Ebertz J M, Hirshman C A, Kettelkamp N S, Uno H, Hanifin J M
J Invest Dermatol. 1987 Jun;88(6):682-5. doi: 10.1111/1523-1747.ep12470339.
Substance P is an undecapeptide found in multiple sites throughout the central and peripheral nervous systems including small unmyelinated (type C) cutaneous nerve fibers. Previous studies demonstrated that antidromic stimulation results in substance P (SP) release from nerve endings, SP stimulates histamine release (HR) from rat mast cells in vitro, and intradermal SP in humans produces wheals identical to those induced by histamine. These studies suggest a possible role for SP as a link between neurologic events and cutaneous mast cell-mediated reactions. We therefore investigated SP-induced HR in an in vitro preparation of human skin mast cells. Human foreskin sections were incubated with varying concentrations of SP. Histamine was assayed using automated fluorimetry and release was calculated as a percentage of total tissue histamine. Substance P caused dose-dependent HR over a range from 10(-5) M (1.3%) to 5 X 10(-4) M (25.1%). Histamine release was optimal at 3 mM calcium and was blocked by pretreatment with calcium chelation. Naloxone failed to block HR. These studies suggest that HR from skin mast cells by SP may play a role in neural modulation of poorly understood inflammatory skin conditions.
P物质是一种十一肽,存在于中枢和外周神经系统的多个部位,包括无髓鞘的小(C型)皮肤神经纤维。先前的研究表明,逆向刺激会导致P物质(SP)从神经末梢释放,SP在体外刺激大鼠肥大细胞释放组胺(HR),并且人皮内注射SP会产生与组胺诱导的风团相同的风团。这些研究表明SP可能作为神经事件与皮肤肥大细胞介导的反应之间的联系发挥作用。因此,我们在人皮肤肥大细胞的体外制备中研究了SP诱导的HR。将人包皮切片与不同浓度的SP一起孵育。使用自动荧光法测定组胺,并将释放量计算为总组织组胺的百分比。P物质在10(-5)M(1.3%)至5×10(-4)M(25.1%)的范围内引起剂量依赖性的HR。组胺释放在3 mM钙时最佳,并被钙螯合预处理阻断。纳洛酮未能阻断HR。这些研究表明,SP引起的皮肤肥大细胞HR可能在对了解甚少的炎症性皮肤病的神经调节中起作用。