Gao X P, Rubinstein I
Department of Medicine, University of Illinois at Chicago, USA.
Am J Physiol. 1995 Nov;269(5 Pt 2):H1648-55. doi: 10.1152/ajpheart.1995.269.5.H1648.
The purpose of this study was to determine whether the stable cyclic peptide analogue of human vasoactive intestinal peptide, Ro 24-9981, modulates bradykinin-induced plasma exudation in the oral mucosa and if so, to determine the mechanisms that mediated these responses. Using intravital microscopy, we found that suffusion of Ro 24-9981 had no significant effects on leaky site formation and clearance of fluorescein-isothiocyanate-dextran (mol mass 70 kDa) in the hamster cheek pouch. However, Ro 24-9981 significantly potentiated bradykinin-induced increases in leaky site formation and clearance of fluorescein-isothiocyanate-dextran (P < 0.05). These effects were specific because Ro 24-9981 had no significant effects on adenosine and calcium ionophore A23187-induced increases in leaky site formation and clearance of fluorescein-isothiocyanate-dextran. Furthermore, they were not mediated by cyclooxygenase products of arachidonic acid metabolism because indomethacin was ineffective. NG-nitro-L-arginine methyl ester, a selective inhibitor of nitric oxide synthase, but not NG-nitro-D-arginine methyl ester, significantly attenuated the effects of both bradykinin and Ro 24-9981 with bradykinin (P < 0.05). These responses were restored by L-arginine but not D-arginine. Collectively, these data indicate that bradykinin-induced plasma exudation in the oral mucosa was potentiated by Ro 24-9981 in a specific receptor-mediated fashion. These responses were mediated, in part, by the L-arginine/nitric oxide biosynthetic pathway.
本研究的目的是确定人血管活性肠肽的稳定环肽类似物Ro 24-9981是否能调节缓激肽诱导的口腔黏膜血浆渗出,若能调节,则确定介导这些反应的机制。通过活体显微镜观察,我们发现Ro 24-9981灌注对仓鼠颊囊中的渗漏部位形成以及异硫氰酸荧光素-葡聚糖(分子量70 kDa)的清除没有显著影响。然而,Ro 24-9981能显著增强缓激肽诱导的渗漏部位形成增加以及异硫氰酸荧光素-葡聚糖的清除(P<0.05)。这些作用具有特异性,因为Ro 24-9981对腺苷和钙离子载体A23187诱导的渗漏部位形成增加以及异硫氰酸荧光素-葡聚糖的清除没有显著影响。此外,它们不是由花生四烯酸代谢的环氧化酶产物介导的,因为吲哚美辛无效。一氧化氮合酶的选择性抑制剂NG-硝基-L-精氨酸甲酯而非NG-硝基-D-精氨酸甲酯,能显著减弱缓激肽和Ro 24-9981的作用(与缓激肽相比,P<0.05)。L-精氨酸可恢复这些反应,而D-精氨酸则不能。总体而言,这些数据表明Ro 24-9981以特异性受体介导的方式增强了缓激肽诱导的口腔黏膜血浆渗出。这些反应部分由L-精氨酸/一氧化氮生物合成途径介导。