Kókai Dávid, Paróczai Dóra, Virok Dezső Peter, Endrész Valéria, Gáspár Renáta, Csont Tamás, Bozó Renáta, Burián Katalin
Department of Medical Microbiology and Immunobiology, University of Szeged, Dóm Square 10, 6720 Szeged, Hungary.
Metabolic Diseases and Cell Signaling (MEDICS) Research Group, Interdisciplinary Center of Excellence, Department of Biochemistry, University of Szeged, Dóm Square 9, 6720 Szeged, Hungary.
Microorganisms. 2021 Apr 20;9(4):880. doi: 10.3390/microorganisms9040880.
Ambroxol (Ax) is used as a mucolytics in the treatment of respiratory tract infections. Ax, at a general dose for humans, does not alter growth in mice. Therefore, we aimed to investigate the potential anti-chlamydial effect of Ax at a concentration four timed higher than that used in human medicine. Mice were infected with and 5-mg/kg Ax was administered orally. The number of recoverable inclusion-forming units (IFUs) in Ax-treated mice was significantly lower than that in untreated mice. mRNA expression levels of several cytokines, including interleukin 12 (IL-12), IL-23, IL-17F, interferon gamma (IFN-γ), and surfactant protein (SP)-A, increased in infected mice treated with Ax. The IFN-γ protein expression levels were also significantly higher in infected and Ax-treated mice. Furthermore, the in vitro results suggested that the ERK 1/2 activity was decreased, which is essential for the replication. SP-A and SP-D treatments significantly decreased the number of viable IFUs and significantly increased the attachment of to macrophage cells. Based on our results, a dose of 5 mg/kg of Ax exhibited an anti-chlamydial effect in mice, probably an immunomodulating effect, and may be used as supporting drug in respiratory infections caused by .
氨溴索(Ax)作为黏液溶解剂用于治疗呼吸道感染。Ax在人类常用剂量下不会改变小鼠的生长。因此,我们旨在研究Ax在高于人类医学用药浓度四倍时的潜在抗衣原体作用。用[具体衣原体名称未给出]感染小鼠,并口服给予5mg/kg的Ax。接受Ax治疗的小鼠中可恢复的包涵体形成单位(IFU)数量显著低于未治疗的小鼠。在用Ax治疗的感染小鼠中,包括白细胞介素12(IL-12)、IL-23、IL-17F、干扰素γ(IFN-γ)和表面活性蛋白(SP)-A在内的几种细胞因子的mRNA表达水平升高。在用Ax治疗的感染小鼠中,IFN-γ蛋白表达水平也显著更高。此外,体外实验结果表明,细胞外调节蛋白激酶1/2(ERK 1/2)活性降低,这对[具体衣原体名称未给出]的复制至关重要。SP-A和SP-D处理显著降低了存活的[具体衣原体名称未给出]IFU数量,并显著增加了[具体衣原体名称未给出]与巨噬细胞的附着。基于我们的结果,5mg/kg剂量的Ax在小鼠中表现出抗衣原体作用,可能是一种免疫调节作用,可作为由[具体衣原体名称未给出]引起的呼吸道感染的辅助药物。