Albores-Garcia Damaris, Acosta-Saavedra Leonor C, Hernandez Alberto J, Loera Miriam J, Calderón-Aranda Emma S
Departamento de Toxicología, CINVESTAV, 07360 México, DF, Mexico.
Biomed Res Int. 2016;2016:6532108. doi: 10.1155/2016/6532108. Epub 2016 Jan 13.
Few studies have assessed the effects of developmental methylmercury (MeHg) exposure on learning and memory at different ages. The possibility of the amelioration or worsening of the effects has not been sufficiently investigated. This study aimed to assess whether low-dose MeHg exposure in utero and during suckling induces differential disturbances in learning and memory of periadolescent and young adult rats. Four experimental groups of pregnant Sprague-Dawley rats were orally exposed to MeHg or vehicle from gestational day 5 to weaning: (1) control (vehicle), (2) 250 μg/kg/day MeHg, (3) 500 μg/kg/day MeHg, and (4) vehicle, and treated on the test day with MK-801 (0.15 mg/kg i.p.), an antagonist of the N-methyl D-aspartate receptor. The effects were evaluated in male offspring through the open field test, object recognition test, Morris water maze, and conditioned taste aversion. For each test and stage assessed, different groups of animals were used. MeHg exposure, in a dose-dependent manner, disrupted exploratory behaviour, recognition memory, spatial learning, and acquisition of aversive memories in periadolescent rats, but alterations were not observed in littermates tested in young adulthood. These results suggest that developmental low-dose exposure to MeHg induces age-dependent detrimental effects. The relevance of decreasing exposure to MeHg in humans remains to be determined.
很少有研究评估发育过程中甲基汞(MeHg)暴露对不同年龄段学习和记忆的影响。其影响改善或恶化的可能性尚未得到充分研究。本研究旨在评估子宫内和哺乳期低剂量MeHg暴露是否会对青春期前后和年轻成年大鼠的学习和记忆产生不同程度的干扰。将四组怀孕的斯普拉格-道利大鼠从妊娠第5天至断奶期间经口给予MeHg或赋形剂:(1)对照组(赋形剂),(2)250μg/kg/天MeHg,(3)500μg/kg/天MeHg,以及(4)赋形剂,并在测试当天用N-甲基-D-天冬氨酸受体拮抗剂MK-801(0.15mg/kg腹腔注射)进行处理。通过旷场试验、物体识别试验、莫里斯水迷宫试验和条件性味觉厌恶试验对雄性后代的影响进行评估。对于每个评估的试验和阶段,使用不同组的动物。MeHg暴露以剂量依赖的方式破坏了青春期前后大鼠的探索行为、识别记忆、空间学习和厌恶记忆的获得,但在年轻成年期测试的同窝幼崽中未观察到改变。这些结果表明,发育过程中低剂量的MeHg暴露会产生年龄依赖性的有害影响。减少人类MeHg暴露的相关性仍有待确定。