Hägermark O, Hökfelt T, Pernow B
J Invest Dermatol. 1978 Oct;71(4):233-5. doi: 10.1111/1523-1747.ep12515092.
Intradermal injection of synthetic substance P (10(-7)--10(-5) M in humans produced flare, wheal and itching. These responses were inhibited by oral pretreatment of the subjects with an antihistaminic drug (chlorcyclizine) or by local pretreatment with Compound 48/80 administered to deplete the local stores of mast-cell bound histamine. The findings indicate that the responses induced by substance P were mainly mediated by histamine released from the dermal mast cells. In contrast to previously studied histamine liberators, substance P was less potent when acting on rat mast cells in vitro than on human skin mast cells in vivo. When incubated with rat peritoneal mast cells, about 100 times higher concentrations (10(-5) M) were required to induce histamine release than in the in vivo studies on humans. It was concluded that substance P is a potent histamine liberator in human skin.
皮内注射合成的P物质(人体中浓度为10⁻⁷ - 10⁻⁵ M)可产生风团、潮红和瘙痒。口服抗组胺药物(氯环嗪)预处理受试者或局部预处理给予48/80化合物以耗尽局部肥大细胞结合的组胺储备,这些反应会受到抑制。研究结果表明,P物质诱导的反应主要由真皮肥大细胞释放的组胺介导。与先前研究的组胺释放剂不同,P物质在体外作用于大鼠肥大细胞时的效力低于在体内作用于人类皮肤肥大细胞时的效力。当与大鼠腹膜肥大细胞一起孵育时,诱导组胺释放所需的浓度(10⁻⁵ M)比人体体内研究高约100倍。得出的结论是,P物质是人体皮肤中一种有效的组胺释放剂。