Fukuyama Tomoki, Ehling Sarah, Wilzopolski Jenny, Bäumer Wolfgang
Department of Molecular Biomedical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, NC, USA.
Institute of Pharmacology and Toxicology, Faculty of Veterinary Medicine, Freie Universität Berlin, Koserstraße 20, 14195, Berlin, Germany.
BMC Pharmacol Toxicol. 2018 Jul 3;19(1):37. doi: 10.1186/s40360-018-0232-3.
Topical administration of PR022, 0.05% hypochlorous acid (HOCl) in gel has been demonstrated to be beneficial in a chronic murine atopic dermatitis model. In a follow up study we tested a higher concentration (0.1%) of PR022 HOCl gel in comparison to the Janus kinase inhibitor tofacitinib, both of which are currently in clinical phase studies for treatment of human atopic dermatitis.
The effect of topically administered HOCl (0.1%) in gel was compared to a topical formulation of tofacitinib (0.5%) in a therapeutic setting on atopic dermatitis-like lesions in NC/Nga mice as well as itch behaviour. NC/Nga mice were sensitized with house dust mite allergen. After reaching visible lesions, mice were treated either topically with HOCl or tofacitinib or gel vehicle for 17 days. After termination of the study, dorsal root ganglia were isolated for ex vivo stimulation and skin samples were taken for cytokine determination in inflamed skin.
When administered onto lesional skin of NC/Nga mice, both HOCl and tofacitinib reduced lesions and scratching behaviour. The reduced inflammatory response by HOCl and tofacitinib treatment was demonstrated by diminished inflammatory cytokines in affected skin tissue from NC/Nga mice. Dorsal root ganglia neurons re-stimulated with a range of mediators of itch showed a reduced response compared to the vehicle control mice, when isolated from tofacitinib or HOCl treated mice.
These data indicate a similar beneficial potential of topical high dose PR022 HOCl (0.1%) in gel and tofacitinib, in a translational murine model of atopic dermatitis.
在慢性小鼠特应性皮炎模型中,已证明局部施用PR022(凝胶中的0.05%次氯酸(HOCl))有益。在一项后续研究中,我们测试了浓度更高(0.1%)的PR022 HOCl凝胶,并与Janus激酶抑制剂托法替布进行比较,这两种药物目前都处于治疗人类特应性皮炎的临床研究阶段。
在治疗环境中,将凝胶中局部施用的HOCl(0.1%)与托法替布(0.5%)的局部制剂在NC/Nga小鼠的特应性皮炎样病变以及瘙痒行为方面的效果进行比较。用屋尘螨过敏原使NC/Nga小鼠致敏。在出现可见病变后,小鼠分别局部用HOCl、托法替布或凝胶赋形剂治疗17天。研究结束后,分离背根神经节进行离体刺激,并采集皮肤样本用于测定炎症皮肤中的细胞因子。
当施用于NC/Nga小鼠的病变皮肤时,HOCl和托法替布均能减轻病变和抓挠行为。NC/Nga小鼠受影响皮肤组织中炎症细胞因子减少,证明了HOCl和托法替布治疗可减轻炎症反应。与赋形剂对照小鼠相比,从托法替布或HOCl治疗的小鼠中分离出的背根神经节神经元在受到一系列瘙痒介质再刺激时反应减弱。
在特应性皮炎的转化小鼠模型中,这些数据表明凝胶中局部高剂量PR022 HOCl(0.1%)和托法替布具有相似的有益潜力。