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首页> 外文期刊>Japanese Journal of Pharmacology >COMPARATIVE STUDIES OF CEREBRAL VASODILATORS ON RELAXATION ACTIVITIES IN ISOLATED BASILAR, MESENTERIC AND PULMONARY ARTERIES OF RABBITS
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COMPARATIVE STUDIES OF CEREBRAL VASODILATORS ON RELAXATION ACTIVITIES IN ISOLATED BASILAR, MESENTERIC AND PULMONARY ARTERIES OF RABBITS

机译:脑血管舒张剂对兔离体基底,中肠和肺动脉中松弛活性的比较研究

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References(27) Cited-By(2) Effects of cerebral vasodilators such as bencyclane, cinnarizine, and papaverine were comparatively studied using helically cut basilar and superior mesenteric arteries and radial muscle preparations of pulmonary arteries with the sympathetic nerve isolated from rabbits. The order of relaxation activities on high K+-induced contractures was cinnarizine bencyclanepapaverine in basilar strips and cinnarizinepapaverine bencyclane in mesenteric strips. Relaxation responses of basilar strips to cinnarizine and bencyclane were faster and more marked than those seen in mesenteric strips. Responses to papaverine were equipotent in both preparations. The action of cinnarizine alone was irreversible. In mesenteric strips, the order of the sensitivity of contractile responses to cumulatively applied biogenic amines was serotoninnoradrenalinehistamine. Cinnarizine produced an antihistaminergic action, while bencyclane produced an antiserotonergic action. In pulmonary arteries, 6×10-6 g/ml papaverine inhibited contractile responses to 2, 5, and 25 Hz nerve stimulation in a frequency-independent manner together with inhibition of responses to noradrenaline. Bencyclane at 6×10-6 and 10-5 g/ml selectively inhibited in a dose-dependent manner contractile responses only to 25 Hz without inhibition of responses to noradrenaline. These results were discussed in comparison with findings of the cerebral vasodilators obtained using other experimental techniques. Spiral strips of basilar arteries from rabbits in combination with peripheral arteries may be used as a simple, quantitative, and reproducible screening method in a preclinical stage for drug evaluation of cerebral vasodilators.
机译:参考文献(27)(2)引用本研究使用螺旋切开的基底动脉和肠系膜上动脉以及radial动脉的radial肌制备了从兔中分离出的交感神经,比较研究了脑血管扩张剂如苯环烷,肉桂酸和罂粟碱的作用。高钾离子引起的挛缩时松弛活动的顺序为基底带中的肉桂那嗪>苯环烷>罂粟碱,肠系膜带中的肉桂那嗪>罂粟碱>苯环烷。与肠系膜条相比,基底条对肉桂酸和苯环烷的弛豫响应更快,更明显。两种制剂对罂粟碱的反应均等。单独的肉桂利嗪作用是不可逆的。在肠系膜条中,对累积施用的生物胺的收缩反应敏感性的顺序为:血清素>去甲肾上腺素>组胺。肉桂利嗪产生抗组胺药作用,而苯环烷产生抗血清素作用。在肺动脉中,6×10-6 g / ml罂粟碱以与频率无关的方式抑制对2、5和25 Hz神经刺激的收缩反应,同时抑制对去甲肾上腺素的反应。浓度为6×10-6和10-5 g / ml的苯环烷以剂量依赖性方式选择性抑制仅25 Hz的收缩反应,而没有抑制去甲肾上腺素的反应。与使用其他实验技术获得的脑血管扩张剂的发现进行了比较,讨论了这些结果。来自兔的基底动脉螺旋带与周围动脉的结合可在临床前阶段用作简单,定量和可重现的筛查方法,用于脑血管扩张药的药物评估。

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