摘要
用TBA法测定了青蒿琥酯(Sodiumartesunate,SA)中毒大鼠骨髓脂质过氧化作用产物——丙二醛(malonaldehyde,MDA)含量以探济该药的造血毒性机制。结果表明,100~333mg/kgSA引起骨髓MDA含量与剂量呈正相关线性增高;相关系灵敏r=0.9566;骨髓MDA增殖(IMDA)时间-反应曲线表明,达峰时间为16.5h,IMDA峰反应消除一半需76.5h。骨髓IMDA变化时程与骨髓细胞膜系结构损伤及造血抑制的发生、发展和恢复的时间规律基本一致。
The mechanism of sodium artesunate (SA) induced hemotoxicity was probed by TBA method to detect the product of lipid peroxidation(LPO),malonaldehyde(MDA),in in vivo SA treated rat bone marrow cells.A dose related increase of bone marrow MDA level was found at 24 h after SA 100 333 mg/kg iv.The regression coefficient was 0 956 6 The time I DMA responce curve showed that the peak responce occurred at 16 5 h and the elimination half peak response was at 76 5 h which was consistent with the couse of development of biomembrane injuries and the inhibition of hematopoiesis in SA poisoned bone marrow cells.These results seem to indicate that the drug free radical membrane LPO may be the possible mechanism of hemotoxic and genotoxic effects induced by SA.
出处
《军事医学科学院院刊》
CSCD
北大核心
1996年第1期5-7,共3页
Bulletin of the Academy of Military Medical Sciences
关键词
青蒿琥酯
大鼠
骨髓细胞
生物膜
脂质过氧化
sodium artesunate
lipid peroxidation
malonaldehyde
bone marrow cells
biomembranes