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可乐定对自家血灌流毁脑脊髓大鼠后肢血管平滑肌的作用

Effects of clonidine on vascular smooth muscles in the perfused hindquarter of pithed rats

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【作者】 金万宝蔡际群赵乃才张克义

【Author】 JIN Wan-bao, CAI Ji-qun, ZHAO Nai-cai, ZHANG Ke-yi (Dept pharmacology, China Medical University, Shenyang 110001)

【机构】 中国医科大学药理教研室中国医科大学药理教研室 沈阳 110001沈阳 110001沈阳 110001

【摘要】 本实验观察了可乐定对自家血恒速灌流的毁脑脊髓大鼠(pithed rat)后肢血管平滑肌的作用和该处突融后膜两种α受体亚型的存在。可乐定引起灌流压(PP)升高,呈剂量依赖关系,但效能远比选择性α1受体激动剂苯福林低。对预先用利血平处理的大鼠,可乐定的作用被显著增强。高度选择性的α1受体阻断剂哌唑嗪0.3mg/kg iv可部分阻断可乐定100μg ia的作用,增加哌唑嗪的剂量并不能进一步增加对可乐定的阻断作用。对于哌唑嗪不能阻断的部分,α1受体阻断剂育亨宾却能表现出十分明显的抑制作用。这些结果提示在大鼠后肢血管平滑肌突触后膜上存在有α1和α2肾上腺素受体,但α1受体似乎占优势。

【Abstract】 The effects of clonidine on vascular smooth muscle in the perfused hindquarters of pithed rats and the existence of postsynaptic α-adrenoceptor subtypes on these sites were observed. Clonidine dose-depen-dently increased perfused pressure, but the efficacy was much smaller than that of phenylephrine,a selective α1-adrenoceptor agonist. The effects of clonidine was significantly potentiated by pretreatment of reset-pine. Prazosin, a highly selective α2-adrenoceptor blocker,did not completely antagonize the elevation ofperfused pressure induced by clonidine 100μg ia,but the prazosin-resis-tant part of the effect of clonidine was significantly inhibited by yo-himbine, an α2-adrenoceptor blocker. These results suggest that the hind-quarter vascular smooth muscle of rat has α1-and α2-adrenoceptors, and α1-receptor seems to be dominant.

【基金】 中国科学院科学基金
  • 【文献出处】 中国药理学与毒理学杂志 ,Chinese Journal of Pharmacology and Toxicology , 编辑部邮箱 ,1986年01期
  • 【下载频次】38
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