陈维洲, 朱巧贞, 丁光生. 莲子心生物碱Nn-9的降压机制J. 药学学报, 1962, 9(5): 271-276.
引用本文: 陈维洲, 朱巧贞, 丁光生. 莲子心生物碱Nn-9的降压机制J. 药学学报, 1962, 9(5): 271-276.
CHEN WEI-ZHOU CHU CHIAO-CHEN TING KUANG-SHENG, . HYPOTENSIVE MECHANISM OF THE ALKALOID Nn-9 FROM NELUMBO NUCIFERAJ. Acta Pharmaceutica Sinica, 1962, 9(5): 271-276.
Citation: CHEN WEI-ZHOU CHU CHIAO-CHEN TING KUANG-SHENG, . HYPOTENSIVE MECHANISM OF THE ALKALOID Nn-9 FROM NELUMBO NUCIFERAJ. Acta Pharmaceutica Sinica, 1962, 9(5): 271-276.

莲子心生物碱Nn-9的降压机制

HYPOTENSIVE MECHANISM OF THE ALKALOID Nn-9 FROM NELUMBO NUCIFERA

  • 摘要: 蓮子心非結晶生物碱Nn-9对麻醉猫靜脉注射1-2毫克/公斤可降低原血压水平約50%,維持2-3小时。狗血压于1/2小时卽恢复,兔子不降压。有快速耐受性。經苯海拉明及异丙嗪处理猫再注射Nn-9碱2—3.5毫克/公斤,降压作用明显減弱。对靜脉注射組織胺引起的降压被Nn-9所減弱。猫靜脉注射2毫克/公斤的Nn-9后,血压下降伴随脑血管阻力減低,动脉注射0.2毫克/公斤使脑血流及后肢血流均增加,血管阻力減低。脊猫靜脉注射2毫克/公斤,有明显的降压出现。靜脉注射腎上腺素、去甲腎上腺素及脑垂体后叶素或在第七頸椎以下加高脊髓腔压所引起的升压反应均被抑制,历1/2—1小时恢复。电刺激頸交感神經节节前纤維所致的瞬膜收縮也受到抑制。对副交感神經节及M-胆碱反应系統无明显影响。頸动脉注射药液也出现降压,并抑制頸总动脉血流阻断所引起的升压反应。总結实驗結果,Nn-9的降压机制主要是释放組織胺,使外周血管扩张,其次神經因素也有关。

     

    Abstract: Nn-9 was a non-crystalline alkaloid isolated from the embryo of the seeds of the Asiatic lotus, Nelumbo nucifera. In anesthetized cats, iv.injections of 1—2 mg/kg lowered, after a delay of 1/2—1 minute, the blood pressure by about 50% from the original level, lasting 2—3 hours. In dogs, the blood pressure returned to normal in 1/2 hour. This dosage was ineffective in rabbits. Tachyphylaxis developed on repeated administrations. After the cats were pretreated with Diphenhydramine or Promethazine, the hypotensive effect of Nn-9 was remarkably diminished. Pretreatment with Nn-9 also lessened the hypotensive action of histamine. When the cats were given 2 mg/kg of Nn-9 intravenously, the hypotension was accompanied by a reduction of cerebral vascular resistance. Intra-arterial injections yielded an increase of both cerebral and femoral blood flows, associated with a diminution of the vascular resistance. In spinal cats, i.v. injection of 2 mg/kg produced a significant drop of blood pressure. The pressor responses elicited by i.v. adrenalin, noradrenalin, pituitrin, or by spinal compression below C-7 were all inhibited for 1/2—1 hour. The retraction of nictitating membrane by preganglionic faradization was also inhibited. But it had no apparent influence on parasympathetic ganglion and M-cholinergic reactive system. Intracarotid injections produced a hypotension, together with a decrease of the carotid occlusion reflex pressor response. In conclusion, Nn-9 seems to act primarily through histamine release. Secondarily, a nervous factor is also involved.

     

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