Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Buenos Aires 1113, Argentina.
Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Instituto de Investigaciones Farmacológicas (ININFA), Universidad de Buenos Aires, Buenos Aires 1113, Argentina.
Cells. 2021 Nov 5;10(11):3026. doi: 10.3390/cells10113026.
Antihistamines and glucocorticoids (GCs) are often used together in the clinic to treat several inflammation-related situations. Although there is no rationale for this association, clinical practice has assumed that, due to their concomitant anti-inflammatory effects, there should be an intrinsic benefit to their co-administration. In this work, we evaluated the effects of the co-treatment of several antihistamines on dexamethasone-induced glucocorticoid receptor transcriptional activity on the expression of various inflammation-related genes in A549 and U937 cell lines. Our results show that all antihistamines potentiate GCs' anti-inflammatory effects, presenting ligand-, cell- and gene-dependent effects. Given that treatment with GCs has strong adverse effects, particularly on bone metabolism, we also examined the impact of antihistamine co-treatment on the expression of bone metabolism markers. Using MC3T3-E1 pre-osteoblastic cells, we observed that, though the antihistamine azelastine reduces the expression of dexamethasone-induced bone loss molecular markers, it potentiates osteoblast apoptosis. Our results suggest that the synergistic effect could contribute to reducing GC clinical doses, ineffective by itself but effective in combination with an antihistamine. This could result in a therapeutic advantage, as the addition of an antihistamine may reinforce the wanted effects of GCs, while related adverse effects could be diminished or at least mitigated. By modulating the patterns of gene activation/repression mediated by GR, antihistamines could enhance only the desired effects of GCs, allowing their effective dose to be reduced. Further research is needed to correctly determine the clinical scope, benefits, and potential risks of this therapeutic strategy.
抗组胺药和糖皮质激素(GCs)经常在临床上联合使用,以治疗几种与炎症相关的情况。尽管这种联合使用没有理论依据,但临床实践认为,由于它们同时具有抗炎作用,联合使用应该会有内在的益处。在这项工作中,我们评估了几种抗组胺药联合治疗对地塞米松诱导的糖皮质激素受体转录活性在 A549 和 U937 细胞系中各种炎症相关基因表达的影响。我们的结果表明,所有的抗组胺药都增强了 GCs 的抗炎作用,表现出配体、细胞和基因依赖性的作用。由于 GCs 的治疗有很强的副作用,特别是对骨代谢,我们还研究了抗组胺药联合治疗对骨代谢标志物表达的影响。使用 MC3T3-E1 前成骨细胞,我们观察到,尽管抗组胺药氮卓斯汀降低了地塞米松诱导的骨丢失分子标志物的表达,但它增强了成骨细胞凋亡。我们的结果表明,这种协同作用可能有助于减少 GC 的临床剂量,单独使用无效,但与抗组胺药联合使用有效。这可能会带来治疗优势,因为添加抗组胺药可能会增强 GCs 的所需作用,同时减轻相关的不良反应或至少缓解这些不良反应。通过调节 GR 介导的基因激活/抑制模式,抗组胺药可以增强 GCs 的所需作用,从而减少其有效剂量。需要进一步的研究来正确确定这种治疗策略的临床范围、益处和潜在风险。