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.
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 [...]