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吸入1,3 - 丁二烯的小鼠和大鼠T细胞中存在年龄、性别和物种依赖性致突变性。

Age-, gender-, and species-dependent mutagenicity in T cells of mice and rats exposed by inhalation to 1,3-butadiene.

作者信息

Meng Quanxin, Walker Dale M, McDonald Jake D, Henderson Rogene F, Carter Meghan M, Cook Dennis L, McCash Consuelo L, Torres Salina M, Bauer Michael J, Seilkop Steven K, Upton Patricia B, Georgieva Nadia I, Boysen Gunnar, Swenberg James A, Walker Vernon E

机构信息

Lovelace Respiratory Research Institute, 2425 Ridgecrest Dr. SE, Albuquerque, NM 87108, USA.

出版信息

Chem Biol Interact. 2007 Mar 20;166(1-3):121-31. doi: 10.1016/j.cbi.2006.07.005. Epub 2006 Jul 26.

Abstract

Experiments were performed: (i) to investigate potential age- and gender-dependent differences in mutagenic responses in T cells following exposures of B6C3F1 mice and F344 rats by inhalation for 2 weeks to 0 or 1250 ppm butadiene (BD), and (ii) to determine if exposures for 2 weeks to 62.5 ppm BD produce a mutagenic effect in female rats. To evaluate the effect of age on mutagenic response, mutant manifestation curves for splenic T cells of female mice exposed at 8-9 weeks of age were defined by measuring Hprt mutant frequencies (MFs) at multiple time points after BD exposure using a T cell cloning assay and comparing the resulting mutagenic potency estimate (calculated as the difference of areas under the mutant manifestation curves of treated versus control animals) to that reported for female mice exposed to BD in the same fashion beginning at 4-5 weeks of age. The shapes of the mutant T cell manifestation curves for spleens were different [e.g., the maximum BD-induced MFs in older mice (8.0+/-1.0 [S.D.]x10(-6)) and younger mice (17.8+/-6.1 x 10(-6)) were observed at 8 and 5 weeks post-exposure, respectively], but the mutagenic burden was the same for both age groups. To assess the effect of gender on mutagenic response, female and male rodents were exposed to BD at 4-5 weeks of age and Hprt MFs were measured when maximum MFs are expected to occur post-exposure. The resulting data demonstrated that the pattern for mutagenic susceptibility from high-level BD exposure is female mice>male mice>female rats>male rats. Exposures of female rats to 62.5 ppm BD caused a minor but significant mutagenic response compared with controls (n=16/group; P=0.03). These results help explain part of the differing outcomes/interpretations of data in earlier Hprt mutation studies in BD-exposed rodents.

摘要

进行了以下实验

(i) 研究B6C3F1小鼠和F344大鼠经吸入2周暴露于0或1250 ppm丁二烯(BD)后,T细胞诱变反应中潜在的年龄和性别依赖性差异;(ii) 确定雌性大鼠经2周暴露于62.5 ppm BD是否产生诱变效应。为评估年龄对诱变反应的影响,通过使用T细胞克隆测定法在BD暴露后的多个时间点测量次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(Hprt)突变频率(MFs),并将所得诱变效力估计值(计算为处理组与对照组动物突变表现曲线下面积之差)与4 - 5周龄开始以相同方式暴露于BD的雌性小鼠的报告值进行比较,确定8 - 9周龄暴露的雌性小鼠脾脏T细胞的突变表现曲线。脾脏突变T细胞表现曲线的形状不同[例如,老年小鼠(8.0±1.0 [标准差]×10⁻⁶)和幼年小鼠(17.8±6.1×10⁻⁶)在暴露后第8周和第5周分别观察到最大BD诱导的MFs],但两个年龄组的诱变负担相同。为评估性别对诱变反应的影响,雌性和雄性啮齿动物在4 - 5周龄时暴露于BD,并在暴露后预期出现最大MFs时测量Hprt MFs。所得数据表明,高剂量BD暴露的诱变易感性模式为雌性小鼠>雄性小鼠>雌性大鼠>雄性大鼠。与对照组相比,雌性大鼠暴露于62.5 ppm BD引起了轻微但显著的诱变反应(每组n = 16;P = 0.03)。这些结果有助于解释早期BD暴露啮齿动物Hprt突变研究中部分不同的数据结果/解释。

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