Zhu Zhi-wei, Yang Ru-lai, Dong Gui-juan, Zhao Zheng-yan
Affiliated Children's Hospital, School of Medicine, Zhejiang University, Hangzhou, China.
J Zhejiang Univ Sci B. 2005 Jul;6(7):686-92. doi: 10.1631/jzus.2005.B0686.
To investigate effects of developmental lead exposure on nitric oxide synthase (NOS) activity in different brain regions and on N-methyl-D-aspartate (NMDA) receptor mRNA expression in the hippocampus of rats. On the basis of these observations, we explored possible mechanisms by which lead exposure leads to impaired learning and memorizing abilities in children.
A series of rat animal models exposed to low levels of lead during the developing period was established (drinking water containing 0.025%, 0.05% and 0.075% lead acetate). NOS activities in the hippocampus, the cerebral cortex, the cerebellum and the brain stem were determined with fluorescence measurement and levels of mRNA expression of the NMDA receptor 2A (NR2A) subunit and NMDA receptor 2B (NR2B) subunit in the rat hippocampus were measured with Retro-translation (RT-PCR).
There were no differences in the body weight of rat pups between any of the groups at any given time (P>0.05). The blood lead level of Pb-exposed rat pups showed a systematic pattern of change: at 14 d of age, it was lower than that at 7 d of age, then rising to the peak level at 21 d and finally falling to lower levels at 28 d. The hippocampal NOS activities of lead-exposed groups were all lower than that of the control group on the 21st and 28th day (P<0.01). NOS activities in the cerebellum of lead-exposed groups were all lower than that of the control group on the 21st and 28th day (P<0.001) and the NOS activity of the 0.025% group was significantly lower than that of the 0.05% and 0.075% groups on the 28th day (P<0.05). NOS activity in the cerebral cortex of the 0.075% group was significantly lower than that of the control, 0.025% and 0.05% groups on the four day spans (P<0.001). There was no significant difference of NOS activity in the brain stem between any lead-exposed group and the control group on the four day spans. In the 0.05% and the 0.075% groups, the level of NR2A mRNA expression was higher than that in the control group at 7 d and 14 d of age (P<0.05). In the 0.025% group, the level of NR2A was found to be higher than that in the control group at 7 d of age only (P<0.05). No significant differences were found for the levels of NR2B mRNA expression between any of the groups at any given time.
NOS activity in the hippocampus, the cerebral cortex and the cerebellum are inhibited by lead exposure. The degree of the inhibitory effect depends on the time span of exposure and the lead concentration. Developmental low-level lead exposure was found to raise the level of NR2A mRNA expression in the hippocampus of rats. Developmental low-level lead exposure does not affect the level of NR2B mRNA expression in the hippocampus.
研究发育期铅暴露对大鼠不同脑区一氧化氮合酶(NOS)活性及海马中N-甲基-D-天冬氨酸(NMDA)受体mRNA表达的影响。基于这些观察结果,我们探讨了铅暴露导致儿童学习记忆能力受损的可能机制。
建立一系列在发育期暴露于低水平铅的大鼠动物模型(饮用含0.025%、0.05%和0.075%醋酸铅的水)。用荧光测量法测定海马、大脑皮层、小脑和脑干中的NOS活性,并用逆转录聚合酶链反应(RT-PCR)测量大鼠海马中NMDA受体2A(NR2A)亚基和NMDA受体2B(NR2B)亚基的mRNA表达水平。
在任何给定时间,各实验组幼鼠体重均无差异(P>0.05)。铅暴露幼鼠的血铅水平呈现出系统性变化模式:14日龄时低于7日龄,然后在21日龄时升至峰值水平,最后在28日龄时降至较低水平。在第21天和第28天,铅暴露组的海马NOS活性均低于对照组(P<0.01)。在第21天和第28天,铅暴露组的小脑NOS活性均低于对照组(P<0.001),且在第28天,0.025%组的NOS活性显著低于0.05%和0.075%组(P<0.05)。在四个时间跨度内,0.075%组大脑皮层的NOS活性显著低于对照组、0.025%组和0.05%组(P<0.001)。在四个时间跨度内,任何铅暴露组与对照组脑干的NOS活性均无显著差异。在0.05%和0.075%组中,7日龄和14日龄时NR2A mRNA表达水平高于对照组(P<0.05)。在0.025%组中,仅在7日龄时发现NR2A水平高于对照组(P<0.05)。在任何给定时间,各实验组之间NR2B mRNA表达水平均无显著差异。
铅暴露可抑制海马、大脑皮层和小脑中的NOS活性。抑制作用的程度取决于暴露时间跨度和铅浓度。发现发育期低水平铅暴露可提高大鼠海马中NR2A mRNA表达水平。发育期低水平铅暴露不影响海马中NR2B mRNA表达水平。