Stabilizing effect of green tea extract and epigallocatechin-3-gallate (EGCG) on mast cell : an in vivo study.

IF 5.3 2区 医学 Q2 IMMUNOLOGY
Md Mominul Islam, Nadiah Syafiqah Nor Azman, Sreemoy Kanti Das, Mohd Gousuddin, Md Abu Hasan Rasel, Md Robiul Islam, Nadia Izbeta Bini
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引用次数: 0

Abstract

Mast cells are vital participants in the pathophysiology of allergic reactions by a process of degranulation where bioactive mediators such as histamine, leukotrienes, interleukins and prostaglandins are released to create the local inflammatory milieu. These mediators play an important role in the onset and advancements of allergic diseases, causing bronchoconstriction, as well as increased vascular permeability and local tissue inflammation. Stabilisation of mast cells is one of the essential therapeutic approaches to prevent excessive degranulation and consequent inflammatory aftermaths in allergic conditions. A major polyphenolic component of green tea, epigallocatechin gallate (EGCG), has been postulated to have mast cell-stabilising effects due to its antioxidant and anti-inflammatory effects. It has been reported that EGCG modulates immune responses through inhibition of oxidative stress and control of proinflammatory cytokines secretion. Due to its natural origin and excellent safety profile, EGCG emerges as an alternative treatment for allergic diseases in comparison to the traditional anti-allergic pharmacotherapy such as antihistamines and corticosteroids which have adverse effects long-term usage. In the present study, in vivo anti-allergic activity of EGCG was assessed using bovine serum albumin (BSA)-induced allergy model in male Brown Norway rats. Different levels of EGCG were administered to the experimental groups, while markers of allergic responses were investigated including the histamine concentration and cytokine profiles. The administration of EGCG led to a dose-dependent inhibition of proinflammatory cytokines and histamine concentrations, which implies strong suppression of degranulation of mast cells. These findings indicate that EGCG has therapeutic promise in addressing the mast cell-based allergic diseases.

绿茶提取物和表没食子儿茶素-3-没食子酸酯(EGCG)对肥大细胞稳定作用的体内研究。
肥大细胞是过敏反应病理生理的重要参与者,在脱芽过程中,生物活性介质如组胺、白三烯、白细胞介素和前列腺素被释放,创造局部炎症环境。这些介质在过敏性疾病的发生和发展中起重要作用,引起支气管收缩,以及血管通透性增加和局部组织炎症。肥大细胞的稳定是必不可少的治疗方法之一,以防止过度脱颗粒和随之而来的炎症后遗症在过敏性条件。绿茶的一种主要多酚成分,表没食子儿茶素没食子酸酯(EGCG),由于其抗氧化和抗炎作用,被认为具有肥大细胞稳定作用。据报道,EGCG通过抑制氧化应激和控制促炎细胞因子的分泌来调节免疫反应。由于其天然来源和良好的安全性,与传统的抗过敏药物治疗(如抗组胺药和皮质类固醇)相比,EGCG成为过敏性疾病的替代治疗方法,这些药物长期使用会产生不良反应。本研究采用牛血清白蛋白(BSA)诱导的雄性褐威大鼠过敏模型,评价EGCG的体内抗过敏活性。实验组给予不同水平的EGCG,同时研究过敏反应的标志物,包括组胺浓度和细胞因子谱。EGCG的施用导致促炎细胞因子和组胺浓度的剂量依赖性抑制,这意味着对肥大细胞脱颗粒的强烈抑制。这些发现表明EGCG在治疗肥大细胞过敏性疾病方面具有治疗前景。
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来源期刊
Inflammopharmacology
Inflammopharmacology IMMUNOLOGYTOXICOLOGY-TOXICOLOGY
CiteScore
8.00
自引率
3.40%
发文量
200
期刊介绍: Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas: -Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states -Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs -Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents -Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain -Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs -Muscle-immune interactions during inflammation [...]
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