Avaliação do espectro de absorção e da viabilidade de linhagens celulares cultivadas sob estresse nutricional e submetidas à fotobiomodulação

Detalhes bibliográficos
Ano de defesa: 2020
Autor(a) principal: Nobile, Juliana Estephan lattes
Orientador(a): Rodrigues, Maria Fernanda Setúbal Destro lattes
Banca de defesa: Rodrigues, Maria Fernanda Setúbal Destro lattes, Silva, Daniela de Fátima Teixeira da lattes, Moreira, Maria Stella Nunes Araujo lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Nove de Julho
Programa de Pós-Graduação: Programa de Pós-Graduação em Biofotônica Aplicada às Ciências da Saúde
Departamento: Saúde
País: Brasil
Palavras-chave em Português:
LED
Palavras-chave em Inglês:
LED
Área do conhecimento CNPq:
Link de acesso: http://bibliotecatede.uninove.br/handle/tede/2782
Resumo: Absorbance is the fraction of light energy that is absorbed by a specific thickness of a material. It means the ability of a material os absorbing light. In a cell cultura where photobiomodulation is used to biostimulate or bioinhibit cell reactions, the knowlogde spctrum of cell lines (HACAT, DOK, fibroblasts, CA1, LUC4 and SCC9) cultivated under a nutricional stress before and after a PBM and analyze the cell viability thorugh the assay MTT. The cell lines was cultured in médium DMEM-F12 with 10% FBS and suplementes, to evaluate the effect od nutritional stress on the light absorption spectra, cells were cultured for 24 h under the following conditions: DMEM-F12 +10% FBS, DMEM-F12 + 5% FBS and DMEM-F12. After this period, 105 cells from each experimental condition were collectes and ressuspended in 1 ml of phosphate buffer solution (PBS) to measure the absorbance in the spectrophotometer. The cells lines that showed statical difference in absorption spectrum were subjected to FBM with LED in the parameters: 6J, 660nm, 240 s. Two treatments were performed: in the first, the cells were cultivated in 48 hours under nutritional stress and through a single irradiation; the other, the same cell lines stay 96 hours under nutritional stress and were treated for three consecutive days with the LED. There is no difference between CA1, LUC4 and fibroblasts when cultivated for 24 hours in nutritional stress. The cell lines HACAT, DOK and SCC9 showed higher absorption when cultivated with higher FBS concentration. There is no statistically diferences between HACAT, DOK and SCC9 cell lines treated with one or three irradiations when cultivated for 48 and 96 houres under nutritional stress. Nutritional stress of the evaluated cell lines showed no effect on absorbance before or after PBM, nor on cell viability.