840 research outputs found

    In Vitro Wound Healing Improvement By Low-level Laser Therapy Application In Cultured Gingival Fibroblasts

    Get PDF
    The aim of this study was to determine adequate energy doses using specific parameters of LLLT to produce biostimulatory effects on human gingival fibroblast culture. Cells (3 10 4 cells/cm 2) were seeded on 24-well acrylic plates using plain DMEM supplemented with 10 fetal bovine serum. After 48-hour incubation with 5 CO2 at 37C, cells were irradiated with a InGaAsP diode laser prototype (LASERTable; 780 3 nm; 40mW) with energy doses of 0.5, 1.5, 3, 5, and 7J/cm 2. Cells were irradiated every 24h totalizing 3 applications. Twenty-four hours after the last irradiation, cell metabolism was evaluated by the MTT assay and the two most effective doses (0.5 and 3J/cm 2) were selected to evaluate the cell number (trypan blue assay) and the cell migration capacity (wound healing assay; transwell migration assay). Data were analyzed by the Kruskal-Wallis and Mann-Whitney nonparametric tests with statistical significance of 5. Irradiation of the fibroblasts with 0.5 and 3J/cm 2 resulted in significant increase in cell metabolism compared with the nonrradiated group (P 0.05). Both energy doses promoted significant increase in the cell number as well as in cell migration (P 0.05). These results demonstrate that, under the tested conditions, LLLT promoted biostimulation of fibroblasts in vitro. Copyright © 2012 Fernanda G. Basso et al.Hkkinen, L., Uitto, V.J., Larjava, H., Cell biology of gingival wound healing (2000) Periodontology 2000, 24 (1), pp. 127-152Kreisler, M., Christoffers, A.B., Al-Haj, H., Willershausen, B., D'Hoedt, B., Low level 809-nm diode laser-induced in vitro stimulation of the proliferation of human gingival fibroblasts (2002) Lasers in Surgery and Medicine, 30 (5), pp. 365-369. , DOI 10.1002/lsm.10060Posten, W., Wrone, D.A., Dover, J.S., Arndt, K.A., Silapunt, S., Alam, M., Low-level laser therapy for wound healing: Mechanism and efficacy (2005) Dermatologic Surgery, 31 (3), pp. 334-340Saygun, I., Karacay, S., Serdar, M., Ural, A.U., 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 (2008) Lasers in Medical Science, 23 (2), pp. 211-215. , DOI 10.1007/s10103-007-0477-3Skopin, M.D., Molitor, S.C., Effects of near-infrared laser exposure in a cellular model of wound healing (2009) Photodermatology Photoimmunology and Photomedicine, 25 (2), pp. 75-80Hakki, S.S., Bozkurt, S.B., Effects of different setting of diode laser on the mRNA expression of growth factors and type i collagen of human gingival fibroblasts (2012) Lasers in Medical Science, 27 (2), pp. 325-331Peplow, P.V., Chung, T.Y., Baxter, G.D., Laser photobiomodulation of proliferation of cells in culture: A review of human and animal studies (2010) Photomedicine and Laser Surgery, 28, pp. 3-S40. , supplement 1Basso, F.G., Oliveira, C.F., Kurachi, C., Hebling, J., Costa, C.A., Biostimulatory effect of low-level laser therapy on keratinocytes in vitro Lasers in Medical Science, , In pressOliveira, C.F., Basso, F.G., Lins, E.C., Kurachi, C., Hebling, J., Bagnato, V.S., De Souza Costa, C.A., In vitro effect of low-level laser on odontoblast-like cells (2011) Laser Physics Letters, 8 (2), pp. 155-163Mosmann, T., Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays (1983) Journal of Immunological Methods, 65 (1-2), pp. 55-63Wiegand, C., Hipler, U., Methods for the measurement of cell and tissue compatibility including tissue regeneration process (2008) GMS Krankenhaushygiene Interdisziplinr, 3 (1), pp. 1863-5245Hoang, A.M., Oates, T.W., Cochran, D.L., In vitro wound healing responses to enamel matrix derivative (2000) Journal of Periodontology, 71 (8), pp. 1270-1277Liang, C.-C., Park, A.Y., Guan, J.-L., In vitro scratch assay: A convenient and inexpensive method for analysis of cell migration in vitro (2007) Nature Protocols, 2 (2), pp. 329-333. , DOI 10.1038/nprot.2007.30, PII NPROT.2006.30Cceres, M., Romero, A., Copaja, M., Daz-Araya, G., Martnez, J., Smith, P.C., Simvastatin alters fibroblastic cell responses involved in tissue repair (2011) Journal of Periodontal Research, 46 (4), pp. 456-463Chor, A., De Azevedo, A.M., Maiolino, A., Nucci, M., Successful treatment of oral lesions of chronic lichenoid graft-vs.-host disease by the addition of low-level laser therapy to systemic immunosuppression (2004) European Journal of Haematology, 72 (3), pp. 222-224. , DOI 10.1046/j.0902-4441.2003.00202.xAbramoff, M.M.F., Lopes, N.N.F., Lopes, L.A., Dib, L.L., Guilherme, A., Caran, E.M., Barreto, A.D., Petrilli, A.S., Low-level laser therapy in the prevention and treatment of chemotherapy-induced oral mucositis in young patients (2008) Photomedicine and Laser Surgery, 26 (4), pp. 393-400Woodruff, L.D., Bounkeo, J.M., Brannon, W.M., Dawes Jr., K.S., Barham, C.D., Waddell, D.L., Enwemeka, C.S., The efficacy of laser therapy in wound repair: A meta-analysis of the literature (2004) Photomedicine and Laser Surgery, 22 (3), pp. 241-247. , DOI 10.1089/1549541041438623Damante, C.A., De Micheli, G., Miyagi, S.P.H., Feist, I.S., Marques, M.M., Effect of laser phototherapy on the release of fibroblast growth factors by human gingival fibroblasts (2009) Lasers in Medical Science, 24 (6), pp. 885-891Almeida-Lopes, L., Rigau, J., Zangaro, R.A., Guidugli-Neto, J., Jaeger, M.M.M., Comparison of the low level laser therapy effects on cultured human gingival fibroblasts proliferation using different irradiance and same fluence (2001) Lasers in Surgery and Medicine, 29 (2), pp. 179-184. , DOI 10.1002/lsm.1107Alghamdi, K.M., Kumar, A., Moussa, N.A., Low-level laser therapy: A useful technique for enhancing the proliferation of various cultured cells (2011) Lasers in Medical Science, 27 (1), pp. 237-249Gao, X., Xing, D., Molecular mechanisms of cell proliferation induced by low power laser irradiation (2009) Journal of Biomedical Science, 164Karu, T.I., Pyatibrat, L.V., Kolyakov, S.F., Afanasyeva, N.I., Absorption measurements of a cell monolayer relevant to phototherapy: Reduction of cytochrome c oxidase under near IR radiation (2005) Journal of Photochemistry and Photobiology B: Biology, 81 (2), pp. 98-106. , DOI 10.1016/j.jphotobiol.2005.07.002, PII S1011134405001302Eells, J.T., Henry, M.M., Summerfelt, P., Wong-Riley, M.T.T., Buchmann, E.V., Kane, M., Whelan, N.T., Whelan, H.T., Therapeutic photobiomodulation for methanol-induced retinal toxicity (2003) Proceedings of the National Academy of Sciences of the United States of America, 100 (6), pp. 3439-3444. , DOI 10.1073/pnas.0534746100Zhang, L., Xing, D., Gao, X., Wu, S., Low-power laser irradiation promotes cell proliferation by activating PI3K/Akt pathway (2009) Journal of Cellular Physiology, 219 (3), pp. 553-562Azevedo, L.H., De Paula Eduardo, F., Moreira, M.S., De Paula Eduardo, C., Marques, M.M., Influence of different power densities of LILT on cultured human fibroblast growth: A pilot study (2006) Lasers in Medical Science, 21 (2), pp. 86-89. , DOI 10.1007/s10103-006-0379-9Lagan, K.M., Alyson Clements, B., McDonough, S., David Baxter, G., Low intensity laser therapy (830nm) in the management of minor postsurgical wounds: A controlled clinical study (2001) Lasers in Surgery and Medicine, 28 (1), pp. 27-32. , DOI 10.1002/1096-9101(2 001)28:13.0.CO;2-

    In Vitro Effect Of Low-level Laser Therapy On Typical Oral Microbial Biofilms

    Get PDF
    The aim of this study was to evaluate the effect of specific parameters of low-level laser therapy (LLLT) on biofilms formed by Streptococcus mutans, Candida albicans or an association of both species. Single and dual-species biofilms - SSB and DSB - were exposed to laser doses of 5, 10 or 20 J/cm 2 from a near infrared InGaAsP diode laser prototype (LASERTable; 780 ± 3 nm, 0.04 W). After irradiation, the analysis of biobilm viability (MTT assay), biofilm growth (cfu/mL) and cell morphology (SEM) showed that LLLT reduced cell viability as well as the growth of biofilms. The response of S. mutans (SSB) to irradiation was similar for all laser doses and the biofilm growth was dose dependent. However, when associated with C. albicans (DSB), S. mutans was resistant to LLLT. For C. albicans, the association with S. mutans (DSB) caused a significant decrease in biofilm growth in a dose-dependent fashion. The morphology of the microorganisms in the SSB was not altered by LLLT, while the association of microbial species (DSB) promoted a reduction in the formation of C. albicans hyphae. LLLT had an inhibitory effect on the microorganisms, and this capacity can be altered according to the interactions between different microbial species.226502510Marques, M.M., Pereira, A.N., Fujihara, N.A., Nogueira, F.N., Eduardo, C.P., Effect of low-power laser irradiation on protein synthesis and ultrastructure of human gingival fibroblasts (2004) Lasers Surg Med, 34, pp. 260-265Damante, C.A., de Micheli, G., Miyagi, S.P.H., Feist, I.S., Marques, M.M., Effect of laser phototherapy on the release of fibroblast growth factors by human gingival fibroblasts (2009) Lasers Med Sci, 24, pp. 885-891Moritz, A., Schoop, U., Goharkhay, K., Schauer, P., Doertbudak, O., Wernisch, J., Treatment of periodontal pockets with a diode laser (1998) Lasers Surg Med, 22, pp. 302-311Nussbaum, E.L., Lilge, L., Mazzulli, T., Effects of 630-, 660-, 810-, and 905-nm laser irradiation delivering radiant exposure of 1-50 J/cm 2 on three species of bacteria in vitro (2002) J Clin Laser Med Surg, 20, pp. 325-333Nussbaum, E.L., Lilge, L., Mazzulli, T., Effects of low-level laser therapy (LLLT) of 810 nm upon in vitro growth of bacteria: Relevance of irradiance and radiant exposure (2003) J Clin Laser Med Surg, 21, pp. 283-290Lino, M.D.M.C., Carvalho, F.B., Oliveira, L.R., Magalhães, E.B., Pinheiro, A.L.B., Ramalho, L.M.P., Laser phototherapy as a treatment for radiotherapy-induced oral mucositis (2011) Braz Dent J, 22, pp. 162-165Maver-Biscanin, M., Mravak-Stipetic, M., Jerolimov, V., Biscanin, A., Fungicidal effect of diode laser irradiation in patients with denture stomatitis (2004) Lasers Surg Med, 35, pp. 259-262Dworkin, M., Endogenous photosensitization in a carotinoidless mutant of Rhodopseudomonas speroides (1958) J Gen Physiol, 43, pp. 1099-1112Rosenberg, B., Kemeny, G., Switzer, R.C., Hamilton, T.C., Quantitative evidence for protein denaturation as the cause of thermal death (1971) Nature, 232, pp. 471-473Krespi, Y.P., Kizhner, V., Nistico, L., Hall-Stoodley, L., Stoodley, P., Laser disruption and killing of methicillin-resistant Staphylococcus aureus biofilms (2011) Am J Otolaryngol, 32, pp. 198-202Shirtliff, M.E., Peters, B.M., Jabra-Rizk, M.A., Cross-kingdom interactions: Candida albicans and bacteria (2009) FEMS Microbiol Lett, 299, pp. 1-8Pereira-Cenci, T., Deng, D.M., Kraneveld, E.A., Manders, E.M.M., del Bel, C.A.A., ten Cate, J.M., The effect of Streptococcus mutans and Candida glabrata on Candida albicans biofilms formed on different surfaces (2008) Arch Oral Biol, 53, pp. 755-764Marsh, P.D., Microbial ecology of dental plaque and its significance in health and disease (1994) Adv Dent Res, 8, pp. 263-271Karkowska-Kuleta, J., Rapala-Kozik, M., Kozik, A., Fungi pathogenic to humans: Molecular bases of virulence of Candida albicans, Cryptococcus neoformans and Aspergillus fumigatus (2009) Acta Biochim Pol, 56, pp. 211-224Thein, Z.M., Samaranayake, Y.H., Samaranayake, L.P., Dietary sugars, serum and the biocide chlorhexidine digluconate modify the population and structural dynamics of mixed Candida albicans and Escherichia coli biofilms (2007) APMIS, 115, pp. 1241-1251Kwieciński, J., Eick, S., Wójcik, K., Effects of tea tre (Melaleuca alternifolia) oil on Staphylococcus aureus in biofilms and stationary phase (2009) Int J Antimicrob Agents, 33, pp. 343-347Wang, Z.C., Fan, L.Y., Jiang, J.Q., Cai, W., Ding, Y., Study on the counting of Streptococcus mutans, Streptococcus sanguis, Haemophilus actinomycetemcomitans by methyl thiazolyl tetrazolium colorimetric method (2010) Hua Xi Kou Qiang Yi Xue Za Zhi, 28, pp. 306-310Nguyen, P.T.M., Abranches, J., Phan, T., Marquis, R.E., Repressed respiration of oral Streptococci grow in biofilms (2002) Curr Microbiol, 44, pp. 262-266Singleton, S., Treloar, R., Warren, P., Watson, G.K., Hodgson, R., Allison, C., Methods for microscopic characterization of oral biofilms: Analysis of colonization, microstructure, and molecular transport phenomena (1997) Adv Dent Res, 11, pp. 133-149Jarosz, L.M., Deng, D.M., van der Mei, H.C., Crielaard, W., Krom, B.P., Streptococcus mutans competence-stimulating peptide inhibits Candida albicans hypha formation (2009) Eukaryot Cell, 8, pp. 1658-1664Dortbudak, O., Haas, R., Bernhart, T., Mailath-Pokorny, G., Lethal photosensitization for decontamination of implant surface in the treatment of peri-implantitis (2001) Clin Oral Implant Res, 12, pp. 104-10
    corecore