Regal J F, Hardy T M, Casey F B, Chakrin L W
Immunopharmacology. 1983 Apr;5(4):315-27. doi: 10.1016/0162-3109(83)90047-4.
C5a, a product of complement system activation, causes a significant contraction of the isolated guinea pig trachea, and the antihistamine diphenhydramine does not alter the rate, amplitude, or duration of the contraction (Regal et al., 1980). The present study demonstrates that over the range of C5a concentrations investigated, the C5a-induced contractile response of the trachea maximized, whereas the contraction of lung parenchymal strips and the release of histamine from chopped lung did not. In addition, the antihistamines, diphenhydramine and pyrilamine, caused a significant delay in the onset of the C5a-induced contraction of lung parenchymal strips. When parenchymal strips from nonperfused lung were used, the maximum of the contraction was also reduced by pyrilamine. Aspirin and indomethacin effectively inhibited the C5a-induced contraction of lung parenchymal strips, and inhibition by a combination of aspirin and pyrilamine was the sum of the inhibition by aspirin and the inhibition by pyrilamine. The SRS-A antagonist, FPL 55712, caused a more rapid relaxation of the C5a-induced response over control. These studies suggest that products of the cyclo-oxygenase pathway are mediators involved in the C5a-induced contraction of lung parenchyma, with histamine and leukotrienes contributing as well.
补体系统激活产物C5a可使离体豚鼠气管显著收缩,而抗组胺药苯海拉明不会改变收缩的速率、幅度或持续时间(雷加尔等人,1980年)。本研究表明,在所研究的C5a浓度范围内,气管对C5a诱导的收缩反应达到最大值,而肺实质条带的收缩和切碎肺组织中组胺的释放则未达到最大值。此外,抗组胺药苯海拉明和吡苄明可显著延迟C5a诱导的肺实质条带收缩的起始时间。当使用未灌注肺的实质条带时,吡苄明也会降低收缩的最大值。阿司匹林和吲哚美辛可有效抑制C5a诱导的肺实质条带收缩,阿司匹林和吡苄明联合使用的抑制作用为阿司匹林的抑制作用与吡苄明的抑制作用之和。SRS-A拮抗剂FPL 55712可使C5a诱导的反应比对照组更快地松弛。这些研究表明,环氧化酶途径的产物是参与C5a诱导的肺实质收缩的介质,组胺和白三烯也起作用。