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1.
J Photochem Photobiol B ; 129: 135-42, 2013 Dec 05.
Article in English | MEDLINE | ID: mdl-24231378

ABSTRACT

The aim of this study was to investigate the analgesic and anti-inflammatory activity of low-level laser therapy (LLLT) on the nociceptive behavioral as well as histomorphological aspects induced by injection of formalin and carrageenan into the rat temporomandibular joint. The 2.5% formalin injection (FRG group) induced behavioral responses characterized by rubbing the orofacial region and flinching the head quickly, which were quantified for 45 min. The pretreatment with systemic administration of diclofenac sodium-DFN group (10 mg/kg i.p.) as well as the irradiation with LLLT infrared (LST group, 780 nm, 70 mW, 30 s, 2.1 J, 52.5 J/cm(2), GaAlAs) significantly reduced the formalin-induced nociceptive responses. The 1% carrageenan injection (CRG group) induced inflammatory responses over the time-course of the study (24 h, and 3 and 7 days) characterized by the presence of intense inflammatory infiltrate rich in neutrophils, scanty areas of liquefactive necrosis and intense interstitial edema, extensive hemorrhagic areas, and enlargement of the joint space on the region. The DFN and LST groups showed an intensity of inflammatory response that was significantly lower than in CRG group over the time-course of the study, especially in the LST group, which showed exuberant granulation tissue with intense vascularization, and deposition of newly formed collagen fibers (3 and 7 days). It was concluded that the LLLT presented an anti-nociceptive and anti-inflammatory response on the inflammation induced in the temporomandibular joint of rodents.


Subject(s)
Inflammation/radiotherapy , Low-Level Light Therapy , Temporomandibular Joint/radiation effects , Animals , Anti-Inflammatory Agents/chemistry , Anti-Inflammatory Agents/pharmacology , Anti-Inflammatory Agents/therapeutic use , Carrageenan/chemistry , Carrageenan/pharmacology , Carrageenan/therapeutic use , Formaldehyde/chemistry , Formaldehyde/pharmacology , Formaldehyde/therapeutic use , Inflammation/drug therapy , Male , Pain Measurement/drug effects , Pain Measurement/radiation effects , Rats , Rats, Wistar , Temporomandibular Joint/drug effects , Temporomandibular Joint/pathology
2.
J Photochem Photobiol B ; 105(1): 51-9, 2011 Oct 05.
Article in English | MEDLINE | ID: mdl-21803596

ABSTRACT

This paper aimed to evaluate the improvement of burn wounds healing by sodium alginate/chitosan-based films and laser therapy. Natural polymers with different biological activities are widely used as film dressings to improve wound healing. Lasers arrays accelerate the healing repair of soft tissue injuries. Burn procedures were performed on the backs of 60 male rats assigned into six groups: untreated (CTR), dressed with cellulose films (CL), dressed with sodium alginate/chitosan-based films (SC), laser-irradiated undressed wounds (LT), laser-irradiated wounds with cellulose (CLLT) and sodium alginate/chitosan-based films (SCLT). Laser therapy was applied for 7 days. Animals of each group were euthanised 8 and 14 days after the burn procedures. The inflammatory reaction was significantly more intense in the CTR group than in the irradiated groups after 8 and 14 days. Laser therapy stimulated myofibroblastic differentiation in 8 days, with or without dressing films. Combined laser therapy and both dressings improved epithelisation, blood vessels formation and collagenization, promoted rapid replacement of type III for type I collagen and favored the better arrangement of the newly formed collagen fibres. The combination of laser therapy and sodium alginate/chitosan-based dressing improves burn healing, apparently by modulating the epithelisation, blood vessels formation and collagenization processes.


Subject(s)
Alginates/pharmacology , Burns/radiotherapy , Chitosan/pharmacology , Low-Level Light Therapy , Actins/metabolism , Animals , Burns/pathology , Collagen Type I/analysis , Fibroblasts/metabolism , Glucuronic Acid/pharmacology , Hexuronic Acids/pharmacology , Male , Neovascularization, Physiologic/drug effects , Neovascularization, Physiologic/radiation effects , Rats , Wound Healing/drug effects , Wound Healing/radiation effects
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