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Depressor and regionally-selective vasodilator effects of human and rat urotensin II in conscious rats

机译:人和大鼠尾加压素II在清醒大鼠中的降压和区域选择性血管舒张作用

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摘要

The regional haemodynamic effects of rat or human urotensin II (U-II) 3, 30, 300 and 3000 pmol kg−1, i.v.) were assessed in separate groups of conscious, unrestrained, male, Sprague-Dawley rats (n=8 in each). Rat and human U-II had similar effects. At a dose of 3 pmol kg−1, neither peptide had any significant action, while at a dose of 30 pmol kg−1, there was a transient mesenteric vasodilatation (significant only for rat U-II). At doses of 300 and 3000 pmol kg−1, there were dose-dependent tachycardias, and mesenteric and hindquarters hyperaemic vasodilatations. Thus, in conscious rats, the predominant cardiovascular action of rat and human U-II is vasodilatation. This is in contrast to recent findings with human U-II in non-human primates, but is consistent with effects on human isolated resistance vessels.
机译:分别在有意识的,不受约束的,雄性的,斯普拉格- Dawley大鼠(每只n = 8)。大鼠和人类U-II的作用相似。剂量为3 pmol kg -1 时,两种肽均无明显作用,而剂量为30 pmol kg -1 时,肠系膜有短暂的血管扩张作用(显着仅适用于大鼠U-II)。在300和3000 pmol kg −1 的剂量下,存在剂量依赖性心动过速,肠系膜和后肢充血性血管舒张。因此,在有意识的大鼠中,大鼠和人U-II的主要心血管作用是血管舒张。这与最近在非人灵长类动物中使用人U-II的发现相反,但与对人分离的抗性血管的作用一致。

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