Erin N, Ersoy Y, Ercan F, Akici A, Oktay S
Central Research Lab, Faculty of Medicine, Akdeniz University Antalya, Turkey.
Clin Exp Dermatol. 2004 Nov;29(6):644-8. doi: 10.1111/j.1365-2230.2004.01613.x.
Mast 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.
肥大细胞与应激诱导的炎症性皮肤病如银屑病有关。然而,应激诱导肥大细胞脱颗粒的机制尚不完全清楚。在此,我们探讨了P物质(SP)受体(NK-1)激活在大鼠暴露于应激时肥大细胞脱颗粒中的作用。使用一种特异性非肽类NK-1拮抗剂CP99994对大鼠进行外周或脑室内治疗。由于大脑中SP活性增加可能介导应激反应,我们还检查了中枢注射SP后皮肤肥大细胞的脱颗粒情况。应激以及中枢注射SP均增加了肥大细胞脱颗粒。中枢和外周注射CP99994均可预防应激诱导的肥大细胞脱颗粒。令人惊讶的是,应激与SP联合使用可减少肥大细胞脱颗粒,表明高水平的SP可能抵消应激反应。该动物模型的结果表明,NK-1拮抗剂可用于治疗应激诱导的炎症性皮肤病;然而,药物剂量应谨慎选择。