvesting: randomized clinical trial. Lasers Med Sci 2015;30:1695–1702
    1. Aras MH, Güngörmüş M. Placebo-controlled randomized clinical trial of the effect two different low-level laser therapies (LLLT)—intraoral and extraoral—on trismus and facial swelling following surgical extraction of the lower third molar. Lasers Med Sci 2010;25:641–645
    1. Sezer U, Eltas A, Ustün K, Senyurt SZ, Erciyas K, Aras MH. Effects of low-level laser therapy as an adjunct to standard therapy in acute pericoronitis, and its impact on oral health-related quality of life. Photomed Laser Surg 2012;30:592–597
    1. Vescovi P, Meleti M, Merigo E, et al. . Case series of 589 tooth extractions in patients under bisphosphonates therapy. Proposal of a clinical protocol supported by Nd:YAG low-level laser therapy. Med Oral Patol Oral Cir Bucal 2013;18:680–685
    1. Vescovi P, Giovannacci I, Merigo E, et al. . Tooth extractions in high-risk patients under bisphosphonate therapy and previously affected with osteonecrosis of the jaws: surgical protocol supported by low-level laser therapy. J Craniofac Surg 2015;26:696–699
    1. Luomanen M, Alaluusua S. Treatment of bisphosphonate-induced osteonecrosis of the jaws with Nd:YAG laser biostimulation. Lasers Med Sci 2012;27:251–255
    1. Chellini F, Sassoli C, Nosi D, et al. . Low pulse energy Nd:YAG laser irradiation exerts a biostimulative effect on different cells of the oral microenvironment: “an in vitro study”. Lasers Surg Med 2010;42:527–539
    1. Usumez A, Cengiz B, Oztuzcu S, Demir T, Aras MH, Gutknecht N. Effects of laser irradiation at different wavelengths (660, 810, 980, and 1,064 nm) on mucositis in an animal model of wound healing. Lasers Med Sci 2014;29:1807–1813
    1. Susin C, Fiorini T, Lee J, De Stefano JA, Dickinson DP, Wikesjö UM. Wound healing following surgical and regenerative periodontal therapy. Periodontology 2000 2015;68:83–98
    1. Polimeni G, Xiropaidis AV, Wikesjö UM. Biology and principles of periodontal wound healing/regeneration. Periodontol 2000 2006;41:30–47
    1. Häkkinen L, Uitto VJ, Larjava H. Cell biology of gingival wound healing. Periodontol 2000 2000;24:127–152
    1. Barrientos S, Stojadinovic O, Golinko MS, Brem H, Tomic–Canic M. Growth factors and cytokines in wound healing. Wound Repair Regen 2008;16:585–601
    1. Bartold PM, Narayanan AS. Molecular and cell biology of healthy and diseased periodontal tissues. Periodontol 2000 2006;40:29–49
    1. Ray AK, Jones AC, Carnes DL, Cochran DL, Mellonig JT, Oates TW., Jr. Platelet-derived growth factor-BB stimulated cell migration mediated through p38 signal transduction pathway in periodontal cells. J Periodontol 2003;74:1320–1328
    1. Mumford JH, Carnes DL, Cochran DL, Oates TW. The effects of platelet-derived growth factor-BB on periodontal cells in an in vitro wound model. J Periodontol 2001;72:331–340
    1. Javed F, Al-Askar M, Al-Rasheed A, Al-Hezaimi K. Significance of the platelet-derived growth factor in periodontal tissue regeneration. Arch Oral Biol 2011;56:1476–1484
    1. Fujita T, Yoshimoto T, Matsuda S, et al. . Interleukin-8 induces DNA synthesis, migration and down-regulation of cleaved caspase-3 in cultured human gingival epithelial cells. J Periodontal Res 2015;50:479–485
    1. Gillitzer R, Goebeler M. Chemokines in cutaneous wound healing. J Leukoc Biol 2001;69:513–521
    1. Silva CO, Ribeiro Edel P, Sallum AW, Tatakis DN. Free gingival grafts: graft shrinkage and donor-site healing in smokers and non-smokers. J Periodontol 2010;81:692–701
    1. Curtis MA, Griffiths GS, Price SJ, Coulthurst SK, Johnson NW. The total protein concentration of gingival crevicular fluid. Variation with sampling time and gingival inflammation. J Clin Periodontol 1988;15:628–632
    1. Widgerow AD. Wound fluid intervention: influencing wound healing from the outside. Wound Healing Southern Africa 2011;4:12–15
    1. Drinkwater SL, Smith A, Burnand KG. What can wound fluids tell us about the venous ulcer microenvironment? Int J Low Extrem Wounds 2002;1:184–190
    1. Yager DR, Kulina RA, Gilman LA. Wound fluids: a window into the wound environment? Int J Low Extrem Wounds 2007;6:262–272
    1. Safavi SM, Kazemi B, Esmaeili M, Fallah A, Modarresi A, Mir M. Effects of low-level He-Ne laser irradiation on the gene expression of IL-1beta, TNF-alpha, IFN-gamma, TGF-beta, bFGF, and PDGF in rat's gingiva. Lasers Med Sci 2008;23:331–335
    1. Wang CY, Tsai SC, Yu MC, Lin YF, Chen CC, Chang PC. Light-emitting diode irradiation promotes donor site wound healing of the free gingival graft. J Periodontol 2015;86:674–681
    1. Almeida AL, Esper LA, Sbrana MC, Ribeiro IW, Kaizer RO. Utilization of low-intensity laser during healing of free gingival grafts. Photomed Laser Surg 2009;27:561–564
    1. Fernandes–Dias SB, de Marco AC, Santamaria M, Jr, Kerbauy WD, Jardini MA, Santamaria MP. Connective tissue graft associated or not with low laser therapy to treat gingival recession: randomized clinical trial. J Clin Periodontol 2015;42:54–61
    1. Amorim JC, de Sousa GR, de Barros Silveira L, Prates RA, Pinotti M, Ribeiro MS. Clinical study of the gingiva healing after gingivectomy and low-level laser therapy. Photomed Laser Surg 2006;24:588–594
    1. Ozcelik O, Cenk Haytac M, Kunin A, Seydaoglu G. Improved wound healing by low-level laser irradiation after gingivectomy operations: a controlled clinical pilot study. J Clin Periodontol 2008;35:250–254
    1. Damante CA, Greghi SL, Sant'ana AC, Passanezi E. Clinical evaluation of the effects of low-intensity laser (GaAlAs) on wound healing after gingivoplasty in humans. J Appl Oral Sci 2004;12:133–136
    1. Dinh T, Braunagel S, Rosenblum BI. Growth factors in wound healing: the present and the future? Clin Podiatr Med Surg 2015;32:109–119
    1. Damante CA, De Micheli G, Miyagi SP, Feist IS, Marques MM. Effect of laser phototherapy on the release of fibroblast growth factors by human gingival fibroblasts. Lasers Med Sci 2009;24:885–891
    1. Meckmongkol TT, Harmon R, McKeown-Longo P, Van De Water L. The fibronectin synergy site modulates TGF- beta-dependent fibroblast contraction. Biochem Biophys Res Commun 2007;360:709–714
    1. Lin H, Chen B, Sun W, Zhao W, Zhao Y, Dai J. The effect of collagen-targeting platelet-derived growth factor on cellurization and vascularization of collagen scaffolds. Biomaterials 2006;27:5708–5714
    1. Rhee S, Grinnell F. P21-activated kinase 1: convergence point in PDGF- and LPA-stimulated collagen matrix contraction by human fibroblasts. J Cell Biol 2006;172:423–432
    1. Jinnin M, Ihn H, Mimura Y, Asano Y, Yamane K, Tamaki K. Regulation of fibrogenic/fibrolytic genes by platelet-derived growth factor C, a novel growth factor, in human dermal fibroblasts. J Cell Physiol 2005;202:510–517
    1. Niessen FB, Andriessen MP, Schalkwijk J, Visser L, Timens W. Keratinocyte-derived growth factors play a role in the formation of hypertrophic scars. J Pathol 2001;194:207–216
    1. Devalaraja RM, Nanney LB, Du J, et al. . Delayed wound healing in CXCR2 knockout mice. J Invest Dermatol 2000;115:234–244
    1. Rennekampff HO, Hansbrough JF, Kiessig V, Doré C, Sticherling M, Schröder JM. Bioactive interleukin-8 is expressed in wounds and enhances wound healing. J Surg Res 2000;93:41–54
    1. Iocono JA, Colleran KR, Remick DG, Gillespie BW, Ehrlich HP, Garner WL. Interleukin-8 levels and activity in delayed-healing human thermal wounds. Wound Repair Regen 2000;8:216–225
    1. Basso FG, Pansani TN, Soares DG, et al. . Biomodulation of inflammatory cytokines related to oral mucositis by low-level laser therapy. Photochem Photobiol 2015;91:952–956
    1. Qadri T, Bohdanecka P, Tunér J, Miranda L, Altamash M, Gustafsson A. The importance of coherence length in laser phototherapy of gingival inflammation: a pilot study. Lasers Med Sci 2007;22:245–251
    1. Saglam M, Kantarci A, Dundar N, Hakki SS. Clinical and biochemical effects of diode laser as an adjunct to nonsurgical treatment of chronic periodontitis: a randomized, controlled clinical trial. Lasers Med Sci. 2014;29:37–46

Source: PubMed

3
Iratkozz fel