Laboratório de Biologia Celular de Fungos, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Avenida Carlos Chagas Filho 373, Centro de Ciências da Saúde, Bloco G, Sala G0-044, Rio de Janeiro, RJ, 21941-902, Brazil.
Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Braz J Microbiol. 2021 Mar;52(1):101-106. doi: 10.1007/s42770-020-00327-9. Epub 2020 Jul 2.
The in vitro activity of ibuprofen, a nonsteroidal anti-inflammatory drug, was evaluated against Sporothrix brasiliensis and S. schenckii, either alone or in combination with amphotericin B, itraconazole, or terbinafine. The inhibitory activity of ibuprofen as a single agent was determined according to minimum inhibitory concentration (MIC) values, while the effect of ibuprofen combined with amphotericin B, itraconazole, or terbinafine was estimated by microdilution checkerboard methodology. The ultrastructural alterations of S. schenckii after exposure to the combination of ibuprofen and amphotericin B were evaluated by scanning electron microscopy (SEM) and flow cytometry analysis. As a single agent, ibuprofen inhibited Sporothrix growth with a MIC median of 256 μg/mL, while the MIC medians of ibuprofen in combination with antifungals were 16 μg/mL and 128 μg/mL. The MIC values of amphotericin B, itraconazole, and terbinafine were reduced when isolates were co-incubated with ibuprofen, mainly the polyene. The major alteration after treatment with the ibuprofen/amphotericin B combination was the increase in the presence of filamentous forms and high membrane damage with loss of plasma membrane integrity. In summary, we demonstrated that ibuprofen increases the in vitro activity of antifungals, mainly amphotericin B, against S. brasiliensis and S. schenckii. Future in vivo studies exploring combination therapy with ibuprofen and antifungals in animal models are needed to confirm its efficacy.
非甾体抗炎药布洛芬对巴西利什孢子丝菌和申克孢子丝菌的体外活性进行了评估,单独使用或与两性霉素 B、伊曲康唑或特比萘芬联合使用。根据最低抑菌浓度 (MIC) 值确定布洛芬作为单一药物的抑制活性,而通过微量稀释棋盘法评估布洛芬与两性霉素 B、伊曲康唑或特比萘芬联合使用的效果。通过扫描电子显微镜 (SEM) 和流式细胞术分析评估了布洛芬与两性霉素 B 联合使用后对申克孢子丝菌超微结构的改变。作为单一药物,布洛芬抑制孢子丝菌生长的 MIC50 中位数为 256μg/mL,而与抗真菌药物联合使用时的 MIC50 中位数分别为 16μg/mL 和 128μg/mL。当分离物与布洛芬共同孵育时,两性霉素 B、伊曲康唑和特比萘芬的 MIC 值降低,主要是多烯类。与布洛芬/两性霉素 B 联合治疗后,主要改变是丝状形式的增加和高膜损伤,导致质膜完整性丧失。总之,我们证明布洛芬可增加巴西利什孢子丝菌和申克孢子丝菌对抗真菌药物(主要是两性霉素 B)的体外活性。需要在动物模型中进行探索布洛芬与抗真菌药物联合治疗的未来体内研究,以确认其疗效。