Agren P, van der Sterren S, Cogolludo A L, Frazziano G, de Mey J G R, Blanco C E, Villamor E
Department of Pediatrics, Maastricht University Hospital, Research Institute Growth and Development, University of Maastricht, Maastricht, The Netherlands.
J Physiol Pharmacol. 2008 Mar;59(1):55-76.
We tested the hypothesis that endothelium-dependent relaxation in the chicken ductus arteriosus (DA) is developmentally regulated. Isolated DA rings from 15-, 19- and 21-day-old (externally pipped) chicken embryos relaxed to acetylcholine (ACh). This relaxation was unaffected by indomethacin but impaired by endothelium removal, by the NO synthase inhibitor L-NAME, and by the soluble guanylate cyclase inhibitor ODQ, suggesting the involvement of NO. This NO production was confirmed with the fluorescent probe DAF-2DA. The combination of apamin and charybdotoxin with L-NAME produced a further inhibition of ACh-induced relaxation, suggesting the participation of a putative EDHF. In the 21-day DA, the relaxations induced by ACh and sodium nitroprusside (SNP) were markedly reduced and scanning electron microscopy demonstrated an irregular endothelial lining with protrusion and detachment of endothelial cells. The relaxations induced by BAY 41-2272 and 8-Br cGMP were not affected by age. When compared with 5%, lower (0%) and higher (21, 95%) O(2) concentrations impaired ACh-induced relaxation. In summary, we found that ACh induces endothelium-dependent relaxation of the chicken DA and that NO and EDHF are involved in this response. During chicken DA closure, endothelial cells undergo morphologic and functional alterations that result in the lack of endothelium-dependent relaxation.
我们检验了鸡动脉导管(DA)中内皮依赖性舒张受发育调控这一假说。从15日龄、19日龄和21日龄(已破壳)鸡胚分离出的DA环对乙酰胆碱(ACh)产生舒张反应。这种舒张不受吲哚美辛影响,但内皮去除、一氧化氮合酶抑制剂L-NAME和可溶性鸟苷酸环化酶抑制剂ODQ可损害其舒张,提示一氧化氮(NO)参与其中。用荧光探针DAF-2DA证实了这种NO的产生。蜂毒明肽和卡律蝎毒素与L-NAME联合使用可进一步抑制ACh诱导的舒张,提示一种假定的内皮依赖性超极化因子(EDHF)参与其中。在21日龄的DA中,ACh和硝普钠(SNP)诱导的舒张明显减弱,扫描电子显微镜显示内皮衬里不规则,有内皮细胞突出和脱落。BAY 41-2272和8-溴环鸟苷酸(8-Br cGMP)诱导的舒张不受年龄影响。与5%相比,较低(0%)和较高(21%、95%)的氧(O₂)浓度会损害ACh诱导的舒张。总之,我们发现ACh可诱导鸡DA的内皮依赖性舒张,且NO和EDHF参与了这一反应。在鸡DA闭合过程中,内皮细胞发生形态和功能改变,导致内皮依赖性舒张缺乏。