Effect of low intensity helium-neon (HeNe) laser irradiation on experimental paracoccidioidomycotic wound healing dynamics

Photochemistry and Photobiology

Volumn 85, Issue 1, 2009, Pages 227-233

  Ferreira, Maria Carolina ^a   Gameiro, Jacy ^a   Nagib, Patrícia Resende Alo ^a   Brito, Vânia Nieto ^b   Vasconcellos, Elza Da Costa Cruz ^a   Verinaud, Liana ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

^b INSTITUTO LAURO DE SOUZA LIMA   (Brazil)

Author keywords

[No Author keywords available]

Indexed keywords

CXCL10 PROTEIN, MOUSE; GAMMA INTERFERON INDUCIBLE PROTEIN 10; INTERLEUKIN 10; INTERLEUKIN 1BETA;

ANIMAL; ARTICLE; BAGG ALBINO MOUSE; LASER; LOW LEVEL LASER THERAPY; MALE; METABOLISM; MOUSE; PATHOLOGY; RADIATION EXPOSURE; SOUTH AMERICAN BLASTOMYCOSIS; WOUND HEALING;

ANIMALS; CHEMOKINE CXCL10; INTERLEUKIN-10; INTERLEUKIN-1BETA; LASER THERAPY, LOW-LEVEL; LASERS, GAS; MALE; MICE; MICE, INBRED BALB C; PARACOCCIDIOIDOMYCOSIS; WOUND HEALING;

ANIMALIA;

EID: 58349100798     PISSN: 00318655     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1751-1097.2008.00423.x     Document Type: Article

References (40)

1. Borges-Walmsley, M. I., D. Chen, X. Shu A. R. Walmsley (2002) The pathobiology of Paracoccidioides brasiliensis. Trends Microbiol. 10, 80 87.
2. Restrepo, A. (2000) Morphological aspects of Paracoccidioides brasiliensis in lymph nodes: Implications for the prolonged latency of paracoccidioidomycosis? Med. Mycol. 38, 317 322.
3. Lupi, O., S. K. Tyring M. R. McGinnis (2005) Tropical dermatology: Fungal tropical diseases. J. Am. Acad. Dermatol. 53, 931 951.
4. Trent, J. T. R. S. Kirsner (2003) Identifying and treating mycotic skin infections. Adv. Skin Wound Care 16, 122 129.
5. Wong, T., J. A. McGrath H. Navsaria (2007) The role of fibroblasts in tissue engineering and regeneration. Br. J. Dermatol. 156, 1149 1155.
6. Darby, I. A. T. D. Hewitson (2007) Fibroblast differentiation in wound healing and fibrosis. Int. Rev. Cytol. 257, 143 147.
7. Romagnani, P., L. Lasagni, F. Annunziato, M. Serio S. Romagnani (2004) CXC chemokines: The regulatory link between inflammation and angiogenesis. Trends Immunol. 25, 201 209.
8. Qadri, T., L. Miranda, J. Tunér A. Gustafsson (2005) The short-term effects of low-level lasers as adjunct therapy in the treatment of periodontal inflammation. J. Clin. Periodontol. 32, 714 719.
9. Safavi, S. M., B. Kazemi, M. Esmaeili, A. Fallah, A. Modarresi M. Mir (2007) 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. 23, 331 335.
10. Ferreira, M. C., V. N. Brito, J. Gameiro, M. R. Costa, E. C. Vasconcellos, M. A. Cruz-Hofling L. Verinaud (2006) Effects of HeNe laser irradiation on experimental paracoccidioidomycotic lesions. J. Photochem. Photobiol. B, Biol. 84, 141 149.
11. Sano, A., N. Kurite, K. Iabuki, R. Coelho, K. Takeo, K. Nishimura M. Miyaji (1993) A comparative study of four different staining methods for estimation of live yeast form cells of Paracoccidioides brasiliensis. Mycopathologia 124, 157 161.
12. Fleiss, J. L. (1973) Statistical Methods for Rates and Proportions. Wiley, New York.
13. Klebanov, G. I. A. Poltanov (2003) Primary and secondary molecular-cellular mechanisms behind laser therapy. Laser Phys. 20, 1 14.
14. Vladimirov, Y. A., A. N. Osipov G. I. Klebanov (2004) Photobiological principles of therapeutic applications of laser radiation. Biochemistry (Mosc) 69, 81 90.
15. Azarova, V. S., M. F. Popova S. H. G. Il'iasova (1990) Effects of autotransplantation of minced muscle tissue and subsequent laser therapy on recovery of the muscle injured by irradiation. Biull. Eksp. Biol. Med. 110, 313 316.
16. Buliakova, N. V. (1989) Effect of helium-neon laser rays on the processes of postradiation recovery in the skeletal muscles of old rats. Biull. Eksp. Biol. Med. 107, 345 347.
17. Buliakova, N. V., T. A. Telegina, S. H. G. Il'iasova, I. D. Bekhoev V. S. Azarova (1992) Effects of helium-neon laser on regeneration capacity of skeletal muscles of adult guinea pigs. Biull. Eksp. Biol. Med. 113, 411 414.
18. Pober, J. S., M. P. Bevilacqua, D. L. Mendrick, L. A. Lapierre, W. Fiers M. A. Gimbrone, Jr. (1986) Two distinct monokines, interleukin 1 and tumor necrosis factor, each independently induced biosynthesis and transient expression of the same antigen on the surface of cultured human vascular endothelial cells. J. Immunol. 136, 1680 1687.
19. Pohlman, T. H., K. A. Stanness, P. G. Beatty, H. D. Ochs J. M. Harlan (1986) An endothelial cell surface factor(s) induced in vitro by lipopolysaccharide, interleukin 1, and tumor necrosis factor-α increases neutrophil adherence by a CDw18-dependent mechanism. J. Immunol. 136, 4548 4553.
20. Matsushima, K., K. Morishita, T. Yoshimura, S. Lavu, Y. Kobayashi, W. Lew, E. Appella, H. F. Kung, E. J. Leonard J. J. Oppenheim (1988) Molecular cloning of a human monocyte- derived neutrophil chemotactic factor (MDNCF) and the induction of MDNCF mRNA by interleukin 1 and tumor necrosis factor. J. Exp. Med. 167, 1883 1893.
21. Lindley, I., H. Aschauer, J. M. Siefert, C. Lam, W. Brunowsky, E. Kownatzki, M. Thelen, P. Peveri, B. Dewald, V. von Tscharner, A. Walz M. Baggiolini (1988) Synthesis and expression in Escherichia coli of the gene encoding monocyte-derived neutrophil-activating factor: Biological equivalence between natural and recombinant neutrophil-activating factor. Proc. Natl Acad. Sci. USA 85, 9199 9203.
22. Dufour, J. H., M. Dziejman, M. T. Liu, J. H. Leung, T. E. Lane A. D. Luster (2002) IFN-gamma-inducible protein 10 (IP-10; CXCL10)-deficient mice reveal a role for IP-10 in effector T cell generation and trafficking. J. Immunol. 168, 3195 3204.
23. Angiolillo, A. L., C. Sgadari, D. D. Taub, F. Liao, J. M. Farber, S. Maheshwari, H. K. Kleinman, G. H. Reaman G. Tosato (1995) Human interferon-inducible protein 10 is a potent inhibitor of angiogenesis in vivo. J. Exp. Med. 182, 155 162.
24. Detmar, M., L. F. Brown, B. Berse, R. W. Jackman, B. M. Elicker, H. F. Dvorak K. P. Claffey (1997) Hypoxia regulates the expression of vascular permeability factor/vascular endothelial growth factor (VPF/VEGF) and its receptors in human skin. J. Invest. Dermatol. 108, 263 268.
25. Detmar, M., L. F. Brown, K. P. Claffey, K. T. Yeo, O. Kocher, R. W. Jackman, B. Berse H. F. Dvorak (1994) Overexpression of vascular permeability factor/vascular endothelial growth factor and its receptors in psoriasis. J. Exp. Med. 180, 11421 1146.
26. Brown, L. F., S. M. Olbricht, B. Berse, R. W. Jackman, G. Matsueda, K. A. Tognazzi, E. J. Manseau, H. F. Dvorak L. van de Water (1995) Overexpression of vascular permeability factor (VPF/VEGF) and its endothelial cell receptors in delayed hypersensitivity skin reactions. J. Immunol. 154, 2801 2807.
27. Brown, L. F., K. T. Yeo, B. Berse, T. K. Yeo, D. R. Senger, H. F. Dvorak L. van de Water (1992) Expression of vascular permeability factor (vascular endothelial growth factor) by epidermal keratinocytes during wound healing. J. Exp. Med. 176, 1375 1379.
28. Saaristo, A., T. Tammela, A. Farkkila, M. Karkkainen, E. Suominen, S. Yla-Herttuala K. Alitalo (2006) Vascular endothelial growth factor-C accelerates diabetic wound healing. Am. J. Pathol. 169, 1080 1087.
29. Frank, S., G. Hubner, G. Breier, M. T. Longaker, D. G. Greenhalgh S. Werner (1995) Regulation of vascular endothelial growth factor expression in cultured keratinocytes: Implications for normal and impaired wound healing. J. Biol. Chem. 270, 12607 12613.
30. Reddy, G. K., L. Stehno-Bittel C. S. Enwemeka (1998) Laser photostimulation of collagen production in healing rabbit Achilles tendons. Lasers Surg. Med. 22, 281 287.
31. Medrado, A. R., L. S. Pugliese, S. R. Reis Z. A. Andrade (2003) Influence of low level laser therapy on wound healing and its biological action upon myofibroblasts. Lasers Surg. Med. 32, 239 244.
32. Posten, W., D. A. Wrone, J. S. Dover, K. A. Arndt, S. Silapunt M. Alam (2005) Low-level laser therapy for wound healing: Mechanism and efficacy. Dermatol. Surg. 31, 334 340.
33. De Carvalho, P. T., N. Mazzer, F. A. dos Reis, A. C. Belchior I. S. Silva (2006) Analysis of the influence of low-power HeNe laser on the healing of skin wounds in diabetic and non-diabetic rats. Acta Cir. Bras. 21, 177 183.
34. Hawkins, D. H. H. Abrahamse (2006) The role of laser fluence in cell viability, proliferation, and membrane integrity of wounded human skin fibroblasts following helium-neon laser irradiation. Lasers Surg. Med. 38, 74 83.
35. Yu, W., J. O. Naim R. J. Lanzafame (1997) Effects of photostimulation on wound healing in diabetic mice. Lasers Surg. Med. 20, 56 63.
36. Pereira, A. N., C. P. Eduardo, E. Matson M. M. Marques (2002) Effect of low-power laser irradiation on cell growth and procollagen synthesis of cultured fibroblasts. Lasers Surg. Med. 31, 263 267.
37. Regan, M. C., S. J. Kirk, M. Hurson, M. Sodeyama, H. L. Wasserkrug A. Barbul (1993) Tumor necrosis factor-alpha inhibits in vivo collagen synthesis. Surgery 113, 173 177.
38. Mori, R., T. Kondo, T. Ohshima, Y. Ishida N. Mukaida (2002) Accelerated wound healing in tumor necrosis factor receptor p55-deficient mice with reduced leukocyte infiltration. FASEB J. 16, 963 974.
39. Solis-Herruzo, J. A., D. A. Brenner M. Chojkier (1998) Tumor necrosis factor alpha inhibits collagen gene transcription and collagen synthesis in cultured human fibroblasts. J. Biol. Chem. 263, 5841 5845.
40. Centrella, M., T. L. MaCarthy E. Canalis (1998) Tumor necrosis factor-α inhibits collagen synthesis and alkaline phosphatase activity independently of its effect on dodexyribonucleic acid synthesis in osteoblast-enriched bone cell cultures. Endocrinology 123, 1442 1448.