使用含有与 β-环糊精复配的抗真菌剂的组织调节剂治疗大鼠义齿口腔炎模型的组织反应。

Carolina Yoshi Campos Sugio, Tânia Mary Cestari, Amanda Aparecida Maia Neves Garcia, Gustavo Simão Moraes, Thaís Albach, Thais Marchini de Oliveira, Gustavo Pompermaier Garlet, Vanessa Migliorini Urban, Karin Hermana Neppelenbroek
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引用次数: 0

摘要

简介。使用抗真菌剂改良的组织调节剂是义齿口腔炎(DS)治疗的一种潜在替代方法。在临床应用之前,缺乏有关组织对这种治疗方法反应的信息。本研究旨在评估抗真菌剂修饰的组织调节剂在大鼠假牙口腔炎模型中的组织反应。在抗生素治疗下诱导 DS 4 天后,Wistar 大鼠的口内装置(IODs)重新衬上了不含 Softone(Soft)或含或不含与 β-环糊精复合物(Nys:βCD 和 Chx:βCD)的奈司他丁(Nystatin,Nys)或洗必泰(Chlorhexidine,Chx)对白色念珠菌的 MIC 值的组织调节剂。其中包括三个对照组:健康大鼠[阴性对照组(Nc)]、使用无菌 IOD 的大鼠[无菌装置(Sd)]和未接受治疗的 DS 大鼠(DS)。治疗 4 天后,对 IOD 下的腭粘膜进行组织学处理,以进行形态病理学和组织计量学分析、胶原纤维形态学(双折射)、细胞增殖(增殖细胞核抗原)和细胞因子(IL-1β)表达的免疫组化。Nc 组和 Sd 组的情况相似(P>0.05),上皮组织和结缔组织没有发生任何明显变化。DS 组和 Soft 组则表现出明显的上皮改变、细胞增殖和细胞因子 IL-1β 的表达。在使用药物(Nys、Chx、Nys:βCD 和 Chx:βCD)治疗的组别中,所有样本都显示组织炎症减轻或完全恢复,上皮符合健康状况。在免疫组化指标方面,Chx、Nys:βCD 和 Chx:βCD 组与 Nc 组具有可比性(P>0.05)。所建议的治疗方法对 DS 很有希望,因为它能使腭粘膜组织恢复。然而,与改良组织调节剂配方中的非复方药物相比,要获得类似或更高程度的组织反应,所需的复方抗真菌药物浓度要低得多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tissue response in a rat model of denture stomatitis treated with tissue conditioner containing antifungal complexed with β-cyclodextrin.

Introduction. Tissue conditioners modified with antifungals are a potential alternative to denture stomatitis (DS) treatment.Gap Statement. Information on tissue response to this treatment before its clinical application is lacking.Aim. This study aimed to evaluate the tissue response of a tissue conditioner modified with antifungals in a rat model of DS.Methodology. After DS induction for 4 days under antibiotic therapy, Wistar rats had their intraoral devices (IODs) relined with the tissue conditioner Softone without (Soft) or with the MICs against Candida albicans of nystatin (Nys) or chlorhexidine (Chx) complexed or not with β-cyclodextrin (Nys:βCD and Chx:βCD). Three controls were included: healthy rats [negative control (Nc)], rats using a sterile IOD [sterile device (Sd)] and rats with DS that did not receive treatment (DS). After 4 days of treatment, the palatal mucosa under the IODs underwent histological processing for morphohistopathological and histometric analyses, morphology of collagen fibres (birefringence), immunohistochemistry for the expression of cell proliferation (proliferating cell nuclear antigen) and cytokine (IL-1β).Results. The Nc and Sd groups were similar (P>0.05), displaying epithelial and connective tissues without any discernible changes in the parameters assessed. The DS and Soft groups exhibited pronounced epithelial alterations, cell proliferation and expression of the cytokine IL-1β. In groups treated with drug incorporation (Nys, Chx, Nys:βCD and Chx:βCD), all samples demonstrated a reduction in tissue inflammation or complete tissue recovery, with an epithelium compatible with health. For the immunohistochemical parameters, the Chx, Nys:βCD and Chx:βCD groups were comparable with Nc (P>0.05).Conclusion. The proposed treatment could be promising for DS, as it led to the tissue recovery of the palatal mucosa. Nevertheless, much lower concentrations of complexed antifungals were required to achieve a similar or higher degree of tissue response compared with uncomplexed drugs in a modified tissue conditioner formulation.

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