首页> 外文期刊>Chronobiology international >Circadian variation of cytotoxicity and genotoxicity induced by an immunosuppressive agent 'Mycophenolate Mofetil' in rats
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Circadian variation of cytotoxicity and genotoxicity induced by an immunosuppressive agent 'Mycophenolate Mofetil' in rats

机译:免疫抑制剂“ Mycophenolate Mofetil”在大鼠中引起的细胞毒性和遗传毒性的昼夜变化

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Immunosuppressive drugs such as Mycophenolate Mofetil (MMF) are used to suppress the immune system activity in transplant patients and reduce the risk of organ rejection. The present study investigates whether the potential cytotoxicity and genotoxicity varied according to MMF dosing-time in Wistar Rat. A potentially toxic MMF dose (300 mg/kg) was acutely administered by the i.p. route in rats at four different circadian stages (1, 7, 13 and 19 hours after light onset, HALO). Rats were sacrificed 3 days following injection, blood and bone marrow were removed for determination of cytotoxicity and genotoxicity analysis. The genotoxic effect of this pro-drug was investigated using the comet assay and the micronucleus test. Hematological changes were also evaluated according to circadian dosing time. MMF treatment induced a significant decrease at 7 HALO in red blood cells, in the hemoglobin rate and in white blood cells. These parameters followed a circadian rhythm in controls or in treated rats with an acrophase located at the end of the light-rest phase. A significant, thrombocytopenia was observed according to MMF circadian dosing time. Furthermore, abnormally shaped red cells, sometimes containing micronuclei, poikilocytotic in red cells and hypersegmented neutrophil nuclei were observed with MMF treatment. The micronucleus test revealed damage to chromosomes in rat bone marrow; the comet assay showed significant DNA damage. This damage varied according to circadian MMF dosing time. The injection of MMF in the middle of the dark-activity phase produced a very mild hematological toxicity and low genotoxicity. Conversely, it induced maximum hematological toxicity and genotoxicity when the administration occurred in the middle of the light-rest phase, which is physiologically analogous to the end of the activity of the diurnal phase in human patients.
机译:免疫抑制药物,例如Mycophenolate Mofetil(MMF)可用于抑制移植患者的免疫系统活性并降低器官排斥的风险。本研究调查了潜在的细胞毒性和遗传毒性是否随Wistar大鼠的MMF给药时间而异。 i.p.急性给予了潜在毒性的MMF剂量(300 mg / kg)。在四个不同的昼夜节律阶段(光晕后1、7、13和19小时,HALO)在大鼠体内进行免疫途径研究。注射后3天处死大鼠,取出血液和骨髓以测定细胞毒性和遗传毒性分析。使用彗星试验和微核试验研究了这种前药的遗传毒性作用。还根据昼夜给药时间评估血液学变化。 MMF治疗在红细胞,血红蛋白发生率和白细胞中在7 HALO时显着降低。这些参数遵循对照或在轻休息期结束时具有顶峰相的经治疗大鼠的昼夜节律。根据MMF的昼夜给药时间观察到明显的血小板减少症。此外,用MMF处理观察到异常形状的红细胞,有时含有微核,红细胞中的卵母细胞增多,并且中性粒细胞核超节。微核试验显示大鼠骨髓染色体受损;彗星试验显示出明显的DNA损伤。这种损害根据昼夜MMF给药时间而异。在暗活动期的中间注射MMF产生非常轻微的血液毒性和低遗传毒性。相反,当在轻度休息阶段的中间进行给药时,它会引起最大的血液学毒性和遗传毒性,这在生理上类似于人类患者昼夜活动的结束。

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