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新型造血前列腺素 D 合酶抑制剂 TAS-205 与不同类型抗过敏药物对实验性变应性鼻炎豚鼠模型鼻塞的协同作用。

Potential synergistic effects of novel hematopoietic prostaglandin D synthase inhibitor TAS-205 and different types of anti-allergic medicine on nasal obstruction in a Guinea pig model of experimental allergic rhinitis.

机构信息

Discovery and Preclinical Research Division, Taiho Pharmaceutical Co. Ltd, 3 Okubo, Tsukuba, Ibaraki, 300-2611, Japan; Laboratory of Pharmacotherapy of Life-Style Related Diseases, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, 980-8578, Miyagi, Japan.

Discovery and Preclinical Research Division, Taiho Pharmaceutical Co. Ltd, 3 Okubo, Tsukuba, Ibaraki, 300-2611, Japan.

出版信息

Eur J Pharmacol. 2020 May 15;875:173030. doi: 10.1016/j.ejphar.2020.173030. Epub 2020 Feb 19.

Abstract

Nasal obstruction is one of the most bothersome symptoms of allergic rhinitis (AR) affecting sleep-related quality of life in AR patients. Although several treatments were tested to control nasal obstruction, some patients with moderate to severe AR do not respond to current treatments, including the combined administration of different types of anti-allergic medicine. Thus, new options for AR treatment are needed. This study aimed to evaluate the effects of combined treatment with a novel inhibitor of hematopoietic prostaglandin D synthase (HPGDS), TAS-205, and different types of anti-allergic medicine on nasal obstruction in AR. Firstly, we demonstrated that TAS-205 selectively inhibited prostaglandin D (PGD) synthesis in an enzymatic assay in a cell-based assay and in vivo models of AR. Moreover, treatment with TAS-205 alone suppressed eosinophil infiltration into the nasal cavity and late phase nasal obstruction. The combined administration of TAS-205 with montelukast, a cysteinyl leukotriene receptor 1 antagonist, showed significant additive inhibitory effects on eosinophil infiltration and late phase nasal obstruction compared to treatment with each agent alone. In contrast, concomitant treatment with TAS-205 and fexofenadine, a histamine H blocker, showed inhibitory effects on late phase and early phase nasal obstruction, although the magnitude of the inhibitory effects upon combined administration was comparable to that of each single treatment. These results suggest that combined treatment with an HPGDS inhibitor and different types of anti-allergic medicine may be a promising strategy to control nasal obstruction in AR patients.

摘要

鼻塞是变应性鼻炎(AR)最恼人的症状之一,影响 AR 患者的睡眠相关生活质量。尽管已经测试了几种治疗方法来控制鼻塞,但一些中重度 AR 患者对当前的治疗方法没有反应,包括不同类型的抗过敏药物联合使用。因此,需要新的 AR 治疗选择。本研究旨在评估新型造血前列腺素 D 合酶(HPGDS)抑制剂 TAS-205 与不同类型抗过敏药物联合治疗对 AR 患者鼻塞的影响。首先,我们证明 TAS-205 在细胞测定和 AR 体内模型中的酶测定中选择性抑制前列腺素 D(PGD)的合成。此外,TAS-205 单独治疗可抑制嗜酸性粒细胞浸润鼻腔和晚期鼻塞。与每种药物单独治疗相比,TAS-205 与孟鲁司特(半胱氨酰白三烯受体 1 拮抗剂)联合治疗对嗜酸性粒细胞浸润和晚期鼻塞具有显著的相加抑制作用。相比之下,TAS-205 与依巴斯汀(组胺 H 阻滞剂)联合治疗对晚期和早期鼻塞具有抑制作用,尽管联合治疗的抑制作用幅度与每种单一治疗相当。这些结果表明,HPGDS 抑制剂与不同类型的抗过敏药物联合治疗可能是控制 AR 患者鼻塞的一种有前途的策略。

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