IDIBAPS, Hospital Clínic, CIBER de Enfermedades Respiratorias (CIBERES), Villarroel 170, Barcelona, 08036, Catalonia, Spain.
Respir Res. 2011 Feb 27;12(1):23. doi: 10.1186/1465-9921-12-23.
Although antihistamines and topical corticosteroids are used in combination to treat allergic rhinitis, their additive effect has not been yet demonstrated. The aim was investigate the antiinflammatory additive effect of mometasone and desloratadine on cytokine and sICAM-1 secretion by epithelial cells, and on eosinophil survival stimulated by human epithelial cells secretions from nasal mucosa and polyps.
Epithelial cells obtained from nasal mucosa or polyps were stimulated with 10% fetal bovine serum in presence of mometasone (10(-11) M-10(-5) M) with/without desloratadine (10(-5) M). Cytokine and sICAM-1 concentrations in supernatants were measured by ELISA. Peripheral blood eosinophils were incubated during 4 days with epithelial cell secretions with (10(-11) M-10(-5) M) and/or desloratadine (10(-5) M) and survival assessed by Trypan blue. Results are expressed as percentage (mean ± SEM) compared to control.
Fetal bovine serum stimulated IL-6, IL-8, GM-CSF and sICAM-1 secretion. In mucosa and polyp epithelial cells, mometasone inhibited this induced secretion while desloratadine inhibited IL-6 and IL-8. The combination of 10(-5) M desloratadine and 10(-9) M mometasone reduced IL-6 secretion (48 ± 11%, p < 0.05) greater extent than mometasone alone (68 ± 10%) compared to control (100%). Epithelial cell secretions induced eosinophil survival from day 1 to 4, this effect being inhibited by mometasone. At day 4, the combination of mometasone (10(-11) M) and desloratadine (10(-5) M) provoked an increased inhibition of eosinophil survival induced by cell secretions (27 ± 5%, p < 0.01) than mometasone (44 ± 7%) or desloratadine (46 ± 7%) alone.
These results suggest that the combination of desloratadine and mometasone furoate have a greater antinflammatory effect in an in vitro model of eosinophil inflammation than those drugs administered alone.
尽管抗组胺药和局部皮质类固醇联合用于治疗过敏性鼻炎,但它们的相加作用尚未得到证实。本研究旨在探讨糠酸莫米松和地氯雷他定对上皮细胞细胞因子和 sICAM-1 分泌以及人鼻黏膜和息肉上皮细胞分泌物刺激嗜酸性粒细胞存活的抗炎相加作用。
用 10%胎牛血清刺激鼻黏膜或息肉上皮细胞,同时用/不用糠酸莫米松(10(-11) M-10(-5) M)和/或地氯雷他定(10(-5) M)处理。通过 ELISA 测量上清液中细胞因子和 sICAM-1 的浓度。外周血嗜酸性粒细胞在 4 天内与上皮细胞分泌物(10(-11) M-10(-5) M)和/或地氯雷他定(10(-5) M)孵育,并通过台盼蓝评估存活情况。结果表示为与对照相比的百分比(平均值±SEM)。
胎牛血清刺激 IL-6、IL-8、GM-CSF 和 sICAM-1 分泌。在黏膜和息肉上皮细胞中,糠酸莫米松抑制这种诱导的分泌,而地氯雷他定抑制 IL-6 和 IL-8。10(-5) M 地氯雷他定和 10(-9) M 糠酸莫米松联合减少 IL-6 分泌(48±11%,p<0.05),比单独使用糠酸莫米松(68±10%)更显著(与对照相比为 100%)。上皮细胞分泌物从第 1 天到第 4 天诱导嗜酸性粒细胞存活,这种作用被糠酸莫米松抑制。第 4 天,糠酸莫米松(10(-11) M)和地氯雷他定(10(-5) M)联合使用可增强细胞分泌物诱导的嗜酸性粒细胞存活的抑制作用(27±5%,p<0.01),比单独使用糠酸莫米松(44±7%)或地氯雷他定(46±7%)更强。
这些结果表明,在嗜酸性粒细胞炎症的体外模型中,地氯雷他定和糠酸莫米松联合使用比单独使用这些药物具有更强的抗炎作用。