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首页> 外文期刊>Academic Journal of Xian Jiaotong University >Alteration in Contractile Response to Noradrenaline, 5-Hydroxytryptamine, Sarafotoxin 6c, and Angiotensin II in Rat Mesenteric Artery During Organ Culture
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Alteration in Contractile Response to Noradrenaline, 5-Hydroxytryptamine, Sarafotoxin 6c, and Angiotensin II in Rat Mesenteric Artery During Organ Culture

机译:器官培养过程中大鼠肠系膜动脉对去甲肾上腺素,5-羟色胺,Sarafotoxin 6c和血管紧张素II的收缩反应的改变

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Objective To compare the vasoconstrictive effects of 9 mediators on fresh and incubated mesenteric arteries of rats. Methods The superior mesenteric artery of rat was removed and the endothelium was denuded. The vessels were cut into 1 mm long cylindrical segments and subjected to organ culture for 24 hours. Fresh or incubated segments were immersed into tissue baths and the concentration-response curves were obtained by cumulative administration of the vasoconstrictors. Results In fresh mesenteric artery, endothelin-1 (ET-1), 5-hydroxytryptamine (5-HT), noradrenaline (NA), 5-carboxamidotryptamine (5-CT), and angiotensin n (Ang II) induced potent and sustained constrictions in a concentration-dependent manner. The contraction induced by sarafotoxin 6c (S6c) was weak, while bradykinin (BK) , des-Arg-bradykinin (DA-BK), and human urotensin II (hUT-II) showed no detectable contraction. The concentraion-response curves in order of slopes was ET-1, NA, 5-HT, 5-CT, and Ang fl . The order of the maximum contractions was ET-1 > NA = 5-HT = 5-CT> Ang II >S6c. After organ culture, the concentration-response curves induced by S6c, NA, and 5-HT were significantly increased, while that induced by Ang II was decreased as comparing to fresh arteries. BK contracted the artery only weakly. Conclusion Organ culture changed the phenotypes towards an increased efficacy of NA, 5-HT, S6c, and a reduced efficacy of Ang II , which is in accordance with the results of pharmacological characterization in some human vascular disease.
机译:目的比较9种介质对大鼠新鲜和温育肠系膜动脉的血管收缩作用。方法切除大鼠肠系膜上动脉,剥除内皮细胞。将容器切成1mm长的圆柱形部分,并进行器官培养24小时。将新鲜的或孵育的片段浸入组织浴中,并通过累积施用血管收缩剂获得浓度-反应曲线。结果在新鲜的肠系膜动脉中,内皮素-1(ET-1),5-羟基色胺(5-HT),去甲肾上腺素(NA),5-羧酰胺基色胺(5-CT)和血管紧张素n(Ang II)诱导了强效和持续性收缩以浓度依赖的方式。 sarafotoxin 6c(S6c)引起的收缩较弱,而缓激肽(BK),des-Arg-缓激肽(DA-BK)和人尿素II(hUT-II)则未显示可检测到的收缩。浓度-响应曲线的斜率顺序为ET-1,NA,5-HT,5-CT和Ang fl。最大收缩的顺序是ET-1> NA = 5-HT = 5-CT> Ang II> S6c。器官培养后,与新鲜动脉相比,S6c,NA和5-HT诱导的浓度-反应曲线显着增加,而Ang II诱导的浓度-反应曲线降低。 BK仅微弱地收缩了动脉。结论器官培养改变了表型,使NA,5-HT,S6c的功效增加,而Ang II的功效降低,这与某些人类血管疾病的药理学表征结果相符。

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