Eduard Gondáš, Jozef Mažerik, Matúš Dohál, Soňa Bálentová, Michal Pokusa, Daniela Vargová, Lukáš Smieško, Martina Šutovská, Marta Jošková, Soňa Fraňová
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引用次数: 0
Abstract
Background: Allergic asthma is a chronic inflammatory disease characterized by airway hyperresponsiveness, inflammation and remodeling. ROCK inhibitors have now been shown to have the potential to alleviate these symptoms, although the specific effects of a new ROCK inhibitor, GSK429286 A, remain underexplored.
Objective: The aim of this study was to evaluate the therapeutic effects of a novel ROCK inhibitor, GSK429286 A, which exhibits a high affinity for both ROCK1 and ROCK2 isoforms, on allergic asthma in a guinea pig model, focusing on its effects on airway hyperresponsiveness, inflammation, and remodeling.
Methods: To induce allergic asthma, guinea pigs were sensitized with ovalbumin for 28 days, and in the middle of sensitization they were treated with different doses of the RoCK inhibitor, GSK429286 A. The study evaluated the effect of the administered doses on the reduction of airway hyperresponsiveness, by measuring specific airway resistance (sRaw), and the number of coughs after citric acid inhalation. We also monitored the anti-inflammatory effect by measuring levels of inflammatory cytokines, IL-2, IL-4, IL-5, IL-13, and remodeling markers, such as collagen deposition, and goblet cell hyperplasia. In addition, we monitored the possible anti-remodeling effect of GSK429286 A by histopathological examination.
Results: The ROCK inhibitor, GSK429286 A, showed an effect on suppressing airway hyperresponsiveness by reducing sRaw and the number of coughs in treated guinea pigs compared to controls. Our investigated drug suppressed the release of key mediators of inflammation, including IL-2, IL-4, and IL-5, thus demonstrating the effect of this ROCK inhibitor on the suppression of inflammation in the airways. Finally, GSK429286 A reduced markers of airway remodeling such as collagen deposition and goblet cell hyperplasia.
Conclusion: GSK429286 A, an inhibitor of the ROCK pathway, exhibits significant anti-inflammatory and antiremodeling effects in a guinea pig model of allergic asthma. Indeed, we demonstrate its effect on suppressing airway hyperreactivity and reducing cough frequency. These findings suggest that GSK429286 A may be a promising therapeutic agent for allergic asthma, although further studies are needed to investigate its long-term efficacy, underlying mechanisms, and optimal dosing strategy.
背景:过敏性哮喘是一种以气道高反应性、炎症和重塑为特征的慢性炎症性疾病。尽管新型 ROCK 抑制剂 GSK429286 A 的具体作用仍未得到充分探索,但 ROCK 抑制剂目前已被证明具有缓解这些症状的潜力:本研究旨在评估新型 ROCK 抑制剂 GSK429286 A 对豚鼠模型中过敏性哮喘的治疗效果,重点关注其对气道高反应性、炎症和重塑的影响:为了诱发过敏性哮喘,我们用卵清蛋白对豚鼠进行了为期 28 天的致敏试验,并在致敏中期用不同剂量的 RoCK 抑制剂 GSK429286 A 对豚鼠进行了治疗。研究通过测量特定气道阻力(sRaw)和吸入柠檬酸后的咳嗽次数,评估了给药剂量对降低气道高反应性的影响。我们还通过测量炎症细胞因子(IL-2、IL-4、IL-5、IL-13)和重塑标志物(如胶原沉积和小管细胞增生)的水平来监测抗炎效果。此外,我们还通过组织病理学检查监测了 GSK429286 A 可能的抗重塑作用:结果:与对照组相比,ROCK抑制剂GSK429286 A通过减少豚鼠的sRaw和咳嗽次数,显示出抑制气道高反应性的作用。我们研究的药物抑制了包括 IL-2、IL-4 和 IL-5 在内的主要炎症介质的释放,从而证明了这种 ROCK 抑制剂对抑制气道炎症的作用。最后,GSK429286 A 还能减少气道重塑的标志物,如胶原沉积和小管细胞增生:结论:GSK429286 A 是一种 ROCK 通路抑制剂,在豚鼠过敏性哮喘模型中具有显著的抗炎和抗重塑作用。事实上,我们证明了它在抑制气道过度反应和降低咳嗽频率方面的作用。这些研究结果表明,GSK429286 A 可能是一种很有前景的过敏性哮喘治疗药物,尽管还需要进一步研究其长期疗效、潜在机制和最佳剂量策略。
期刊介绍:
International Journal of Immunopathology and Pharmacology is an Open Access peer-reviewed journal publishing original papers describing research in the fields of immunology, pathology and pharmacology. The intention is that the journal should reflect both the experimental and clinical aspects of immunology as well as advances in the understanding of the pathology and pharmacology of the immune system.