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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/64215
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dc.contributor.authorGomes, J. C.-
dc.date.accessioned2014-05-27T11:17:27Z-
dc.date.accessioned2016-10-25T18:12:52Z-
dc.date.available2014-05-27T11:17:27Z-
dc.date.available2016-10-25T18:12:52Z-
dc.date.issued1992-01-01-
dc.identifier.citationAgents and Actions, v. 36, n. SUPPL., p. 87-95, 1992.-
dc.identifier.issn0065-4299-
dc.identifier.urihttp://hdl.handle.net/11449/64215-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/64215-
dc.description.abstractIt is well known that histamine is found in high concentration in mast cell granules(1). The histamine content of these granules may be released to the extracellular space if an appropriate stimulus is provided(2). Besides histamine, other preformed active substances like enzymes, chemotatic factors and proteoglycans, as well as newly generated mediators like eicosanoids, platelet activating factor and adenosine are released during the secretion process of mast cells(3). The activation of mast cell degranulation has been associated with a number of pathologic disorders, most frequently, diseases derived from the atopic state(4). It is now evident that mast cells are the primary effector cells in the early reaction in both allergic and non-allergic asthma(5,6), although some authors doubt that the late reaction of asthma is a mast cell dependent event(6). Other studies point towards basophils as cellular elements involved in the secondary phase of inflammation in allergic diseases(7). Secretion would depend on a histamine releasing factor, and on the presence of IgE on the basophil's surface(8). There is also evidence suggesting involvement of mast cells in some non-allergic inflammatory processes like arthritis(9). The pharmacological management of these diseases basically consists in the use of methylxantines, beta 2-adrenergic agonists, glucocorticoids, sodium cromoglycate-like drugs, anticholinergic and antihistaminic H 1 antagonists(10). Their therapeutic effects include bronchodilatation, receptor and physiological antagonism, prevention of inflammatory responses induced by secondary cells, and finally, inhibition of mast cell activation(11). This review is concerned with compounds having inhibitory action on mast cell activation, and their possible importance on the pathophysiology of mast cell-related diseases.en
dc.format.extent87-95-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectadenosine-
dc.subjectadrenalin-
dc.subjectazatadine-
dc.subjectazelastine-
dc.subjectcalcimycin-
dc.subjectcalcium channel blocking agent-
dc.subjectceterizine-
dc.subjectconcanavalin a-
dc.subjectcromoglycate disodium-
dc.subjectdextran-
dc.subjecthistamine h1 receptor antagonist-
dc.subjecthistamine release inhibitor-
dc.subjecticosanoid-
dc.subjectisoprenaline-
dc.subjectketotifen-
dc.subjectnedocromil-
dc.subjectphenothiazine derivative-
dc.subjectplant extract-
dc.subjectproteoglycan-
dc.subjectterfenadine-
dc.subjecttheophylline-
dc.subjectthrombocyte activating factor-
dc.subjectunclassified drug-
dc.subjectanimal tissue-
dc.subjectantiinflammatory activity-
dc.subjectconference paper-
dc.subjecthistamine release-
dc.subjecthuman-
dc.subjecthuman tissue-
dc.subjectmast cell-
dc.subjectmast cell degranulation-
dc.subjectnonhuman-
dc.subjectpriority journal-
dc.subjectAnimal-
dc.subjectHistamine Antagonists-
dc.subjectHistamine Release-
dc.subjectHuman-
dc.titleAgents that inhibit histamine release: A reviewen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartment of Pharmacology Institute of Biosciences, Unesp, Botucatu, SP-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofAgents and Actions-
dc.identifier.scopus2-s2.0-0026587010-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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