刘昌孝, 黄文通, 刘仁富, 叶桂珍, 向家进, 张振伦, 胡建程. 硝硫氰胺在血吸虫病患者体内的清除和药物对大鼠肝胆系统毒性的研究J. 药学学报, 1983, 18(2): 86-89.
引用本文: 刘昌孝, 黄文通, 刘仁富, 叶桂珍, 向家进, 张振伦, 胡建程. 硝硫氰胺在血吸虫病患者体内的清除和药物对大鼠肝胆系统毒性的研究J. 药学学报, 1983, 18(2): 86-89.
LIU Chang-xiao, HUANG Wen-tong, LIU Ren-fu, YE Gui-zhen, XIANG Jia-jin, ZHANG Zhen-lun, , HU Jian-cheng. STUDIES ON THE ELIMINATION OF NITHIOCYAMIINE FROM-PATIENTs WITH SCHISTOSOMIASIS AND ITS TOXICITIES TO THE LIVER-BILE SYSTEM OF RATSJ. Acta Pharmaceutica Sinica, 1983, 18(2): 86-89.
Citation: LIU Chang-xiao, HUANG Wen-tong, LIU Ren-fu, YE Gui-zhen, XIANG Jia-jin, ZHANG Zhen-lun, , HU Jian-cheng. STUDIES ON THE ELIMINATION OF NITHIOCYAMIINE FROM-PATIENTs WITH SCHISTOSOMIASIS AND ITS TOXICITIES TO THE LIVER-BILE SYSTEM OF RATSJ. Acta Pharmaceutica Sinica, 1983, 18(2): 86-89.

硝硫氰胺在血吸虫病患者体内的清除和药物对大鼠肝胆系统毒性的研究

STUDIES ON THE ELIMINATION OF NITHIOCYAMIINE FROM-PATIENTs WITH SCHISTOSOMIASIS AND ITS TOXICITIES TO THE LIVER-BILE SYSTEM OF RATS

  • 摘要: 本文报告日本血吸虫病患者口服硝硫氰胺后,药物在体内的分布与清除及药物对大鼠肝胆系统的影响。硝硫氰胺350 mg分3天口服的47例血吸虫病患者,首次给药后48小时的全血药浓度的平均值为1.56±0.18 μg/ml。末次给药后16天,血药浓度还维持在0.10 μg/ml。但药物主要存在于血浆中,血细胞与其它有形成分的含药量则较少。给药期原药经由尿的排泄量大于停药后的排泄量,药物的排出可持续到19天以上。在一例因其它疾病死亡的尸检脏器组织中,测得肝、肾、心、脾的药物含量均高于肌肉、脑、脂肪与血清中的含药量。大鼠口服硝硫氰胺100 mg/kg/d×7,胆汁分泌量明显减少,与对照组比较胆汁量减少58.3%。药物能抑制肝脏分泌胆汁的能力,并使动物黄疸指数和胆红素升高。

     

    Abstract: Forty-seven patients with schistosomiasis were treated orally with nithiocyamine at the total dosage of 350 mg/kg for 3 days. The blood concentration of the drug reached 1.56+0.18μg/ml 48 hours after initiation of oral administration. By the 16th day after treatment, the blood drug concentration was still 0.1μg/ml. In the blood, plasma took up more drug than the blood cells and other blood constituents. Urinary excretion in patients usually lasted more than 19 days after three consecutive. dosages.Determination of nithiocyamine in tissues of one patient at autopsy showed that the concentrations in the liver, kidney, heart and spleen were higher than those in the muscle, brain, fat and plasma.The drug when given orally to rats at dosage of 100mg/kg/day for 7 days induced a marked reduction of bile secretion through the liver and a marked increasein bilirubin and icterus index in the Serum of rats.

     

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