Woodward D F, Spada C S, Hawley S B, Nieves A L
Invest Ophthalmol Vis Sci. 1986 Oct;27(10):1495-503.
The present histological studies have demonstrated that histamine causes dose-dependent eosinophil infiltration into the conjunctiva. A highly directional movement toward the conjunctival epithelium was observed, and the presence of large numbers of degranulating eosinophils appeared to result in epithelial cell damage and goblet cell discharge. Blockade of H2-receptors by systemic cimetidine pretreatment significantly inhibited the eosinophil infiltration elicited by an intermediate histamine dose, whereas the H1-receptor blockade produced by systemic pyrilamine pretreatment markedly reduced the response to all histamine doses. The pyrilamine-insensitive residual eosinophil infiltrate was not affected by administering a cimetidine-pyrilamine combination. In animals presensitized to ovalbumin, antigen challenge evoked extensive and directional emigration of eosinophils toward the conjunctival epithelium with resultant exfoliation and depletion of goblet cell populations. In conjunctival immediate hypersensitivity, neither cimetidine nor pyrilamine alone produced an inhibitory effect, but a cimetidine-pyrilamine combination caused a significant reduction in the number of infiltrating eosinophils and prevented epithelial damage and goblet cell depletion. These results suggest that histamine may participate in the recruitment of eosinophils during immediate hypersensitivity reactions. The differential effect of pyrilamine on the eosinophil infiltration evoked by histamine or immediate hypersensitivity may, perhaps, reflect the importance of increased microvascular permeability in facilitating eosinophil emigration.
目前的组织学研究表明,组胺可引起剂量依赖性嗜酸性粒细胞浸润结膜。观察到嗜酸性粒细胞向结膜上皮呈高度定向移动,大量脱颗粒的嗜酸性粒细胞的存在似乎导致上皮细胞损伤和杯状细胞排出。全身给予西咪替丁预处理阻断H2受体,可显著抑制中等剂量组胺引起的嗜酸性粒细胞浸润,而全身给予吡苄明预处理产生的H1受体阻断作用则明显降低了对所有组胺剂量的反应。吡苄明不敏感的残余嗜酸性粒细胞浸润不受西咪替丁 - 吡苄明联合用药的影响。在对卵清蛋白致敏的动物中,抗原激发引起嗜酸性粒细胞广泛且定向地向结膜上皮迁移,导致杯状细胞剥脱和数量减少。在结膜速发型超敏反应中,单独使用西咪替丁或吡苄明均未产生抑制作用,但西咪替丁 - 吡苄明联合用药可显著减少浸润的嗜酸性粒细胞数量,并防止上皮损伤和杯状细胞减少。这些结果表明,组胺可能参与速发型超敏反应期间嗜酸性粒细胞的募集。吡苄明对组胺或速发型超敏反应引起的嗜酸性粒细胞浸润的不同作用,可能反映了微血管通透性增加在促进嗜酸性粒细胞迁移中的重要性。