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Learning and memory retention in MAO A knockout mice

机译:MAO A基因敲除小鼠的学习和记忆力保留

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Transgenic Tg8 mice provide an experimental model of selective lack of the gene encoding monoamine oxidase A (MAO A), and correspond to analogous human genetic pathology found in a Dutch family. To investigate the possible consequences of the effect of the lack of a major enzyme in serotonin and catecholamine metabolism on cognitive functions, MAO A-deficient mice were subjected to a passive avoidance task. Significant differences in the learning ability and in the retention of passive avoidance response between Tg8 mice and the wild-type mice C3H/HeJ were found. MAO A-deficient mice demonstrated increased step-through latency and a longer retention of memory trace for 11 experimental days as compared to wild-type mice. We found that Tg8 mice are more resistant to detention-induced amnesia and show better social memory in social recognition test than C3H mice. The findings show an enhancement of learning and memory retention in the MAO A-deficient mice.
机译:转基因Tg8小鼠提供了选择性缺乏编码单胺氧化酶A(MAO A)的基因的实验模型,并且对应于在荷兰家庭中发现的类似人类遗传病理学。为了研究5-羟色胺和儿茶酚胺代谢中主要酶的缺乏对认知功能的影响的可能后果,对MAO A缺陷小鼠进行被动回避任务。发现在Tg8小鼠和野生型小鼠C3H / HeJ之间的学习能力和保留被动回避反应的能力上存在显着差异。与野生型小鼠相比,MAO A缺陷型小鼠表现出增加的逐步潜伏时间和11天的实验迹线保留时间。我们发现,Tg8小鼠比C3H小鼠对拘留诱发的健忘症更具抵抗力,并且在社交识别测试中显示出更好的社交记忆。这些发现表明,MAO A缺陷小鼠的学习和记忆力得以增强。

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