Siquier-Dameto Gabriel, Iguaran-Pérez Ainhoa, Gimeno-Beltrán Javier, Bellia Gilberto, Giori Andrea Maria, Boadas-Vaello Pere, Verdú Enrique
Research Group of Clinical Anatomy, Embryology and Neuroscience (NEOMA), Department of Medical Sciences, University of Girona, 17003 Girona, Spain.
Dameto Clinics International, 07310 Campanet, Spain.
J Clin Med. 2025 Mar 3;14(5):1701. doi: 10.3390/jcm14051701.
Intraperitoneal sensitization combined with topical and/or epicutaneous treatment using an ovalbumin (OVA)-aluminum salt solution (OVA-AL) represents a model for inducing atopic dermatitis (AD). However, the combination of sensitization with subcutaneous treatment and cutaneous application of OVA-AL via a brush has not been explored as a method for inducing AD. Adult mice were subcutaneously injected with OVA-AL following sensitization on days 0, 7, and 14 and were treated with OVA-AL via brush application to the dorsal skin fortnightly until days 35 and 49. Concomitant alloknesis and skin changes were assessed. Mice of the Balb/c and ICR-CD1 strains were treated with OVA-AL until day 35, with only the ICR-CD1 strain continuing treatment until day 49. Control animals received saline. At 35 and 49 days, dorsal skin was harvested and processed for histological analysis. Mice treated with OVA-AL developed dry skin, with no scratching or alloknesis. Histological examination of dorsal skin revealed an increase in mast cells and collagen deposition. Dermatitis-like symptoms were observed in mice treated with OVA-AL using this administration method.
腹腔致敏联合使用卵清蛋白(OVA)-铝盐溶液(OVA-AL)进行局部和/或表皮治疗是诱导特应性皮炎(AD)的一种模型。然而,皮下治疗致敏与通过刷子在皮肤上涂抹OVA-AL相结合作为诱导AD的方法尚未得到探索。成年小鼠在第0、7和14天致敏后皮下注射OVA-AL,并每两周通过刷子将OVA-AL涂抹于背部皮肤,直至第35天和第49天。评估伴随的触觉异常和皮肤变化。Balb/c和ICR-CD1品系的小鼠用OVA-AL治疗至第35天,只有ICR-CD1品系继续治疗至第49天。对照动物接受生理盐水。在第35天和第49天,采集背部皮肤并进行组织学分析。用OVA-AL治疗的小鼠出现皮肤干燥,无抓挠或触觉异常。背部皮肤的组织学检查显示肥大细胞增多和胶原沉积。使用这种给药方法,在用OVA-AL治疗的小鼠中观察到了类似皮炎的症状。