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灯盏花素对大鼠主动脉肌环的松弛作用

The Effect of Breviscapln on the Relaxation of Aortic Rings in Rats

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【作者】 陈一岳王胜涛曾文珊朱颖虹傅咏梅江涛

【Author】 Chen Yiyue; Wang Shentao; Zhen Wenshan;Zhu Yinhong; Fu Yongmei ;Jiang Tao(Department of Pharmacology, Medical and)Pharmaceutical College, Guangzhou 510224)

【机构】 广东药学院心血管药理研究室

【摘要】 用苯肾上腺素及氯化钡引起血管环收缩,并测定五种血管扩张药对这两种激动剂缩血管作用的拮抗作用的比值。结果表明,灯盏花素的作用与三氟拉嗪相似,是以抑制细胞内钙释放为主。在去除血管内皮的实验中发现,灯盏花素的松弛血管平滑肌的作用,与三氟拉嗪、脑益嗪及硝吡啶均相似,即并不依赖血管内皮的完整性,但从量效曲线来看,灯盏花素与前两者(尤其是与三氟拉嗪)相平行。然而,灯盏花素对五羟色胺的缩血管作用无任何拮抗作用,三氟拉嗪在低浓度时未显示拮抗作用,在高浓度时,可使量效曲线明显右移。这些结果说明灯盏花素的作用可能与拮抗钙调素的作用有关,但确切的机理仍有待进一步探讨。

【Abstract】 The antagonism of five kinds of vasodilators against the vasoconstriction induced byphenylephrine and barium chloride was studied. The results showed that the action ofbreviscapin (Bre) was similar to that of trifluoperazine (TFP), chiefly inhibiting therelease of intracellular calcium. In the experiment of eliminating vascular endothelium,it was found that the vasodilating action of Bre was independent of the integrity ofvascular endothelium, which was similar to that of TFP, cinnarizine and nifedipine, andthe dose-response curve of Bre was paralled to that to TFP. However, Bre did notantagonize the vasoconstriction induced by 5-HT, and TFP also elicited no antagonismin low dosage but markedly shifted the dose-response curve to the right in high dosage.It is indicated that the mechanism of Bre is probably related to the antagonism againstcalmodulin .

  • 【文献出处】 中药新药与临床药理 ,TRADITIONAL CHINESE DRUG RESEARCH & CLINICAL PHARMACOLOGY , 编辑部邮箱 ,1994年02期
  • 【分类号】R285.5
  • 【被引频次】61
  • 【下载频次】150
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