Orsolic N, Sirovina D, Krbavcic M, Car N
1Department of Animal Physiology, Faculty of Science, University of Zagreb, Zagreb, Croatia.
Hum Exp Toxicol. 2013 Aug 7. doi: 10.1177/0960327113499048.
Hyperthermia enhanced the clastogenicity of alkylating agents. We investigated whether quercetin (QU; 3,3',4',5,7-pentahydroxy flavone) or naringenin (NAR) can sensitize Ehrlich ascites tumour (EAT) to cisplatin (CP) hyperthermal intraperitoneal chemotherapy treatment and whether these flavonoids in combination with CP can ameliorate CP-induced micronuclei (MNs) in peripheral blood reticulocytes of mice. QU or NAR were administered to mice 7 and 3 days before implantation of EAT cells, while CP (5 or 10 mg kg) was injected intraperitoneally to normothermic or hyperthermic-treated mice 3 days after implantation of EAT cells (2 10). Our study supports the claim that the QU or NAR in combined treatment with CP has the potential to inhibit tumour growth in both normothermic and hyperthermic conditions and attenuate number of MNs in the peripheral blood reticulocytes of mice at normothermic condition but enhanced the clastogenicity of CP agents in hyperthermal condition.
热疗增强了烷化剂的致断裂性。我们研究了槲皮素(QU;3,3',4',5,7-五羟基黄酮)或柚皮素(NAR)是否能使艾氏腹水瘤(EAT)对顺铂(CP)热腹腔化疗治疗敏感,以及这些类黄酮与CP联合使用是否能改善CP诱导的小鼠外周血网织红细胞中的微核(MNs)。在接种EAT细胞前7天和3天给小鼠施用QU或NAR,而在接种EAT细胞3天后(2×10),给正常体温或热疗处理的小鼠腹腔注射CP(5或10mg/kg)。我们的研究支持以下观点:QU或NAR与CP联合治疗有可能在正常体温和热疗条件下抑制肿瘤生长,并在正常体温条件下减少小鼠外周血网织红细胞中的MNs数量,但在热疗条件下增强了CP制剂的致断裂性。