Ferlemi Anastasia-Varvara, Avgoustatos Dionisis, Kokkosis Alexandros G, Protonotarios Vasilis, Constantinou Caterina, Margarity Marigoula
Laboratory of Human & Animal Physiology, Department of Biology, University of Patras, 26500 Patras, Greece.
Lavrion Technology and Cultural Park, 1 Athinon-Lavriou Avenue, 19500 Lavrion, Greece.
Physiol Behav. 2014 May 28;131:115-22. doi: 10.1016/j.physbeh.2014.04.033. Epub 2014 Apr 24.
The aim of the present study was to investigate whether the underlying mechanism of lead (Pb)-induced effects on learning/memory and fear/anxiety behavior involves changes either on AChE G4 (most abundant in brain) or on G1 isoform activity, and/or to a putative local disruption of oxidant/antioxidant balance. Adult male mice were randomly divided into two groups (18 animals/group): a vehicle group [500ppm (mg/L) CH3COONa/day for 4weeks in their drinking water] and a Pb-treated group [500ppm Pb(CH3COO)2/day for 4weeks in their drinking water]. At the end of the treatment period, mice were subjected to the behavioral tasks. Learning/memory was tested by step-through passive avoidance test, whereas fear/anxiety was studied using the elevated plus-maze and thigmotaxis tests. Pb levels in mice brain were determined using atomic absorption spectrometry. AChE activity was determined colorimetrically, and GSH and MDA levels fluorometrically in whole brain minus cerebellum, cerebral cortex, midbrain, hippocampus, striatum and cerebellum. The possible correlations between learning/memory or fear/anxiety behavior with the AChE activity and/or the lipid peroxidation levels and GSH content were also examined. Pb consumption caused significant deficits on mice learning/memory ability and increased anxiety. The consumption of the Pb solution inhibited the activity of the two AChE isoforms in all brain regions tested. Moreover, Pb exposure increased lipid peroxidation and decreased GSH levels in all brain regions examined. Spearman correlation analysis revealed that the coefficients between the particular behaviors, AChE activity and redox balance were brain region- and AChE isoform-specific.
本研究的目的是调查铅(Pb)诱导的对学习/记忆及恐惧/焦虑行为的潜在机制是否涉及大脑中最丰富的乙酰胆碱酯酶G4或G1同工型活性的变化,和/或假定的氧化剂/抗氧化剂平衡的局部破坏。成年雄性小鼠被随机分为两组(每组18只动物):溶剂对照组[饮用水中含500ppm(mg/L)醋酸钠,持续4周]和铅处理组[饮用水中含500ppm醋酸铅,持续4周]。在处理期结束时,对小鼠进行行为任务测试。通过穿梭式被动回避试验测试学习/记忆,而使用高架十字迷宫和趋触性试验研究恐惧/焦虑。使用原子吸收光谱法测定小鼠脑中的铅水平。用比色法测定乙酰胆碱酯酶活性,用荧光法测定全脑(不含小脑)、大脑皮层、中脑、海马、纹状体和小脑中的谷胱甘肽(GSH)和丙二醛(MDA)水平。还检查了学习/记忆或恐惧/焦虑行为与乙酰胆碱酯酶活性和/或脂质过氧化水平及谷胱甘肽含量之间的可能相关性。摄入铅导致小鼠学习/记忆能力显著缺陷并增加焦虑。饮用铅溶液抑制了所有测试脑区中两种乙酰胆碱酯酶同工型的活性。此外,铅暴露增加了所有检查脑区的脂质过氧化并降低了谷胱甘肽水平。Spearman相关性分析表明,特定行为、乙酰胆碱酯酶活性和氧化还原平衡之间的系数具有脑区和乙酰胆碱酯酶同工型特异性。