Baluk P, Bertrand C, Geppetti P, McDonald D M, Nadel J A
Cardiovascular Research Institute, University of California, San Francisco, USA.
Exp Lung Res. 1996 Jul-Aug;22(4):409-18. doi: 10.3109/01902149609046032.
The involvement of neurokinin NK1 receptors in cigarette-induced adhesion of neutrophils and eosinophils to venules of the airway mucosa was investigated. Rats were pretreated with the NK1 receptor antagonist CP-99,994 (4 mg/kg IV), its vehicle, or its inactive enantiomer CP-100,263 before exposure to cigarette smoke. Adherent neutrophils and eosinophils were stained histochemically for endogenous peroxidase activity and were counted in tracheal whole mounts. Plasma leakage was quantified be stereological measurements of the extravasation of Monastral blue. Cigarette smoke induced the adhesion of 104 + 17 neutrophils and 10.4 +/- 1.7 eosinophils per square millimeter of mucosa. CP-99,994 reduced neutrophil and eosinophil adhesion by 66 and 61%, respectively, and reduced plasma extravasation by 61% (p < .05), but CP-100,263 had no significant effect. The inhibitory effects of CP-99,994 appeared to be specific because CP-99,994 had no effect on neutrophil and eosinophil adhesion, or on plasma extravasation induced by platelet activating factor, an inflammatory stimulus acting independently of NK1 receptors. These results suggest that NK1 receptors are involved in cigarette smoke-induced adhesion of neutrophils and eosinophils to the endothelium of venules in the rat tracheal mucosa.
研究了神经激肽NK1受体在香烟诱导的中性粒细胞和嗜酸性粒细胞与气道黏膜小静脉黏附中的作用。在暴露于香烟烟雾之前,用NK1受体拮抗剂CP - 99,994(4毫克/千克静脉注射)、其溶媒或其无活性对映体CP - 100,263对大鼠进行预处理。对黏附的中性粒细胞和嗜酸性粒细胞进行内源性过氧化物酶活性的组织化学染色,并在气管整装片中计数。通过对莫纳斯特蓝外渗的体视学测量来定量血浆渗漏。香烟烟雾诱导每平方毫米黏膜有104±17个中性粒细胞和10.4±1.7个嗜酸性粒细胞黏附。CP - 99,994分别使中性粒细胞和嗜酸性粒细胞黏附减少66%和61%,并使血浆外渗减少61%(p<0.05),但CP - 100,263没有显著作用。CP - 99,994的抑制作用似乎具有特异性,因为CP - 99,994对中性粒细胞和嗜酸性粒细胞黏附以及对由血小板活化因子诱导的血浆外渗没有影响,血小板活化因子是一种独立于NK1受体起作用的炎症刺激物。这些结果表明,NK1受体参与了香烟烟雾诱导的大鼠气管黏膜小静脉内皮细胞与中性粒细胞和嗜酸性粒细胞的黏附。