Publication:
NK-1 antagonist CP99994 inhibits stress-induced mast cell degranulation in rats

dc.contributor.authorAKICI, AHMET
dc.contributor.authorERCAN, FERİHA
dc.contributor.authorsErin, N; Ersoy, Y; Ercan, F; Akici, A; Oktay, S
dc.date.accessioned2022-03-12T17:17:34Z
dc.date.accessioned2026-01-11T18:28:26Z
dc.date.available2022-03-12T17:17:34Z
dc.date.issued2004
dc.description.abstractMast cells are implicated in stress-induced inflammatory skin diseases such as psoriasis. Mechanisms of stress-induced mast cell degranulation however, are not entirely clear. Here we explore the role of activation of a Substance P (SP) receptor (NK-1) on mast cell degranulation upon exposure to stress in rats. A specific nonpeptide NK-1 antagonist, CP99994 was used to treat the rats either peripherally or intracerebroventricularly. Because increased SP activity in the brain may mediate the stress response, we also examined cutaneous mast cell degranulation after central injection of SP. Stress, as well as SP injected centrally, increased mast cell degranulation. Both central and peripheral injection of CP99994 prevented stress-induced mast cell degranulation. Surprisingly, the combination of stress with SP decreased mast cell degranulation, suggesting that high levels of SP may counteract the stress responses. Results in this animal model suggest that NK-1 antagonists may be used therapeutically to treat stress-induced inflammatory skin diseases; however, drug doses should be chosen carefully.
dc.identifier.doi10.1111/j.1365-2230.2004.01613.x
dc.identifier.eissn1365-2230
dc.identifier.issn0307-6938
dc.identifier.pubmed15550145
dc.identifier.urihttps://hdl.handle.net/11424/227867
dc.identifier.wosWOS:000225436900019
dc.language.isoeng
dc.publisherWILEY
dc.relation.ispartofCLINICAL AND EXPERIMENTAL DERMATOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCORTICOTROPIN-RELEASING HORMONE
dc.subjectINDUCED HISTAMINE-RELEASE
dc.subjectENDOGENOUS SUBSTANCE-P
dc.subjectRECEPTORS
dc.subjectNK1
dc.titleNK-1 antagonist CP99994 inhibits stress-induced mast cell degranulation in rats
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage648
oaire.citation.issue6
oaire.citation.startPage644
oaire.citation.titleCLINICAL AND EXPERIMENTAL DERMATOLOGY
oaire.citation.volume29

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