Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
1.
Acta cir. bras ; 34(2): e201900210, 2019. tab, graf
Artigo em Inglês | LILACS | ID: biblio-989058

RESUMO

Abstract Purpose: To analyze aspects of the biomodulating effect of light in biological tissues, bone cells from surgical explants of the femur of rats were irradiated with low intensity laser. Methods: Bone cells were cultured and irradiated with LASER light (GaAlAs). Growth, cell viability, mineralized matrix formation, total protein dosage, immunostimulatory properties, cytochemical analysis, gene expression of bone proteins were examined using live cell imaging and cell counting by colorimetric assay. The gene expression of: alkaline phosphatase (ALP), type 1 collagen, osteocalcin and osteopontin through the real-time polymerase chain reaction. Results: At 8 days, the viability of the irradiated culture was 82.3% and 72.4% in non-irradiated cells. At 18 days, the cellular viability (with laser) was 77.42% and 47.62% without laser. At 8 days, the total protein concentration was 21.622 mg / mol in the irradiated group and 16, 604 mg / mol in the non-irradiated group and at 18 days the concentration was 37.25 mg / mol in the irradiated group and 24, 95 mg / mol in the non-irradiated group. Conclusion: The laser interfered in the histochemical reaction, cell viability, matrix mineralization, and maintained the cellular expression of proteins


Assuntos
Animais , Ratos , Osteoblastos/efeitos da radiação , Diferenciação Celular/efeitos da radiação , Sobrevivência Celular/efeitos da radiação , Terapia com Luz de Baixa Intensidade/métodos , Fatores de Tempo , Células Cultivadas , Ratos Wistar , Relação Dose-Resposta à Radiação
2.
Rev. Col. Bras. Cir ; 37(4): 295-302, jul.-ago. 2010.
Artigo em Português | LILACS | ID: lil-564253

RESUMO

O uso da luz laser de baixa intensidade vem sendo utilizado como terapia coadjuvante ou de forma terapêutica isolada em várias especialidades odontológicas. Suas principais indicações incluem ação anti-inflamatória, analgésica e indutora da reparação tecidual. O poder cicatrizante do laser de baixa potência é discutido neste trabalho assim como os mecanismos de biomodulação e estimulação da mitose. Estas propriedades, já estudadas em células benignas, quando aplicadas em células neoplásicas malignas, abrem espaço para discussões. O objetivo do presente trabalho foi realizar uma revisão da literatura sobre os aspectos indutivos do laser no processo de proliferação celular principalmente no que se refere a estes mecanismos em células neoplásicas malignas.


Low energy laser has been used as an adjuvant therapy or as a therapeutic tool in many different areas of Dentistry. It is recognized by its anti-inflammatory and analgesic properties, and also as a tissue repair inductor. Low intensity laser property in stimulate cell proliferation during wound healing and its biomodulation mechanisms are discussed in this paper. These properties have already been established for cultured benign cells, but there is a controversy when extended to the spectrum of the malignant neoplastic process, normally generating great discussions. The objective of this work was to perform a literature review about the low intensity laser capacity in induce cell proliferation. The discussion is specially concerned about its effects on malignant cells.


Assuntos
Humanos , Diferenciação Celular/efeitos da radiação , Proliferação de Células/efeitos da radiação , Terapia a Laser/métodos , Neoplasias/patologia
3.
Artigo em Inglês | IMSEAR | ID: sea-139893

RESUMO

Objective: The present study histologically and radiologically evaluates the muscle tissue of rats after implantation of bone morphogenic protein (rhBMP-2) in a natural inorganic bone mineral scaffold from a bull calf femur and irradiation with low-power light laser. Materials and Methods: The right and left hind limbs of 16 rats were shaved and an incision was made in the muscle on the face corresponding to the median portion of the tibia, into which rhBMP-2 in a scaffold of inorganic bone was implanted. Two groups of limbs were formed: control (G1) and laser irradiation (G2). G2 received diode laser light applied in the direction of the implant, at a dose of 8 J/cm2 for three minutes. On the 7th, 21st, 40th and 112th days after implantation, hind limbs of 4 animals were radiographed and their implants removed together with the surrounding tissue for study under the microscope. The histological results were graded as 0=absence, 1=slight presence, 2=representative and 3=very representative, with regard to the following events: formation of osteoid structure, acute inflammation, chronic inflammation, fibrin deposition, neovascularization, foreign-body granuloma and fibrosis. Results: There were no statistically significant differences in these events at each evaluation times, between the two groups (P>0.05; Mann-Whitney test). Nevertheless, it could be concluded that the natural inorganic bone matrix with rhBMP-2, from the femur of a bull calf, is a biocompatible combination. Conclusions: Under these conditions, the inductive capacity of rhBMP-2 for cell differentiation was inhibited. There was a slight acceleration in tissue healing in the group that received irradiation with low-power laser light.


Assuntos
Implantes Absorvíveis , Animais , Materiais Biocompatíveis/uso terapêutico , Matriz Óssea/efeitos dos fármacos , Matriz Óssea/efeitos da radiação , Matriz Óssea/transplante , Proteína Morfogenética Óssea 2 , Proteínas Morfogenéticas Ósseas/administração & dosagem , Proteínas Morfogenéticas Ósseas/efeitos da radiação , Proteínas Morfogenéticas Ósseas/uso terapêutico , Bovinos , Diferenciação Celular/efeitos dos fármacos , Diferenciação Celular/efeitos da radiação , Fibrina/análise , Fibrose , Granuloma de Corpo Estranho/etiologia , Granuloma de Corpo Estranho/patologia , Inflamação , Terapia com Luz de Baixa Intensidade/métodos , Lasers Semicondutores/uso terapêutico , Masculino , Músculo Esquelético/patologia , Músculo Esquelético/diagnóstico por imagem , Músculo Esquelético/cirurgia , Neovascularização Fisiológica/efeitos dos fármacos , Neovascularização Fisiológica/efeitos da radiação , Osteogênese/efeitos dos fármacos , Osteogênese/efeitos da radiação , Doses de Radiação , Ratos , Ratos Wistar , Proteínas Recombinantes/administração & dosagem , Proteínas Recombinantes/efeitos da radiação , Proteínas Recombinantes/uso terapêutico , Fatores de Tempo , Alicerces Teciduais , Fator de Crescimento Transformador beta/administração & dosagem , Fator de Crescimento Transformador beta/efeitos da radiação , Fator de Crescimento Transformador beta/uso terapêutico , Cicatrização/efeitos dos fármacos , Cicatrização/efeitos da radiação
4.
Yonsei Medical Journal ; : 852-861, 2006.
Artigo em Inglês | WPRIM | ID: wpr-141741

RESUMO

This study investigated that whether a 2 mT, 60 Hz, sinusoidal electromagnetic field (EMF) alters the structure and function of cells. This research compared the effects of EMF on four kinds of cell lines: hFOB 1.19 (fetal osteoblast), T/G HA-VSMC (aortic vascular smooth muscle cell), RPMI 7666 (B lymphoblast), and HCN-2 (cortical neuronal cell). Over 14 days, cells were exposed to EMF for 1, 3, or 6 hours per day (hrs/d). The results pointed to a cell type-specific reaction to EMF exposure. In addition, the cellular responses were dependent on duration of EMF exposure. In the present study, cell proliferation was the trait most sensitive to EMF. EMF treatment promoted growth of hFOB 1.19 and HCN-2 compared with control cells at 7 and 14 days of incubation. When the exposure time was 3 hrs/d, EMF enhanced the proliferation of RPMI 7666 but inhibited that of T/G HA- VSMC. On the other hand, the effects of EMF on cell cycle distribution, cell differentiation, and actin distribution were unclear. Furthermore, we hardly found any correlation between EMF exposure and gap junctional intercellular communication in hFOB 1.19. This study revealed that EMF might serve as a potential tool for manipulating cell proliferation.


Assuntos
Humanos , Transdução de Sinais , Citoesqueleto de Actina/efeitos da radiação , Junções Comunicantes/metabolismo , Campos Eletromagnéticos , Proliferação de Células/efeitos da radiação , Fenômenos Fisiológicos Celulares/efeitos da radiação , Linhagem Celular , Diferenciação Celular/efeitos da radiação , Ciclo Celular/efeitos da radiação
5.
Yonsei Medical Journal ; : 852-861, 2006.
Artigo em Inglês | WPRIM | ID: wpr-141740

RESUMO

This study investigated that whether a 2 mT, 60 Hz, sinusoidal electromagnetic field (EMF) alters the structure and function of cells. This research compared the effects of EMF on four kinds of cell lines: hFOB 1.19 (fetal osteoblast), T/G HA-VSMC (aortic vascular smooth muscle cell), RPMI 7666 (B lymphoblast), and HCN-2 (cortical neuronal cell). Over 14 days, cells were exposed to EMF for 1, 3, or 6 hours per day (hrs/d). The results pointed to a cell type-specific reaction to EMF exposure. In addition, the cellular responses were dependent on duration of EMF exposure. In the present study, cell proliferation was the trait most sensitive to EMF. EMF treatment promoted growth of hFOB 1.19 and HCN-2 compared with control cells at 7 and 14 days of incubation. When the exposure time was 3 hrs/d, EMF enhanced the proliferation of RPMI 7666 but inhibited that of T/G HA- VSMC. On the other hand, the effects of EMF on cell cycle distribution, cell differentiation, and actin distribution were unclear. Furthermore, we hardly found any correlation between EMF exposure and gap junctional intercellular communication in hFOB 1.19. This study revealed that EMF might serve as a potential tool for manipulating cell proliferation.


Assuntos
Humanos , Transdução de Sinais , Citoesqueleto de Actina/efeitos da radiação , Junções Comunicantes/metabolismo , Campos Eletromagnéticos , Proliferação de Células/efeitos da radiação , Fenômenos Fisiológicos Celulares/efeitos da radiação , Linhagem Celular , Diferenciação Celular/efeitos da radiação , Ciclo Celular/efeitos da radiação
6.
Indian J Exp Biol ; 2003 May; 41(5): 419-23
Artigo em Inglês | IMSEAR | ID: sea-59131

RESUMO

Yield of ultraweak photon emission in a cell culture model for biophotonic measurements using fibroblastic differentiation depended on the temperature of photonic measurement. The ultraweak photon emission of medium was significantly higher at 37 degrees C than at 25 degrees C and after UVB-irradiation this difference was even more pronounced. While with cells in the medium no temperature dependence could be determined in unirradiated samples, after UVB-irradiation of cells an increase of biophotonic emission was observed in postmitotic fibroblasts. While after several UVB exposures normal cells begin to absorb the ultraviolet light, cells from patients with the disease Xeroderma Pigmentosum loose this capacity. In view that fibroblasts play an essential role in skin aging, skin carcinogenesis and wound healing, the biophotonic model using the fibroblastic differentiation system provides to be a new and powerful non-invasive tool for the development of skin science.


Assuntos
Diferenciação Celular/efeitos da radiação , Fibroblastos/citologia , Humanos , Fótons , Luz Solar , Temperatura
7.
Indian J Pathol Microbiol ; 1996 Apr; 39(2): 105-9
Artigo em Inglês | IMSEAR | ID: sea-75387

RESUMO

The UV response of marginal melanocytes in vitiliginous skin was studied using a whole skin organ culture technique. This method assesses the plasticity of melanocytes in response to UV. It is observed that there is a sequential increase in catecholoxidase production and in the volume and dendricity of the melanocytes on exposure to a single pulse of UV, reaching a peak at 3 1/2 h. From this study it is evident that the melanocyte shows a prominent structural and functional plasticity in response to UV. Implicit is the utilisation and transduction of UV energy by the melanocyte, for transcriptional and translational activity, enhancing catecholoxidase and cell structural protein production.


Assuntos
Catecol Oxidase/metabolismo , Diferenciação Celular/efeitos da radiação , Fase G2 , Humanos , Melanócitos/citologia , Técnicas de Cultura de Órgãos , Raios Ultravioleta , Vitiligo/enzimologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA