张覃沐, 赵国举, 吕富华. 汉防己甲素及乙素对心血管系统的作用J. 药学学报, 1958, 6(3): 147-154.
引用本文: 张覃沐, 赵国举, 吕富华. 汉防己甲素及乙素对心血管系统的作用J. 药学学报, 1958, 6(3): 147-154.
CHANG TAN-MU CHAO KUO-CHUE LUE FU-HUA, . THE CARDIOVASCULAR EFFECTS OF TETRANDRINE AND DEMETHYL-TETRANDRINEJ. Acta Pharmaceutica Sinica, 1958, 6(3): 147-154.
Citation: CHANG TAN-MU CHAO KUO-CHUE LUE FU-HUA, . THE CARDIOVASCULAR EFFECTS OF TETRANDRINE AND DEMETHYL-TETRANDRINEJ. Acta Pharmaceutica Sinica, 1958, 6(3): 147-154.

汉防己甲素及乙素对心血管系统的作用

THE CARDIOVASCULAR EFFECTS OF TETRANDRINE AND DEMETHYL-TETRANDRINE

  • 摘要: 1.以汉防已甲素或乙素3毫克/公斤靜脉注射、肌肉注射或灌胃,均可使麻醉猫的血压明显下降,甲素之降压作用較乙素大而持久,甲素靜脉注射时,降压作用急驟而持久,可維持1—5小时;肌肉注射及灌胃时,降压作用較緩慢,但亦甚持久。2.乙素之降压作用較甲素弱而短暫,靜脉給药之作用較肌肉注射为强,灌胃之降压作用又較肌肉注射为弱。3.静脉注射甲素或乙素3毫克/公斤,在血压下降的同时,可見暫时性心收縮力減弱;但肌肉注射同样或更大剂量(5毫克/公斤),則不出現心力抑制現象,甲素对心率之影响較少,乙素則往往引起心率減慢,心动电流圖上仅見R波幅度之減小,对P-R間歇及T波等均無影响。4.甲素及乙素可使脾容积增加,但在血压急剧下降时,則可使脾容积縮小。5.甲素及乙素均可使离体兎耳血管扩張,直接对平滑肌之抑制作用及神經反射机制均参加在內.甲素之血管扩張作用較乙素及罂粟硷为大而持久。

     

    Abstract: The analgesic, antiphlogistic, anti-anaphylactoid shock and anti-amebic effects of tetrandrine and demethyl-tetrandrine have been reported previously. Further studies on their cardiovascular effects were undertaken with the following results: (1) By intravenous and intramuscular injection as well as per oral administration, tetrandrine and demethyl-tetrandrine caused a profound hypotensive effect in urethan-anesthetized cats. The hypotensive effect of tetrandrine was found to be stronger and more sustained than that of demethyl-tetrandrine. The blood pressure was reduced by more than 50% in the case of tetrandrine and the effect lasted for several hours at a dose of 3 mg/kg regardless of its route of administration. (2) Large doses of the two alkaloids, when injected intravenously, but not intramuscularly, caused a decrease in the contractile force of the cat's heart, which returned to normal within 2-5 minutes. (3) During the fall of the blood pres ure induced by tetrandrine and demethyltetrandrine, the splenic volume of the animals was invariably increased, but it might be reduced in size when the fall of blood pressure was abrupt and severe. (4) These two alkaloids, 1.5-3.0 mg/kg given intravenously, did not cause any significant change in EKG except the reduction of the amplitude of the R wave. The P-R interval was unaltered but sometimes it became shortened under tetrandrine and lengthened under demethyl-tetrandrine; (5) In perfused isolated rabbit's ears, these two alkaloids showed direct vasodilating effects, the minimal effective concentrations of tetrandrine and demethyl-tetrandrine being 1:20,000 and 1:4,000 respectively. In equimolar concentrations, the vasodilating effect of tetrandrine was more prominent and lasted for a longer time in contrast with papaverine. (6) In perfused isolated rabbit's ears with the innervation intact, these two alkaloids and papaverine, at the dosage of 3 mg/kg intravenously, produced reflex vasodilatation. The effect of tetrandrine appeared to be the strongest and lasted the longest, papaverine being the weakest.

     

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