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WR-2721: inhibitor of cisplatin-induced micronuclei.

机译:WR-2721:顺铂诱导的微核抑制剂。

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The modulatory effect of S-2-/3-aminopropylamino/ethyl-phosphorothioic acid, (WR-2721, Amifostine) on induction of micronuclei by cis-diamminedichloroplatinum[II] (CDDP) was studied. The adult, male Swiss mice were treated with WR-2721, at a dose of 200 mg/kg or 400 mg/kg body weight, and/or with CDDP, at a dose 5 mg/kg or 10 mg/kg body weight. WR-2721 was given alone or 30 min before CDDP administration. The frequency of micronucleated polychromatic erythrocytes (MNPCEs) and also the number of polychromatic erythrocytes (PCEs) in the bone marrow and peripheral blood, at 24 h after the drug application, were determined. After administration of CDDP, the frequency of MNPCEs distinctly increased, and the number of PCEs decreased. As compared with the animals injected with CDDP only, in mice treated with WR-2721 before CDDP application, the number of MNPCEs was reduced and the frequency of PCEs was increased. However, WR-2721 given alone, without subsequent administration of cis-diamminedichloroplatinum[II], caused an increase in the number of micronucleated polychromatic erythrocytes and a decrease in the number of PCEs. The geno- and cyto-toxicity and chemoprotection were dependent on the doses of the agents WR-2721 and CDDP applied. In mice injected with CDDP and/or WR-2721, the patterns of changes in the frequency of MNPCEs and PCEs were similar in the bone marrow and peripheral blood, respectively. The protective effect of the aminothiol compound WR-2721 against induction of micronuclei and apoptotic cell death in the erythropoietic system by CDDP was shown.
机译:研究了S-2- / 3-氨基丙基氨基/乙基硫代磷酸(WR-2721,氨磷汀)对顺二氨二氯铂[II](CDDP)诱导微核的调节作用。用WR-2721,以200 mg / kg或400 mg / kg体重的剂量和/或以CDDP,以5 mg / kg或10 mg / kg体重的剂量治疗成年雄性瑞士小鼠。 WR-2721单独给药或在CDDP给药前30分钟给药。在应用药物后24小时,测定了微核多色红细胞(MNPCE)的频率以及骨髓和外周血中多色红细胞(PCE)的数量。施用CDDP后,MNPCE的频率明显增加,而PCE的数量减少。与仅注射CDDP的动物相比,在CDDP施用前用WR-2721治疗的小鼠中,MNPCE的数量减少,PCE的频率增加。然而,单独给予WR-2721,而未随后给予顺式二甲基二氯铂[II],则会导致微核多色红细胞数量增加,而PCE数量减少。基因和细胞毒性以及化学保护作用取决于所用试剂WR-2721和CDDP的剂量。在注射了CDDP和/或WR-2721的小鼠中,骨髓和外周血中MNPCE和PCE的频率变化模式分别相似。显示了氨基硫醇化合物WR-2721对CDDP促红细胞系统中微核的诱导和凋亡细胞死亡的保护作用。

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