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首页> 外文期刊>Basic & clinical pharmacology & toxicology. >Transcriptional up-regulation in expression of 5-hydroxytryptamine2A and transcriptional down-regulation of angiotensin II type 1 receptors during organ culture of rat mesenteric artery.
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Transcriptional up-regulation in expression of 5-hydroxytryptamine2A and transcriptional down-regulation of angiotensin II type 1 receptors during organ culture of rat mesenteric artery.

机译:大鼠肠系膜动脉器官培养过程中5-羟色胺2A表达的转录上调和血管紧张素II 1型受体的转录下调。

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The purpose of this study was to investigate in rat mesenteric artery if there is up-regulation of 5-hydroxytryptamine (5-HT) receptors and angiotensin II receptors and the potential role of protein kinase C activation in the smooth muscle cells during organ culture. Angiotensin II, 5-HT and potassium induced contraction of ring segments without endothelium, monitored by a sensitive in vitro pharmacology method. After the culture of the arterial ring segments for 24 hr, the concentration-contraction curves induced by 5-HT slightly shifted towards to the left with pEC(50) from 6.64+/-0.11 to 6.84+/-0.11 and a significant increase in E(max) from 147+/-11% to 246+/-15% (P<0.05), compared with that obtained in fresh segments. In contrast, the angiotensin II concentration-contraction curve only showed a significant decrease in E(max) from 99+/-10% to 37+/-8%. Specific antagonists for the 5-HT type 2A receptors (5-HT(2A)) and angiotensin II type 1 receptors (AT(1)) demonstrated that the contractions occurred via 5-HT(2A) and AT(1) receptors, respectively. Real-time PCR revealed that the 5-HT(2A) receptor mRNA was up-regulated in parallel with the contractile response while there was a down-regulation of AT(1) receptor mRNA. Transcriptional inhibitor actinomycin D and specific protein kinase C inhibitor Ro31-8220 demonstrated that it was a transcriptional mechanism with involvement of protein kinase C that regulated the enhanced expression of 5-HT(2A) receptors in the mesenteric artery.
机译:这项研究的目的是调查大鼠肠系膜动脉中5-羟色胺(5-HT)受体和血管紧张素II受体的上调以及器官培养过程中平滑肌细胞中蛋白激酶C激活的潜在作用。通过敏感的体外药理学方法监测血管紧张素II,5-HT和钾诱导的无内皮环段的收缩。培养了24小时的动脉环段后,5-HT诱导的浓度-收缩曲线在pEC(50)从6.64 +/- 0.11略微向左移动到6.84 +/- 0.11,并且显着增加与新鲜部分相比,E(max)从147 +/- 11%增至246 +/- 15%(P <0.05)。相比之下,血管紧张素II浓度-收缩曲线仅显示E(max)从99 +/- 10%显着降低到37 +/- 8%。 5-HT 2A受体(5-HT(2A))和血管紧张素II 1型受体(AT(1))的特异性拮抗剂表明收缩分别通过5-HT(2A)和AT(1)受体发生。实时PCR显示5-HT(2A)受体mRNA与收缩反应同时上调,而AT(1)受体mRNA则下调。转录抑制剂放线菌素D和特定的蛋白激酶C抑制剂Ro31-8220表明,这是一种转录机制,涉及蛋白激酶C调节肠系膜动脉中5-HT(2A)受体的表达增强。

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