• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

抑制造血前列腺素 D 合酶可改善豚鼠变应性鼻阻塞。

Inhibition of hematopoietic prostaglandin D synthase improves allergic nasal blockage in guinea pigs.

机构信息

Department of Pharmacology, Kyoto Pharmaceutical University, Nakauchi, Misasagi, Yamashina, Japan.

出版信息

Prostaglandins Other Lipid Mediat. 2011 Aug;95(1-4):27-34. doi: 10.1016/j.prostaglandins.2011.05.001. Epub 2011 May 10.

DOI:10.1016/j.prostaglandins.2011.05.001
PMID:21601002
Abstract

Although it has been suggested that prostaglandin (PG) D(2) is involved in the pathogenesis of allergic rhinitis, whether the inhibition of hematopoietic PGD(2) synthase (H-PGDS) shows beneficial effects on allergic rhinitis has been unclear. We evaluated the effects of a selective H-PGDS inhibitor, TFC-007, on nasal symptoms on Japanese cedar pollen-induced allergic rhinitis of guinea pigs. Sensitized animals were challenged with the pollen once a week. TFC-007 (30mg/kg, p.o.) given once before a challenge almost completely suppressed PGD(2) production in the nasal tissue early and late after the challenge. Although pre-treatment did not affect the incidences of sneezing and early phase nasal blockage, late phase nasal blockage was partially but significantly attenuated; however, nasal eosinophilia was not suppressed. In contrast, when TFC-007 was given once 1.5h after the challenge, the late phase response was not affected. Collectively, PGD(2) produced by H-PGDS early after an antigen challenge can participate in the induction of late phase nasal blockage, although the mechanism may be independent of eosinophil infilatration. The strategy for H-PGDS inhibition may be beneficial for allergic rhinitis therapy.

摘要

尽管已经有人提出前列腺素(PG)D(2)参与了过敏性鼻炎的发病机制,但抑制造血 PGDS(H-PGDS)是否对过敏性鼻炎有有益作用尚不清楚。我们评估了一种选择性 H-PGDS 抑制剂 TFC-007 对豚鼠日本雪松花粉诱导的过敏性鼻炎的鼻部症状的影响。致敏动物每周接受一次花粉挑战。在挑战前给予 TFC-007(30mg/kg,po)一次几乎完全抑制了挑战后早期和晚期鼻组织中 PGD(2)的产生。虽然预处理不影响打喷嚏和早期鼻塞的发生率,但晚期鼻塞部分但显著减轻;然而,鼻嗜酸性粒细胞浸润并未被抑制。相比之下,当 TFC-007 在挑战后 1.5 小时给予一次时,晚期反应不受影响。总之,抗原挑战后早期由 H-PGDS 产生的 PGD(2)可参与诱导晚期鼻塞,尽管其机制可能与嗜酸性粒细胞浸润无关。H-PGDS 抑制策略可能有益于过敏性鼻炎的治疗。

相似文献

1
Inhibition of hematopoietic prostaglandin D synthase improves allergic nasal blockage in guinea pigs.抑制造血前列腺素 D 合酶可改善豚鼠变应性鼻阻塞。
Prostaglandins Other Lipid Mediat. 2011 Aug;95(1-4):27-34. doi: 10.1016/j.prostaglandins.2011.05.001. Epub 2011 May 10.
2
Role of hematopoietic prostaglandin D synthase in biphasic nasal obstruction in guinea pig model of experimental allergic rhinitis.造血前列腺素 D 合酶在实验性变应性鼻炎豚鼠模型中双相性鼻阻塞中的作用。
Eur J Pharmacol. 2011 Sep 30;667(1-3):389-95. doi: 10.1016/j.ejphar.2011.05.041. Epub 2011 Jun 1.
3
Effect of Ganoderma lucidum on pollen-induced biphasic nasal blockage in a guinea pig model of allergic rhinitis.灵芝对变应性鼻炎豚鼠模型花粉诱导的双相性鼻阻塞的影响。
Phytother Res. 2012 Mar;26(3):325-32. doi: 10.1002/ptr.3557. Epub 2011 Jun 23.
4
Important roles of tachykinins in the development of allergic nasal hyperresponsiveness in guinea-pigs.速激肽在豚鼠变应性鼻高反应性发展中的重要作用。
Clin Exp Allergy. 2009 Jan;39(1):138-46. doi: 10.1111/j.1365-2222.2008.03097.x. Epub 2008 Sep 4.
5
Involvement of peroxynitrite in pollen-induced nasal blockage in guinea pigs.过氧亚硝酸盐在豚鼠花粉诱导的鼻阻塞中的作用。
Eur J Pharmacol. 2008 Mar 17;582(1-3):139-44. doi: 10.1016/j.ejphar.2007.12.007. Epub 2008 Jan 14.
6
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.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。
Eur J Pharmacol. 2020 May 15;875:173030. doi: 10.1016/j.ejphar.2020.173030. Epub 2020 Feb 19.
7
Effect of local nasal immunotherapy on nasal blockage in pollen-induced allergic rhinitis of Guinea pigs.局部鼻免疫疗法对豚鼠花粉诱导性变应性鼻炎鼻阻塞的影响。
Allergol Int. 2008 Dec;57(4):419-27. doi: 10.2332/allergolint.08-OA-0013. Epub 2008 Nov 1.
8
Absence of nasal blockage in a Japanese cedar pollen-induced allergic rhinitis model mouse.日本柳杉花粉诱导的变应性鼻炎模型小鼠中无鼻阻塞现象。
Allergol Int. 2009 Jun;58(2):171-8. doi: 10.2332/allergolint.08-OA-0021. Epub 2009 Feb 25.
9
Effects of KP-496, a novel dual antagonist of leukotriene D(4) and thromboxane A (2) receptors on nasal blockage in guinea pig models of allergic rhinitis.新型白三烯D4和血栓素A2受体双重拮抗剂KP-496对变应性鼻炎豚鼠模型鼻阻塞的影响
Inflamm Res. 2008 Jun;57(6):247-51. doi: 10.1007/s00011-007-7067-5.
10
Evaluation of nasal barrier dysfunction at acute- and late-phase reactions in a guinea pig model of allergic rhinitis.在豚鼠变应性鼻炎模型中评估急性和晚期反应时的鼻屏障功能障碍。
Vascul Pharmacol. 2005 Oct;43(4):267-76. doi: 10.1016/j.vph.2005.08.016. Epub 2005 Oct 27.

引用本文的文献

1
Optimizing linker rigidity to improve intracellular behavior of PROTACs targeting hematopoietic prostaglandin D synthase.优化连接体刚性以改善靶向造血前列腺素D合酶的PROTACs的细胞内行为。
RSC Med Chem. 2025 Sep 2. doi: 10.1039/d5md00396b.
2
In Silico Design, Synthesis, and Evaluation of PROTAC Against Hematopoietic Prostaglandin D Synthase.基于计算机的设计、合成及对造血前列腺素 D 合酶的 PROTAC 评价。
Methods Mol Biol. 2024;2780:345-359. doi: 10.1007/978-1-0716-3985-6_18.
3
Computer-Aided Designing Peptide Inhibitors of Human Hematopoietic Prostaglandin D2 Synthase Combined Molecular Docking and Molecular Dynamics Simulation.
计算机辅助设计人源造血前列腺素 D2 合酶抑制剂肽的分子对接和分子动力学模拟。
Molecules. 2023 Aug 7;28(15):5933. doi: 10.3390/molecules28155933.
4
Structure-activity relationship study of PROTACs against hematopoietic prostaglandin D synthase.针对造血前列腺素 D 合酶的 PROTACs 的构效关系研究
RSC Med Chem. 2022 Sep 23;13(12):1495-1503. doi: 10.1039/d2md00284a. eCollection 2022 Dec 14.
5
Biochemical and Structural Characteristics, Gene Regulation, Physiological, Pathological and Clinical Features of Lipocalin-Type Prostaglandin D Synthase as a Multifunctional Lipocalin.脂联素型前列腺素D合成酶作为一种多功能脂联素的生化与结构特征、基因调控、生理、病理及临床特征
Front Physiol. 2021 Oct 22;12:718002. doi: 10.3389/fphys.2021.718002. eCollection 2021.
6
Development of a Hematopoietic Prostaglandin D Synthase-Degradation Inducer.造血前列腺素D合酶降解诱导剂的研发
ACS Med Chem Lett. 2021 Jan 14;12(2):236-241. doi: 10.1021/acsmedchemlett.0c00605. eCollection 2021 Feb 11.
7
The Biology of Prostaglandins and Their Role as a Target for Allergic Airway Disease Therapy.前列腺素的生物学及其作为变态反应性气道疾病治疗靶点的作用。
Int J Mol Sci. 2020 Mar 8;21(5):1851. doi: 10.3390/ijms21051851.
8
Therapeutic Potential of Hematopoietic Prostaglandin D Synthase in Allergic Inflammation.造血前列腺素 D 合酶在过敏性炎症中的治疗潜力。
Cells. 2019 Jun 20;8(6):619. doi: 10.3390/cells8060619.
9
Effects of anticholinergic agent on miRNA profiles and transcriptomes in a murine model of allergic rhinitis.抗胆碱能药物对变应性鼻炎小鼠模型中 miRNA 谱和转录组的影响。
Mol Med Rep. 2017 Nov;16(5):6558-6569. doi: 10.3892/mmr.2017.7411. Epub 2017 Aug 31.
10
Prostaglandins and Their Receptors in Eosinophil Function and As Therapeutic Targets.前列腺素及其受体在嗜酸性粒细胞功能中的作用以及作为治疗靶点
Front Med (Lausanne). 2017 Jul 19;4:104. doi: 10.3389/fmed.2017.00104. eCollection 2017.