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Cyclophosphamide‐induced cytogenetic effects in mouse bone marrow and spleen cells in in vivo and in vivo/in vitro assays

机译:环磷酰胺诱导的小鼠骨髓和脾脏细胞体内和体内/体外测定的细胞遗传学效应

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AbstractSister chromatid exchange (SCE) and chromosomal aberration studies have been used to monitor human populations for genotoxic exposure to chemical substances. These monitoring techniques involve collection of blood and/or bone marrow from the exposed subjects and culturing cells for one or two cell cycles with various treatments in culture. The results obtained from such in vivo/in vitro studies may lead to an over‐or underestimation of the damage that could occur in vivo. In the present study, which uses a mouse model, the in vivo/in vitro cytogenetic assays (SCEs and chromosomal aberrations) have been compared with similar in vivo systems in bone marrow and spleen cells treated with various doses of cyclophosphamide (CPA). The results indicate a significant difference in CPA‐induced cytogenetic endpoints between in vivo and in vivo/in vitro conditions in both organs. However, linear relationships were found between CPA dose and cytogenetic end point analyzed under both conditions. Based on these results it appears that the in vivo/in vitro assay is a useful technique for indicating potential in vivo damage of chemic
机译:摘要姊妹染色单体交换(SCE)和染色体畸变研究已被用于监测人群对化学物质的遗传毒性暴露。这些监测技术包括从暴露的受试者身上收集血液和/或骨髓,并在培养中通过各种处理将细胞培养一个或两个细胞周期。从这种体内/体外研究中获得的结果可能会导致高估或低估体内可能发生的损害。在本研究中,使用小鼠模型,体内/体外细胞遗传学测定(SCE和染色体畸变)已与用不同剂量的环磷酰胺(CPA)处理的骨髓和脾脏细胞中的类似体内系统进行了比较。结果表明,在体内和体内/体外条件下,CPA诱导的细胞遗传学终点在两个器官中存在显着差异。然而,在两种条件下,CPA剂量和细胞遗传学终点之间的线性关系都得到了分析。基于这些结果,体内/体外测定似乎是一种有用的技术,用于指示化学的潜在体内损伤

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