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Antimicrobial Photodynamic Therapy in Combination with Nystatin in the Treatment of Experimental Oral Candidiasis Induced by Candida albicans Resistant to Fluconazole
Background: It has been demonstrated that azole-resistant strains of Candida albicans have a greater resistance to antimicrobial photodynamic therapy (aPDT) when compared to their more susceptible counterparts. For this reason, the present study evaluated the efficacy of aPDT, together with nystatin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789856/ https://www.ncbi.nlm.nih.gov/pubmed/31540476 http://dx.doi.org/10.3390/ph12030140 |
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author | Janeth Rimachi Hidalgo, Karem Cabrini Carmello, Juliana Carolina Jordão, Cláudia Aboud Barbugli, Paula de Sousa Costa, Carlos Alberto Garcia de Oliveira Mima, Ewerton Pavarina, Ana Claudia |
author_facet | Janeth Rimachi Hidalgo, Karem Cabrini Carmello, Juliana Carolina Jordão, Cláudia Aboud Barbugli, Paula de Sousa Costa, Carlos Alberto Garcia de Oliveira Mima, Ewerton Pavarina, Ana Claudia |
author_sort | Janeth Rimachi Hidalgo, Karem |
collection | PubMed |
description | Background: It has been demonstrated that azole-resistant strains of Candida albicans have a greater resistance to antimicrobial photodynamic therapy (aPDT) when compared to their more susceptible counterparts. For this reason, the present study evaluated the efficacy of aPDT, together with nystatin (NYS), in the treatment of oral candidiasis in vivo. Methods: Mice were infected with fluconazole-resistant C. albicans (ATCC 96901). To perform the combined therapy, aPDT, mediated by Photodithazine (PDZ) and LED light, was used together with NYS. The efficacy of the treatments was evaluated by microbiological, macroscopic, histopathological and Confocal Scanning Laser Microscopy analyses of the lesions. The expression of p21 and p53, proteins associated with cell death, from the tongues of mice, was also performed. Results: The combined therapy reduced the fungal viability by around 2.6 log(10) and decreased the oral lesions and the inflammatory reaction. Additionally, it stimulated the production of p53 and p21. Conclusions: The combined therapy is a promising alternative treatment for oral candidiasis induced by C. albicans resistant to fluconazole. |
format | Online Article Text |
id | pubmed-6789856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67898562019-10-16 Antimicrobial Photodynamic Therapy in Combination with Nystatin in the Treatment of Experimental Oral Candidiasis Induced by Candida albicans Resistant to Fluconazole Janeth Rimachi Hidalgo, Karem Cabrini Carmello, Juliana Carolina Jordão, Cláudia Aboud Barbugli, Paula de Sousa Costa, Carlos Alberto Garcia de Oliveira Mima, Ewerton Pavarina, Ana Claudia Pharmaceuticals (Basel) Article Background: It has been demonstrated that azole-resistant strains of Candida albicans have a greater resistance to antimicrobial photodynamic therapy (aPDT) when compared to their more susceptible counterparts. For this reason, the present study evaluated the efficacy of aPDT, together with nystatin (NYS), in the treatment of oral candidiasis in vivo. Methods: Mice were infected with fluconazole-resistant C. albicans (ATCC 96901). To perform the combined therapy, aPDT, mediated by Photodithazine (PDZ) and LED light, was used together with NYS. The efficacy of the treatments was evaluated by microbiological, macroscopic, histopathological and Confocal Scanning Laser Microscopy analyses of the lesions. The expression of p21 and p53, proteins associated with cell death, from the tongues of mice, was also performed. Results: The combined therapy reduced the fungal viability by around 2.6 log(10) and decreased the oral lesions and the inflammatory reaction. Additionally, it stimulated the production of p53 and p21. Conclusions: The combined therapy is a promising alternative treatment for oral candidiasis induced by C. albicans resistant to fluconazole. MDPI 2019-09-18 /pmc/articles/PMC6789856/ /pubmed/31540476 http://dx.doi.org/10.3390/ph12030140 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Janeth Rimachi Hidalgo, Karem Cabrini Carmello, Juliana Carolina Jordão, Cláudia Aboud Barbugli, Paula de Sousa Costa, Carlos Alberto Garcia de Oliveira Mima, Ewerton Pavarina, Ana Claudia Antimicrobial Photodynamic Therapy in Combination with Nystatin in the Treatment of Experimental Oral Candidiasis Induced by Candida albicans Resistant to Fluconazole |
title | Antimicrobial Photodynamic Therapy in Combination with Nystatin in the Treatment of Experimental Oral Candidiasis Induced by Candida albicans Resistant to Fluconazole |
title_full | Antimicrobial Photodynamic Therapy in Combination with Nystatin in the Treatment of Experimental Oral Candidiasis Induced by Candida albicans Resistant to Fluconazole |
title_fullStr | Antimicrobial Photodynamic Therapy in Combination with Nystatin in the Treatment of Experimental Oral Candidiasis Induced by Candida albicans Resistant to Fluconazole |
title_full_unstemmed | Antimicrobial Photodynamic Therapy in Combination with Nystatin in the Treatment of Experimental Oral Candidiasis Induced by Candida albicans Resistant to Fluconazole |
title_short | Antimicrobial Photodynamic Therapy in Combination with Nystatin in the Treatment of Experimental Oral Candidiasis Induced by Candida albicans Resistant to Fluconazole |
title_sort | antimicrobial photodynamic therapy in combination with nystatin in the treatment of experimental oral candidiasis induced by candida albicans resistant to fluconazole |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6789856/ https://www.ncbi.nlm.nih.gov/pubmed/31540476 http://dx.doi.org/10.3390/ph12030140 |
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