Chahoud Ibrahim, Paumgarttem Francisco J R
Institut für Klinische Pharmakologie und Toxikologie, Charité - Universitätsmedizin Berlin, Berlin, Deutschland.
Laboratório de Toxicologia Ambiental, Escola Nacional de Saúde Pública, Fundação Oswaldo Cruz, Rio de Janeiro, RJ, Brazil.
An Acad Bras Cienc. 2017 May;89(1 Suppl 0):635-647. doi: 10.1590/0001-3765201720160483.
The development of DBA/2J mouse strain embryos is nearly 12 h - or 6 somite pairs - delayed as compared to the outbred NMRI mouse embryos of the same age on gestation days (GD) 8-12. To evaluate inter-strain differences in susceptibility to teratogens, dams were treated with methylnitrosourea (MNU, 5 mg/kg body weight i.p.) on defined gestation days (NMRI: GD 9, 91/2 or 10; DBA/2J: GD 10 or 101/2). Skeletal anomalies produced by MNU on both mouse strains varied with the GD of treatment. The pattern of anomalies produced by MNU on a given GD markedly differed between the two mouse strains, yet they were similar -with a few exceptions- when exposures at equivalent embryonic stages are compared. Findings from this study indicated that strain-dependent differences in the developmental stage of mouse embryos of the same gestational age occur, a possibility that has been often neglected when inter-strain differences in susceptibility to developmental toxicants are interpreted.
与相同孕期(妊娠第8 - 12天)的远交系NMRI小鼠胚胎相比,DBA/2J小鼠品系胚胎的发育延迟了近12小时或6对体节。为了评估不同品系对致畸剂易感性的差异,在特定的妊娠天数对孕鼠进行甲基亚硝基脲(MNU,腹腔注射5 mg/kg体重)处理(NMRI:妊娠第9天、9.5天或10天;DBA/2J:妊娠第10天或10.5天)。MNU在两种小鼠品系上产生的骨骼异常随处理的妊娠天数而变化。在给定的妊娠天数,MNU在两种小鼠品系上产生的异常模式明显不同,但当比较相同胚胎阶段的暴露情况时,它们(有一些例外)是相似的。本研究结果表明,相同胎龄的小鼠胚胎发育阶段存在品系依赖性差异,在解释不同品系对发育毒物易感性差异时,这一可能性常常被忽视。