...
首页> 外文期刊>Japanese Journal of Pharmacology >Chronotropic and Inotropic Effects of Kampo Extracts in the Canine Isolated, Blood-Perfused Heart Preparations
【24h】

Chronotropic and Inotropic Effects of Kampo Extracts in the Canine Isolated, Blood-Perfused Heart Preparations

机译:汉普提取物对犬离体血液灌流心脏制剂的时间变质和变力作用

获取原文
           

摘要

References(9) Cited-By(6) Cardiac effects of drugs used for circulatory disorders in traditional Japanese medicine based on ancient Chinese medicine (Kampo Medicine): Saikoka-ryukotsu-borei-to, Oren-gedoku-to, Toki-shakuyaku-san, Shimbu-to, Moku-boi-to, Ryo-kei-jutsu-kan-to, Sha-kanzo-to, Keishi-ninjin-to, Toki-to and Ryo-kan-kyo-mi-shin-ge-nin-to were investigated using canine isolated, blood-perfused sinoatrial node and papillary muscle preparations. Single injections of small doses of Oren-gedoku-to, Moku-boi-to and Ryo-kan-kyo-mi-shin-ge-nin-to (0.1 to 3 mg) dosedependently increased the sinoatrial rate and the developed tension of papillary muscle, while other drugs showed almost no effect on these parameters. All the drugs had almost no effect on the blood flow through the nutrient arteries of each preparation. The positive chronotropic and inotropic effects induced by Oren-gedoku-to, Moku-boi-to and Ryo-kan-kyo-mi-shin-ge-nin-to did not show tachyphylaxis and were not affected after pharmacological denervation by tetrodotoxin treatment or by reserpine pretreatment, but were significantly suppressed by atenolol. These results indicate that these three drugs act as beta-adrenoceptor agonists to produce clinically useful cardiac effects.
机译:参考文献(9)被引用的(6)基于古代中药(Kampo Medicine)的传统中医药中用于循环系统疾病的药物的心脏作用:Saikoka-ryukotsu-borei-to,Oren-gedoku-to,Toki-shakuyaku- san,Shimbu-to,Moku-boi-to,Ryo-kei-jutsu-kan-to,Sha-kanzo-to,Keishi-Ninjin-to,Toki-to和Ryo-kan-kyo-mi-shin-ge-使用犬分离的,血液灌注的窦房结和乳头肌制剂进行了nin-to研究。小剂量Oren-gedoku-to,Moku-boi-to和Ryo-kan-kyo-mi-shin-ge-nin-to的单次剂量(0.1至3 mg)剂量依赖性地提高窦房率和乳头状肌发达的张力肌肉,而其他药物对这些参数几乎没有影响。所有药物对每种制剂的营养动脉的血流几乎没有影响。 Oren-gedoku-to,Moku-boi-to和Ryo-kan-kyo-mi-shin-ge-nin-to诱导的正性变力和变力作用没有表现出速激肽抑制作用,并且在通过河豚毒素处理或通过利血平预处理,但被阿替洛尔显着抑制。这些结果表明这三种药物充当β-肾上腺素受体激动剂,可产生临床上有用的心脏作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号