Pruett Stephen B, Fan Ruping, Zheng Qiang, Schwab Carlton
Department of Cellular Biology & Anatomy, Louisiana State University Health Sciences Center, Shreveport, Louisiana 71130, USA.
Toxicol Sci. 2009 Jun;109(2):265-75. doi: 10.1093/toxsci/kfp073. Epub 2009 Apr 7.
Previous studies have demonstrated that the stress response induced by some drugs and chemicals contributes in a predictable way to alteration of particular immunological parameters in mice. It has not been determined if mice can become tolerant or habituated with regard to the stress response and consequent immunological effects. Addressing this issue was the purpose of the present study. Mice were dosed daily for 28 days with atrazine, ethanol, propanil, or subjected to restraint, which are known to induce neuroendocrine stress responses and thereby to alter several immunological parameters. On day 29, a blood sample was taken and the spleen was removed for analysis of cellular phenotypes, differential cell counts (for blood), and natural killer (NK) cell activity. Corticosterone concentration at various times after dosing (or restraint) was also measured. Comparison of these results with results from previous studies with a single acute exposure revealed that the corticosterone response was almost completely absent in mice treated with ethanol, reduced in mice treated with restraint and propanil, and for atrazine the response was the same as noted for acute exposure. In most cases, the changes in immunological parameters were consistent with expectations based on these corticosterone responses. However, in a few cases (e.g., NK cell activity), it was clear that there were effects not mediated by stress. These results indicate that the nature of the stressor determines whether mice become tolerant with regard to the stress response and consequent immunological effects. This finding has practical implications for safety testing in mice.
先前的研究表明,某些药物和化学物质诱导的应激反应以可预测的方式导致小鼠特定免疫参数的改变。尚未确定小鼠是否会对应激反应及随之产生的免疫效应产生耐受性或适应性。本研究的目的就是解决这个问题。给小鼠每日服用阿特拉津、乙醇、敌稗28天,或对其进行束缚,已知这些会诱导神经内分泌应激反应,从而改变多个免疫参数。在第29天,采集血样并取出脾脏,用于分析细胞表型、细胞分类计数(针对血液)和自然杀伤(NK)细胞活性。还测量了给药(或束缚)后不同时间的皮质酮浓度。将这些结果与之前单次急性暴露研究的结果进行比较,发现乙醇处理的小鼠几乎完全没有皮质酮反应,束缚和敌稗处理的小鼠反应减弱,阿特拉津处理的小鼠反应与急性暴露时相同。在大多数情况下,免疫参数的变化与基于这些皮质酮反应的预期一致。然而,在少数情况下(如NK细胞活性),很明显存在并非由应激介导的效应。这些结果表明,应激源的性质决定了小鼠是否会对应激反应及随之产生的免疫效应产生耐受性。这一发现对小鼠安全性测试具有实际意义。