超声羧甲基葡聚糖对环磷酰胺致突变性的影响

Darina Chorvatovičová , Eva Machová , Josef Šandula
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引用次数: 29

摘要

采用超声降低分子量(0.89 × 105)的羧甲基葡聚糖(CMG)在注射环磷酰胺(CP)前分别腹腔、静脉或口服给药,观察其对小鼠骨髓微核频率的影响。CMG经肠外(腹腔和静脉)和口服均能降低CP的致裂作用。静脉和腹腔给药对CP的保护作用呈浓度依赖性,200 mg/kg给药对CP的保护作用大于100 mg/kg给药。低剂量CMG静脉给药与CP注射间隔2小时。口服CMG预处理小鼠骨髓多染红细胞微核出现频率有统计学意义。超声解聚CMG在口服给药时也有效,这表明较小的CMG分子可以通过胃肠道壁。
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Effect of ultrasonicated carboxymethylglucan on cyclophosphamide induced mutagenicity

Carboxymethylglucan (CMG) with ultrasonically lowered molecular weight (0.89 × 105) was administered either intraperitoneally, intravenously or orally prior to cyclophosphamide (CP) injection and its effect on the frequency of micronuclei in mouse bone marrow was evaluated. Both parenteral (intraperitoneal and intravenous) and oral administration of CMG decreased the clastogenic effect of CP. The protective effect induced by intravenous and intraperitoneal administration was concentration-dependent, with a higher decrease achieved by 200 mg/kg than by 100 mg/kg body weight. With the lower dose of CMG a 2-h interval was necessary between intravenous CMG administration and CP injection. Oral pretreatment of mice with CMG decreased statistically significantly the frequency of micronuclei in polychromatic erythrocytes of the bone marrow. The fact that ultrasonically depolymerized CMG was effective also on oral administration is indicative of the passage of smaller CMG molecules through the wall of the gastrointestinal tract.

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