摘要
目的:研究骆驼蓬总碱的毒性。方法:用骆驼蓬总硷对小鼠进行急性毒性,大鼠进行亚急性毒性实验。结果:小鼠急性毒性实验测出骆驼蓬总硷,于腹腔、静脉注射及灌胃3种给药途径1次给药的LD50,以及可信限分别为:144mg/kg(131.7~157.9mg/kg)、56mg/kg(48.3~64.9mg/kg)、289mg/kg(218.5~382.3mg/kg)。在大鼠亚急性毒性实验可见300mg/kg骆驼蓬总碱引起肾病变和尿素氮升高,停药后肾毒性程度可降低。结论:骆驼蓬总碱毒性的靶器官是肾脏,在停药之后肾脏病变在一定程度上是可逆的。
Objective: To study toxicity of total alkaloid of Peganum harmala(TAH). Methods: Mice and rats were used for detecting acute and subacute toxicity of TAH. Results: In mice LD_50 and 95% confident limit of TAH by i.p, i.v and p.o administration were 144mg/kg(131.7~157.9mg/kg), 56mg/kg(48.3~64.9mg/kg) and 289mg/kg(218.5~382.3mg/kg) respectively. Subancute toxicity test in rats showed that 300mg/kg of TAH can induce renal pathological change and higher BUN level, the degree of nephro-toxicity can reduce after stopping administration. Conclusion: Kidney is the toxic target organ of TAH, to some degree the nephro-toxicity can reverse after stopping administration.
出处
《中山医科大学学报》
CSCD
1998年第3期170-171,178,共3页
Academic Journal of Sun Yat-sen University of Medical Sciences
基金
国家自然科学基金
关键词
毒理学
抗肿瘤药
骆驼蓬总碱
harmine/toxicity
harmaline/toxicity
antitumor drug/toxicity