Zylicz Z, Wagener D J, van Rennes H, Wessels J M, van der Kleijn E, de Grip W J, Ottenheijm H C, van den Broek L A
Cancer Lett. 1986 Jul;32(1):53-9. doi: 10.1016/0304-3835(86)90038-8.
The influence of protein synthesis inhibition by sparsomycin (Sm) on in vivo cisplatin activity has been studied on BALBc X DBA2: F1 mice bearing L1210 leukemia i.p. Sm alone at the dose range from 0.5 to 3.0 mg/kg did not significantly improve animal survival. Sm potentiated cisplatin activity only when given 3 or 6 h prior to cisplatin (P less than 0.001). Sm 0.5-1.5 mg/kg 3 h prior to cisplatin resulted in a significant prolongation of animal survival (P less than 0.001) and 66% cures in each group versus 0% due to cisplatin alone. Sm pretreatment decreased weight loss due to cisplatin suggesting that it probably is able to decrease cisplatin toxicity.
在经腹腔接种L1210白血病的BALBc X DBA2: F1小鼠身上,研究了稀疏霉素(Sm)抑制蛋白质合成对顺铂体内活性的影响。单独使用剂量范围为0.5至3.0 mg/kg的Sm不会显著提高动物存活率。仅在顺铂给药前3或6小时给予Sm时,Sm会增强顺铂的活性(P小于0.001)。在顺铂给药前3小时给予0.5 - 1.5 mg/kg的Sm可显著延长动物存活时间(P小于0.001),每组有66%的治愈率,而单独使用顺铂时治愈率为0%。Sm预处理减少了顺铂导致的体重减轻,这表明它可能能够降低顺铂的毒性。