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Antihistamines as Important Tools for Regulating Inflammation 抗组胺药是调节炎症的重要工具
Pub Date : 2005-01-31 DOI: 10.2174/1568014053005372
E. Nettis, M. C. Colanardi, A. Ferrannini, A. Tursi
Allergic disorders are characterized by typical symptoms and an infiltrate of cells, including Th2 lymphocytes, eosinophils and mast cells. Activated mast cell mediators cause the early appearance of symptoms, and cytokines induce a cascade of inflammatory events. Both resident and infiltrating cells are important sources of those mediators and cytokines which maintain and enhance the allergic inflammatory response. The predominant preformed mediator released by mast cells and basophils is histamine, which binds to specific cell receptors to produce its clinical effects. Therapeutic intervention in allergic disease has thus commonly focused on blocking the action of histamine. Ever since Arunlakshana demonstrated, in 1953, the ability of antihistamines to inhibit histamine release by mast cells, numerous studies have been conducted, both in vivo and in vitro , to determine the H1 antihistamines additional properties which contribute to their clinical efficacy in the treatment of allergic disease. It has been reported that some antihistamines can also regulate the expression and/or release of cytokines, chemokines, adhesion molecules, and or/inflammatory mediators. Such properties make these agents important tools for the continuous long- term regulation of both early and late-phase allergic reactions. It appears likely that antihistamines exert these anti- inflammatory effects by means of both receptor-dependent and receptor-independent mechanisms. The receptor- dependent mechanisms seem to involve inhibition of the generation of NF-kB dependent cytokines and adhesion proteins. The latter mechanisms, which require higher drug concentrations, appear to include the release by inflammatory cells of pre-formed mediators, such as histamine and eosinophil proteins as well as eicosanoid generation and oxygen free radicals production. Herein, we review the current state of knowledge of the anti-inflammatory properties of antihistamine s and their mechanisms.
过敏性疾病的特点是典型症状和细胞浸润,包括Th2淋巴细胞、嗜酸性粒细胞和肥大细胞。激活的肥大细胞介质引起症状的早期出现,细胞因子诱导一系列炎症事件。驻留细胞和浸润细胞都是维持和增强过敏性炎症反应的介质和细胞因子的重要来源。肥大细胞和嗜碱性细胞释放的主要预形成介质是组胺,它与特定的细胞受体结合产生临床效果。因此,过敏性疾病的治疗干预通常集中在阻断组胺的作用上。自从Arunlakshana在1953年证明抗组胺药抑制肥大细胞释放组胺的能力以来,已经进行了大量的体内和体外研究,以确定H1抗组胺药的其他特性,这些特性有助于其治疗过敏性疾病的临床疗效。据报道,一些抗组胺药还可以调节细胞因子、趋化因子、粘附分子和/或炎症介质的表达和/或释放。这些特性使这些药物成为持续长期调节早期和晚期过敏反应的重要工具。似乎抗组胺药通过受体依赖性和受体非依赖性机制发挥这些抗炎作用。受体依赖机制似乎涉及抑制NF-kB依赖的细胞因子和粘附蛋白的产生。后一种机制需要更高的药物浓度,似乎包括炎症细胞释放预先形成的介质,如组胺和嗜酸性粒细胞蛋白,以及类二十烷的产生和氧自由基的产生。本文就抗组胺药抗炎特性及其作用机制的研究现状进行综述。
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引用次数: 23
Innate Immune Receptors and IRF Family Transcription Factors 先天免疫受体和IRF家族转录因子
Pub Date : 2005-01-31 DOI: 10.2174/1568014053005291
T. Yoneyama
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引用次数: 0
Novel Therapeutic Targets for Somatostatin in Inflammatory Chronic Diseases 生长抑素治疗炎症性慢性疾病的新靶点
Pub Date : 2005-01-31 DOI: 10.2174/1568014053005354
N. Vaysse, H. Lahlou, Géraldine Ferjoux, C. Susini
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引用次数: 6
SIGIRR/TIR8: A negative regulator of Toll-IL-1R signaling SIGIRR/TIR8: Toll-IL-1R信号的负调控因子
Pub Date : 2005-01-31 DOI: 10.2174/1568014053005309
Xiaoxia Li, J. Qin
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引用次数: 0
Chemokines in Allergic Inflammation: Human Disease and Animal Models 变应性炎症中的趋化因子:人类疾病和动物模型
Pub Date : 2004-11-30 DOI: 10.2174/1568014043355203
H. Hogenesch
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引用次数: 4
Lymphocyte Homing to the Liver 淋巴细胞归巢到肝脏
Pub Date : 2004-11-30 DOI: 10.2174/1568014043355258
Tohru Sato, H. Thorlacius, E. Butcher
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引用次数: 1
Small-Molecule Chemokine Receptor Antagonists: Potential Targets for Inflammatory and Allergic Disorders 小分子趋化因子受体拮抗剂:炎症和过敏性疾病的潜在靶点
Pub Date : 2004-11-30 DOI: 10.2174/1568014043355230
T. Saeki
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引用次数: 1
Stromal cell derived factor-1/CXCL12, CXCR4 and CD26 in the mobilization and homing of hematopoietic stem and progenitor cells 造血干细胞和祖细胞的动员和归巢中的基质细胞衍生因子-1/CXCL12、CXCR4和CD26
Pub Date : 2004-11-30 DOI: 10.2174/1568014043355249
H. Broxmeyer, K. Christopherson
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引用次数: 7
Preface [Hot Topic: Chemokines (Guest Editor: Chang H. Kim)] 前言[热门话题:趋化因子(客座编辑:Chang H. Kim)]
Pub Date : 2004-11-30 DOI: 10.2174/1568014043355212
C. Kim
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引用次数: 0
Trafficking Potentials of Unconventional T Cell Subsets 非常规T细胞亚群的转运潜力
Pub Date : 2004-11-30 DOI: 10.2174/1568014043355267
C. Johnson
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引用次数: 4
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Current medicinal chemistry. Anti-inflammatory & anti-allergy agents
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