徐叔云, 邢文(钅荣). 臭梧桐的药理研究 Ⅰ.臭梧桐热浸剂及提出物的毒性和降血压作用J. 药学学报, 1962, 9(12): 734-740.
引用本文: 徐叔云, 邢文(钅荣). 臭梧桐的药理研究 Ⅰ.臭梧桐热浸剂及提出物的毒性和降血压作用J. 药学学报, 1962, 9(12): 734-740.
HSU SHU-YUN HSING WEN-RONG, . STUDIES ON THE PHARMACOLOGY OF THE CHINESE DRUG CHOU-WU-TUNG(AERIAL PARTS OF CLERODENDRON TRICHOTOMUM THUNB.)——Ⅰ.THE TOXICITY AND HYPOTENSIVE EFFECT OF INFUSION AND CRUDE EXTRACT OF CHOU-WU-TUNGJ. Acta Pharmaceutica Sinica, 1962, 9(12): 734-740.
Citation: HSU SHU-YUN HSING WEN-RONG, . STUDIES ON THE PHARMACOLOGY OF THE CHINESE DRUG CHOU-WU-TUNG(AERIAL PARTS OF CLERODENDRON TRICHOTOMUM THUNB.)——Ⅰ.THE TOXICITY AND HYPOTENSIVE EFFECT OF INFUSION AND CRUDE EXTRACT OF CHOU-WU-TUNGJ. Acta Pharmaceutica Sinica, 1962, 9(12): 734-740.

臭梧桐的药理研究 Ⅰ.臭梧桐热浸剂及提出物的毒性和降血压作用

STUDIES ON THE PHARMACOLOGY OF THE CHINESE DRUG CHOU-WU-TUNG(AERIAL PARTS OF CLERODENDRON TRICHOTOMUM THUNB.)——Ⅰ.THE TOXICITY AND HYPOTENSIVE EFFECT OF INFUSION AND CRUDE EXTRACT OF CHOU-WU-TUNG

  • 摘要: 1.本文就臭梧桐的一般性质作了实验性研究,结果证明其降血压成分易溶于水,难溶或不溶于乙醚、乙醇和氯仿,对热稳定,在碱性溶液中可被氯化钙沉淀出来。臭梧桐降血压效果可因产地而不同。开花前的和新鲜的臭梧桐降血压作用分别较开花后的和经长时间保存的要强。2.臭梧桐毒性甚小,其热浸剂和提出物给小鼠静脉注射时半数致死量分别为19.4克/公斤和0.98±0.075克/公斤。给大鼠每天用热浸剂(0.25—2.5克/公斤)灌胃经60天,除少数动物出现安静、轻度收缩压下降和大便变稀外,未发现其他毒性反应。3.臭梧桐提出物(50—100毫克/公斤)和热浸剂(150毫克/公斤)给麻醉大鼠和狗静脉注射时,可引起两度血压下降,但肌肉注射或经口给药,仅引起第二度降血压作用,其作用可维持2—3小时。静脉注射煎剂(麻醉大鼠和狗实验)仅出现第一度降血压作用,经口给药时无效。乙醚、乙醇和氯仿的浸出液不论静脉注射或经口给药,均不引起麻醉动物的血压下降。给肾型高血压大鼠每天经口投予臭梧桐热浸剂(0.5—5克/公斤)和提出物(50毫克/公斤)时,给药的第3—10天卽口出现血压下降,在给药的第二周和停药后的第一周,血压下降最明显,最大降血压作用可达原值的57.4%。多数高血压大鼠的血压在停药后的第二周恢复,少数在停药的2—4天或4周后恢复。

     

    Abstract: The LD50 in mice was found to be 19.4 g/kg and 0.98±0.075 g/kg respectively for the infusion and crude extract of Chou-wu-tung, given by intravenous injections. The subacute toxicity is negligible when the infusion was crally administered to rats (0.25—2.5 g/kg/day) for 60 days, except that some animals showed quietness, slight fall of systolic pressure and soft stool. No apparent toxic effects were observed. A crude extract and infusion of Chou-wu-tung, when injected intravenously at respective dosages of 50—100 mg/kg and 150 mg/kg, produced primary and secondary falls of blood pressure on anaesthetized rats and dogs, but with intramuscular injection or oral administration, only the secondary fall of blood pressure was apparent. This hypotensive effect might last for 2—3 hours. Intravenous injection of the decoction to anaesthetized animals produced only primary fall of blood pressure, the infusions of alcohol, ether and ,chloroform, given by the same route, did not lower the blood pressure. Twenty-eight renal hypertensive rats were divided into three groups, the first (11 rats) and the second (7 rats) groups were treated with the infusion at respective dosages of 0.5 g/kg/day and 5 g/kg/day, and the third (10 rats) with the crude extract at 50 mg/kg/day. The drug was given to all the rats for 2 weeks by oral administration. Hypotensive effect was observed in 3—10 days after medication, and became more remarkable in the second week of the therapeutic period or the first week after cessation of medication; the blood pressure dropped 57.4%. The blood pressure in most rats returned in 2 weeks, and in some rats in 2—4 days or 4 weeks after the stopping of medication.

     

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