Proctor J W, Waters R V, Jones G H, Gorecka-Tisera A, Yamamura Y
Oncodev Biol Med. 1982;3(2-3):179-90.
Various doses of coded samples of the parent muramyl dipeptide entity and eight synthetic analogues were injected intravenously into C57BL/6J mice, and the extent of clearance of intravenously injected 5-[125I]iodo-2-deoxyuridine (125I-dUrd) radioactively labeled B16 tumor cells from the lung was measured 3 days later. The results of between one and four experiments with each compound demonstrated that five compounds, including the parent compound, produced dose-dependent increases in the loss of tumor cells from the lung. The same five compounds also caused an increase in the clearance of intravascular carbon clearance. Monitoring of serum lysozyme levels revealed no significant increases compared to controls at doses of up to 1 mg/mouse following muramyl dipeptide (MDP) administration i.v., i.p. or s.c. at any time up to 30 days after administration. Increased pulmonary tumor cell clearance did not occur after s.c. MDP administration and peaked 3 days after i.p. or i.v. MDP, reaching near normal levels by Day 7.
将不同剂量的母体胞壁酰二肽实体及其八种合成类似物的编码样品静脉注射到C57BL/6J小鼠体内,3天后测量静脉注射的5-[125I]碘-2-脱氧尿苷(125I-dUrd)放射性标记的B16肿瘤细胞从肺中的清除程度。对每种化合物进行的一到四项实验结果表明,包括母体化合物在内的五种化合物使肺中肿瘤细胞的损失呈剂量依赖性增加。同样的五种化合物还导致血管内碳清除率增加。对血清溶菌酶水平的监测显示,在静脉内、腹腔内或皮下给予胞壁酰二肽(MDP)后,在长达30天的任何时间,剂量高达1mg/小鼠时,与对照组相比血清溶菌酶水平无显著升高。皮下注射MDP后未出现肺肿瘤细胞清除增加的情况,腹腔内或静脉内注射MDP后3天达到峰值,到第7天接近正常水平。