GSK Research Centre Zagreb Ltd., Zagreb, Croatia.
Transl Res. 2012 Aug;160(2):137-45. doi: 10.1016/j.trsl.2012.02.001. Epub 2012 Feb 25.
The murine model of cantharidin-induced ear inflammation was profiled in detail for its alignment with the human model and to explore the mechanism of anti-inflammatory activity of the macrolide antibiotics, clarithromycin and azithromycin. Ear swelling in CD1 mice persisted for 7 days, with peak intensity at 16 h after inflammation induction. As in humans, cantharidin (12.5 μg/ear) generated macrophage-inflammatory protein (MIP)-2, monocyte chemoattractant protein (MCP)-1, keratinocyte-derived chemokine (KC), interleukin (IL)-6, IL-1β, and myeloperoxidase (MPO) production, as well as neutrophil accumulation in mouse ear tissue. The tested macrolides, clarithromycin and azithromycin, administered orally (2 × 150 mg/kg) 0.5 h before and 5 h after cantharidin challenge, reduced MIP-2, MCP-1, KC, and MPO concentrations and thereby decreased ear swelling. Our results suggest that cantharidin-induced acute inflammation represents an excellent model for translational research of novel anti-inflammatories.
详细描述了斑蝥素诱导的耳炎小鼠模型,以使其与人类模型一致,并探索大环内酯类抗生素,克拉霉素和阿奇霉素的抗炎活性机制。CD1 小鼠的耳部肿胀持续 7 天,在炎症诱导后 16 小时达到峰值强度。与人类一样,斑蝥素(12.5μg/耳)可产生巨噬细胞炎性蛋白(MIP)-2、单核细胞趋化蛋白(MCP)-1、角质细胞衍生趋化因子(KC)、白细胞介素(IL)-6、IL-1β 和髓过氧化物酶(MPO)的产生,以及中性粒细胞在小鼠耳部组织中的聚集。测试的大环内酯类药物克拉霉素和阿奇霉素在斑蝥素挑战前 0.5 小时和 5 小时口服(2×150mg/kg)给药,可降低 MIP-2、MCP-1、KC 和 MPO 浓度,从而减轻耳部肿胀。我们的结果表明,斑蝥素诱导的急性炎症代表了一种用于新型抗炎药转化研究的优秀模型。